Roles of brca2 (fancd1) in oocyte nuclear architecture, gametogenesis, gonad tumors, and genome stability in zebrafish - Wikidata - awgldk - TriplyDB

Roles of brca2 (fancd1) in oocyte nuclear architecture, gametogenesis, gonad tumors, and genome stability in zebrafish

Roles of brca2 (fancd1) in oocyte nuclear architecture, gametogenesis, gonad tumors, and genome stability in zebrafish

http://www.wikidata.org/entity/Q27342643

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Zebrafish: A Versatile Animal Model for Fertility Research Connecting by breaking and repairing: mechanisms of DNA strand exchange in meiotic recombination The zebrafish reference genome sequence and its relationship to the human genome Multiple sex-associated regions and a putative sex chromosome in zebrafish revealed by RAD mapping and population genomics.Simple methods for generating and detecting locus-specific mutations induced with TALENs in the zebrafish genome.DNA double strand breaks but not interstrand crosslinks prevent progress through meiosis in fully grown mouse oocytes.Wild sex in zebrafish: loss of the natural sex determinant in domesticated strains Retinoic acid metabolic genes, meiosis, and gonadal sex differentiation in zebrafish.Homologous recombination and its regulation Comparison of age at natural menopause in BRCA1/2 mutation carriers with a non-clinic-based sample of women in northern California Sox9-related signaling controls zebrafish juvenile ovary-testis transformation.BRCA2 and TP53 collaborate in tumorigenesis in zebrafish.Next generation mothers: Maternal control of germline development in zebrafish.Loss of the chromatin modifier Kdm2aa causes BrafV600E-independent spontaneous melanoma in zebrafish.The zebrafish kidney mutant zeppelin reveals that brca2/fancd1 is essential for pronephros development.Loss of the homologous recombination gene rad51 leads to Fanconi anemia-like symptoms in zebrafish.Zebrafish models for human cancer.Accurate quantification of homologous recombination in zebrafish: brca2 deficiency as a paradigm.Distinct and Cooperative Roles of amh and dmrt1 in Self-Renewal and Differentiation of Male Germ Cells in Zebrafish.Development of Cre-loxP technology in zebrafish to study the regulation of fish reproduction.[Fanconi anemia animal models - How differences can teach us as much as similarities…].The age of heterozygous telomerase mutant parents influences the adult phenotype of their offspring irrespective of genotype in zebrafish.Scaling up to study brca2: the zeppelin zebrafish mutant reveals a role for brca2 in embryonic development of kidney mesoderm.

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Roles of brca2 (fancd1) in oocyte nuclear architecture, gametogenesis, gonad tumors, and genome stability in zebrafish

http://www.wikidata.org/entity/Q27342643

description

2011 nî lūn-bûn

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2011 թուականի Մարտին հրատարակուած գիտական յօդուած

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2011 թվականի մարտին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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Roles of brca2 (fancd1) in ooc ...... genome stability in zebrafish

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Roles of brca2 (fancd1) in ooc ...... genome stability in zebrafish

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Roles of brca2 (fancd1) in ooc ...... genome stability in zebrafish

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Roles of brca2 (fancd1) in ooc ...... genome stability in zebrafish

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Roles of brca2 (fancd1) in ooc ...... genome stability in zebrafish

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Roles of brca2 (fancd1) in ooc ...... genome stability in zebrafish

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Roles of brca2 (fancd1) in ooc ...... genome stability in zebrafish

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Roles of brca2 (fancd1) in ooc ...... genome stability in zebrafish

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Roles of brca2 (fancd1) in ooc ...... genome stability in zebrafish

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Roles of brca2 (fancd1) in ooc ...... genome stability in zebrafish

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Adam Johnston

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Adriana Rodríguez-Marí

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Ruth A BreMiller

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P2860

Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype

The BRC repeats in BRCA2 are critical for RAD51 binding and resistance to methyl methanesulfonate treatment

Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

Preservation of duplicate genes by complementary, degenerative mutations

Genome duplication, a trait shared by 22000 species of ray-finned fish

How the fanconi anemia pathway guards the genome

A simple method for displaying the hydropathic character of a protein

BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure

Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia

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Cristian Cañestro

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