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You searched for subject:(Fanconi anemia). Showing records 1 – 30 of 91 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


Vrije Universiteit Amsterdam

2. Haitjema, A. Towards Elucidating the Fanconi Anemia Network Through Genomic and Proteomic Approaches .

Degree: 2015, Vrije Universiteit Amsterdam

Subjects/Keywords: Fanconi anemia

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APA (6th Edition):

Haitjema, A. (2015). Towards Elucidating the Fanconi Anemia Network Through Genomic and Proteomic Approaches . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/53529

Chicago Manual of Style (16th Edition):

Haitjema, A. “Towards Elucidating the Fanconi Anemia Network Through Genomic and Proteomic Approaches .” 2015. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 20, 2020. http://hdl.handle.net/1871/53529.

MLA Handbook (7th Edition):

Haitjema, A. “Towards Elucidating the Fanconi Anemia Network Through Genomic and Proteomic Approaches .” 2015. Web. 20 Oct 2020.

Vancouver:

Haitjema A. Towards Elucidating the Fanconi Anemia Network Through Genomic and Proteomic Approaches . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2015. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/1871/53529.

Council of Science Editors:

Haitjema A. Towards Elucidating the Fanconi Anemia Network Through Genomic and Proteomic Approaches . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2015. Available from: http://hdl.handle.net/1871/53529

3. 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


University of Minnesota

4. Luebben, Spencer William. The Fanconi anemia pathway and HELQ work alongside dormant replication origins to suppress replication-associated genome instability.

Degree: PhD, 2014, University of Minnesota

 DNA replication is continually impeded by endogenous lesions that cause the stalling of replication forks. If left unchecked, this threatens the integrity of the genome… (more)

Subjects/Keywords: Cancer; chaos3; Fancc; Fanconi anemia; Helq; Replication

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APA (6th Edition):

Luebben, S. W. (2014). The Fanconi anemia pathway and HELQ work alongside dormant replication origins to suppress replication-associated genome instability. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/165753

Chicago Manual of Style (16th Edition):

Luebben, Spencer William. “The Fanconi anemia pathway and HELQ work alongside dormant replication origins to suppress replication-associated genome instability.” 2014. Doctoral Dissertation, University of Minnesota. Accessed October 20, 2020. http://hdl.handle.net/11299/165753.

MLA Handbook (7th Edition):

Luebben, Spencer William. “The Fanconi anemia pathway and HELQ work alongside dormant replication origins to suppress replication-associated genome instability.” 2014. Web. 20 Oct 2020.

Vancouver:

Luebben SW. The Fanconi anemia pathway and HELQ work alongside dormant replication origins to suppress replication-associated genome instability. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/11299/165753.

Council of Science Editors:

Luebben SW. The Fanconi anemia pathway and HELQ work alongside dormant replication origins to suppress replication-associated genome instability. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/165753

5. 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

6. 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

7. Selenti, Nikoletta. Κυτταρογενετική και μοριακή διερεύνηση της αναιμίας fanconi.

Degree: 2014, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Fanconi anaemia (FA) is a rare genetic disorder, characterised by progressive pancytopenia, variable congenital anomalies, susceptibility to malignancies and induced chromosomal instability. 15 subtypes are… (more)

Subjects/Keywords: Αναιμία fanconi; Kυτταρογενετική και μοριακή διερεύνηση; Fanconi anemia; Cytogenetic and molecular diagnosis

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APA (6th Edition):

Selenti, N. (2014). Κυτταρογενετική και μοριακή διερεύνηση της αναιμίας fanconi. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/40541

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):

Selenti, Nikoletta. “Κυτταρογενετική και μοριακή διερεύνηση της αναιμίας fanconi.” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 20, 2020. http://hdl.handle.net/10442/hedi/40541.

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

MLA Handbook (7th Edition):

Selenti, Nikoletta. “Κυτταρογενετική και μοριακή διερεύνηση της αναιμίας fanconi.” 2014. Web. 20 Oct 2020.

Vancouver:

Selenti N. Κυτταρογενετική και μοριακή διερεύνηση της αναιμίας fanconi. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10442/hedi/40541.

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

Council of Science Editors:

Selenti N. Κυτταρογενετική και μοριακή διερεύνηση της αναιμίας fanconi. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/40541

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


Universidade Estadual de Campinas

8. 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

9. 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

10. 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

11. Timmers, Cynthia D. Identification and initial characterization of the Fanconi anemia complementation group D gene.

Degree: PhD, 1999, Oregon Health Sciences University

Subjects/Keywords: Fanconi Anemia  – genetics; Phenotype

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APA (6th Edition):

Timmers, C. D. (1999). Identification and initial characterization of the Fanconi anemia complementation group D gene. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4PG1Q2T ; http://digitalcommons.ohsu.edu/etd/3378

Chicago Manual of Style (16th Edition):

Timmers, Cynthia D. “Identification and initial characterization of the Fanconi anemia complementation group D gene.” 1999. Doctoral Dissertation, Oregon Health Sciences University. Accessed October 20, 2020. doi:10.6083/M4PG1Q2T ; http://digitalcommons.ohsu.edu/etd/3378.

MLA Handbook (7th Edition):

Timmers, Cynthia D. “Identification and initial characterization of the Fanconi anemia complementation group D gene.” 1999. Web. 20 Oct 2020.

Vancouver:

Timmers CD. Identification and initial characterization of the Fanconi anemia complementation group D gene. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1999. [cited 2020 Oct 20]. Available from: doi:10.6083/M4PG1Q2T ; http://digitalcommons.ohsu.edu/etd/3378.

Council of Science Editors:

Timmers CD. Identification and initial characterization of the Fanconi anemia complementation group D gene. [Doctoral Dissertation]. Oregon Health Sciences University; 1999. Available from: doi:10.6083/M4PG1Q2T ; http://digitalcommons.ohsu.edu/etd/3378


Kyoto University / 京都大学

12. Yoshikiyo, Kazunori. KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents. : KIAA1018/FAN1ヌクレアーゼはDNA鎖間架橋剤により誘導されるゲノム不安定性に対して細胞を保護する.

Degree: 博士(医学), 2013, Kyoto University / 京都大学

Kazunori Yoshikiyo, Katja Kratz, Kouji Hirota, Kana Nishihara, Minoru Takata, Hitoshi Kurumizaka, Satoshi Horimoto, Shunichi Takeda, and Josef Jiricny "KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents" PNAS 2010 107 (50) 21553-21557; published ahead of print November 29, 2010, doi:10.1073/pnas.1011081107

新制・論文博士

乙第12772号

論医博第2063号

Subjects/Keywords: KIAA1018/FAN1; DNA Interstrand crosslink; Fanconi Anemia; DT40

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APA (6th Edition):

Yoshikiyo, K. (2013). KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents. : KIAA1018/FAN1ヌクレアーゼはDNA鎖間架橋剤により誘導されるゲノム不安定性に対して細胞を保護する. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/180458 ; http://dx.doi.org/10.14989/doctor.r12772

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):

Yoshikiyo, Kazunori. “KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents. : KIAA1018/FAN1ヌクレアーゼはDNA鎖間架橋剤により誘導されるゲノム不安定性に対して細胞を保護する.” 2013. Thesis, Kyoto University / 京都大学. Accessed October 20, 2020. http://hdl.handle.net/2433/180458 ; http://dx.doi.org/10.14989/doctor.r12772.

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

MLA Handbook (7th Edition):

Yoshikiyo, Kazunori. “KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents. : KIAA1018/FAN1ヌクレアーゼはDNA鎖間架橋剤により誘導されるゲノム不安定性に対して細胞を保護する.” 2013. Web. 20 Oct 2020.

Vancouver:

Yoshikiyo K. KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents. : KIAA1018/FAN1ヌクレアーゼはDNA鎖間架橋剤により誘導されるゲノム不安定性に対して細胞を保護する. [Internet] [Thesis]. Kyoto University / 京都大学; 2013. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/2433/180458 ; http://dx.doi.org/10.14989/doctor.r12772.

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

Council of Science Editors:

Yoshikiyo K. KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents. : KIAA1018/FAN1ヌクレアーゼはDNA鎖間架橋剤により誘導されるゲノム不安定性に対して細胞を保護する. [Thesis]. Kyoto University / 京都大学; 2013. Available from: http://hdl.handle.net/2433/180458 ; http://dx.doi.org/10.14989/doctor.r12772

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

13. 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


University of Newcastle

14. Yuen, Wai Shan. DNA repair and the Fanconi Anemia pathway: insights into female meiosis and mitosis.

Degree: PhD, 2012, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

There are numerous intrinsic and extrinsic factors that cause DNA damage. Without proper DNA repair, such damage would… (more)

Subjects/Keywords: meiosis; mitosis; DNA repair; Fanconi Anemia; DNA damage

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APA (6th Edition):

Yuen, W. S. (2012). DNA repair and the Fanconi Anemia pathway: insights into female meiosis and mitosis. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1036684

Chicago Manual of Style (16th Edition):

Yuen, Wai Shan. “DNA repair and the Fanconi Anemia pathway: insights into female meiosis and mitosis.” 2012. Doctoral Dissertation, University of Newcastle. Accessed October 20, 2020. http://hdl.handle.net/1959.13/1036684.

MLA Handbook (7th Edition):

Yuen, Wai Shan. “DNA repair and the Fanconi Anemia pathway: insights into female meiosis and mitosis.” 2012. Web. 20 Oct 2020.

Vancouver:

Yuen WS. DNA repair and the Fanconi Anemia pathway: insights into female meiosis and mitosis. [Internet] [Doctoral dissertation]. University of Newcastle; 2012. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/1959.13/1036684.

Council of Science Editors:

Yuen WS. DNA repair and the Fanconi Anemia pathway: insights into female meiosis and mitosis. [Doctoral Dissertation]. University of Newcastle; 2012. Available from: http://hdl.handle.net/1959.13/1036684


Vrije Universiteit Amsterdam

15. Bakker, S.T. FANCM, the mouse that roared .

Degree: 2011, Vrije Universiteit Amsterdam

Subjects/Keywords: Fanconi anemia; DNA repair; muismodellen

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APA (6th Edition):

Bakker, S. T. (2011). FANCM, the mouse that roared . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/28779

Chicago Manual of Style (16th Edition):

Bakker, S T. “FANCM, the mouse that roared .” 2011. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 20, 2020. http://hdl.handle.net/1871/28779.

MLA Handbook (7th Edition):

Bakker, S T. “FANCM, the mouse that roared .” 2011. Web. 20 Oct 2020.

Vancouver:

Bakker ST. FANCM, the mouse that roared . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2011. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/1871/28779.

Council of Science Editors:

Bakker ST. FANCM, the mouse that roared . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2011. Available from: http://hdl.handle.net/1871/28779

16. 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


University of Dundee

17. Hain, Karolina Ottilia. Characterisation of human SLX4/FANCP, a coordinator of DNA repair nucleases.

Degree: PhD, 2012, University of Dundee

 Budding yeast Slx4 binds to the structure-specific DNA repair nucleases Slx1 and Rad1XPF-Rad10ERCC1, and it was reported that Slx4 is essential for DNA flap cleavage… (more)

Subjects/Keywords: 572.8; DNA damage; Fanconi anemia; Interstrand crosslink repair; SLX4

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APA (6th Edition):

Hain, K. O. (2012). Characterisation of human SLX4/FANCP, a coordinator of DNA repair nucleases. (Doctoral Dissertation). University of Dundee. Retrieved from https://discovery.dundee.ac.uk/en/studentTheses/bf9a5ba3-7cea-4d25-8e8c-aa4cd5de3fae ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578875

Chicago Manual of Style (16th Edition):

Hain, Karolina Ottilia. “Characterisation of human SLX4/FANCP, a coordinator of DNA repair nucleases.” 2012. Doctoral Dissertation, University of Dundee. Accessed October 20, 2020. https://discovery.dundee.ac.uk/en/studentTheses/bf9a5ba3-7cea-4d25-8e8c-aa4cd5de3fae ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578875.

MLA Handbook (7th Edition):

Hain, Karolina Ottilia. “Characterisation of human SLX4/FANCP, a coordinator of DNA repair nucleases.” 2012. Web. 20 Oct 2020.

Vancouver:

Hain KO. Characterisation of human SLX4/FANCP, a coordinator of DNA repair nucleases. [Internet] [Doctoral dissertation]. University of Dundee; 2012. [cited 2020 Oct 20]. Available from: https://discovery.dundee.ac.uk/en/studentTheses/bf9a5ba3-7cea-4d25-8e8c-aa4cd5de3fae ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578875.

Council of Science Editors:

Hain KO. Characterisation of human SLX4/FANCP, a coordinator of DNA repair nucleases. [Doctoral Dissertation]. University of Dundee; 2012. Available from: https://discovery.dundee.ac.uk/en/studentTheses/bf9a5ba3-7cea-4d25-8e8c-aa4cd5de3fae ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578875


University of Minnesota

18. Thompson, Elizabeth. The Role of Fanconi Anemia Proteins in DNA Repair, Replication Stress and Genome Stability.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2017, University of Minnesota

Fanconi anemia (FA) is a genetic chromosomal instability disorder characterized by progressive bone marrow failure and a strong predisposition to cancer. The FA proteins work… (more)

Subjects/Keywords: DNA repair; FANCD2; FANCI; FANCN; Fanconi anemia; PALB2

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APA (6th Edition):

Thompson, E. (2017). The Role of Fanconi Anemia Proteins in DNA Repair, Replication Stress and Genome Stability. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/192684

Chicago Manual of Style (16th Edition):

Thompson, Elizabeth. “The Role of Fanconi Anemia Proteins in DNA Repair, Replication Stress and Genome Stability.” 2017. Doctoral Dissertation, University of Minnesota. Accessed October 20, 2020. http://hdl.handle.net/11299/192684.

MLA Handbook (7th Edition):

Thompson, Elizabeth. “The Role of Fanconi Anemia Proteins in DNA Repair, Replication Stress and Genome Stability.” 2017. Web. 20 Oct 2020.

Vancouver:

Thompson E. The Role of Fanconi Anemia Proteins in DNA Repair, Replication Stress and Genome Stability. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/11299/192684.

Council of Science Editors:

Thompson E. The Role of Fanconi Anemia Proteins in DNA Repair, Replication Stress and Genome Stability. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/192684

19. Bick, Gregory P. Uncovering the roles of RNF8 ubiquitin signaling networks and BRCA1 in recruiting Fanconi Anemia proteins to DNA damage.

Degree: PhD, Medicine: Molecular and Developmental Biology, 2016, University of Cincinnati

Fanconi Anemia is a multigenic DNA damage repair disorder and cancer predisposition syndrome. The 20 proteins in the FA pathway are all linked by their… (more)

Subjects/Keywords: Cellular Biology; PALB2; RNF8; DNA damage; FANCD2; Fanconi Anemia; ubiquitin

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APA (6th Edition):

Bick, G. P. (2016). Uncovering the roles of RNF8 ubiquitin signaling networks and BRCA1 in recruiting Fanconi Anemia proteins to DNA damage. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1467987940

Chicago Manual of Style (16th Edition):

Bick, Gregory P. “Uncovering the roles of RNF8 ubiquitin signaling networks and BRCA1 in recruiting Fanconi Anemia proteins to DNA damage.” 2016. Doctoral Dissertation, University of Cincinnati. Accessed October 20, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1467987940.

MLA Handbook (7th Edition):

Bick, Gregory P. “Uncovering the roles of RNF8 ubiquitin signaling networks and BRCA1 in recruiting Fanconi Anemia proteins to DNA damage.” 2016. Web. 20 Oct 2020.

Vancouver:

Bick GP. Uncovering the roles of RNF8 ubiquitin signaling networks and BRCA1 in recruiting Fanconi Anemia proteins to DNA damage. [Internet] [Doctoral dissertation]. University of Cincinnati; 2016. [cited 2020 Oct 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1467987940.

Council of Science Editors:

Bick GP. Uncovering the roles of RNF8 ubiquitin signaling networks and BRCA1 in recruiting Fanconi Anemia proteins to DNA damage. [Doctoral Dissertation]. University of Cincinnati; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1467987940


Université Paris-Sud – Paris XI

20. 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

21. 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 (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


Vrije Universiteit Amsterdam

22. Stone, S.N. Xenopus Laevis as a Model System for Evaluating the Function of Fanconi Anemia Proteins .

Degree: 2008, Vrije Universiteit Amsterdam

Subjects/Keywords: Role of Fanconi anemia proteins in genomic maintenance; Fanconi Anemia; DNA repair

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APA (6th Edition):

Stone, S. N. (2008). Xenopus Laevis as a Model System for Evaluating the Function of Fanconi Anemia Proteins . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/15482

Chicago Manual of Style (16th Edition):

Stone, S N. “Xenopus Laevis as a Model System for Evaluating the Function of Fanconi Anemia Proteins .” 2008. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 20, 2020. http://hdl.handle.net/1871/15482.

MLA Handbook (7th Edition):

Stone, S N. “Xenopus Laevis as a Model System for Evaluating the Function of Fanconi Anemia Proteins .” 2008. Web. 20 Oct 2020.

Vancouver:

Stone SN. Xenopus Laevis as a Model System for Evaluating the Function of Fanconi Anemia Proteins . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2008. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/1871/15482.

Council of Science Editors:

Stone SN. Xenopus Laevis as a Model System for Evaluating the Function of Fanconi Anemia Proteins . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2008. Available from: http://hdl.handle.net/1871/15482


Universitat Pompeu Fabra

23. 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

24. 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


University of Toronto

25. Lee, Eva I-Hua. Distinctive Roles for FANCD2 and FANCJ in the Resection of Radiation-induced DNA Double-strand Breaks in Human Cells.

Degree: 2016, University of Toronto

Fanconi anemia (FA) patients are hypersensitive to ionizing radiation and other agents that generate DNA double-strand breaks (DSBs). The major error-free DSB repair pathway in… (more)

Subjects/Keywords: DNA repair; Double strand breaks; DSB resection; FANCD2; FANCJ; Fanconi Anemia; 0369

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APA (6th Edition):

Lee, E. I. (2016). Distinctive Roles for FANCD2 and FANCJ in the Resection of Radiation-induced DNA Double-strand Breaks in Human Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72732

Chicago Manual of Style (16th Edition):

Lee, Eva I-Hua. “Distinctive Roles for FANCD2 and FANCJ in the Resection of Radiation-induced DNA Double-strand Breaks in Human Cells.” 2016. Masters Thesis, University of Toronto. Accessed October 20, 2020. http://hdl.handle.net/1807/72732.

MLA Handbook (7th Edition):

Lee, Eva I-Hua. “Distinctive Roles for FANCD2 and FANCJ in the Resection of Radiation-induced DNA Double-strand Breaks in Human Cells.” 2016. Web. 20 Oct 2020.

Vancouver:

Lee EI. Distinctive Roles for FANCD2 and FANCJ in the Resection of Radiation-induced DNA Double-strand Breaks in Human Cells. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/1807/72732.

Council of Science Editors:

Lee EI. Distinctive Roles for FANCD2 and FANCJ in the Resection of Radiation-induced DNA Double-strand Breaks in Human Cells. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/72732


Harvard University

26. Cherry, Anne Blanche Cresswell. Reprogramming Pediatric Genetic Disorders: Pearson Syndrome, Ring 14 Syndrome, and Fanconi Anemia.

Degree: PhD, Biology: Medical Sciences, Division of, 2014, Harvard University

 The effect of a single genetic mutation can vary greatly between different types of cells. The mutated gene may not be expressed in one tissue… (more)

Subjects/Keywords: Biology; Molecular biology; Cellular biology; Disease model; Fanconi Anemia; Heteroplasmy; iPS; Pearson syndrome; Ring 14

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APA (6th Edition):

Cherry, A. B. C. (2014). Reprogramming Pediatric Genetic Disorders: Pearson Syndrome, Ring 14 Syndrome, and Fanconi Anemia. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274294

Chicago Manual of Style (16th Edition):

Cherry, Anne Blanche Cresswell. “Reprogramming Pediatric Genetic Disorders: Pearson Syndrome, Ring 14 Syndrome, and Fanconi Anemia.” 2014. Doctoral Dissertation, Harvard University. Accessed October 20, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274294.

MLA Handbook (7th Edition):

Cherry, Anne Blanche Cresswell. “Reprogramming Pediatric Genetic Disorders: Pearson Syndrome, Ring 14 Syndrome, and Fanconi Anemia.” 2014. Web. 20 Oct 2020.

Vancouver:

Cherry ABC. Reprogramming Pediatric Genetic Disorders: Pearson Syndrome, Ring 14 Syndrome, and Fanconi Anemia. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2020 Oct 20]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274294.

Council of Science Editors:

Cherry ABC. Reprogramming Pediatric Genetic Disorders: Pearson Syndrome, Ring 14 Syndrome, and Fanconi Anemia. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274294


Texas Medical Center

27. Huang, Yaling. MODULATED FUNCTIONS OF THE FANCONI ANEMIA CORE COMPLEX.

Degree: PhD, 2014, Texas Medical Center

  Cells derived from Fanconi anemia (FA) patients are characterized by hypersensitivity to DNA interstrand crosslinks (ICLs), suggesting that FA genes play a role in… (more)

Subjects/Keywords: Fanconi anemia; interstrand crosslink; DNA repair; Cancer Biology; Medical Genetics; Molecular Genetics

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APA (6th Edition):

Huang, Y. (2014). MODULATED FUNCTIONS OF THE FANCONI ANEMIA CORE COMPLEX. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/429

Chicago Manual of Style (16th Edition):

Huang, Yaling. “MODULATED FUNCTIONS OF THE FANCONI ANEMIA CORE COMPLEX.” 2014. Doctoral Dissertation, Texas Medical Center. Accessed October 20, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/429.

MLA Handbook (7th Edition):

Huang, Yaling. “MODULATED FUNCTIONS OF THE FANCONI ANEMIA CORE COMPLEX.” 2014. Web. 20 Oct 2020.

Vancouver:

Huang Y. MODULATED FUNCTIONS OF THE FANCONI ANEMIA CORE COMPLEX. [Internet] [Doctoral dissertation]. Texas Medical Center; 2014. [cited 2020 Oct 20]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/429.

Council of Science Editors:

Huang Y. MODULATED FUNCTIONS OF THE FANCONI ANEMIA CORE COMPLEX. [Doctoral Dissertation]. Texas Medical Center; 2014. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/429


Vrije Universiteit Amsterdam

28. Zeeburg, H.J.T. van. Oncolytic adenoviruses for treatment of oral cancer and precancer in sporadic and genetically predisposed patients .

Degree: 2010, Vrije Universiteit Amsterdam

Subjects/Keywords: HNSCC; adenovirus; preneoplastic lesions; Fanconi anemia

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APA (6th Edition):

Zeeburg, H. J. T. v. (2010). Oncolytic adenoviruses for treatment of oral cancer and precancer in sporadic and genetically predisposed patients . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/16285

Chicago Manual of Style (16th Edition):

Zeeburg, H J T van. “Oncolytic adenoviruses for treatment of oral cancer and precancer in sporadic and genetically predisposed patients .” 2010. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 20, 2020. http://hdl.handle.net/1871/16285.

MLA Handbook (7th Edition):

Zeeburg, H J T van. “Oncolytic adenoviruses for treatment of oral cancer and precancer in sporadic and genetically predisposed patients .” 2010. Web. 20 Oct 2020.

Vancouver:

Zeeburg HJTv. Oncolytic adenoviruses for treatment of oral cancer and precancer in sporadic and genetically predisposed patients . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2010. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/1871/16285.

Council of Science Editors:

Zeeburg HJTv. Oncolytic adenoviruses for treatment of oral cancer and precancer in sporadic and genetically predisposed patients . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2010. Available from: http://hdl.handle.net/1871/16285


Univerzitet u Beogradu

29. Filipović-Tričković, Jelena, 1985- 14881383. Molekularno-citogenetička karakterizacija hromozomskih prekida u limfocitima periferne krvi pacijenata obolelih od Fankonijeve anemije u različitim fazama bolesti.

Degree: Biološki fakultet, 2019, Univerzitet u Beogradu

Biologija - Genetika / Biology - Genetics

Česta fragilna mesta (CFS) su hromozomski regioni skloni lezijama, suženjima i prekidima u uslovima replikativnog stresa in vitro.… (more)

Subjects/Keywords: CFS; Fanconi anemia; telomere fusions; radials; FANCD2 variants; deep intonic variants; bone marrow failure

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APA (6th Edition):

Filipović-Tričković, Jelena, 1. (2019). Molekularno-citogenetička karakterizacija hromozomskih prekida u limfocitima periferne krvi pacijenata obolelih od Fankonijeve anemije u različitim fazama bolesti. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:19564/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):

Filipović-Tričković, Jelena, 1985-. “Molekularno-citogenetička karakterizacija hromozomskih prekida u limfocitima periferne krvi pacijenata obolelih od Fankonijeve anemije u različitim fazama bolesti.” 2019. Thesis, Univerzitet u Beogradu. Accessed October 20, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:19564/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):

Filipović-Tričković, Jelena, 1985-. “Molekularno-citogenetička karakterizacija hromozomskih prekida u limfocitima periferne krvi pacijenata obolelih od Fankonijeve anemije u različitim fazama bolesti.” 2019. Web. 20 Oct 2020.

Vancouver:

Filipović-Tričković, Jelena 1. Molekularno-citogenetička karakterizacija hromozomskih prekida u limfocitima periferne krvi pacijenata obolelih od Fankonijeve anemije u različitim fazama bolesti. [Internet] [Thesis]. Univerzitet u Beogradu; 2019. [cited 2020 Oct 20]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19564/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:

Filipović-Tričković, Jelena 1. Molekularno-citogenetička karakterizacija hromozomskih prekida u limfocitima periferne krvi pacijenata obolelih od Fankonijeve anemije u različitim fazama bolesti. [Thesis]. Univerzitet u Beogradu; 2019. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19564/bdef:Content/get

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


Freie Universität Berlin

30. Schmiester, Maren. Investigation of hSNM1B/Apollo's role within the FA/BRCA pathway.

Degree: 2017, Freie Universität Berlin

 Objectives: Fanconi Anemia (FA) is a genetic disorder manifesting in congenital defects, increased risk of cancer and bone marrow failure. The primary defect lies in… (more)

Subjects/Keywords: Fanconi Anemia; DNA damage; hSNM1B/Apollo; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Schmiester, M. (2017). Investigation of hSNM1B/Apollo's role within the FA/BRCA pathway. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-14221

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):

Schmiester, Maren. “Investigation of hSNM1B/Apollo's role within the FA/BRCA pathway.” 2017. Thesis, Freie Universität Berlin. Accessed October 20, 2020. http://dx.doi.org/10.17169/refubium-14221.

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

MLA Handbook (7th Edition):

Schmiester, Maren. “Investigation of hSNM1B/Apollo's role within the FA/BRCA pathway.” 2017. Web. 20 Oct 2020.

Vancouver:

Schmiester M. Investigation of hSNM1B/Apollo's role within the FA/BRCA pathway. [Internet] [Thesis]. Freie Universität Berlin; 2017. [cited 2020 Oct 20]. Available from: http://dx.doi.org/10.17169/refubium-14221.

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

Council of Science Editors:

Schmiester M. Investigation of hSNM1B/Apollo's role within the FA/BRCA pathway. [Thesis]. Freie Universität Berlin; 2017. Available from: http://dx.doi.org/10.17169/refubium-14221

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

[1] [2] [3] [4]

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