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You searched for subject:(POLYCYSTIC KIDNEY AUTOSOMAL RECESSIVE physiopathology). Showing records 1 – 30 of 3256 total matches.

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1. Olteanu, Dragos S. Dysregulated ENAC and NHE function in cilium-deficient renal collecting duct cell monolayers : a model of polycystic kidney disease.

Degree: PhD, 2007, University of Alabama – Birmingham

Polycystic kidney disease in both its recessive and dominant forms involves the remodeling of the kidney and extra-renal tissues where parts of the tissue break… (more)

Subjects/Keywords: Cilia  – metabolism<; br>; Epithelial Cells<; br>; Kidney<; br>; Polycystic Kidney, Autosomal Recessive  – metabolism<; br>; Sodium  – metabolism<; br>; Sodium Channels  – metabolism

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APA (6th Edition):

Olteanu, D. S. (2007). Dysregulated ENAC and NHE function in cilium-deficient renal collecting duct cell monolayers : a model of polycystic kidney disease. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,610

Chicago Manual of Style (16th Edition):

Olteanu, Dragos S. “Dysregulated ENAC and NHE function in cilium-deficient renal collecting duct cell monolayers : a model of polycystic kidney disease.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed October 27, 2020. http://contentdm.mhsl.uab.edu/u?/etd,610.

MLA Handbook (7th Edition):

Olteanu, Dragos S. “Dysregulated ENAC and NHE function in cilium-deficient renal collecting duct cell monolayers : a model of polycystic kidney disease.” 2007. Web. 27 Oct 2020.

Vancouver:

Olteanu DS. Dysregulated ENAC and NHE function in cilium-deficient renal collecting duct cell monolayers : a model of polycystic kidney disease. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2020 Oct 27]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,610.

Council of Science Editors:

Olteanu DS. Dysregulated ENAC and NHE function in cilium-deficient renal collecting duct cell monolayers : a model of polycystic kidney disease. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,610

2. Menezes, Luis Fernando Carvalho de. "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva".

Degree: PhD, Fisiopatologia Experimental, 2004, University of São Paulo

O gene PKHD1, mutado na doença renal policística autossômica recessiva, apresenta um padrão de splicing complexo associado a múltiplos transcritos alternativos. Neste trabalho estudamos o… (more)

Subjects/Keywords: BLOTTING WESTERN/methods; CÍLIOS/patologia; IMMUNOHISTOCHEMISTRY/methods; IMUNOHISTOQUÍMICA/métodos; ISOFORMAS DE PROTEÍNAS/análise; KIDNEY TUBULES COLLECTING/pathology; KIDNEY TUBULES COLLECTING/physiopathology; MEMBRANE PROTEINS/analysis; MICROSCOPIA IMUNOELETRÔNICA/métodos/ MICROSCOPIA DE FLUORESCÊNCIA/méto; MICROSCOPY FLUORESCENCE/methods; MICROSCOPY IMMUNOELECTRON/methods; POLYCYSTIC KIDNEY AUTOSOMAL RECESSIVE/etiology; POLYCYSTIC KIDNEY AUTOSOMAL RECESSIVE/genetics; POLYCYSTIC KIDNEY AUTOSOMAL RECESSIVE/physiopathology; PROTEIN ISOFORMS/analysis; PROTEÍNAS DE MEMBRANA/análise; RIM POLICÍSTICO AUTOSSÔMICO RECESSIVO/etiologia; RIM POLICÍSTICO AUTOSSÔMICO RECESSIVO/fisiopatologia; RIM POLICÍSTICO AUTOSSÔMICO RECESSIVO/genética; TÚBULOS COLETORES RENAIS/fisiopatologia; TÚBULOS COLETORES RENAIS/patologia; WESTERN BLOTTING/métodos

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APA (6th Edition):

Menezes, L. F. C. d. (2004). "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva". (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;

Chicago Manual of Style (16th Edition):

Menezes, Luis Fernando Carvalho de. “"Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva".” 2004. Doctoral Dissertation, University of São Paulo. Accessed October 27, 2020. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;.

MLA Handbook (7th Edition):

Menezes, Luis Fernando Carvalho de. “"Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva".” 2004. Web. 27 Oct 2020.

Vancouver:

Menezes LFCd. "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva". [Internet] [Doctoral dissertation]. University of São Paulo; 2004. [cited 2020 Oct 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;.

Council of Science Editors:

Menezes LFCd. "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva". [Doctoral Dissertation]. University of São Paulo; 2004. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;


Freie Universität Berlin

3. Oberländer, Natalie. Zystennierenentfernungen an der Charité Campus Mitte von 2005–2018.

Degree: 2020, Freie Universität Berlin

Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic disorders, affecting 12.5 million people worldwide. The disease causes the growth of… (more)

Subjects/Keywords: nephrektomy; kidney transplantation; autosomal dominant polycystic kidney disease; ddc:610

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APA (6th Edition):

Oberländer, N. (2020). Zystennierenentfernungen an der Charité Campus Mitte von 2005–2018. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-26994

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Oberländer, Natalie. “Zystennierenentfernungen an der Charité Campus Mitte von 2005–2018.” 2020. Thesis, Freie Universität Berlin. Accessed October 27, 2020. http://dx.doi.org/10.17169/refubium-26994.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Oberländer, Natalie. “Zystennierenentfernungen an der Charité Campus Mitte von 2005–2018.” 2020. Web. 27 Oct 2020.

Vancouver:

Oberländer N. Zystennierenentfernungen an der Charité Campus Mitte von 2005–2018. [Internet] [Thesis]. Freie Universität Berlin; 2020. [cited 2020 Oct 27]. Available from: http://dx.doi.org/10.17169/refubium-26994.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Oberländer N. Zystennierenentfernungen an der Charité Campus Mitte von 2005–2018. [Thesis]. Freie Universität Berlin; 2020. Available from: http://dx.doi.org/10.17169/refubium-26994

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

4. Boddu, Ravindra. Characterizing The Transcriptional Complexity Of Pkhd1/pkhd1.

Degree: 2012, University of Alabama – Birmingham

Mutations in <italic>PKHD1</italic> gene cause autosomal recessive polycystic kidney disease. Our previous studies have shown that human <italic>PKHD1</italic> and its mouse orthologue, <italic>Pkhd1</italic>, undergo an… (more)

Subjects/Keywords: Alternative Splicing<; br>; Disease Models, Animal<; br>; Kidney Tubules, Collecting – metabolism.<; br>; Polycystic Kidney, Autosomal Recessive – genetics.<; br>; Receptors, Cell Surface – genetics.<; br>; Translocation, Genetic

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APA (6th Edition):

Boddu, R. (2012). Characterizing The Transcriptional Complexity Of Pkhd1/pkhd1. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1504

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Boddu, Ravindra. “Characterizing The Transcriptional Complexity Of Pkhd1/pkhd1.” 2012. Thesis, University of Alabama – Birmingham. Accessed October 27, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1504.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Boddu, Ravindra. “Characterizing The Transcriptional Complexity Of Pkhd1/pkhd1.” 2012. Web. 27 Oct 2020.

Vancouver:

Boddu R. Characterizing The Transcriptional Complexity Of Pkhd1/pkhd1. [Internet] [Thesis]. University of Alabama – Birmingham; 2012. [cited 2020 Oct 27]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1504.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Boddu R. Characterizing The Transcriptional Complexity Of Pkhd1/pkhd1. [Thesis]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1504

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of New South Wales

5. Mallawaarachchi, Amali. Molecular diagnosis in inherited polycystic kidney disease.

Degree: Garvan Institute of Medical Research, 2019, University of New South Wales

Polycystic Kidney Disease (PKD) incorporates a number of genetically but not always phenotypically distinct inherited cystic kidney disorders. Autosomal Dominant Polycystic Kidney Disease (ADPKD) is… (more)

Subjects/Keywords: PKD2; Autosomal dominant polycystic kidney disease; PKD1; Whole genome sequencing

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APA (6th Edition):

Mallawaarachchi, A. (2019). Molecular diagnosis in inherited polycystic kidney disease. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/62980 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:59489/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Mallawaarachchi, Amali. “Molecular diagnosis in inherited polycystic kidney disease.” 2019. Doctoral Dissertation, University of New South Wales. Accessed October 27, 2020. http://handle.unsw.edu.au/1959.4/62980 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:59489/SOURCE02?view=true.

MLA Handbook (7th Edition):

Mallawaarachchi, Amali. “Molecular diagnosis in inherited polycystic kidney disease.” 2019. Web. 27 Oct 2020.

Vancouver:

Mallawaarachchi A. Molecular diagnosis in inherited polycystic kidney disease. [Internet] [Doctoral dissertation]. University of New South Wales; 2019. [cited 2020 Oct 27]. Available from: http://handle.unsw.edu.au/1959.4/62980 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:59489/SOURCE02?view=true.

Council of Science Editors:

Mallawaarachchi A. Molecular diagnosis in inherited polycystic kidney disease. [Doctoral Dissertation]. University of New South Wales; 2019. Available from: http://handle.unsw.edu.au/1959.4/62980 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:59489/SOURCE02?view=true


University of Manitoba

6. Koohgoli, Roxanna Yasmin. Oxylipin profiles in an orthologous mouse model of autosomal dominant polycystic kidney disease.

Degree: Food and Human Nutritional Sciences, 2020, University of Manitoba

Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the growth of renal cysts, which ultimately causes renal failure. Previous studies have suggested that whole… (more)

Subjects/Keywords: Autosomal dominant polycystic kidney disease; Oxylipins; Flaxseed; Sex effects; Healthy vs disease oxylipins

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APA (6th Edition):

Koohgoli, R. Y. (2020). Oxylipin profiles in an orthologous mouse model of autosomal dominant polycystic kidney disease. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/34540

Chicago Manual of Style (16th Edition):

Koohgoli, Roxanna Yasmin. “Oxylipin profiles in an orthologous mouse model of autosomal dominant polycystic kidney disease.” 2020. Masters Thesis, University of Manitoba. Accessed October 27, 2020. http://hdl.handle.net/1993/34540.

MLA Handbook (7th Edition):

Koohgoli, Roxanna Yasmin. “Oxylipin profiles in an orthologous mouse model of autosomal dominant polycystic kidney disease.” 2020. Web. 27 Oct 2020.

Vancouver:

Koohgoli RY. Oxylipin profiles in an orthologous mouse model of autosomal dominant polycystic kidney disease. [Internet] [Masters thesis]. University of Manitoba; 2020. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1993/34540.

Council of Science Editors:

Koohgoli RY. Oxylipin profiles in an orthologous mouse model of autosomal dominant polycystic kidney disease. [Masters Thesis]. University of Manitoba; 2020. Available from: http://hdl.handle.net/1993/34540

7. Sousa, Mauri Félix de. "Efeitos renais da haploinsuficiência do gene Pkd1 (Polycystic kidney disease 1) em camundongos".

Degree: PhD, Nefrologia, 2005, University of São Paulo

Vários estudos mostram que na doença renal policística autossômica dominante os cistos surgem a partir de um mecanismo de "dois-golpes". A patogênese das manifestações não-císticas,… (more)

Subjects/Keywords: CAMUNDONGOS KNOCKOUT; CAPACIDADE DE CONCENTRAÇÃO RENAL; GLOMERULAR FILTRATION RATE; GLOMÉRULOS RENAIS/anatomia & histologia; KIDNEY CONCENTRATING ABILITY; KIDNEY GLOMERULUS/anatomy & histology; MICE KNOCKOUT; POLYCYSTIC KIDNEY AUTOSOMAL DOMINANT/physiopathology; RIM POLICÍSTICO AUTOSSÔMICO DOMINANTE/fisiopatologia; TAXA DE FILTRAÇÃO GLOMERULAR

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APA (6th Edition):

Sousa, M. F. d. (2005). "Efeitos renais da haploinsuficiência do gene Pkd1 (Polycystic kidney disease 1) em camundongos". (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5148/tde-21122005-163447/ ;

Chicago Manual of Style (16th Edition):

Sousa, Mauri Félix de. “"Efeitos renais da haploinsuficiência do gene Pkd1 (Polycystic kidney disease 1) em camundongos".” 2005. Doctoral Dissertation, University of São Paulo. Accessed October 27, 2020. http://www.teses.usp.br/teses/disponiveis/5/5148/tde-21122005-163447/ ;.

MLA Handbook (7th Edition):

Sousa, Mauri Félix de. “"Efeitos renais da haploinsuficiência do gene Pkd1 (Polycystic kidney disease 1) em camundongos".” 2005. Web. 27 Oct 2020.

Vancouver:

Sousa MFd. "Efeitos renais da haploinsuficiência do gene Pkd1 (Polycystic kidney disease 1) em camundongos". [Internet] [Doctoral dissertation]. University of São Paulo; 2005. [cited 2020 Oct 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-21122005-163447/ ;.

Council of Science Editors:

Sousa MFd. "Efeitos renais da haploinsuficiência do gene Pkd1 (Polycystic kidney disease 1) em camundongos". [Doctoral Dissertation]. University of São Paulo; 2005. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-21122005-163447/ ;

8. Larissa Collis Vendramini. Avaliação do consumo de cafeína em pacientes com Doença Renal Policística Autossômica Dominante (DRPAD).

Degree: 2010, Universidade Federal de São Paulo

 A cafeína tem sido considerada um fator de risco para o crescimento dos cistos na Doença Renal Policística Autossômica Dominante (DRPAD) devido ao aumento de… (more)

Subjects/Keywords: Doença renal policística; Rins policísticos; Cafeína; Adenosina monofosfato cíclico; Volume Renal; NEFROLOGIA; Autosomal Dominant Polycystic Kidney Disease; Caffeine; Cyclic AMP; Nutrition

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APA (6th Edition):

Vendramini, L. C. (2010). Avaliação do consumo de cafeína em pacientes com Doença Renal Policística Autossômica Dominante (DRPAD). (Thesis). Universidade Federal de São Paulo. Retrieved from http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=1458

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Vendramini, Larissa Collis. “Avaliação do consumo de cafeína em pacientes com Doença Renal Policística Autossômica Dominante (DRPAD).” 2010. Thesis, Universidade Federal de São Paulo. Accessed October 27, 2020. http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=1458.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Vendramini, Larissa Collis. “Avaliação do consumo de cafeína em pacientes com Doença Renal Policística Autossômica Dominante (DRPAD).” 2010. Web. 27 Oct 2020.

Vancouver:

Vendramini LC. Avaliação do consumo de cafeína em pacientes com Doença Renal Policística Autossômica Dominante (DRPAD). [Internet] [Thesis]. Universidade Federal de São Paulo; 2010. [cited 2020 Oct 27]. Available from: http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=1458.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Vendramini LC. Avaliação do consumo de cafeína em pacientes com Doença Renal Policística Autossômica Dominante (DRPAD). [Thesis]. Universidade Federal de São Paulo; 2010. Available from: http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=1458

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Texas A&M University

9. Kondru, Vijaya. The Impact of Hypophosphatemia on Chondrocyte Fate.

Degree: MS, Oral Biology, 2017, Texas A&M University

 Dentin Matrix Protein 1(DMP1) is a non-collagenous phosphoprotein, belonging to the Small Integrin small integrin-binding ligand, N-linked glycoprotein (SIBLING) family, the deficiency or mutation of… (more)

Subjects/Keywords: DMP1; Autosomal Recessive Hypophosphatemic Rickets; SIBLING proteins

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APA (6th Edition):

Kondru, V. (2017). The Impact of Hypophosphatemia on Chondrocyte Fate. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/165846

Chicago Manual of Style (16th Edition):

Kondru, Vijaya. “The Impact of Hypophosphatemia on Chondrocyte Fate.” 2017. Masters Thesis, Texas A&M University. Accessed October 27, 2020. http://hdl.handle.net/1969.1/165846.

MLA Handbook (7th Edition):

Kondru, Vijaya. “The Impact of Hypophosphatemia on Chondrocyte Fate.” 2017. Web. 27 Oct 2020.

Vancouver:

Kondru V. The Impact of Hypophosphatemia on Chondrocyte Fate. [Internet] [Masters thesis]. Texas A&M University; 2017. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1969.1/165846.

Council of Science Editors:

Kondru V. The Impact of Hypophosphatemia on Chondrocyte Fate. [Masters Thesis]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/165846


Queen Mary, University of London

10. Bland, Philip James. The genetic and functional role of ABCA12 in Harlequin Ichthyosis.

Degree: PhD, 2016, Queen Mary, University of London

 Harlequin Ichthyosis (HI) is the most severe disorder in the family of autosomal recessive congenital ichthyosis (ARCI). Recessive mutations in the ABC transporter ABCA12 were… (more)

Subjects/Keywords: Harlequin Ichthyosis; autosomal recessive congenital ichthyosis; ABCA12

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APA (6th Edition):

Bland, P. J. (2016). The genetic and functional role of ABCA12 in Harlequin Ichthyosis. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/12571 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775189

Chicago Manual of Style (16th Edition):

Bland, Philip James. “The genetic and functional role of ABCA12 in Harlequin Ichthyosis.” 2016. Doctoral Dissertation, Queen Mary, University of London. Accessed October 27, 2020. http://qmro.qmul.ac.uk/xmlui/handle/123456789/12571 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775189.

MLA Handbook (7th Edition):

Bland, Philip James. “The genetic and functional role of ABCA12 in Harlequin Ichthyosis.” 2016. Web. 27 Oct 2020.

Vancouver:

Bland PJ. The genetic and functional role of ABCA12 in Harlequin Ichthyosis. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2016. [cited 2020 Oct 27]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/12571 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775189.

Council of Science Editors:

Bland PJ. The genetic and functional role of ABCA12 in Harlequin Ichthyosis. [Doctoral Dissertation]. Queen Mary, University of London; 2016. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/12571 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775189


University of the Western Cape

11. Magwebu, Zandisiwe Emilia Z.E. Molecular genetics: strategies to identify congenital cataract genes in captive-bred vervet monkeys .

Degree: 2013, University of the Western Cape

 Molecular genetics: strategies to indentify congenital cataract genes in captive-bred Vervet monkeys Zandisiwe Emilia Magwebu MSc thesis, Department of Medical Biosciences, University of the Western… (more)

Subjects/Keywords: Vervet monkeys; Congenital cataract; Autosomal recessive cataract

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APA (6th Edition):

Magwebu, Z. E. Z. E. (2013). Molecular genetics: strategies to identify congenital cataract genes in captive-bred vervet monkeys . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/4265

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Magwebu, Zandisiwe Emilia Z E. “Molecular genetics: strategies to identify congenital cataract genes in captive-bred vervet monkeys .” 2013. Thesis, University of the Western Cape. Accessed October 27, 2020. http://hdl.handle.net/11394/4265.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Magwebu, Zandisiwe Emilia Z E. “Molecular genetics: strategies to identify congenital cataract genes in captive-bred vervet monkeys .” 2013. Web. 27 Oct 2020.

Vancouver:

Magwebu ZEZE. Molecular genetics: strategies to identify congenital cataract genes in captive-bred vervet monkeys . [Internet] [Thesis]. University of the Western Cape; 2013. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/11394/4265.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Magwebu ZEZE. Molecular genetics: strategies to identify congenital cataract genes in captive-bred vervet monkeys . [Thesis]. University of the Western Cape; 2013. Available from: http://hdl.handle.net/11394/4265

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

12. Raptis, Vasileios. Ο ρόλος της ασύμμετρης διμεθυλαργινίνης (ADMA) στην παθογένεια της νεφρικής ανεπάρκειας σε ασθενείς με αυτοσωματική επικρατούσα πολυκυστική νόσο νεφρών (ΑΕΠΚΝ).

Degree: 2015, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

 ADPKD is the most frequently occurring inherited disorder that causes CKD worldwide, leading to about 5% of patients in the final stage, both in Europe… (more)

Subjects/Keywords: Αυτοσωματική επικρατούσα πολυκυστική νόσος νεφρών; Χρόνια νεφρική νόσος; Ασύμμετρη Διμεθυλαργινίνη; Οξειδωτικό stress; Autosomal dominant polycystic kidney disease; Chronic kidney disease; Asymmetric dimethylarginine; Oxidative stress

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Raptis, V. (2015). Ο ρόλος της ασύμμετρης διμεθυλαργινίνης (ADMA) στην παθογένεια της νεφρικής ανεπάρκειας σε ασθενείς με αυτοσωματική επικρατούσα πολυκυστική νόσο νεφρών (ΑΕΠΚΝ). (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/35847

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Raptis, Vasileios. “Ο ρόλος της ασύμμετρης διμεθυλαργινίνης (ADMA) στην παθογένεια της νεφρικής ανεπάρκειας σε ασθενείς με αυτοσωματική επικρατούσα πολυκυστική νόσο νεφρών (ΑΕΠΚΝ).” 2015. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed October 27, 2020. http://hdl.handle.net/10442/hedi/35847.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Raptis, Vasileios. “Ο ρόλος της ασύμμετρης διμεθυλαργινίνης (ADMA) στην παθογένεια της νεφρικής ανεπάρκειας σε ασθενείς με αυτοσωματική επικρατούσα πολυκυστική νόσο νεφρών (ΑΕΠΚΝ).” 2015. Web. 27 Oct 2020.

Vancouver:

Raptis V. Ο ρόλος της ασύμμετρης διμεθυλαργινίνης (ADMA) στην παθογένεια της νεφρικής ανεπάρκειας σε ασθενείς με αυτοσωματική επικρατούσα πολυκυστική νόσο νεφρών (ΑΕΠΚΝ). [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2015. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10442/hedi/35847.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Raptis V. Ο ρόλος της ασύμμετρης διμεθυλαργινίνης (ADMA) στην παθογένεια της νεφρικής ανεπάρκειας σε ασθενείς με αυτοσωματική επικρατούσα πολυκυστική νόσο νεφρών (ΑΕΠΚΝ). [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2015. Available from: http://hdl.handle.net/10442/hedi/35847

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

13. Balbo, Bruno Eduardo Pedroso. Camundongos com deficiência em Pkd1 apresentam  disfunção cardíaca, fenótipo atenuado por knockout de galectina-3.

Degree: PhD, Nefrologia, 2014, University of São Paulo

Anormalidades miocárdicas destacam-se entre as manifestações cardiovasculares da doença renal policística autossômica dominante (DRPAD). Para investigar a patogênese dessas manifestações, analisamos o fenótipo cardíaco em… (more)

Subjects/Keywords: Apoptose; Apoptosis; Autosomal dominant polycystic Kidney disease; Biologia molecular; Camundongos; Cardiomyopathies; Echocardiography; Ecocardiografia; Fibrose; Fibrosis; Galectin 3; Galectina 3; Mice; Miocardiopatias; Molecular biology; Rim policístico autossômico dominante; Ultrasonography; Ultrassonografia

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Balbo, B. E. P. (2014). Camundongos com deficiência em Pkd1 apresentam  disfunção cardíaca, fenótipo atenuado por knockout de galectina-3. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5148/tde-09122014-123524/ ;

Chicago Manual of Style (16th Edition):

Balbo, Bruno Eduardo Pedroso. “Camundongos com deficiência em Pkd1 apresentam  disfunção cardíaca, fenótipo atenuado por knockout de galectina-3.” 2014. Doctoral Dissertation, University of São Paulo. Accessed October 27, 2020. http://www.teses.usp.br/teses/disponiveis/5/5148/tde-09122014-123524/ ;.

MLA Handbook (7th Edition):

Balbo, Bruno Eduardo Pedroso. “Camundongos com deficiência em Pkd1 apresentam  disfunção cardíaca, fenótipo atenuado por knockout de galectina-3.” 2014. Web. 27 Oct 2020.

Vancouver:

Balbo BEP. Camundongos com deficiência em Pkd1 apresentam  disfunção cardíaca, fenótipo atenuado por knockout de galectina-3. [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2020 Oct 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-09122014-123524/ ;.

Council of Science Editors:

Balbo BEP. Camundongos com deficiência em Pkd1 apresentam  disfunção cardíaca, fenótipo atenuado por knockout de galectina-3. [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-09122014-123524/ ;


University of Otago

14. Bowden, Sarah. Genome-Wide DNA Methylation in Polycystic Kidney Disease .

Degree: University of Otago

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a heritable renal disease that causes the enlargement of kidneys due to the bilateral development of fluid-filled cysts.… (more)

Subjects/Keywords: Autosomal Dominant Polycystic Kidney Disease; ADPKD; DNA Methylation; miRNA; RRBS

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bowden, S. (n.d.). Genome-Wide DNA Methylation in Polycystic Kidney Disease . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/9536

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Chicago Manual of Style (16th Edition):

Bowden, Sarah. “Genome-Wide DNA Methylation in Polycystic Kidney Disease .” Masters Thesis, University of Otago. Accessed October 27, 2020. http://hdl.handle.net/10523/9536.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

MLA Handbook (7th Edition):

Bowden, Sarah. “Genome-Wide DNA Methylation in Polycystic Kidney Disease .” Web. 27 Oct 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Bowden S. Genome-Wide DNA Methylation in Polycystic Kidney Disease . [Internet] [Masters thesis]. University of Otago; [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10523/9536.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Council of Science Editors:

Bowden S. Genome-Wide DNA Methylation in Polycystic Kidney Disease . [Masters Thesis]. University of Otago; Available from: http://hdl.handle.net/10523/9536

Note: this citation may be lacking information needed for this citation format:
No year of publication.

15. Zhao, Yang. Mutation analysis of the USH2A gene in Japanese patients with non-syndromic autosomal recessive retinitis pigmentosa : 非症候群性の常染色体劣性網膜色素変性の日本人患者におけるUSH2A遺伝子の変異解析.

Degree: 博士(医学), 2013, Hamamatsu University School of Medicine / 浜松医科大学

Objective: To identify disease-causing USH2A (Usher syndrome 2A) gene mutations in Japanese patients with non-syndromic retinitis pigmentosa (RP). Design: Case series.Participants: Hundred unrelated Japanese patients… (more)

Subjects/Keywords: Retinitis pigmentosa; autosomal recessive; USH2A gene; Japanese patient

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APA (6th Edition):

Zhao, Y. (2013). Mutation analysis of the USH2A gene in Japanese patients with non-syndromic autosomal recessive retinitis pigmentosa : 非症候群性の常染色体劣性網膜色素変性の日本人患者におけるUSH2A遺伝子の変異解析. (Thesis). Hamamatsu University School of Medicine / 浜松医科大学. Retrieved from http://hdl.handle.net/10271/2768

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zhao, Yang. “Mutation analysis of the USH2A gene in Japanese patients with non-syndromic autosomal recessive retinitis pigmentosa : 非症候群性の常染色体劣性網膜色素変性の日本人患者におけるUSH2A遺伝子の変異解析.” 2013. Thesis, Hamamatsu University School of Medicine / 浜松医科大学. Accessed October 27, 2020. http://hdl.handle.net/10271/2768.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zhao, Yang. “Mutation analysis of the USH2A gene in Japanese patients with non-syndromic autosomal recessive retinitis pigmentosa : 非症候群性の常染色体劣性網膜色素変性の日本人患者におけるUSH2A遺伝子の変異解析.” 2013. Web. 27 Oct 2020.

Vancouver:

Zhao Y. Mutation analysis of the USH2A gene in Japanese patients with non-syndromic autosomal recessive retinitis pigmentosa : 非症候群性の常染色体劣性網膜色素変性の日本人患者におけるUSH2A遺伝子の変異解析. [Internet] [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2013. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10271/2768.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zhao Y. Mutation analysis of the USH2A gene in Japanese patients with non-syndromic autosomal recessive retinitis pigmentosa : 非症候群性の常染色体劣性網膜色素変性の日本人患者におけるUSH2A遺伝子の変異解析. [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2013. Available from: http://hdl.handle.net/10271/2768

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

16. Takeda, Ikuko. Autosomal recessive Andersen-Tawil syndrome with a novel mutation L94P in Kir2.1 : Kir2.1に新規ミスセンス変異(L94P)を認める常染色体劣性遺伝形式のAndersen-Tawil症候群.

Degree: 博士(医学), 2014, Hiroshima University / 広島大学

 Aim: Dominant negative mutations of the inwardly rectifying K+ channel Kir2.1 cause Andersen-Tawil syndrome, an autosomal dominant disorder. Here, we identified a novel Kir2.1 mutation… (more)

Subjects/Keywords: Andersen-Tawil syndrome; KCNJ2; Kir2.1; autosomal recessive; patch clamp

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Takeda, I. (2014). Autosomal recessive Andersen-Tawil syndrome with a novel mutation L94P in Kir2.1 : Kir2.1に新規ミスセンス変異(L94P)を認める常染色体劣性遺伝形式のAndersen-Tawil症候群. (Thesis). Hiroshima University / 広島大学. Retrieved from http://ir.lib.hiroshima-u.ac.jp/00036281

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Takeda, Ikuko. “Autosomal recessive Andersen-Tawil syndrome with a novel mutation L94P in Kir2.1 : Kir2.1に新規ミスセンス変異(L94P)を認める常染色体劣性遺伝形式のAndersen-Tawil症候群.” 2014. Thesis, Hiroshima University / 広島大学. Accessed October 27, 2020. http://ir.lib.hiroshima-u.ac.jp/00036281.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Takeda, Ikuko. “Autosomal recessive Andersen-Tawil syndrome with a novel mutation L94P in Kir2.1 : Kir2.1に新規ミスセンス変異(L94P)を認める常染色体劣性遺伝形式のAndersen-Tawil症候群.” 2014. Web. 27 Oct 2020.

Vancouver:

Takeda I. Autosomal recessive Andersen-Tawil syndrome with a novel mutation L94P in Kir2.1 : Kir2.1に新規ミスセンス変異(L94P)を認める常染色体劣性遺伝形式のAndersen-Tawil症候群. [Internet] [Thesis]. Hiroshima University / 広島大学; 2014. [cited 2020 Oct 27]. Available from: http://ir.lib.hiroshima-u.ac.jp/00036281.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Takeda I. Autosomal recessive Andersen-Tawil syndrome with a novel mutation L94P in Kir2.1 : Kir2.1に新規ミスセンス変異(L94P)を認める常染色体劣性遺伝形式のAndersen-Tawil症候群. [Thesis]. Hiroshima University / 広島大学; 2014. Available from: http://ir.lib.hiroshima-u.ac.jp/00036281

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Debrecen

17. Rizvi, Danial. Pharmacological Management of Cystic Fibrosis .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 Cystic fibrosis (CF) is an autosomal recessive defect occurring in approximately one in 3,500 live births based on data from neonatal screening. CF is clinically… (more)

Subjects/Keywords: Cystic Fibrosis; CFTR; Autosomal Recessive

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Rizvi, D. (n.d.). Pharmacological Management of Cystic Fibrosis . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/273747

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rizvi, Danial. “Pharmacological Management of Cystic Fibrosis .” Thesis, University of Debrecen. Accessed October 27, 2020. http://hdl.handle.net/2437/273747.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rizvi, Danial. “Pharmacological Management of Cystic Fibrosis .” Web. 27 Oct 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Rizvi D. Pharmacological Management of Cystic Fibrosis . [Internet] [Thesis]. University of Debrecen; [cited 2020 Oct 27]. Available from: http://hdl.handle.net/2437/273747.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Rizvi D. Pharmacological Management of Cystic Fibrosis . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/273747

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of New South Wales

18. Pan, Annie Ying-Hui. Disease gene identification in Australian kelpies.

Degree: Biotechnology & Biomolecular Sciences, 2012, University of New South Wales

 The Australian Kelpie was generated from three pairs of working Scottish Collie dogs in 1870. The new breed was developed in an effort to ease… (more)

Subjects/Keywords: Ataxia; Australian Kelpie; Cerebellar Abiotrophy; Dog; Canine model; Autosomal recessive disease

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Pan, A. Y. (2012). Disease gene identification in Australian kelpies. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51889 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10558/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Pan, Annie Ying-Hui. “Disease gene identification in Australian kelpies.” 2012. Masters Thesis, University of New South Wales. Accessed October 27, 2020. http://handle.unsw.edu.au/1959.4/51889 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10558/SOURCE02?view=true.

MLA Handbook (7th Edition):

Pan, Annie Ying-Hui. “Disease gene identification in Australian kelpies.” 2012. Web. 27 Oct 2020.

Vancouver:

Pan AY. Disease gene identification in Australian kelpies. [Internet] [Masters thesis]. University of New South Wales; 2012. [cited 2020 Oct 27]. Available from: http://handle.unsw.edu.au/1959.4/51889 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10558/SOURCE02?view=true.

Council of Science Editors:

Pan AY. Disease gene identification in Australian kelpies. [Masters Thesis]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/51889 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10558/SOURCE02?view=true


University of Otago

19. Lett, Bron. Genetics of an Ovine PKD Model .

Degree: 2011, University of Otago

Autosomal recessive polycystic kidney disease (ARPKD) is an important cause of renal and liver related perinatal and neonatal death. ARPKD is presented as a gross… (more)

Subjects/Keywords: Polycystic Kidney Disease; Ovine Model

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APA (6th Edition):

Lett, B. (2011). Genetics of an Ovine PKD Model . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/2070

Chicago Manual of Style (16th Edition):

Lett, Bron. “Genetics of an Ovine PKD Model .” 2011. Masters Thesis, University of Otago. Accessed October 27, 2020. http://hdl.handle.net/10523/2070.

MLA Handbook (7th Edition):

Lett, Bron. “Genetics of an Ovine PKD Model .” 2011. Web. 27 Oct 2020.

Vancouver:

Lett B. Genetics of an Ovine PKD Model . [Internet] [Masters thesis]. University of Otago; 2011. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10523/2070.

Council of Science Editors:

Lett B. Genetics of an Ovine PKD Model . [Masters Thesis]. University of Otago; 2011. Available from: http://hdl.handle.net/10523/2070


University of Manitoba

20. Monirujjaman, Md. Effect of dietary oils and protein and cyclooxygenase-2 inhibition on disease progression and oxylipin alterations in cystic kidney disease.

Degree: Food and Human Nutritional Sciences, 2019, University of Manitoba

Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease in humans. In animal models that are non-orthologous to ADPKD, dietary soy… (more)

Subjects/Keywords: Polycystic kidney disease; Oxylipin

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APA (6th Edition):

Monirujjaman, M. (2019). Effect of dietary oils and protein and cyclooxygenase-2 inhibition on disease progression and oxylipin alterations in cystic kidney disease. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/34233

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Monirujjaman, Md. “Effect of dietary oils and protein and cyclooxygenase-2 inhibition on disease progression and oxylipin alterations in cystic kidney disease.” 2019. Thesis, University of Manitoba. Accessed October 27, 2020. http://hdl.handle.net/1993/34233.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Monirujjaman, Md. “Effect of dietary oils and protein and cyclooxygenase-2 inhibition on disease progression and oxylipin alterations in cystic kidney disease.” 2019. Web. 27 Oct 2020.

Vancouver:

Monirujjaman M. Effect of dietary oils and protein and cyclooxygenase-2 inhibition on disease progression and oxylipin alterations in cystic kidney disease. [Internet] [Thesis]. University of Manitoba; 2019. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1993/34233.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Monirujjaman M. Effect of dietary oils and protein and cyclooxygenase-2 inhibition on disease progression and oxylipin alterations in cystic kidney disease. [Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/34233

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

21. Bastos, Ana Paula Almeida. A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos.

Degree: PhD, Nefrologia, 2010, University of São Paulo

A maior parte dos casos de doença renal policística autossômica dominante (DRPAD) é causada por mutações no gene PKD1 (Polycystic Kidney Disease 1). O insulto… (more)

Subjects/Keywords: Autosomal dominant polycystic kidney disease; Cell proliferation; Cyclin-dependent kinase Inhibitor p21; Cystic kidney diseases; Doenças renais císticas; Inibidor de quinase dependente de ciclina p21; Ischemia; Isquemia; Mutação; Mutation; Proliferação de células; Reperfusion injury; Rim policístico autossômico dominante; Traumatismo por reperfusão

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bastos, A. P. A. (2010). A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5148/tde-25082010-112042/ ;

Chicago Manual of Style (16th Edition):

Bastos, Ana Paula Almeida. “A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos.” 2010. Doctoral Dissertation, University of São Paulo. Accessed October 27, 2020. http://www.teses.usp.br/teses/disponiveis/5/5148/tde-25082010-112042/ ;.

MLA Handbook (7th Edition):

Bastos, Ana Paula Almeida. “A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos.” 2010. Web. 27 Oct 2020.

Vancouver:

Bastos APA. A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2020 Oct 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-25082010-112042/ ;.

Council of Science Editors:

Bastos APA. A haploinsuficiência de Pkd1 aumenta a lesão renal e induz formação de microcistos após isquemia/reperfusão em camundongos. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/5/5148/tde-25082010-112042/ ;

22. Cornec-Le Gall, Emilie. Polykystose rénale autosomique dominante : de la génétique moléculaire au développement d'outils pronostiques : Autosomal dominant holycystic kidney disease (ADPKD) : from molecular genetics to the development of prognostic tools.

Degree: Docteur es, Biologie-santé, 2015, Brest

La Polykystose Rénale Autosomique Dominante (PKRAD) est une des pathologies héréditaires les plus fréquentes et affecte environ un individu sur 1000. Elle se caractérise par… (more)

Subjects/Keywords: Polykystose rénale autosomique dominante; Génétique moléculaire; PKD1; PKD2; Insuffisance rénale terminale; Dialyse; Transplantation rénale; Facteurs prédictifs; Médecine personnalisée; Autosomal dominant polycystic kidney disease; Molecular genetics; PKD1; PKD2; End-stage renal disease; Dialysis; Kidney transplantation; Predictive factors; Personalized medicine; 572.8; 616.61

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Cornec-Le Gall, E. (2015). Polykystose rénale autosomique dominante : de la génétique moléculaire au développement d'outils pronostiques : Autosomal dominant holycystic kidney disease (ADPKD) : from molecular genetics to the development of prognostic tools. (Doctoral Dissertation). Brest. Retrieved from http://www.theses.fr/2015BRES0030

Chicago Manual of Style (16th Edition):

Cornec-Le Gall, Emilie. “Polykystose rénale autosomique dominante : de la génétique moléculaire au développement d'outils pronostiques : Autosomal dominant holycystic kidney disease (ADPKD) : from molecular genetics to the development of prognostic tools.” 2015. Doctoral Dissertation, Brest. Accessed October 27, 2020. http://www.theses.fr/2015BRES0030.

MLA Handbook (7th Edition):

Cornec-Le Gall, Emilie. “Polykystose rénale autosomique dominante : de la génétique moléculaire au développement d'outils pronostiques : Autosomal dominant holycystic kidney disease (ADPKD) : from molecular genetics to the development of prognostic tools.” 2015. Web. 27 Oct 2020.

Vancouver:

Cornec-Le Gall E. Polykystose rénale autosomique dominante : de la génétique moléculaire au développement d'outils pronostiques : Autosomal dominant holycystic kidney disease (ADPKD) : from molecular genetics to the development of prognostic tools. [Internet] [Doctoral dissertation]. Brest; 2015. [cited 2020 Oct 27]. Available from: http://www.theses.fr/2015BRES0030.

Council of Science Editors:

Cornec-Le Gall E. Polykystose rénale autosomique dominante : de la génétique moléculaire au développement d'outils pronostiques : Autosomal dominant holycystic kidney disease (ADPKD) : from molecular genetics to the development of prognostic tools. [Doctoral Dissertation]. Brest; 2015. Available from: http://www.theses.fr/2015BRES0030

23. Raman, Archana. THE ROLE OF MATRICELLULAR SIGNALING IN POLYCYSTIC KIDNEY DISEASE.

Degree: PhD, Molecular & Integrative Physiology, 2017, University of Kansas

Polycystic kidney disease (PKD) is characterized by excessive enlargement of the kidney, due to the hyperplastic growth of renal epithelial cells, giving rise to fluid-filled… (more)

Subjects/Keywords: Physiology; Autosomal dominant Polycystic kidney disease; ECM; Integrin-linked kinase; Integrins; Kidney; Periostin

…vasopressin ADPKD: autosomal dominant polycystic kidney disease ARPKD: autosomal Recessive… …xvi Chapter 1. Pathophysiology of autosomal dominant polycystic kidney disease… …1 1.2. Autosomal Dominant Polycystic Kidney Disease (ADPKD)… …AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE 1.1. Polycystic Kidney Disease “Though of simple… …1 1.1. Polycystic Kidney Disease… 

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Raman, A. (2017). THE ROLE OF MATRICELLULAR SIGNALING IN POLYCYSTIC KIDNEY DISEASE. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/26892

Chicago Manual of Style (16th Edition):

Raman, Archana. “THE ROLE OF MATRICELLULAR SIGNALING IN POLYCYSTIC KIDNEY DISEASE.” 2017. Doctoral Dissertation, University of Kansas. Accessed October 27, 2020. http://hdl.handle.net/1808/26892.

MLA Handbook (7th Edition):

Raman, Archana. “THE ROLE OF MATRICELLULAR SIGNALING IN POLYCYSTIC KIDNEY DISEASE.” 2017. Web. 27 Oct 2020.

Vancouver:

Raman A. THE ROLE OF MATRICELLULAR SIGNALING IN POLYCYSTIC KIDNEY DISEASE. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1808/26892.

Council of Science Editors:

Raman A. THE ROLE OF MATRICELLULAR SIGNALING IN POLYCYSTIC KIDNEY DISEASE. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/26892


Texas A&M University

24. Lin, Shuxian. Dmp1 Regulates Osteocyte Function Via Wnt/β-Catenin Signaling Pathway.

Degree: PhD, Biomedical Sciences, 2014, Texas A&M University

 DMP1, dentin matrix protein 1, was cloned from a rat dentin cDNA library 20 years ago. Initially, this non-collagenous matrix protein was thought to be… (more)

Subjects/Keywords: Dentin Matrix Protein 1; Wnt/β-catenin; Autosomal Recessive Hypophosphatemic Rickets; Skeleton; Tooth

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Lin, S. (2014). Dmp1 Regulates Osteocyte Function Via Wnt/β-Catenin Signaling Pathway. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152604

Chicago Manual of Style (16th Edition):

Lin, Shuxian. “Dmp1 Regulates Osteocyte Function Via Wnt/β-Catenin Signaling Pathway.” 2014. Doctoral Dissertation, Texas A&M University. Accessed October 27, 2020. http://hdl.handle.net/1969.1/152604.

MLA Handbook (7th Edition):

Lin, Shuxian. “Dmp1 Regulates Osteocyte Function Via Wnt/β-Catenin Signaling Pathway.” 2014. Web. 27 Oct 2020.

Vancouver:

Lin S. Dmp1 Regulates Osteocyte Function Via Wnt/β-Catenin Signaling Pathway. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1969.1/152604.

Council of Science Editors:

Lin S. Dmp1 Regulates Osteocyte Function Via Wnt/β-Catenin Signaling Pathway. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152604

25. Gancheva, Diana / Ганчева, Диана. Peculiarities in the clinical approach in patients with Wilson’s disease. // Особености в клиничния подход при пациенти с болест на Wilson.

Degree: 2014, Medical University of Varna

 [EN] The dissertation is dedicated to Wilson’s disease (WD) – a rare inherited autosomal recessive disease, related to a disorder of copper metabolism. Its aim… (more)

Subjects/Keywords: Wilson’s disease; inherited autosomal recessive disease; copper metabolism; Вътрешни болести / Internal Diseases; Гастроентерология / Gastroenterology

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Gancheva, Diana / Ганчева, . (2014). Peculiarities in the clinical approach in patients with Wilson’s disease. // Особености в клиничния подход при пациенти с болест на Wilson. (Thesis). Medical University of Varna. Retrieved from http://repository.mu-varna.bg/handle/nls/43

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gancheva, Diana / Ганчева, Диана. “Peculiarities in the clinical approach in patients with Wilson’s disease. // Особености в клиничния подход при пациенти с болест на Wilson.” 2014. Thesis, Medical University of Varna. Accessed October 27, 2020. http://repository.mu-varna.bg/handle/nls/43.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gancheva, Diana / Ганчева, Диана. “Peculiarities in the clinical approach in patients with Wilson’s disease. // Особености в клиничния подход при пациенти с болест на Wilson.” 2014. Web. 27 Oct 2020.

Vancouver:

Gancheva, Diana / Ганчева . Peculiarities in the clinical approach in patients with Wilson’s disease. // Особености в клиничния подход при пациенти с болест на Wilson. [Internet] [Thesis]. Medical University of Varna; 2014. [cited 2020 Oct 27]. Available from: http://repository.mu-varna.bg/handle/nls/43.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gancheva, Diana / Ганчева . Peculiarities in the clinical approach in patients with Wilson’s disease. // Особености в клиничния подход при пациенти с болест на Wilson. [Thesis]. Medical University of Varna; 2014. Available from: http://repository.mu-varna.bg/handle/nls/43

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Freie Universität Berlin

26. Abbasi Moheb, Lia. Identifizierung von drei neuen Genen für autosomal rezessive geistige Behinderung und molekulare Charakterisierung der zugrundeliegenden Gendefekte.

Degree: 2012, Freie Universität Berlin

 Mentale Retardierung (MR), eine der komplexesten Erkrankungen, hat eine weltweite Prävalenz von etwa 2% und ist ein häufiger Grund schwerster Behinderung. Aus diesem Grund ist… (more)

Subjects/Keywords: Intellectual Disability; autosomal recessive; brain; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Abbasi Moheb, L. (2012). Identifizierung von drei neuen Genen für autosomal rezessive geistige Behinderung und molekulare Charakterisierung der zugrundeliegenden Gendefekte. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/11246

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Abbasi Moheb, Lia. “Identifizierung von drei neuen Genen für autosomal rezessive geistige Behinderung und molekulare Charakterisierung der zugrundeliegenden Gendefekte.” 2012. Thesis, Freie Universität Berlin. Accessed October 27, 2020. https://refubium.fu-berlin.de/handle/fub188/11246.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Abbasi Moheb, Lia. “Identifizierung von drei neuen Genen für autosomal rezessive geistige Behinderung und molekulare Charakterisierung der zugrundeliegenden Gendefekte.” 2012. Web. 27 Oct 2020.

Vancouver:

Abbasi Moheb L. Identifizierung von drei neuen Genen für autosomal rezessive geistige Behinderung und molekulare Charakterisierung der zugrundeliegenden Gendefekte. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2020 Oct 27]. Available from: https://refubium.fu-berlin.de/handle/fub188/11246.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Abbasi Moheb L. Identifizierung von drei neuen Genen für autosomal rezessive geistige Behinderung und molekulare Charakterisierung der zugrundeliegenden Gendefekte. [Thesis]. Freie Universität Berlin; 2012. Available from: https://refubium.fu-berlin.de/handle/fub188/11246

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Queen Mary, University of London

27. Duncan, Emma Jane. The neurodegenerative disease Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) : cellular defects due to loss of sacsin function.

Degree: PhD, 2016, Queen Mary, University of London

 Sacsin, which is mutated in the neurodegenerative disease Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS), is a 520 kDa modular protein with regions of homology… (more)

Subjects/Keywords: Endocrinology; Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay; ARSACS; Neurodegenerative Disease; Sacsin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Duncan, E. J. (2016). The neurodegenerative disease Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) : cellular defects due to loss of sacsin function. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/23110 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765788

Chicago Manual of Style (16th Edition):

Duncan, Emma Jane. “The neurodegenerative disease Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) : cellular defects due to loss of sacsin function.” 2016. Doctoral Dissertation, Queen Mary, University of London. Accessed October 27, 2020. http://qmro.qmul.ac.uk/xmlui/handle/123456789/23110 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765788.

MLA Handbook (7th Edition):

Duncan, Emma Jane. “The neurodegenerative disease Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) : cellular defects due to loss of sacsin function.” 2016. Web. 27 Oct 2020.

Vancouver:

Duncan EJ. The neurodegenerative disease Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) : cellular defects due to loss of sacsin function. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2016. [cited 2020 Oct 27]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/23110 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765788.

Council of Science Editors:

Duncan EJ. The neurodegenerative disease Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) : cellular defects due to loss of sacsin function. [Doctoral Dissertation]. Queen Mary, University of London; 2016. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/23110 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765788


Queen Mary, University of London

28. Bradshaw, Teisha Y. The cellular phenotype of the neurodegenerative disease autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Degree: PhD, 2014, Queen Mary, University of London

Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS) is an early onset neurodegenerative disorder resulting from mutations in the SACS gene that encodes the protein… (more)

Subjects/Keywords: 616.8; Medicine; Endocrinology; Autosomal recessive spastic ataxia of Charlevoix Saguenay; Neurodegenerative diseases; SACS gene; Sacsin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bradshaw, T. Y. (2014). The cellular phenotype of the neurodegenerative disease autosomal recessive spastic ataxia of Charlevoix-Saguenay. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/8924 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667309

Chicago Manual of Style (16th Edition):

Bradshaw, Teisha Y. “The cellular phenotype of the neurodegenerative disease autosomal recessive spastic ataxia of Charlevoix-Saguenay.” 2014. Doctoral Dissertation, Queen Mary, University of London. Accessed October 27, 2020. http://qmro.qmul.ac.uk/xmlui/handle/123456789/8924 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667309.

MLA Handbook (7th Edition):

Bradshaw, Teisha Y. “The cellular phenotype of the neurodegenerative disease autosomal recessive spastic ataxia of Charlevoix-Saguenay.” 2014. Web. 27 Oct 2020.

Vancouver:

Bradshaw TY. The cellular phenotype of the neurodegenerative disease autosomal recessive spastic ataxia of Charlevoix-Saguenay. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2014. [cited 2020 Oct 27]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/8924 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667309.

Council of Science Editors:

Bradshaw TY. The cellular phenotype of the neurodegenerative disease autosomal recessive spastic ataxia of Charlevoix-Saguenay. [Doctoral Dissertation]. Queen Mary, University of London; 2014. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/8924 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667309

29. Δημητρίου, Κυπρούλα. Μελέτη αυτοσωματικής επικρατούσας μορφής πολυκυστικής νόσου των νεφρών (ΑΕΠΝΝ) τύπου 1 και 2 στην Κύπρο: κλινικά χαρακτηριστικά και επιδημιολογία της νόσου.

Degree: 2004, University of Crete (UOC); Πανεπιστήμιο Κρήτης

Subjects/Keywords: Αυτοσωματική επικρατούσα πολυκυστική νόσος νεφρών; Τύπος 1; Τύπος 2; Autosomal dominant polycystic kidney disease; Type 1; Type 2

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APA (6th Edition):

Δημητρίου, . . (2004). Μελέτη αυτοσωματικής επικρατούσας μορφής πολυκυστικής νόσου των νεφρών (ΑΕΠΝΝ) τύπου 1 και 2 στην Κύπρο: κλινικά χαρακτηριστικά και επιδημιολογία της νόσου. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/15929

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Δημητρίου, Κυπρούλα. “Μελέτη αυτοσωματικής επικρατούσας μορφής πολυκυστικής νόσου των νεφρών (ΑΕΠΝΝ) τύπου 1 και 2 στην Κύπρο: κλινικά χαρακτηριστικά και επιδημιολογία της νόσου.” 2004. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed October 27, 2020. http://hdl.handle.net/10442/hedi/15929.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Δημητρίου, Κυπρούλα. “Μελέτη αυτοσωματικής επικρατούσας μορφής πολυκυστικής νόσου των νεφρών (ΑΕΠΝΝ) τύπου 1 και 2 στην Κύπρο: κλινικά χαρακτηριστικά και επιδημιολογία της νόσου.” 2004. Web. 27 Oct 2020.

Vancouver:

Δημητρίου . Μελέτη αυτοσωματικής επικρατούσας μορφής πολυκυστικής νόσου των νεφρών (ΑΕΠΝΝ) τύπου 1 και 2 στην Κύπρο: κλινικά χαρακτηριστικά και επιδημιολογία της νόσου. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2004. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10442/hedi/15929.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Δημητρίου . Μελέτη αυτοσωματικής επικρατούσας μορφής πολυκυστικής νόσου των νεφρών (ΑΕΠΝΝ) τύπου 1 και 2 στην Κύπρο: κλινικά χαρακτηριστικά και επιδημιολογία της νόσου. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2004. Available from: http://hdl.handle.net/10442/hedi/15929

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universitat Pompeu Fabra

30. Trujillano Lidón, Daniel, 1987-. Mendelian disease gene identification and diagnosis using targeted next generation sequencing.

Degree: Departament de Ciències Experimentals i de la Salut, 2013, Universitat Pompeu Fabra

 Next Generation Sequencing (NGS) technologies have emerged as a powerful tool for the discovery of causative mutations and novel Mendelian disease genes, and are rapidly… (more)

Subjects/Keywords: Mendelian disease; Diagnostics; Next generation sequencing; Cystic fibrosis; Hyperphenylalaninemias; Autosomal domynant polycystic kidney disease; Malaltia mendeliana; Diagnòstic; Seqüenciació de nova generació; Hipertensió; Fibrosi quística; Hiperfenilalaninèmies; Malaltia poliquística renal autosòmica dominant; 575

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APA (6th Edition):

Trujillano Lidón, Daniel, 1. (2013). Mendelian disease gene identification and diagnosis using targeted next generation sequencing. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/295582

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Trujillano Lidón, Daniel, 1987-. “Mendelian disease gene identification and diagnosis using targeted next generation sequencing.” 2013. Thesis, Universitat Pompeu Fabra. Accessed October 27, 2020. http://hdl.handle.net/10803/295582.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Trujillano Lidón, Daniel, 1987-. “Mendelian disease gene identification and diagnosis using targeted next generation sequencing.” 2013. Web. 27 Oct 2020.

Vancouver:

Trujillano Lidón, Daniel 1. Mendelian disease gene identification and diagnosis using targeted next generation sequencing. [Internet] [Thesis]. Universitat Pompeu Fabra; 2013. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10803/295582.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Trujillano Lidón, Daniel 1. Mendelian disease gene identification and diagnosis using targeted next generation sequencing. [Thesis]. Universitat Pompeu Fabra; 2013. Available from: http://hdl.handle.net/10803/295582

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2] [3] [4] [5] … [109]

.