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You searched for subject:(Anemia de Fanconi). Showing records 1 – 19 of 19 total matches.

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Universidad de Cantabria

1. Prieto Remón, Inés. Estudio integrado sobre la anemia de Fanconi: aproximación a las bases moleculares del fallo medular y de la microftalmia.

Degree: 2013, Universidad de Cantabria

 RESUMEN: La anemia de Fanconi es una enfermedad genética rara. Presenta una gran heterogeneidad de síntomas clínicos, que van desde una aplasia medular precoz (pérdida… (more)

Subjects/Keywords: Anemia de Fanconi

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APA (6th Edition):

Prieto Remón, I. (2013). Estudio integrado sobre la anemia de Fanconi: aproximación a las bases moleculares del fallo medular y de la microftalmia. (Doctoral Dissertation). Universidad de Cantabria. Retrieved from http://hdl.handle.net/10902/1918

Chicago Manual of Style (16th Edition):

Prieto Remón, Inés. “Estudio integrado sobre la anemia de Fanconi: aproximación a las bases moleculares del fallo medular y de la microftalmia.” 2013. Doctoral Dissertation, Universidad de Cantabria. Accessed October 20, 2020. http://hdl.handle.net/10902/1918.

MLA Handbook (7th Edition):

Prieto Remón, Inés. “Estudio integrado sobre la anemia de Fanconi: aproximación a las bases moleculares del fallo medular y de la microftalmia.” 2013. Web. 20 Oct 2020.

Vancouver:

Prieto Remón I. Estudio integrado sobre la anemia de Fanconi: aproximación a las bases moleculares del fallo medular y de la microftalmia. [Internet] [Doctoral dissertation]. Universidad de Cantabria; 2013. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10902/1918.

Council of Science Editors:

Prieto Remón I. Estudio integrado sobre la anemia de Fanconi: aproximación a las bases moleculares del fallo medular y de la microftalmia. [Doctoral Dissertation]. Universidad de Cantabria; 2013. Available from: http://hdl.handle.net/10902/1918

2. Lima, Suelen Cristina. Uso da radiação ionizante no diagnóstico da Anemia de Fanconi .

Degree: 2013, Universidade Federal de Pernambuco

 A Anemia de Fanconi (AF) é uma síndrome genética essencialmente autossômica recessiva, caracterizada clinicamente por anormalidades congênitas, alterações hematológicas e suscetibilidade aumentada ao câncer. Ao… (more)

Subjects/Keywords: Anemia de Fanconi; DEB; Radiação Ionizante

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APA (6th Edition):

Lima, S. C. (2013). Uso da radiação ionizante no diagnóstico da Anemia de Fanconi . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/10150

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):

Lima, Suelen Cristina. “Uso da radiação ionizante no diagnóstico da Anemia de Fanconi .” 2013. Thesis, Universidade Federal de Pernambuco. Accessed October 20, 2020. http://repositorio.ufpe.br/handle/123456789/10150.

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

MLA Handbook (7th Edition):

Lima, Suelen Cristina. “Uso da radiação ionizante no diagnóstico da Anemia de Fanconi .” 2013. Web. 20 Oct 2020.

Vancouver:

Lima SC. Uso da radiação ionizante no diagnóstico da Anemia de Fanconi . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2013. [cited 2020 Oct 20]. Available from: http://repositorio.ufpe.br/handle/123456789/10150.

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

Council of Science Editors:

Lima SC. Uso da radiação ionizante no diagnóstico da Anemia de Fanconi . [Thesis]. Universidade Federal de Pernambuco; 2013. Available from: http://repositorio.ufpe.br/handle/123456789/10150

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

3. Barroca, Vilma. Renouvellement des cellules souches : plasticité des progéniteurs germinaux et rôle du gène Fancg dans la fonction des cellules souches hématopoïétiques : Stem cell renewal : germinal progenitor plasticity and role of the Fancg gene in the hematopoietic stem cell functions.

Degree: Docteur es, Biologie, 2009, Université d'Orléans

La préservation d’un stock de cellules souches fonctionnelles est indispensable pour le maintien de nombreux tissus chez l’adulte. Les cellules souches se multiplient pour s’auto-renouveller… (more)

Subjects/Keywords: Anémie de Fanconi; Gène Fancg; Fanconi anemia; Fancg gene

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APA (6th Edition):

Barroca, V. (2009). Renouvellement des cellules souches : plasticité des progéniteurs germinaux et rôle du gène Fancg dans la fonction des cellules souches hématopoïétiques : Stem cell renewal : germinal progenitor plasticity and role of the Fancg gene in the hematopoietic stem cell functions. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2009ORLE2023

Chicago Manual of Style (16th Edition):

Barroca, Vilma. “Renouvellement des cellules souches : plasticité des progéniteurs germinaux et rôle du gène Fancg dans la fonction des cellules souches hématopoïétiques : Stem cell renewal : germinal progenitor plasticity and role of the Fancg gene in the hematopoietic stem cell functions.” 2009. Doctoral Dissertation, Université d'Orléans. Accessed October 20, 2020. http://www.theses.fr/2009ORLE2023.

MLA Handbook (7th Edition):

Barroca, Vilma. “Renouvellement des cellules souches : plasticité des progéniteurs germinaux et rôle du gène Fancg dans la fonction des cellules souches hématopoïétiques : Stem cell renewal : germinal progenitor plasticity and role of the Fancg gene in the hematopoietic stem cell functions.” 2009. Web. 20 Oct 2020.

Vancouver:

Barroca V. Renouvellement des cellules souches : plasticité des progéniteurs germinaux et rôle du gène Fancg dans la fonction des cellules souches hématopoïétiques : Stem cell renewal : germinal progenitor plasticity and role of the Fancg gene in the hematopoietic stem cell functions. [Internet] [Doctoral dissertation]. Université d'Orléans; 2009. [cited 2020 Oct 20]. Available from: http://www.theses.fr/2009ORLE2023.

Council of Science Editors:

Barroca V. Renouvellement des cellules souches : plasticité des progéniteurs germinaux et rôle du gène Fancg dans la fonction des cellules souches hématopoïétiques : Stem cell renewal : germinal progenitor plasticity and role of the Fancg gene in the hematopoietic stem cell functions. [Doctoral Dissertation]. Université d'Orléans; 2009. Available from: http://www.theses.fr/2009ORLE2023


Universitat Autònoma de Barcelona

4. Trujillo Quintero, Juan Pablo. Genética Clínica de la anemia de Fanconi.

Degree: Departament de Genètica i de Microbiologia, 2013, Universitat Autònoma de Barcelona

Fanconi anemia (FA) is a rare genetic disorder, which is mainly inherited with autosomal recessive pattern. Clinically it is characterized by congenital and endocrine abnormalities,… (more)

Subjects/Keywords: Anemia de Fanconi; Mosaicismo somático; Fanconi-like; Ciències Experimentals; 575

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APA (6th Edition):

Trujillo Quintero, J. P. (2013). Genética Clínica de la anemia de Fanconi. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/129106

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):

Trujillo Quintero, Juan Pablo. “Genética Clínica de la anemia de Fanconi.” 2013. Thesis, Universitat Autònoma de Barcelona. Accessed October 20, 2020. http://hdl.handle.net/10803/129106.

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

MLA Handbook (7th Edition):

Trujillo Quintero, Juan Pablo. “Genética Clínica de la anemia de Fanconi.” 2013. Web. 20 Oct 2020.

Vancouver:

Trujillo Quintero JP. Genética Clínica de la anemia de Fanconi. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2013. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10803/129106.

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

Council of Science Editors:

Trujillo Quintero JP. Genética Clínica de la anemia de Fanconi. [Thesis]. Universitat Autònoma de Barcelona; 2013. Available from: http://hdl.handle.net/10803/129106

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


Universidade Estadual de Campinas

5. Amstalden, Lucila Gobby. Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer.

Degree: 2011, Universidade Estadual de Campinas

 Abstract: Breast Cancer (BC) is the cancer type more commonly occurs among women with estimative of 49.240 new cases in 2010. The BC presents risk… (more)

Subjects/Keywords: Mamas - Câncer; Fanconi, Anemia de; Metástase; Câncer; Sequência de nucleotídeos; Breast - Cancer; Fanconi anemia; Metastasis; Cancer; Nucleotides sequence

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APA (6th Edition):

Amstalden, L. G. (2011). Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/308580

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):

Amstalden, Lucila Gobby. “Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer.” 2011. Thesis, Universidade Estadual de Campinas. Accessed October 20, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/308580.

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

MLA Handbook (7th Edition):

Amstalden, Lucila Gobby. “Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer.” 2011. Web. 20 Oct 2020.

Vancouver:

Amstalden LG. Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer. [Internet] [Thesis]. Universidade Estadual de Campinas; 2011. [cited 2020 Oct 20]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308580.

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

Council of Science Editors:

Amstalden LG. Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer. [Thesis]. Universidade Estadual de Campinas; 2011. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308580

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


Universidade Estadual de Campinas

6. Gonçalves, Claudia Estela, 1970-. Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia.

Degree: 2014, Universidade Estadual de Campinas

 Abstract: The Fanconi Anemia (FA) is a genetic disorder characterized by multiple congenital and hematological abnormalities and predisposition to a variety of tumors. The worldwide… (more)

Subjects/Keywords: Anemia de Fanconi; Neoplasias; Genótipo; Síndromes mielodisplásicas; Mutação; Instabilidade cromossomica; Fanconi anemia; Neoplasms; Genotype; Myelodysplastic syndromes; Mutation; Chromosomal instability

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APA (6th Edition):

Gonçalves, Claudia Estela, 1. (2014). Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/308602

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):

Gonçalves, Claudia Estela, 1970-. “Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia.” 2014. Thesis, Universidade Estadual de Campinas. Accessed October 20, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/308602.

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

MLA Handbook (7th Edition):

Gonçalves, Claudia Estela, 1970-. “Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia.” 2014. Web. 20 Oct 2020.

Vancouver:

Gonçalves, Claudia Estela 1. Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia. [Internet] [Thesis]. Universidade Estadual de Campinas; 2014. [cited 2020 Oct 20]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308602.

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

Council of Science Editors:

Gonçalves, Claudia Estela 1. Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia. [Thesis]. Universidade Estadual de Campinas; 2014. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308602

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


Universitat Autònoma de Barcelona

7. Montanuy Escribano, Helena. Recerca terapèutica en l'anèmia de Fanconi.

Degree: Departament de Genètica i de Microbiologia, 2017, Universitat Autònoma de Barcelona

 Much effort is being made on Fanconi anemia therapeutics to treat bone marrow failure and cancer, the most life threatening signs of the disease. There… (more)

Subjects/Keywords: Anèmia de Fanconi; Anemia de Fanconi; Fanconi anemia; Fragilitat cromosòmica; Fragilidad cromosómica; Chromosome fragility; Cribatge de fàrmacs; Cribaje de fármacos; Drug screening; Ciències de la Salut; 575

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APA (6th Edition):

Montanuy Escribano, H. (2017). Recerca terapèutica en l'anèmia de Fanconi. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/458658

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):

Montanuy Escribano, Helena. “Recerca terapèutica en l'anèmia de Fanconi.” 2017. Thesis, Universitat Autònoma de Barcelona. Accessed October 20, 2020. http://hdl.handle.net/10803/458658.

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

MLA Handbook (7th Edition):

Montanuy Escribano, Helena. “Recerca terapèutica en l'anèmia de Fanconi.” 2017. Web. 20 Oct 2020.

Vancouver:

Montanuy Escribano H. Recerca terapèutica en l'anèmia de Fanconi. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2017. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10803/458658.

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

Council of Science Editors:

Montanuy Escribano H. Recerca terapèutica en l'anèmia de Fanconi. [Thesis]. Universitat Autònoma de Barcelona; 2017. Available from: http://hdl.handle.net/10803/458658

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

8. Federico, María Belén. Relevancia de la vía de Fanconi en el copiado de ADN dañado por luz UV.

Degree: 2016, Universidad de Buenos Aires

Here we show that irradiation with low doses of UV light causes modest accumulation of replication-coupled double strand breaks (DSBs), i.e. collapsed forks. Remarkably, the… (more)

Subjects/Keywords: UV; Vía de Fanconi; Anemia; ADN; Ciencias de la vida

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APA (6th Edition):

Federico, M. B. (2016). Relevancia de la vía de Fanconi en el copiado de ADN dañado por luz UV. (Thesis). Universidad de Buenos Aires. Retrieved from http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1387 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1387.dir/1387.PDF

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):

Federico, María Belén. “Relevancia de la vía de Fanconi en el copiado de ADN dañado por luz UV.” 2016. Thesis, Universidad de Buenos Aires. Accessed October 20, 2020. http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1387 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1387.dir/1387.PDF.

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

MLA Handbook (7th Edition):

Federico, María Belén. “Relevancia de la vía de Fanconi en el copiado de ADN dañado por luz UV.” 2016. Web. 20 Oct 2020.

Vancouver:

Federico MB. Relevancia de la vía de Fanconi en el copiado de ADN dañado por luz UV. [Internet] [Thesis]. Universidad de Buenos Aires; 2016. [cited 2020 Oct 20]. Available from: http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1387 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1387.dir/1387.PDF.

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

Council of Science Editors:

Federico MB. Relevancia de la vía de Fanconi en el copiado de ADN dañado por luz UV. [Thesis]. Universidad de Buenos Aires; 2016. Available from: http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1387 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1387.dir/1387.PDF

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

9. Tatiana Maria Folador Mattioli. Análise sialométrica e das concentrações salivares de cálcio, amilase, uréia e proteínas totais de indivíduos portadores da anemia de Fanconi.

Degree: 2005, Pontifícia Universidade Católica do Paraná

A anemia de Fanconi (AF) é uma doença genética caracterizada por uma instabilidade cromossômica que leva ao desenvolvimento de pancitopenia progressiva e intensa, leucemia e/ou… (more)

Subjects/Keywords: ODONTOLOGIA; Estomatologia; Anemia de Fanconi; Saliva; Doenças hereditárias

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APA (6th Edition):

Mattioli, T. M. F. (2005). Análise sialométrica e das concentrações salivares de cálcio, amilase, uréia e proteínas totais de indivíduos portadores da anemia de Fanconi. (Thesis). Pontifícia Universidade Católica do Paraná. Retrieved from http://www.biblioteca.pucpr.br/tede//tde_busca/arquivo.php?codArquivo=272

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):

Mattioli, Tatiana Maria Folador. “Análise sialométrica e das concentrações salivares de cálcio, amilase, uréia e proteínas totais de indivíduos portadores da anemia de Fanconi.” 2005. Thesis, Pontifícia Universidade Católica do Paraná. Accessed October 20, 2020. http://www.biblioteca.pucpr.br/tede//tde_busca/arquivo.php?codArquivo=272.

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

MLA Handbook (7th Edition):

Mattioli, Tatiana Maria Folador. “Análise sialométrica e das concentrações salivares de cálcio, amilase, uréia e proteínas totais de indivíduos portadores da anemia de Fanconi.” 2005. Web. 20 Oct 2020.

Vancouver:

Mattioli TMF. Análise sialométrica e das concentrações salivares de cálcio, amilase, uréia e proteínas totais de indivíduos portadores da anemia de Fanconi. [Internet] [Thesis]. Pontifícia Universidade Católica do Paraná; 2005. [cited 2020 Oct 20]. Available from: http://www.biblioteca.pucpr.br/tede//tde_busca/arquivo.php?codArquivo=272.

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

Council of Science Editors:

Mattioli TMF. Análise sialométrica e das concentrações salivares de cálcio, amilase, uréia e proteínas totais de indivíduos portadores da anemia de Fanconi. [Thesis]. Pontifícia Universidade Católica do Paraná; 2005. Available from: http://www.biblioteca.pucpr.br/tede//tde_busca/arquivo.php?codArquivo=272

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


Université Paris-Sud – Paris XI

10. Girard, Chloé. FANCM et ses cofacteurs MHF1-MHF2, ainsi que FIDGETIN-Like-1 limitent la formation des crossovers méiotiques chez Arabidopsis thaliana : FANCM and its co-factors MHF1-MHF2, as well as FIDGETIN-Like-1 limit meiotic CO formation in Arabidopsis thaliana.

Degree: Docteur es, Biologie, 2014, Université Paris-Sud – Paris XI

La grand majorité des espèces forment très peu de crossovers (CO) par chromosome en méiose, et ce quelle que soit la taille des chromosomes et… (more)

Subjects/Keywords: Meiose; Crossovers; Chromosomes; FANCM; Anémie de Fanconi; FIDGETIN-Like-1; Recombinaison; Meiosis; Crossovers; Chromosomes; FANCM; Fanconi anemia; FIDGETIN-Like-1; Recombination

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APA (6th Edition):

Girard, C. (2014). FANCM et ses cofacteurs MHF1-MHF2, ainsi que FIDGETIN-Like-1 limitent la formation des crossovers méiotiques chez Arabidopsis thaliana : FANCM and its co-factors MHF1-MHF2, as well as FIDGETIN-Like-1 limit meiotic CO formation in Arabidopsis thaliana. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA112259

Chicago Manual of Style (16th Edition):

Girard, Chloé. “FANCM et ses cofacteurs MHF1-MHF2, ainsi que FIDGETIN-Like-1 limitent la formation des crossovers méiotiques chez Arabidopsis thaliana : FANCM and its co-factors MHF1-MHF2, as well as FIDGETIN-Like-1 limit meiotic CO formation in Arabidopsis thaliana.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 20, 2020. http://www.theses.fr/2014PA112259.

MLA Handbook (7th Edition):

Girard, Chloé. “FANCM et ses cofacteurs MHF1-MHF2, ainsi que FIDGETIN-Like-1 limitent la formation des crossovers méiotiques chez Arabidopsis thaliana : FANCM and its co-factors MHF1-MHF2, as well as FIDGETIN-Like-1 limit meiotic CO formation in Arabidopsis thaliana.” 2014. Web. 20 Oct 2020.

Vancouver:

Girard C. FANCM et ses cofacteurs MHF1-MHF2, ainsi que FIDGETIN-Like-1 limitent la formation des crossovers méiotiques chez Arabidopsis thaliana : FANCM and its co-factors MHF1-MHF2, as well as FIDGETIN-Like-1 limit meiotic CO formation in Arabidopsis thaliana. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2020 Oct 20]. Available from: http://www.theses.fr/2014PA112259.

Council of Science Editors:

Girard C. FANCM et ses cofacteurs MHF1-MHF2, ainsi que FIDGETIN-Like-1 limitent la formation des crossovers méiotiques chez Arabidopsis thaliana : FANCM and its co-factors MHF1-MHF2, as well as FIDGETIN-Like-1 limit meiotic CO formation in Arabidopsis thaliana. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA112259


Université Paris-Sud – Paris XI

11. Renaudin, Xavier. Rôle de FANCA dans la régulation de la neddylation de protéines membranaires. : Role of the FANCA protein in neddylation of membrane associated proteins.

Degree: Docteur es, Sciences de la vie et de la santé, 2014, Université Paris-Sud – Paris XI

Le but de cette thèse était d’identifier de nouveaux substrats au complexe FANC Core,déficient dans l’Anémie de Fanconi, une pathologie génétique rare. Cette maladie estcaractérisée… (more)

Subjects/Keywords: Anémie de Fanconi; Neddylation; Ubiquitination; Récepteurs aux chimiokines; Mobilité cellulaire; Leucémie; Fanconi Anemia; Neddylation; Ubiquitylation; Chemokines receptors; Cell motility; Leukemia

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

APA (6th Edition):

Renaudin, X. (2014). Rôle de FANCA dans la régulation de la neddylation de protéines membranaires. : Role of the FANCA protein in neddylation of membrane associated proteins. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA112187

Chicago Manual of Style (16th Edition):

Renaudin, Xavier. “Rôle de FANCA dans la régulation de la neddylation de protéines membranaires. : Role of the FANCA protein in neddylation of membrane associated proteins.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 20, 2020. http://www.theses.fr/2014PA112187.

MLA Handbook (7th Edition):

Renaudin, Xavier. “Rôle de FANCA dans la régulation de la neddylation de protéines membranaires. : Role of the FANCA protein in neddylation of membrane associated proteins.” 2014. Web. 20 Oct 2020.

Vancouver:

Renaudin X. Rôle de FANCA dans la régulation de la neddylation de protéines membranaires. : Role of the FANCA protein in neddylation of membrane associated proteins. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2020 Oct 20]. Available from: http://www.theses.fr/2014PA112187.

Council of Science Editors:

Renaudin X. Rôle de FANCA dans la régulation de la neddylation de protéines membranaires. : Role of the FANCA protein in neddylation of membrane associated proteins. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA112187

12. Bogliolo, Massimo. Secuenciación del exoma en anemia de Fanconi: del diagnóstico al descubrimiento de un nuevo gen.

Degree: Departament de Genètica i de Microbiologia, 2015, Universitat Autònoma de Barcelona

Fanconi anemia (FA) is a rare genomic instability disorder characterized by progressive bone marrow failure and predisposition to cancer. 19 FA-associated proteins are involved in… (more)

Subjects/Keywords: Anemia de Fanconi; Fanconi anemia; Estudi genètic de exoma complet; Estudio genético de exoma completo; Whole exome sequencing; Reparació del DNA; Reparación del DNA; DNA repair; Ciències Experimentals; 575

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

APA (6th Edition):

Bogliolo, M. (2015). Secuenciación del exoma en anemia de Fanconi: del diagnóstico al descubrimiento de un nuevo gen. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/325160

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):

Bogliolo, Massimo. “Secuenciación del exoma en anemia de Fanconi: del diagnóstico al descubrimiento de un nuevo gen.” 2015. Thesis, Universitat Autònoma de Barcelona. Accessed October 20, 2020. http://hdl.handle.net/10803/325160.

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

MLA Handbook (7th Edition):

Bogliolo, Massimo. “Secuenciación del exoma en anemia de Fanconi: del diagnóstico al descubrimiento de un nuevo gen.” 2015. Web. 20 Oct 2020.

Vancouver:

Bogliolo M. Secuenciación del exoma en anemia de Fanconi: del diagnóstico al descubrimiento de un nuevo gen. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2015. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10803/325160.

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

Council of Science Editors:

Bogliolo M. Secuenciación del exoma en anemia de Fanconi: del diagnóstico al descubrimiento de un nuevo gen. [Thesis]. Universitat Autònoma de Barcelona; 2015. Available from: http://hdl.handle.net/10803/325160

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


Universitat Pompeu Fabra

13. Reina Castillón, Judith, 1989-. Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling.

Degree: Departament de Ciències Experimentals i de la Salut, 2017, Universitat Pompeu Fabra

 El mosaicisme genètic somàtic pot està present en individus sans i en altres amb certes condicions com edat avançada o càncer. La seva detecció en… (more)

Subjects/Keywords: Clonal mosaicism; Fanconi anemia; Chronic lymphothytic leukemia; Rescue uniparental disomy; Genetic counselling; Mosaicisme clonal; Anemia de Fanconi; Leucèmia linfocítica crònica; Disomia uniparental de rescat; Assessorament genetic; 575

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APA (6th Edition):

Reina Castillón, Judith, 1. (2017). Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/666707

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):

Reina Castillón, Judith, 1989-. “Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling.” 2017. Thesis, Universitat Pompeu Fabra. Accessed October 20, 2020. http://hdl.handle.net/10803/666707.

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

MLA Handbook (7th Edition):

Reina Castillón, Judith, 1989-. “Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling.” 2017. Web. 20 Oct 2020.

Vancouver:

Reina Castillón, Judith 1. Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling. [Internet] [Thesis]. Universitat Pompeu Fabra; 2017. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10803/666707.

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

Council of Science Editors:

Reina Castillón, Judith 1. Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling. [Thesis]. Universitat Pompeu Fabra; 2017. Available from: http://hdl.handle.net/10803/666707

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


Universidade Estadual de Campinas

14. Aguilar Rodriguez, David Enrique. Estudo molecular da anemia de Fanconi.

Degree: 2003, Universidade Estadual de Campinas

Subjects/Keywords: Fanconi, Anemia de; Biologia molecular; Genética molecular

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

APA (6th Edition):

Aguilar Rodriguez, D. E. (2003). Estudo molecular da anemia de Fanconi. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/316588

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):

Aguilar Rodriguez, David Enrique. “Estudo molecular da anemia de Fanconi.” 2003. Thesis, Universidade Estadual de Campinas. Accessed October 20, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/316588.

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

MLA Handbook (7th Edition):

Aguilar Rodriguez, David Enrique. “Estudo molecular da anemia de Fanconi.” 2003. Web. 20 Oct 2020.

Vancouver:

Aguilar Rodriguez DE. Estudo molecular da anemia de Fanconi. [Internet] [Thesis]. Universidade Estadual de Campinas; 2003. [cited 2020 Oct 20]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/316588.

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

Council of Science Editors:

Aguilar Rodriguez DE. Estudo molecular da anemia de Fanconi. [Thesis]. Universidade Estadual de Campinas; 2003. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/316588

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

15. Araujo, Melissa Rodrigues de. Estudo clínico, citológico e de prevalência do papilomavírus humano em mucosa oral na Anemia de Fanconi.

Degree: PhD, Estomatologia, 2008, University of São Paulo

A Anemia de Fanconi (AF) é uma doença genética rara de herança recessiva caracterizada por insuficiência da medula óssea, anormalidades de desenvolvimento malformações congênitas. A… (more)

Subjects/Keywords: anemia de fanconi; citologia em base líquida; Fanconis anemia; HPV; human papillomavirus; liquid based cytology; papilomavírus humano; PCR; polymerase chain reaction; reação em cadeia da polimerase; reverse hyb

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

APA (6th Edition):

Araujo, M. R. d. (2008). Estudo clínico, citológico e de prevalência do papilomavírus humano em mucosa oral na Anemia de Fanconi. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/25/25132/tde-02032009-202210/ ;

Chicago Manual of Style (16th Edition):

Araujo, Melissa Rodrigues de. “Estudo clínico, citológico e de prevalência do papilomavírus humano em mucosa oral na Anemia de Fanconi.” 2008. Doctoral Dissertation, University of São Paulo. Accessed October 20, 2020. http://www.teses.usp.br/teses/disponiveis/25/25132/tde-02032009-202210/ ;.

MLA Handbook (7th Edition):

Araujo, Melissa Rodrigues de. “Estudo clínico, citológico e de prevalência do papilomavírus humano em mucosa oral na Anemia de Fanconi.” 2008. Web. 20 Oct 2020.

Vancouver:

Araujo MRd. Estudo clínico, citológico e de prevalência do papilomavírus humano em mucosa oral na Anemia de Fanconi. [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2020 Oct 20]. Available from: http://www.teses.usp.br/teses/disponiveis/25/25132/tde-02032009-202210/ ;.

Council of Science Editors:

Araujo MRd. Estudo clínico, citológico e de prevalência do papilomavírus humano em mucosa oral na Anemia de Fanconi. [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/25/25132/tde-02032009-202210/ ;

16. Poret, Arnaud. Modélisation qualitative des réseaux biologiques pour l'innovation thérapeutique : Qualitative modeling of biological networks for therapeutic innovation.

Degree: Docteur es, Biologie computationnelle, 2015, Université Claude Bernard – Lyon I

 Cette thèse est consacrée à la modélisation qualitative des réseaux biologiques pour l'innovation thérapeutique. Elle étudie comment utiliser les réseaux Booléens, et comment les améliorer,… (more)

Subjects/Keywords: Réseau biologique; Réseau Booléen; Cible thérapeutique; Découverte de médicament; Attracteur; Anémie de Fanconi; Logique multivaluée; Logique floue; Biological network; Boolean network; Therapeutic target; Drug discovery; Attractor; Fanconi anemia; Multivalued logic; Fuzzy logic; 570.15

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APA (6th Edition):

Poret, A. (2015). Modélisation qualitative des réseaux biologiques pour l'innovation thérapeutique : Qualitative modeling of biological networks for therapeutic innovation. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2015LYO10090

Chicago Manual of Style (16th Edition):

Poret, Arnaud. “Modélisation qualitative des réseaux biologiques pour l'innovation thérapeutique : Qualitative modeling of biological networks for therapeutic innovation.” 2015. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed October 20, 2020. http://www.theses.fr/2015LYO10090.

MLA Handbook (7th Edition):

Poret, Arnaud. “Modélisation qualitative des réseaux biologiques pour l'innovation thérapeutique : Qualitative modeling of biological networks for therapeutic innovation.” 2015. Web. 20 Oct 2020.

Vancouver:

Poret A. Modélisation qualitative des réseaux biologiques pour l'innovation thérapeutique : Qualitative modeling of biological networks for therapeutic innovation. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2015. [cited 2020 Oct 20]. Available from: http://www.theses.fr/2015LYO10090.

Council of Science Editors:

Poret A. Modélisation qualitative des réseaux biologiques pour l'innovation thérapeutique : Qualitative modeling of biological networks for therapeutic innovation. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2015. Available from: http://www.theses.fr/2015LYO10090


Université Paris-Sud – Paris XI

17. Nguyen, Thuy Vy. Role for Fanconi anemia pathway in immunoglobulin diversification : Rôle de la voie FANC dans les processus de diversifications des immunoglobuline.

Degree: Docteur es, Biologie, 2013, Université Paris-Sud – Paris XI

Dans le but de reconnaitre et répondre de manière efficace à une très grande variétés d’agents pathogènes, les cellules B ont développé au cours des… (more)

Subjects/Keywords: Voie Anémie de Fanconi; Diversifications des immunoglobulines; Recombinaison V(D)J; Hypermutation somatiques (SHM); Changement de classe par recombinaison (CSR); Fanconi anemia pathway; Immunoglobulin diversification; V(D)J recombination; Somatic hypermutation (SHM); Class switch recombination (CSR)

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

APA (6th Edition):

Nguyen, T. V. (2013). Role for Fanconi anemia pathway in immunoglobulin diversification : Rôle de la voie FANC dans les processus de diversifications des immunoglobuline. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA112268

Chicago Manual of Style (16th Edition):

Nguyen, Thuy Vy. “Role for Fanconi anemia pathway in immunoglobulin diversification : Rôle de la voie FANC dans les processus de diversifications des immunoglobuline.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 20, 2020. http://www.theses.fr/2013PA112268.

MLA Handbook (7th Edition):

Nguyen, Thuy Vy. “Role for Fanconi anemia pathway in immunoglobulin diversification : Rôle de la voie FANC dans les processus de diversifications des immunoglobuline.” 2013. Web. 20 Oct 2020.

Vancouver:

Nguyen TV. Role for Fanconi anemia pathway in immunoglobulin diversification : Rôle de la voie FANC dans les processus de diversifications des immunoglobuline. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2020 Oct 20]. Available from: http://www.theses.fr/2013PA112268.

Council of Science Editors:

Nguyen TV. Role for Fanconi anemia pathway in immunoglobulin diversification : Rôle de la voie FANC dans les processus de diversifications des immunoglobuline. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA112268

18. Castellà Castellà, Maria. Análisis de la variabilidad genética de la anemia de Fanconi en España.

Degree: Departament de Genètica i de Microbiologia, 2009, Universitat Autònoma de Barcelona

Fanconi anemia (FA) is characterized by congenital malformations, bone marrow failure and predisposition to cancer. Bone marrow transplant is the only possible treatment to overcome… (more)

Subjects/Keywords: Mutaciones; Enfermedades raras; Anemia de Fanconi; Ciències Experimentals; 575

…desoxi-ribonucleico ARN Ácido ribonucleico AF Anemia de Fanconi BRCA del inglés… …1. GENERALIDADES SOBRE LA ANEMIA DE FANCONI La anemia de Fanconi (AF) fue… …hermanos que presentaban una variedad de anomalías congénitas, anemia severa, infecciones… …denominada Fanconi/Susceptibilidad al cáncer de mama (FA/BRCA). Así pues, hoy en día se… …fanconi/mutate/). Como ejemplo, para el gen FANCA se han registrado más de 350 mutaciones… 

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

APA (6th Edition):

Castellà Castellà, M. (2009). Análisis de la variabilidad genética de la anemia de Fanconi en España. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/3933

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):

Castellà Castellà, Maria. “Análisis de la variabilidad genética de la anemia de Fanconi en España.” 2009. Thesis, Universitat Autònoma de Barcelona. Accessed October 20, 2020. http://hdl.handle.net/10803/3933.

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

MLA Handbook (7th Edition):

Castellà Castellà, Maria. “Análisis de la variabilidad genética de la anemia de Fanconi en España.” 2009. Web. 20 Oct 2020.

Vancouver:

Castellà Castellà M. Análisis de la variabilidad genética de la anemia de Fanconi en España. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2009. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10803/3933.

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

Council of Science Editors:

Castellà Castellà M. Análisis de la variabilidad genética de la anemia de Fanconi en España. [Thesis]. Universitat Autònoma de Barcelona; 2009. Available from: http://hdl.handle.net/10803/3933

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


Universitat Pompeu Fabra

19. Rodríguez Pizà, Ignasi. Development of xenobiotic-free conditions towards the generation and propagation of clinically-safe human pluripotent stem cells.

Degree: Departament de Ciències Experimentals i de la Salut, 2010, Universitat Pompeu Fabra

 Human embryonic stem cells (hESC) and, more recently, induced pluripotent cells (iPSC) represent a new and unprecedented opportunity for the development of new therapeutic strategies… (more)

Subjects/Keywords: Ectoderm; induced pluripotent stem cells; Haematopoietic stem cells; Cardiomyocyte; Blastocyst; Fanconi's anemia; Xeno-biòtics; Transgens; Teratoma; rebuig immunitari; Queratinòcits; Mesoderm; Fibroblasts; Endoderm; Ectoderm; cèl·lules de pluripotència induïda; cèl·lules mare hematopoètiques; Cardiomiòcits; Blastocist; anemia de Fanconi; Endoderm; Fibroblasts; Mesoderm; Keratinocytes; Immunological rejection; Teratoma; Transgens; Xenobiotics; 576

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APA (6th Edition):

Rodríguez Pizà, I. (2010). Development of xenobiotic-free conditions towards the generation and propagation of clinically-safe human pluripotent stem cells. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/7227

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):

Rodríguez Pizà, Ignasi. “Development of xenobiotic-free conditions towards the generation and propagation of clinically-safe human pluripotent stem cells.” 2010. Thesis, Universitat Pompeu Fabra. Accessed October 20, 2020. http://hdl.handle.net/10803/7227.

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

MLA Handbook (7th Edition):

Rodríguez Pizà, Ignasi. “Development of xenobiotic-free conditions towards the generation and propagation of clinically-safe human pluripotent stem cells.” 2010. Web. 20 Oct 2020.

Vancouver:

Rodríguez Pizà I. Development of xenobiotic-free conditions towards the generation and propagation of clinically-safe human pluripotent stem cells. [Internet] [Thesis]. Universitat Pompeu Fabra; 2010. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10803/7227.

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

Council of Science Editors:

Rodríguez Pizà I. Development of xenobiotic-free conditions towards the generation and propagation of clinically-safe human pluripotent stem cells. [Thesis]. Universitat Pompeu Fabra; 2010. Available from: http://hdl.handle.net/10803/7227

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

.