Rapid positional cloning of zebrafish mutations by linkage and homozygosity mapping using whole-genome sequencing. - Test2 - elhamkhani - TriplyDB

Rapid positional cloning of zebrafish mutations by linkage and homozygosity mapping using whole-genome sequencing.

Rapid positional cloning of zebrafish mutations by linkage and homozygosity mapping using whole-genome sequencing.

http://www.wikidata.org/entity/Q30447155

about

Regulation of zebrafish sleep and arousal states: current and prospective approaches Deep sequencing strategies for mapping and identifying mutations from genetic screens Mutagenesis and phenotyping resources in zebrafish for studying development and human disease Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear.Excessive activation of ionotropic glutamate receptors induces apoptotic hair-cell death independent of afferent and efferent innervation In vivo analysis of hyaloid vasculature morphogenesis in zebrafish: A role for the lens in maturation and maintenance of the hyaloid.Rapid identification of kidney cyst mutations by whole exome sequencing in zebrafish Exploiting the extraordinary genetic polymorphism of ciona for developmental genetics with whole genome sequencing.Cluap1 is essential for ciliogenesis and photoreceptor maintenance in the vertebrate eye.Using zebrafish to study podocyte genesis during kidney development and regeneration.Production of haploid zebrafish embryos by in vitro fertilization.Identification of mutations in zebrafish using next-generation sequencing.Interpreting human genetic variation with in vivo zebrafish assays.SNPfisher: tools for probing genetic variation in laboratory-reared zebrafish.N-Ethylmaleimide-Sensitive Factor b (nsfb) Is Required for Normal Pigmentation of the Zebrafish Retinal Pigment Epithelium.RNA-seq-based mapping and candidate identification of mutations from forward genetic screens Advances in the Study of Heart Development and Disease Using Zebrafish.Multi-allelic phenotyping--a systematic approach for the simultaneous analysis of multiple induced mutations snow white, a zebrafish model of Hermansky-Pudlak Syndrome type 5 The zebrafish as a model for complex tissue regeneration.Mitophagy and neurodegeneration: the zebrafish model system.Using next-generation sequencing to isolate mutant genes from forward genetic screens.Whole Genome Sequencing-Based Mapping and Candidate Identification of Mutations from Fixed Zebrafish Tissue.Next-Generation Sequencing-Based Approaches for Mutation Mapping and Identification in Caenorhabditis elegans.The genetics of hair-cell function in zebrafish.Lmx1b is required for the glutamatergic fates of a subset of spinal cord neurons.Sequence-Based Mapping and Genome Editing Reveal Mutations in Stickleback Hps5 Cause Oculocutaneous Albinism and the casper Phenotype.Kinesin family member 6 (kif6) is necessary for spine development in zebrafish.Interval mapping for red/green skin color in Asian pears using a modified QTL-seq method.Population genetic diversity in zebrafish lines.Use of a Sibling Subtraction Method for Identifying Causal Mutations in Caenorhabditis elegans by Whole-Genome Sequencing.Genetic Screen for Postembryonic Development in the Zebrafish (Danio rerio): Dominant Mutations Affecting Adult Form.Different mutational function of low- and high-linear energy transfer heavy-ion irradiation demonstrated by whole-genome resequencing of Arabidopsis mutants.Lamellar projections in the endolymphatic sac act as a relief valve to regulate inner ear pressure.Elucidating Gene-by-Environment Interactions Associated with Differential Susceptibility to Chemical Exposure

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Rapid positional cloning of zebrafish mutations by linkage and homozygosity mapping using whole-genome sequencing.

http://www.wikidata.org/entity/Q30447155

description

2012 nî lūn-bûn

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2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2012 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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Rapid positional cloning of ze ...... using whole-genome sequencing.

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Rapid positional cloning of ze ...... using whole-genome sequencing.

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Rapid positional cloning of ze ...... using whole-genome sequencing.

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Rapid positional cloning of ze ...... using whole-genome sequencing.

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Alex V Nechiporuk

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Evan Schwab

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Ian A Swinburne

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Nikolaus Obholzer

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Sean G Megason

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Teresa Nicolson

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P2860

Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences

A systematic approach to mapping recessive disease genes in individuals from outbred populations

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

ZFIN: enhancements and updates to the Zebrafish Model Organism Database

Sequencing technologies and genome sequencing

Phoenix is required for mechanosensory hair cell regeneration in the zebrafish lateral line

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23052906

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