About: CATSPER2, a human autosomal nonsyndromic male infertility gene

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description	article (en) artículu científicu (ast) wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2003 (uk) im Juni 2003 veröffentlichter wissenschaftlicher Artikel (de) article scientifique publié en juin 2003 (fr)
publication date	wds:Q57398176-EA312769-0683-4183-94A0-4D8958B50F9A
publication date	2003-06-27 00:00:00Z (xsd:dateTime)
exact match	wds:Q57398176-FBADE56C-0C07-4AED-A96D-E845BCC6B2D7
exact match	https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200991
cites work	wds:Q57398176-041703FB-6901-4E34-B24F-F49DBF9E0F4C wds:Q57398176-0BD63106-8B0D-412B-A48F-1CC41A434F25 wds:Q57398176-3190A9C7-728F-45E4-9DE9-D7AA7345BBC0 wds:Q57398176-3712F482-51AD-49C1-AE56-DF0917E1BBA6 wds:Q57398176-3E79EDD8-5637-4800-BB29-4F6EBFB76392 wds:Q57398176-49DC1359-A3A7-4611-8E9A-74D79FB0FC74 wds:Q57398176-65862206-949A-47AF-9FF5-C38C5A602852 wds:Q57398176-65A1134A-CD5F-4ADC-8D8F-E303B6F17180 wds:Q57398176-686C6A78-68A8-484A-B746-94A6FFF5EE61 wds:Q57398176-68F88C17-FDC6-4FCE-8636-4A9DD0BD9835 wds:Q57398176-715CB48A-63D1-449A-BD3E-6378EBDA3324 wds:Q57398176-800BC843-073F-4C59-8517-94D312576BB7 wds:Q57398176-834AB78D-816A-41D8-8365-17E6952FC69F wds:Q57398176-A0EF0068-A6D1-456C-9A16-728B0B6CFC4E wds:Q57398176-A1DFCA64-695B-4446-8EB4-945EC336C15C wds:Q57398176-C68DEE21-D4E0-4C38-B103-55180AE5C6F0 wds:Q57398176-D50DE784-2FFB-47E0-951E-E1B07E0070CF wds:Q57398176-D58877E3-4397-4263-B19D-3F850E376A18 wds:Q57398176-D9CB1A7B-49FE-4DC3-A546-3B052D418F70 wds:Q57398176-E733C11A-0981-4A74-8AC4-CAE89824DA90 wds:Q57398176-E7E05A94-CCE3-45D4-9D4A-2A7639D53F84 wds:Q57398176-EEB80E42-FA90-4B5D-A228-A6BD3D67F0BF wds:Q57398176-EFF46D21-BCEC-4F4A-B46A-332D40FF8FC7 wds:Q57398176-F94AA05F-FDB1-49AE-AFF5-60AE5F0B065B
cites work	Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia. The androgen receptor gene mutations database The frequency of androgen receptor deficiency in infertile men. Recent segmental duplications in the human genome Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure Human mtDNA haplogroups associated with high or reduced spermatozoa motility Basic local alignment search tool The PROSITE database, its status in 2002 Increased coverage of protein families with the blocks database servers Genome architecture, rearrangements and genomic disorders A new DNA sequence assembly program Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus A voltage-gated ion channel expressed specifically in spermatozoa A sperm ion channel required for sperm motility and male fertility Two-phase liquid culture system models normal human adult erythropoiesis at the molecular level The immotile-cilia syndrome. A congenital ciliary abnormality as an etiologic factor in chronic airway infections and male sterility Cloning and sequencing of human FSH receptor cDNA Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3. Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1 Long RT-PCR Amplification of the entire coding sequence of the polycystic kidney disease 1 (PKD1) gene. '9 + 0' axoneme in spermatozoa and some nasal cilia of a patient with totally immotile spermatozoa associated with thickened sheath and short midpiece Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor gene Familial oligoasthenoteratozoospermia: evidence of autosomal dominant inheritance with sex-limited expression
author name string	wds:Q57398176-07459294-AF94-4E27-BC18-8BD81F77818F wds:Q57398176-2E4B07AF-BBD7-4C84-8CB3-B1CE8DA1FC9C wds:Q57398176-4C55445F-E520-4019-A616-402FDB3898B2 wds:Q57398176-5D6F10A1-5078-4A90-B65F-5278BA67C380 wds:Q57398176-67B3C3A0-29DF-4238-952E-CF763F51FC8D wds:Q57398176-89FC856E-5607-4885-B93C-4EC2C8AC3F78 wds:Q57398176-9D5AE1F0-3427-4389-922E-F8A27D1EF497 wds:Q57398176-A69E3CBE-9FCB-4CEE-9769-9E8CC92ADC16 wds:Q57398176-AA752B7E-9D56-4F28-84E7-709255A0B015 wds:Q57398176-AB36E734-BB9B-4891-8825-FF5BC70E8640 wds:Q57398176-BE87AF0F-DD67-48AC-AE3E-7E600CDDD485 wds:Q57398176-C7D534C9-2DE3-48DD-B534-69C532D7F068 wds:Q57398176-D6762986-1FDA-4EF0-B2C0-33C513AD1EF2 wds:Q57398176-D67F6A10-3617-45C5-A8C1-0E8F5D9962A3 wds:Q57398176-D8E3BDB2-FFEE-4C63-A36B-BB3DCF1E68AA wds:Q57398176-DCC6A7E8-9FF7-4FAA-AE2C-1806A3F0F3CC wds:Q57398176-DD788A4F-513F-49FC-B5F5-2B58A3FBAEBA wds:Q57398176-E4FD6B3E-DE90-4F16-ABFE-30B9940527A8 wds:Q57398176-F0468871-350E-4538-824B-5DD201C61F81
author name string	Jean Delaunay Nili Avidan Hannah Tamary Miriam Khen Marc Fellous Edna Ben-Asher Rina Zaizov Orly Dgany Alexandre Pariente Hanna Shalev Tatyana Krasnov Lea Shalmon Daniel Cattan Nicolas Borot Alain Barthelme Issac Yaniv Lucien Moati Michel Thulliez Tsvyia Olender
rdfs:label	CATSPER2, a human autosomal nonsyndromic male infertility gene (en) CATSPER2, a human autosomal nonsyndromic male infertility gene (nl)
skos:prefLabel	CATSPER2, a human autosomal nonsyndromic male infertility gene (en)

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