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You searched for subject:(Mutations). Showing records 1 – 30 of 726 total matches.

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1. Magdoud, Hajer. Implication fonctionnelle de la protéine adaptatrice Lnk dans les cellules normales et pathologiques du lignage mégacaryocytaire : Functional application of the Lnk adaptor protein in normal and pathological megakaryopoiesis.

Degree: Docteur es, Biologie moléculaire et cellulaire, 2014, Paris 13

 L’adaptateur Lnk est un inhibiteur clé dans le système hématopoïétique. Son invalidation chez la souris entraîne l’hyperprolifération des lignages myéloïdes (mégacaryocytaire et érythoïde). Les cellules… (more)

Subjects/Keywords: Mutations de Lnk; Lnk mutations

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

APA (6th Edition):

Magdoud, H. (2014). Implication fonctionnelle de la protéine adaptatrice Lnk dans les cellules normales et pathologiques du lignage mégacaryocytaire : Functional application of the Lnk adaptor protein in normal and pathological megakaryopoiesis. (Doctoral Dissertation). Paris 13. Retrieved from http://www.theses.fr/2014PA132003

Chicago Manual of Style (16th Edition):

Magdoud, Hajer. “Implication fonctionnelle de la protéine adaptatrice Lnk dans les cellules normales et pathologiques du lignage mégacaryocytaire : Functional application of the Lnk adaptor protein in normal and pathological megakaryopoiesis.” 2014. Doctoral Dissertation, Paris 13. Accessed December 13, 2019. http://www.theses.fr/2014PA132003.

MLA Handbook (7th Edition):

Magdoud, Hajer. “Implication fonctionnelle de la protéine adaptatrice Lnk dans les cellules normales et pathologiques du lignage mégacaryocytaire : Functional application of the Lnk adaptor protein in normal and pathological megakaryopoiesis.” 2014. Web. 13 Dec 2019.

Vancouver:

Magdoud H. Implication fonctionnelle de la protéine adaptatrice Lnk dans les cellules normales et pathologiques du lignage mégacaryocytaire : Functional application of the Lnk adaptor protein in normal and pathological megakaryopoiesis. [Internet] [Doctoral dissertation]. Paris 13; 2014. [cited 2019 Dec 13]. Available from: http://www.theses.fr/2014PA132003.

Council of Science Editors:

Magdoud H. Implication fonctionnelle de la protéine adaptatrice Lnk dans les cellules normales et pathologiques du lignage mégacaryocytaire : Functional application of the Lnk adaptor protein in normal and pathological megakaryopoiesis. [Doctoral Dissertation]. Paris 13; 2014. Available from: http://www.theses.fr/2014PA132003

2. Karkanis, Dimitrios. Mutations économiques et démographiques en Chine : croissance ou développement ? : Economic and Demographic Mutations in China : Growth or Development?.

Degree: Docteur es, Sciences économiques et démographiques, 2016, Université Toulouse I – Capitole

Le processus de croissance économique de la Chine ces dernières décennies, tiré principalement par la dynamique du secteur des exportations, est accompagné par une croissance… (more)

Subjects/Keywords: Mutations démographiques - Chine; Mutations économiques - Chine

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APA (6th Edition):

Karkanis, D. (2016). Mutations économiques et démographiques en Chine : croissance ou développement ? : Economic and Demographic Mutations in China : Growth or Development?. (Doctoral Dissertation). Université Toulouse I – Capitole. Retrieved from http://www.theses.fr/2016TOU10017

Chicago Manual of Style (16th Edition):

Karkanis, Dimitrios. “Mutations économiques et démographiques en Chine : croissance ou développement ? : Economic and Demographic Mutations in China : Growth or Development?.” 2016. Doctoral Dissertation, Université Toulouse I – Capitole. Accessed December 13, 2019. http://www.theses.fr/2016TOU10017.

MLA Handbook (7th Edition):

Karkanis, Dimitrios. “Mutations économiques et démographiques en Chine : croissance ou développement ? : Economic and Demographic Mutations in China : Growth or Development?.” 2016. Web. 13 Dec 2019.

Vancouver:

Karkanis D. Mutations économiques et démographiques en Chine : croissance ou développement ? : Economic and Demographic Mutations in China : Growth or Development?. [Internet] [Doctoral dissertation]. Université Toulouse I – Capitole; 2016. [cited 2019 Dec 13]. Available from: http://www.theses.fr/2016TOU10017.

Council of Science Editors:

Karkanis D. Mutations économiques et démographiques en Chine : croissance ou développement ? : Economic and Demographic Mutations in China : Growth or Development?. [Doctoral Dissertation]. Université Toulouse I – Capitole; 2016. Available from: http://www.theses.fr/2016TOU10017


Wright State University

3. Alsaran, Hadel Mohammed. Functional characterization of cancer-related mutations of ERK3.

Degree: MS, Biochemistry and Molecular Biology, 2016, Wright State University

 Extracellular signal-regulated kinase 3 (ERK3) is an atypical member of the mitogen-activated protein kinase (MAPK) family. Recent studies have shown that ERK3 is highly upregulated… (more)

Subjects/Keywords: Biochemistry; ERK3; mutations

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APA (6th Edition):

Alsaran, H. M. (2016). Functional characterization of cancer-related mutations of ERK3. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1483791134536552

Chicago Manual of Style (16th Edition):

Alsaran, Hadel Mohammed. “Functional characterization of cancer-related mutations of ERK3.” 2016. Masters Thesis, Wright State University. Accessed December 13, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1483791134536552.

MLA Handbook (7th Edition):

Alsaran, Hadel Mohammed. “Functional characterization of cancer-related mutations of ERK3.” 2016. Web. 13 Dec 2019.

Vancouver:

Alsaran HM. Functional characterization of cancer-related mutations of ERK3. [Internet] [Masters thesis]. Wright State University; 2016. [cited 2019 Dec 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1483791134536552.

Council of Science Editors:

Alsaran HM. Functional characterization of cancer-related mutations of ERK3. [Masters Thesis]. Wright State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1483791134536552

4. Wells, Owen Spencer. Cellular and biochemical analyses of TDP1 mediated chromosomal break repair.

Degree: PhD, 2014, University of Sussex

 Tyrosyl DNA phosphodiesterase 1 (TDP1) is an end- rocessing enzyme involved in the repair of abortive topoisomerase I (Top1) complexes. Although not essential for survival,… (more)

Subjects/Keywords: 570; QH0460 Mutations

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APA (6th Edition):

Wells, O. S. (2014). Cellular and biochemical analyses of TDP1 mediated chromosomal break repair. (Doctoral Dissertation). University of Sussex. Retrieved from http://sro.sussex.ac.uk/id/eprint/49564/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618903

Chicago Manual of Style (16th Edition):

Wells, Owen Spencer. “Cellular and biochemical analyses of TDP1 mediated chromosomal break repair.” 2014. Doctoral Dissertation, University of Sussex. Accessed December 13, 2019. http://sro.sussex.ac.uk/id/eprint/49564/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618903.

MLA Handbook (7th Edition):

Wells, Owen Spencer. “Cellular and biochemical analyses of TDP1 mediated chromosomal break repair.” 2014. Web. 13 Dec 2019.

Vancouver:

Wells OS. Cellular and biochemical analyses of TDP1 mediated chromosomal break repair. [Internet] [Doctoral dissertation]. University of Sussex; 2014. [cited 2019 Dec 13]. Available from: http://sro.sussex.ac.uk/id/eprint/49564/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618903.

Council of Science Editors:

Wells OS. Cellular and biochemical analyses of TDP1 mediated chromosomal break repair. [Doctoral Dissertation]. University of Sussex; 2014. Available from: http://sro.sussex.ac.uk/id/eprint/49564/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618903


Queens University

5. Chan, Marina. Studies of the Misprocessing Mutations R1202D and E1204K in the Drug and Organic Anion Transporter, MRP1 (ABCC1) in Cultured HEK cells .

Degree: Pharmacology and Toxicology, 2013, Queens University

 Multidrug resistance protein 1 (MRP1) is a drug and organic anion transporter of the ATP-binding cassette superfamily. Previous studies showed that opposite charge substitutions of… (more)

Subjects/Keywords: Misprocessing Mutations; MRP1

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APA (6th Edition):

Chan, M. (2013). Studies of the Misprocessing Mutations R1202D and E1204K in the Drug and Organic Anion Transporter, MRP1 (ABCC1) in Cultured HEK cells . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8470

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):

Chan, Marina. “Studies of the Misprocessing Mutations R1202D and E1204K in the Drug and Organic Anion Transporter, MRP1 (ABCC1) in Cultured HEK cells .” 2013. Thesis, Queens University. Accessed December 13, 2019. http://hdl.handle.net/1974/8470.

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

MLA Handbook (7th Edition):

Chan, Marina. “Studies of the Misprocessing Mutations R1202D and E1204K in the Drug and Organic Anion Transporter, MRP1 (ABCC1) in Cultured HEK cells .” 2013. Web. 13 Dec 2019.

Vancouver:

Chan M. Studies of the Misprocessing Mutations R1202D and E1204K in the Drug and Organic Anion Transporter, MRP1 (ABCC1) in Cultured HEK cells . [Internet] [Thesis]. Queens University; 2013. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/1974/8470.

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

Council of Science Editors:

Chan M. Studies of the Misprocessing Mutations R1202D and E1204K in the Drug and Organic Anion Transporter, MRP1 (ABCC1) in Cultured HEK cells . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/8470

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


University of Saskatchewan

6. MacAusland-Berg, Josh 1993-. FRK cancer-related mutations: Effect on enzymatic activity and cellular processes.

Degree: 2019, University of Saskatchewan

 Cancer-associated FRK mutations have not been thoroughly studied however, a previous study analyzed six cancer related mutations of BRK L16F, R131L, V253M, N317S, L343F, P450L;… (more)

Subjects/Keywords: Cancer associated mutations

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APA (6th Edition):

MacAusland-Berg, J. 1. (2019). FRK cancer-related mutations: Effect on enzymatic activity and cellular processes. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12357

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):

MacAusland-Berg, Josh 1993-. “FRK cancer-related mutations: Effect on enzymatic activity and cellular processes.” 2019. Thesis, University of Saskatchewan. Accessed December 13, 2019. http://hdl.handle.net/10388/12357.

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

MLA Handbook (7th Edition):

MacAusland-Berg, Josh 1993-. “FRK cancer-related mutations: Effect on enzymatic activity and cellular processes.” 2019. Web. 13 Dec 2019.

Vancouver:

MacAusland-Berg J1. FRK cancer-related mutations: Effect on enzymatic activity and cellular processes. [Internet] [Thesis]. University of Saskatchewan; 2019. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10388/12357.

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

Council of Science Editors:

MacAusland-Berg J1. FRK cancer-related mutations: Effect on enzymatic activity and cellular processes. [Thesis]. University of Saskatchewan; 2019. Available from: http://hdl.handle.net/10388/12357

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

7. Birgy, André. Paysage adaptatif des bêta-lactamases TEM-1 et CTX-M-15 : Adaptative landscape of beta-lactamases TEM-1 and CTX-M-15.

Degree: Docteur es, Sciences de la vie et de la santé. Microbiologie, 2017, Sorbonne Paris Cité

De part leur importance médicale, leur capacité à évoluer et leur facilité de manipulations, les bêta-lactamases TEM-1 et plus récemment CTX-M-15, se sont imposées comme… (more)

Subjects/Keywords: Mutations compensatrices; Distribution de l'effet des mutations; Compensatory mutations; Distribution of the effect of mutations

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APA (6th Edition):

Birgy, A. (2017). Paysage adaptatif des bêta-lactamases TEM-1 et CTX-M-15 : Adaptative landscape of beta-lactamases TEM-1 and CTX-M-15. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2017USPCC261

Chicago Manual of Style (16th Edition):

Birgy, André. “Paysage adaptatif des bêta-lactamases TEM-1 et CTX-M-15 : Adaptative landscape of beta-lactamases TEM-1 and CTX-M-15.” 2017. Doctoral Dissertation, Sorbonne Paris Cité. Accessed December 13, 2019. http://www.theses.fr/2017USPCC261.

MLA Handbook (7th Edition):

Birgy, André. “Paysage adaptatif des bêta-lactamases TEM-1 et CTX-M-15 : Adaptative landscape of beta-lactamases TEM-1 and CTX-M-15.” 2017. Web. 13 Dec 2019.

Vancouver:

Birgy A. Paysage adaptatif des bêta-lactamases TEM-1 et CTX-M-15 : Adaptative landscape of beta-lactamases TEM-1 and CTX-M-15. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2017. [cited 2019 Dec 13]. Available from: http://www.theses.fr/2017USPCC261.

Council of Science Editors:

Birgy A. Paysage adaptatif des bêta-lactamases TEM-1 et CTX-M-15 : Adaptative landscape of beta-lactamases TEM-1 and CTX-M-15. [Doctoral Dissertation]. Sorbonne Paris Cité; 2017. Available from: http://www.theses.fr/2017USPCC261


University of Utah

8. Szerlong, Heather. The nuclear actin-related proteins, Arp7 and Arp9: connecting ARP hetertodimerization to the regulation of chromatin remodling.

Degree: PhD, Oncological Sciences;, 2004, University of Utah

 Actin-related proteins (ARPs) belong to the actin superfamily of proteins with diverse functions in both the cytoplasm and the nucleus. ARPs share limited sequence similarity… (more)

Subjects/Keywords: Purification; Mutations

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APA (6th Edition):

Szerlong, H. (2004). The nuclear actin-related proteins, Arp7 and Arp9: connecting ARP hetertodimerization to the regulation of chromatin remodling. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1999/rec/1197

Chicago Manual of Style (16th Edition):

Szerlong, Heather. “The nuclear actin-related proteins, Arp7 and Arp9: connecting ARP hetertodimerization to the regulation of chromatin remodling.” 2004. Doctoral Dissertation, University of Utah. Accessed December 13, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1999/rec/1197.

MLA Handbook (7th Edition):

Szerlong, Heather. “The nuclear actin-related proteins, Arp7 and Arp9: connecting ARP hetertodimerization to the regulation of chromatin remodling.” 2004. Web. 13 Dec 2019.

Vancouver:

Szerlong H. The nuclear actin-related proteins, Arp7 and Arp9: connecting ARP hetertodimerization to the regulation of chromatin remodling. [Internet] [Doctoral dissertation]. University of Utah; 2004. [cited 2019 Dec 13]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1999/rec/1197.

Council of Science Editors:

Szerlong H. The nuclear actin-related proteins, Arp7 and Arp9: connecting ARP hetertodimerization to the regulation of chromatin remodling. [Doctoral Dissertation]. University of Utah; 2004. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1999/rec/1197


University of Utah

9. Zhang, Jie. Myotonia congenita-associated chloride channelopathies: mutations, function, and structure.

Degree: PhD, Neurology;, 1999, University of Utah

 Myotonia Congenita (MC) is a genetic muscle disorder manifesting myotonia, a delayed relaxation of muscle after contraction. MC includes two inherited forms: autosomal dominant myotonia… (more)

Subjects/Keywords: Physiology; Mutations

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APA (6th Edition):

Zhang, J. (1999). Myotonia congenita-associated chloride channelopathies: mutations, function, and structure. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1478/rec/799

Chicago Manual of Style (16th Edition):

Zhang, Jie. “Myotonia congenita-associated chloride channelopathies: mutations, function, and structure.” 1999. Doctoral Dissertation, University of Utah. Accessed December 13, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1478/rec/799.

MLA Handbook (7th Edition):

Zhang, Jie. “Myotonia congenita-associated chloride channelopathies: mutations, function, and structure.” 1999. Web. 13 Dec 2019.

Vancouver:

Zhang J. Myotonia congenita-associated chloride channelopathies: mutations, function, and structure. [Internet] [Doctoral dissertation]. University of Utah; 1999. [cited 2019 Dec 13]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1478/rec/799.

Council of Science Editors:

Zhang J. Myotonia congenita-associated chloride channelopathies: mutations, function, and structure. [Doctoral Dissertation]. University of Utah; 1999. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1478/rec/799


Louisiana State University

10. Rahman, Sheikh Arafatur. Role of Histone H4 Mutations in DNA Repair Pathways.

Degree: MS, Medicine and Health Sciences, 2016, Louisiana State University

 Histone H3K79 methylation has been shown to play roles in different DNA repair pathways. Histone H4 residues serine 64 to threonine 80 surround histone H3K79… (more)

Subjects/Keywords: Histone H4 Mutations; DNA Repair

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APA (6th Edition):

Rahman, S. A. (2016). Role of Histone H4 Mutations in DNA Repair Pathways. (Masters Thesis). Louisiana State University. Retrieved from etd-07112016-153156 ; https://digitalcommons.lsu.edu/gradschool_theses/1565

Chicago Manual of Style (16th Edition):

Rahman, Sheikh Arafatur. “Role of Histone H4 Mutations in DNA Repair Pathways.” 2016. Masters Thesis, Louisiana State University. Accessed December 13, 2019. etd-07112016-153156 ; https://digitalcommons.lsu.edu/gradschool_theses/1565.

MLA Handbook (7th Edition):

Rahman, Sheikh Arafatur. “Role of Histone H4 Mutations in DNA Repair Pathways.” 2016. Web. 13 Dec 2019.

Vancouver:

Rahman SA. Role of Histone H4 Mutations in DNA Repair Pathways. [Internet] [Masters thesis]. Louisiana State University; 2016. [cited 2019 Dec 13]. Available from: etd-07112016-153156 ; https://digitalcommons.lsu.edu/gradschool_theses/1565.

Council of Science Editors:

Rahman SA. Role of Histone H4 Mutations in DNA Repair Pathways. [Masters Thesis]. Louisiana State University; 2016. Available from: etd-07112016-153156 ; https://digitalcommons.lsu.edu/gradschool_theses/1565


University of Cambridge

11. GARG, SUMEDHA. Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal.

Degree: 2019, University of Cambridge

 Primary aldosteronism (PA) accounts for 5-10% of all hypertension. One of the major causes of PA is sporadic formation of aldosterone-producing adenomas (APAs). These benign… (more)

Subjects/Keywords: aldosterone; adenoma; somatic mutations; hypertension

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APA (6th Edition):

GARG, S. (2019). Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal. (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/289390

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):

GARG, SUMEDHA. “Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal. ” 2019. Thesis, University of Cambridge. Accessed December 13, 2019. https://www.repository.cam.ac.uk/handle/1810/289390.

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

MLA Handbook (7th Edition):

GARG, SUMEDHA. “Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal. ” 2019. Web. 13 Dec 2019.

Vancouver:

GARG S. Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal. [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Dec 13]. Available from: https://www.repository.cam.ac.uk/handle/1810/289390.

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

Council of Science Editors:

GARG S. Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal. [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/289390

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


University of Houston

12. Peng, Fen 1988-. Genetic Background and Environment Influence the Effects of Mutations in pykF and Help Reveal Mechanisms Underlying Their Benefit.

Degree: Biology and Biochemistry, Department of, 2015, University of Houston

 Resolving the relationship between genotypic and their effects remains a central challenge in the study of adaptation. Although parallel mutations, a signature of adaptation, have… (more)

Subjects/Keywords: parallel mutations; pyruvate kinase; epistasis

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APA (6th Edition):

Peng, F. 1. (2015). Genetic Background and Environment Influence the Effects of Mutations in pykF and Help Reveal Mechanisms Underlying Their Benefit. (Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/1978

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):

Peng, Fen 1988-. “Genetic Background and Environment Influence the Effects of Mutations in pykF and Help Reveal Mechanisms Underlying Their Benefit.” 2015. Thesis, University of Houston. Accessed December 13, 2019. http://hdl.handle.net/10657/1978.

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

MLA Handbook (7th Edition):

Peng, Fen 1988-. “Genetic Background and Environment Influence the Effects of Mutations in pykF and Help Reveal Mechanisms Underlying Their Benefit.” 2015. Web. 13 Dec 2019.

Vancouver:

Peng F1. Genetic Background and Environment Influence the Effects of Mutations in pykF and Help Reveal Mechanisms Underlying Their Benefit. [Internet] [Thesis]. University of Houston; 2015. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10657/1978.

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

Council of Science Editors:

Peng F1. Genetic Background and Environment Influence the Effects of Mutations in pykF and Help Reveal Mechanisms Underlying Their Benefit. [Thesis]. University of Houston; 2015. Available from: http://hdl.handle.net/10657/1978

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


University of Illinois – Urbana-Champaign

13. Hou, Jack Pu. DawnRank: discovering personalized driver genes in cancer.

Degree: MS, Bioengineering, 2016, University of Illinois – Urbana-Champaign

 Large-scale cancer genomic studies have revealed that the genetic heterogeneity of the same type of cancer is greater than previously thought. A key question in… (more)

Subjects/Keywords: Computational Biology; Detection; Cancer; Mutations

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APA (6th Edition):

Hou, J. P. (2016). DawnRank: discovering personalized driver genes in cancer. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95431

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):

Hou, Jack Pu. “DawnRank: discovering personalized driver genes in cancer.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed December 13, 2019. http://hdl.handle.net/2142/95431.

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

MLA Handbook (7th Edition):

Hou, Jack Pu. “DawnRank: discovering personalized driver genes in cancer.” 2016. Web. 13 Dec 2019.

Vancouver:

Hou JP. DawnRank: discovering personalized driver genes in cancer. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/2142/95431.

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

Council of Science Editors:

Hou JP. DawnRank: discovering personalized driver genes in cancer. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95431

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


University of Cambridge

14. Garg, Sumedha. Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal.

Degree: PhD, 2019, University of Cambridge

 Primary aldosteronism (PA) accounts for 5-10% of all hypertension. One of the major causes of PA is sporadic formation of aldosterone-producing adenomas (APAs). These benign… (more)

Subjects/Keywords: aldosterone; adenoma; somatic mutations; hypertension

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APA (6th Edition):

Garg, S. (2019). Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/289390 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767736

Chicago Manual of Style (16th Edition):

Garg, Sumedha. “Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal.” 2019. Doctoral Dissertation, University of Cambridge. Accessed December 13, 2019. https://www.repository.cam.ac.uk/handle/1810/289390 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767736.

MLA Handbook (7th Edition):

Garg, Sumedha. “Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal.” 2019. Web. 13 Dec 2019.

Vancouver:

Garg S. Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2019 Dec 13]. Available from: https://www.repository.cam.ac.uk/handle/1810/289390 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767736.

Council of Science Editors:

Garg S. Role of two genes, CACNA1D and CADM1, with common or rare mutations in aldosterone producing adenomas of the adrenal. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/289390 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767736


Queens University

15. Davis, Jordan. Intragenic Rescue of the Function of Long QT Syndrome-Causing Mutant hERG K+ Channels .

Degree: Biomedical and Molecular Sciences, Queens University

 The human-ether-a-go-go-related gene (hERG) encodes the pore forming subunit of the rapidly activating delayed rectifier K+ channel (IKr), which is important for the repolarization phase… (more)

Subjects/Keywords: hERG; Mutations

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APA (6th Edition):

Davis, J. (n.d.). Intragenic Rescue of the Function of Long QT Syndrome-Causing Mutant hERG K+ Channels . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/24476

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):

Davis, Jordan. “Intragenic Rescue of the Function of Long QT Syndrome-Causing Mutant hERG K+ Channels .” Thesis, Queens University. Accessed December 13, 2019. http://hdl.handle.net/1974/24476.

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):

Davis, Jordan. “Intragenic Rescue of the Function of Long QT Syndrome-Causing Mutant hERG K+ Channels .” Web. 13 Dec 2019.

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

Vancouver:

Davis J. Intragenic Rescue of the Function of Long QT Syndrome-Causing Mutant hERG K+ Channels . [Internet] [Thesis]. Queens University; [cited 2019 Dec 13]. Available from: http://hdl.handle.net/1974/24476.

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:

Davis J. Intragenic Rescue of the Function of Long QT Syndrome-Causing Mutant hERG K+ Channels . [Thesis]. Queens University; Available from: http://hdl.handle.net/1974/24476

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


University College London (University of London)

16. Ahmed, Suhaib. An approach for the prevention of thalassaemia in Pakistan.

Degree: PhD, 1998, University College London (University of London)

 The basic aim of this thesis was to identify a suitable approach for prevention of thalassaemia in Pakistan. The overall carrier rate for β-thalassaemia was… (more)

Subjects/Keywords: 610; Mutations

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APA (6th Edition):

Ahmed, S. (1998). An approach for the prevention of thalassaemia in Pakistan. (Doctoral Dissertation). University College London (University of London). Retrieved from https://discovery.ucl.ac.uk/id/1317916/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299931

Chicago Manual of Style (16th Edition):

Ahmed, Suhaib. “An approach for the prevention of thalassaemia in Pakistan.” 1998. Doctoral Dissertation, University College London (University of London). Accessed December 13, 2019. https://discovery.ucl.ac.uk/id/1317916/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299931.

MLA Handbook (7th Edition):

Ahmed, Suhaib. “An approach for the prevention of thalassaemia in Pakistan.” 1998. Web. 13 Dec 2019.

Vancouver:

Ahmed S. An approach for the prevention of thalassaemia in Pakistan. [Internet] [Doctoral dissertation]. University College London (University of London); 1998. [cited 2019 Dec 13]. Available from: https://discovery.ucl.ac.uk/id/1317916/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299931.

Council of Science Editors:

Ahmed S. An approach for the prevention of thalassaemia in Pakistan. [Doctoral Dissertation]. University College London (University of London); 1998. Available from: https://discovery.ucl.ac.uk/id/1317916/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299931


University of Edinburgh

17. Novo, Sonia Marisa. Use of an ex vivo model of human colorectal tumours to study response to the MEK1/2 inhibitor AZD6244.

Degree: PhD, 2013, University of Edinburgh

 Colorectal cancer is the second most common cause of cancer death in Western Europe and North America. Current therapies are largely ineffective and are associated… (more)

Subjects/Keywords: 616.99; MEK1/2; MAPK pathway; KRAS mutations; BRAF mutations; proliferation; apoptosis

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APA (6th Edition):

Novo, S. M. (2013). Use of an ex vivo model of human colorectal tumours to study response to the MEK1/2 inhibitor AZD6244. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/11778

Chicago Manual of Style (16th Edition):

Novo, Sonia Marisa. “Use of an ex vivo model of human colorectal tumours to study response to the MEK1/2 inhibitor AZD6244.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed December 13, 2019. http://hdl.handle.net/1842/11778.

MLA Handbook (7th Edition):

Novo, Sonia Marisa. “Use of an ex vivo model of human colorectal tumours to study response to the MEK1/2 inhibitor AZD6244.” 2013. Web. 13 Dec 2019.

Vancouver:

Novo SM. Use of an ex vivo model of human colorectal tumours to study response to the MEK1/2 inhibitor AZD6244. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/1842/11778.

Council of Science Editors:

Novo SM. Use of an ex vivo model of human colorectal tumours to study response to the MEK1/2 inhibitor AZD6244. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/11778

18. Amamou, Leila. A la recherche d'une nouvelle identité artistique transnationale dans les spots publicitaires tunisiens (1994-2007) : oscillation entre esthétique de l'image et efficacité de la communication : In search of a new transnational artistic identity in tunisian advertising spots (1994-2007) : oscillation between aesthetic image and effective communication.

Degree: Docteur es, Arts et sciences de l'art, 2013, Paris 1

L'objectif de cette thèse est de montrer comment les créateurs des spots publicitaires en Tunisie de 1994 jusqu'à 2007 ont cherché à créer une nouvelle… (more)

Subjects/Keywords: Identité artistique; Tunisie; Mutations culturelles; Artistic identity; Tunisia; Cultural mutations; 730

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APA (6th Edition):

Amamou, L. (2013). A la recherche d'une nouvelle identité artistique transnationale dans les spots publicitaires tunisiens (1994-2007) : oscillation entre esthétique de l'image et efficacité de la communication : In search of a new transnational artistic identity in tunisian advertising spots (1994-2007) : oscillation between aesthetic image and effective communication. (Doctoral Dissertation). Paris 1. Retrieved from http://www.theses.fr/2013PA010625

Chicago Manual of Style (16th Edition):

Amamou, Leila. “A la recherche d'une nouvelle identité artistique transnationale dans les spots publicitaires tunisiens (1994-2007) : oscillation entre esthétique de l'image et efficacité de la communication : In search of a new transnational artistic identity in tunisian advertising spots (1994-2007) : oscillation between aesthetic image and effective communication.” 2013. Doctoral Dissertation, Paris 1. Accessed December 13, 2019. http://www.theses.fr/2013PA010625.

MLA Handbook (7th Edition):

Amamou, Leila. “A la recherche d'une nouvelle identité artistique transnationale dans les spots publicitaires tunisiens (1994-2007) : oscillation entre esthétique de l'image et efficacité de la communication : In search of a new transnational artistic identity in tunisian advertising spots (1994-2007) : oscillation between aesthetic image and effective communication.” 2013. Web. 13 Dec 2019.

Vancouver:

Amamou L. A la recherche d'une nouvelle identité artistique transnationale dans les spots publicitaires tunisiens (1994-2007) : oscillation entre esthétique de l'image et efficacité de la communication : In search of a new transnational artistic identity in tunisian advertising spots (1994-2007) : oscillation between aesthetic image and effective communication. [Internet] [Doctoral dissertation]. Paris 1; 2013. [cited 2019 Dec 13]. Available from: http://www.theses.fr/2013PA010625.

Council of Science Editors:

Amamou L. A la recherche d'une nouvelle identité artistique transnationale dans les spots publicitaires tunisiens (1994-2007) : oscillation entre esthétique de l'image et efficacité de la communication : In search of a new transnational artistic identity in tunisian advertising spots (1994-2007) : oscillation between aesthetic image and effective communication. [Doctoral Dissertation]. Paris 1; 2013. Available from: http://www.theses.fr/2013PA010625

19. Bousard, Aurélie. Etude génétique et épigénétique de l'adénocarcinome du rein à cellules claires : Genetic and epigenetic study of clear cell renal cell carcinoma.

Degree: Docteur es, Génétique et Epigénétique, 2015, Evry-Val d'Essonne

Ce travail de thèse comporte trois projets visant à approfondir la caractérisation moléculaire des adénocarcinomes du rein à cellules claires (ccRCC) et à en améliorer… (more)

Subjects/Keywords: Mutations de l'ADN non-codant; Mutations de l'ADN non-codant

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APA (6th Edition):

Bousard, A. (2015). Etude génétique et épigénétique de l'adénocarcinome du rein à cellules claires : Genetic and epigenetic study of clear cell renal cell carcinoma. (Doctoral Dissertation). Evry-Val d'Essonne. Retrieved from http://www.theses.fr/2015EVRY0004

Chicago Manual of Style (16th Edition):

Bousard, Aurélie. “Etude génétique et épigénétique de l'adénocarcinome du rein à cellules claires : Genetic and epigenetic study of clear cell renal cell carcinoma.” 2015. Doctoral Dissertation, Evry-Val d'Essonne. Accessed December 13, 2019. http://www.theses.fr/2015EVRY0004.

MLA Handbook (7th Edition):

Bousard, Aurélie. “Etude génétique et épigénétique de l'adénocarcinome du rein à cellules claires : Genetic and epigenetic study of clear cell renal cell carcinoma.” 2015. Web. 13 Dec 2019.

Vancouver:

Bousard A. Etude génétique et épigénétique de l'adénocarcinome du rein à cellules claires : Genetic and epigenetic study of clear cell renal cell carcinoma. [Internet] [Doctoral dissertation]. Evry-Val d'Essonne; 2015. [cited 2019 Dec 13]. Available from: http://www.theses.fr/2015EVRY0004.

Council of Science Editors:

Bousard A. Etude génétique et épigénétique de l'adénocarcinome du rein à cellules claires : Genetic and epigenetic study of clear cell renal cell carcinoma. [Doctoral Dissertation]. Evry-Val d'Essonne; 2015. Available from: http://www.theses.fr/2015EVRY0004

20. Crahé, Maxime-Morvan. Le breton de Languidic : étude phonétique, morphologique et syntaxique d'un sous-dialecte du breton vannetais : The Breton Micro-dialect of Languidic : a phonetical, morphlogical and syntaxic study of a variety of the Breton Vannetais.

Degree: Docteur es, Breton et celtique, 2013, Rennes 2

Cette étude apporte un nouveau corpus à la description du paysage linguistique de Basse-Bretagne et participe de ce fait à une meilleure connaissance de la… (more)

Subjects/Keywords: Oralite; Dialectologie; Mutations consonantiques; Orality; Dialectology; Consonant mutations; 491.6

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APA (6th Edition):

Crahé, M. (2013). Le breton de Languidic : étude phonétique, morphologique et syntaxique d'un sous-dialecte du breton vannetais : The Breton Micro-dialect of Languidic : a phonetical, morphlogical and syntaxic study of a variety of the Breton Vannetais. (Doctoral Dissertation). Rennes 2. Retrieved from http://www.theses.fr/2013REN20062

Chicago Manual of Style (16th Edition):

Crahé, Maxime-Morvan. “Le breton de Languidic : étude phonétique, morphologique et syntaxique d'un sous-dialecte du breton vannetais : The Breton Micro-dialect of Languidic : a phonetical, morphlogical and syntaxic study of a variety of the Breton Vannetais.” 2013. Doctoral Dissertation, Rennes 2. Accessed December 13, 2019. http://www.theses.fr/2013REN20062.

MLA Handbook (7th Edition):

Crahé, Maxime-Morvan. “Le breton de Languidic : étude phonétique, morphologique et syntaxique d'un sous-dialecte du breton vannetais : The Breton Micro-dialect of Languidic : a phonetical, morphlogical and syntaxic study of a variety of the Breton Vannetais.” 2013. Web. 13 Dec 2019.

Vancouver:

Crahé M. Le breton de Languidic : étude phonétique, morphologique et syntaxique d'un sous-dialecte du breton vannetais : The Breton Micro-dialect of Languidic : a phonetical, morphlogical and syntaxic study of a variety of the Breton Vannetais. [Internet] [Doctoral dissertation]. Rennes 2; 2013. [cited 2019 Dec 13]. Available from: http://www.theses.fr/2013REN20062.

Council of Science Editors:

Crahé M. Le breton de Languidic : étude phonétique, morphologique et syntaxique d'un sous-dialecte du breton vannetais : The Breton Micro-dialect of Languidic : a phonetical, morphlogical and syntaxic study of a variety of the Breton Vannetais. [Doctoral Dissertation]. Rennes 2; 2013. Available from: http://www.theses.fr/2013REN20062

21. Michot, Pauline. Utilisation des séquences de génome complet pour l'identification de mutations délétères responsables d'anomalies génétiques récessives chez le bovin. : Use of whole genome sequence data to identify new deleterious mutations associated to genetic defects in French dairy and beef cattle breeds.

Degree: Docteur es, Génétique animale, 2017, Paris Saclay

L’effectif génétique réduit des races bovines entraîne une augmentation de consanguinité de l’ordre de 1% par génération et une forte dérive génétique. Cette évolution favorise… (more)

Subjects/Keywords: Génomique; Mutations délétères; Anomalies; Bovins; Genomic; Deleterious mutations; Anomalies; Bovine; 576

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APA (6th Edition):

Michot, P. (2017). Utilisation des séquences de génome complet pour l'identification de mutations délétères responsables d'anomalies génétiques récessives chez le bovin. : Use of whole genome sequence data to identify new deleterious mutations associated to genetic defects in French dairy and beef cattle breeds. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2017SACLA011

Chicago Manual of Style (16th Edition):

Michot, Pauline. “Utilisation des séquences de génome complet pour l'identification de mutations délétères responsables d'anomalies génétiques récessives chez le bovin. : Use of whole genome sequence data to identify new deleterious mutations associated to genetic defects in French dairy and beef cattle breeds.” 2017. Doctoral Dissertation, Paris Saclay. Accessed December 13, 2019. http://www.theses.fr/2017SACLA011.

MLA Handbook (7th Edition):

Michot, Pauline. “Utilisation des séquences de génome complet pour l'identification de mutations délétères responsables d'anomalies génétiques récessives chez le bovin. : Use of whole genome sequence data to identify new deleterious mutations associated to genetic defects in French dairy and beef cattle breeds.” 2017. Web. 13 Dec 2019.

Vancouver:

Michot P. Utilisation des séquences de génome complet pour l'identification de mutations délétères responsables d'anomalies génétiques récessives chez le bovin. : Use of whole genome sequence data to identify new deleterious mutations associated to genetic defects in French dairy and beef cattle breeds. [Internet] [Doctoral dissertation]. Paris Saclay; 2017. [cited 2019 Dec 13]. Available from: http://www.theses.fr/2017SACLA011.

Council of Science Editors:

Michot P. Utilisation des séquences de génome complet pour l'identification de mutations délétères responsables d'anomalies génétiques récessives chez le bovin. : Use of whole genome sequence data to identify new deleterious mutations associated to genetic defects in French dairy and beef cattle breeds. [Doctoral Dissertation]. Paris Saclay; 2017. Available from: http://www.theses.fr/2017SACLA011

22. Krasovec, Marc. Estimation des taux de mutation : implications pour la diversification et l'évolution du phytoplancton eucaryote : Estimation of mutation rates : implications for diversification and evolution of eukaryotic phytoplankton.

Degree: Docteur es, Evolution moléculaire, 2016, Université Pierre et Marie Curie – Paris VI

Les mutations sont la principale source de diversité sur laquelle agit la sélection pour permettre aux espèces de s'adapter. Les études de l'effet des mutations(more)

Subjects/Keywords: Taux de mutation; Phytoplancton; Fitness; Mutations spontanées; Accumulation de mutations; Evolution eucaryote; Mutation rate; Spontaneous mutations; Eucaryote evolution; 579.8

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APA (6th Edition):

Krasovec, M. (2016). Estimation des taux de mutation : implications pour la diversification et l'évolution du phytoplancton eucaryote : Estimation of mutation rates : implications for diversification and evolution of eukaryotic phytoplankton. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066371

Chicago Manual of Style (16th Edition):

Krasovec, Marc. “Estimation des taux de mutation : implications pour la diversification et l'évolution du phytoplancton eucaryote : Estimation of mutation rates : implications for diversification and evolution of eukaryotic phytoplankton.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed December 13, 2019. http://www.theses.fr/2016PA066371.

MLA Handbook (7th Edition):

Krasovec, Marc. “Estimation des taux de mutation : implications pour la diversification et l'évolution du phytoplancton eucaryote : Estimation of mutation rates : implications for diversification and evolution of eukaryotic phytoplankton.” 2016. Web. 13 Dec 2019.

Vancouver:

Krasovec M. Estimation des taux de mutation : implications pour la diversification et l'évolution du phytoplancton eucaryote : Estimation of mutation rates : implications for diversification and evolution of eukaryotic phytoplankton. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2019 Dec 13]. Available from: http://www.theses.fr/2016PA066371.

Council of Science Editors:

Krasovec M. Estimation des taux de mutation : implications pour la diversification et l'évolution du phytoplancton eucaryote : Estimation of mutation rates : implications for diversification and evolution of eukaryotic phytoplankton. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066371


University of Utah

23. Pyne, Michael Terry. Characterization of intronic variants in BRCA1 and BRCA2;.

Degree: MS;, Pathology;, 2000, University of Utah

 Approximately 10% of American women develop breast cancer during their lifetimes. Of the cases of breast cancer, about 10% are attributed to a genetic trait;… (more)

Subjects/Keywords: Breast Cancer; Mutations

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APA (6th Edition):

Pyne, M. T. (2000). Characterization of intronic variants in BRCA1 and BRCA2;. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/880/rec/144

Chicago Manual of Style (16th Edition):

Pyne, Michael Terry. “Characterization of intronic variants in BRCA1 and BRCA2;.” 2000. Masters Thesis, University of Utah. Accessed December 13, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/880/rec/144.

MLA Handbook (7th Edition):

Pyne, Michael Terry. “Characterization of intronic variants in BRCA1 and BRCA2;.” 2000. Web. 13 Dec 2019.

Vancouver:

Pyne MT. Characterization of intronic variants in BRCA1 and BRCA2;. [Internet] [Masters thesis]. University of Utah; 2000. [cited 2019 Dec 13]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/880/rec/144.

Council of Science Editors:

Pyne MT. Characterization of intronic variants in BRCA1 and BRCA2;. [Masters Thesis]. University of Utah; 2000. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/880/rec/144


University of Utah

24. Li, Xinghai. The role of protein phosphatase 2A in regulating Wnt signaling and apoptosis;.

Degree: PhD, Oncological Sciences;, 2001, University of Utah

 Protein phosphatase 2A (PP2A) is a major serine/threonine-specific phosphatase and regulates a significant array of cellular events. This dissertation primarily describes the novel role of… (more)

Subjects/Keywords: Gene Mutations; Neuroblastoma

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APA (6th Edition):

Li, X. (2001). The role of protein phosphatase 2A in regulating Wnt signaling and apoptosis;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1157/rec/1387

Chicago Manual of Style (16th Edition):

Li, Xinghai. “The role of protein phosphatase 2A in regulating Wnt signaling and apoptosis;.” 2001. Doctoral Dissertation, University of Utah. Accessed December 13, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1157/rec/1387.

MLA Handbook (7th Edition):

Li, Xinghai. “The role of protein phosphatase 2A in regulating Wnt signaling and apoptosis;.” 2001. Web. 13 Dec 2019.

Vancouver:

Li X. The role of protein phosphatase 2A in regulating Wnt signaling and apoptosis;. [Internet] [Doctoral dissertation]. University of Utah; 2001. [cited 2019 Dec 13]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1157/rec/1387.

Council of Science Editors:

Li X. The role of protein phosphatase 2A in regulating Wnt signaling and apoptosis;. [Doctoral Dissertation]. University of Utah; 2001. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1157/rec/1387


University of Utah

25. Dohrmann, Paul Richard. Transcriptional regulation by the ACE2 and SWI5 activators in yeast;.

Degree: PhD, Pathology;, 1994, University of Utah

 Two independent transcriptional pathways regulated by the ACE2 and SWI5 genes have been identified in the yeast Saccharomyces cerevisiae. The CTSl and the HO pathways… (more)

Subjects/Keywords: Genetics; Mutations; RNA

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APA (6th Edition):

Dohrmann, P. R. (1994). Transcriptional regulation by the ACE2 and SWI5 activators in yeast;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1343/rec/1416

Chicago Manual of Style (16th Edition):

Dohrmann, Paul Richard. “Transcriptional regulation by the ACE2 and SWI5 activators in yeast;.” 1994. Doctoral Dissertation, University of Utah. Accessed December 13, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1343/rec/1416.

MLA Handbook (7th Edition):

Dohrmann, Paul Richard. “Transcriptional regulation by the ACE2 and SWI5 activators in yeast;.” 1994. Web. 13 Dec 2019.

Vancouver:

Dohrmann PR. Transcriptional regulation by the ACE2 and SWI5 activators in yeast;. [Internet] [Doctoral dissertation]. University of Utah; 1994. [cited 2019 Dec 13]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1343/rec/1416.

Council of Science Editors:

Dohrmann PR. Transcriptional regulation by the ACE2 and SWI5 activators in yeast;. [Doctoral Dissertation]. University of Utah; 1994. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1343/rec/1416

26. Maddaly Ravi. Analysis of somatic cell mutations at the Glycophorina locus in human erythrocytes.

Degree: Human Genetics, 2001, Sri Ramachandra University

Introduction: Dose evaluation of exposed humans to radiation becomes necessary after exposure. Such a dose evaluation can be done by biological dosimetric methods of which… (more)

Subjects/Keywords: Glycophorina; Human erythrocytes; Somatic cell mutations

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APA (6th Edition):

Ravi, M. (2001). Analysis of somatic cell mutations at the Glycophorina locus in human erythrocytes. (Thesis). Sri Ramachandra University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/17910

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):

Ravi, Maddaly. “Analysis of somatic cell mutations at the Glycophorina locus in human erythrocytes.” 2001. Thesis, Sri Ramachandra University. Accessed December 13, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/17910.

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

MLA Handbook (7th Edition):

Ravi, Maddaly. “Analysis of somatic cell mutations at the Glycophorina locus in human erythrocytes.” 2001. Web. 13 Dec 2019.

Vancouver:

Ravi M. Analysis of somatic cell mutations at the Glycophorina locus in human erythrocytes. [Internet] [Thesis]. Sri Ramachandra University; 2001. [cited 2019 Dec 13]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/17910.

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

Council of Science Editors:

Ravi M. Analysis of somatic cell mutations at the Glycophorina locus in human erythrocytes. [Thesis]. Sri Ramachandra University; 2001. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/17910

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


Univerzitet u Beogradu

27. Jakovljević, Ksenija V. 1981-. Analiza učestalosti i tipova mutacija KRAS i BRAF gena u karcinomima kolorektuma u populaciji Srbije.

Degree: Biološki fakultet, 2012, Univerzitet u Beogradu

Molekularna biologija - molekularna genetika / Molecular biology - molecular genetics

Uvod: Kolorektalni kancer (CRC) se po svojoj učestalosti i smrtnosti nalazi u samom vrhu… (more)

Subjects/Keywords: Colorectal carcinoma; KRAS gene; BRAF gene; mutations

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

APA (6th Edition):

Jakovljević, K. V. 1. (2012). Analiza učestalosti i tipova mutacija KRAS i BRAF gena u karcinomima kolorektuma u populaciji Srbije. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:2342/bdef:Content/get

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):

Jakovljević, Ksenija V 1981-. “Analiza učestalosti i tipova mutacija KRAS i BRAF gena u karcinomima kolorektuma u populaciji Srbije.” 2012. Thesis, Univerzitet u Beogradu. Accessed December 13, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:2342/bdef:Content/get.

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

MLA Handbook (7th Edition):

Jakovljević, Ksenija V 1981-. “Analiza učestalosti i tipova mutacija KRAS i BRAF gena u karcinomima kolorektuma u populaciji Srbije.” 2012. Web. 13 Dec 2019.

Vancouver:

Jakovljević KV1. Analiza učestalosti i tipova mutacija KRAS i BRAF gena u karcinomima kolorektuma u populaciji Srbije. [Internet] [Thesis]. Univerzitet u Beogradu; 2012. [cited 2019 Dec 13]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:2342/bdef:Content/get.

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

Council of Science Editors:

Jakovljević KV1. Analiza učestalosti i tipova mutacija KRAS i BRAF gena u karcinomima kolorektuma u populaciji Srbije. [Thesis]. Univerzitet u Beogradu; 2012. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:2342/bdef:Content/get

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


Univerzitet u Beogradu

28. Davidović, Radoslav S., 1977-. Анализа мутационог статуса гена p53 и метилационог статуса промотора гена p14 и p16 у липосаркомима.

Degree: Biološki fakultet, 2016, Univerzitet u Beogradu

Молекуларна биологија - Молекуларна генетика канцера / Molecular biology - Molecular genetics of cancer

Липосаркоми, тумори мезенхималног порекла, представљају најучесталији хистолошки тип саркома меких ткива.… (more)

Subjects/Keywords: liposarcoma; mutations; methylation; expression; p14; p16; p53

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APA (6th Edition):

Davidović, Radoslav S., 1. (2016). Анализа мутационог статуса гена p53 и метилационог статуса промотора гена p14 и p16 у липосаркомима. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:11308/bdef:Content/get

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):

Davidović, Radoslav S., 1977-. “Анализа мутационог статуса гена p53 и метилационог статуса промотора гена p14 и p16 у липосаркомима.” 2016. Thesis, Univerzitet u Beogradu. Accessed December 13, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:11308/bdef:Content/get.

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

MLA Handbook (7th Edition):

Davidović, Radoslav S., 1977-. “Анализа мутационог статуса гена p53 и метилационог статуса промотора гена p14 и p16 у липосаркомима.” 2016. Web. 13 Dec 2019.

Vancouver:

Davidović, Radoslav S. 1. Анализа мутационог статуса гена p53 и метилационог статуса промотора гена p14 и p16 у липосаркомима. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2019 Dec 13]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11308/bdef:Content/get.

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

Council of Science Editors:

Davidović, Radoslav S. 1. Анализа мутационог статуса гена p53 и метилационог статуса промотора гена p14 и p16 у липосаркомима. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11308/bdef:Content/get

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

29. Rios Visconti, Micaela. Genetic and environmental determinants of Paget's disease of bone.

Degree: PhD, 2015, University of Edinburgh

 Genetic factors play an important role in the pathogenesis of Paget’s Disease of Bone (PDB). The most important predisposing gene is SQSTM1 which is mutated… (more)

Subjects/Keywords: 616.7; SQSTM1; p62; severity score; mutations; virus

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

APA (6th Edition):

Rios Visconti, M. (2015). Genetic and environmental determinants of Paget's disease of bone. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/20421

Chicago Manual of Style (16th Edition):

Rios Visconti, Micaela. “Genetic and environmental determinants of Paget's disease of bone.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed December 13, 2019. http://hdl.handle.net/1842/20421.

MLA Handbook (7th Edition):

Rios Visconti, Micaela. “Genetic and environmental determinants of Paget's disease of bone.” 2015. Web. 13 Dec 2019.

Vancouver:

Rios Visconti M. Genetic and environmental determinants of Paget's disease of bone. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/1842/20421.

Council of Science Editors:

Rios Visconti M. Genetic and environmental determinants of Paget's disease of bone. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/20421


University of California – Santa Cruz

30. Radenbaugh, Amie. The Identification and Characterization of Alterations to DNA and RNA in Cancer Using Next-Generation Sequencing Data.

Degree: Biomolecular Engineering and Bioinformatics, 2015, University of California – Santa Cruz

 Much of our current understanding of cancer has come from investigating how normal cells are transformed into malignant cancers through the stepwise acquisition of somatic… (more)

Subjects/Keywords: Bioinformatics; editing; mutations; NGS; RNA; somatic; variants

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

APA (6th Edition):

Radenbaugh, A. (2015). The Identification and Characterization of Alterations to DNA and RNA in Cancer Using Next-Generation Sequencing Data. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/0dt1w1fx

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):

Radenbaugh, Amie. “The Identification and Characterization of Alterations to DNA and RNA in Cancer Using Next-Generation Sequencing Data.” 2015. Thesis, University of California – Santa Cruz. Accessed December 13, 2019. http://www.escholarship.org/uc/item/0dt1w1fx.

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

MLA Handbook (7th Edition):

Radenbaugh, Amie. “The Identification and Characterization of Alterations to DNA and RNA in Cancer Using Next-Generation Sequencing Data.” 2015. Web. 13 Dec 2019.

Vancouver:

Radenbaugh A. The Identification and Characterization of Alterations to DNA and RNA in Cancer Using Next-Generation Sequencing Data. [Internet] [Thesis]. University of California – Santa Cruz; 2015. [cited 2019 Dec 13]. Available from: http://www.escholarship.org/uc/item/0dt1w1fx.

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

Council of Science Editors:

Radenbaugh A. The Identification and Characterization of Alterations to DNA and RNA in Cancer Using Next-Generation Sequencing Data. [Thesis]. University of California – Santa Cruz; 2015. Available from: http://www.escholarship.org/uc/item/0dt1w1fx

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

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