메뉴 건너뛰기




Volumn 16, Issue 12, 2000, Pages 565-572

Towards an understanding of the genetics of human male infertility: Lessons from flies

Author keywords

[No Author keywords available]

Indexed keywords

ACROCEPHALOSYNDACTYLY; ALBRIGHT SYNDROME; ANIMAL MODEL; ASTHENOSPERMIA; AUTOSOMAL RECESSIVE INHERITANCE; AZOOSPERMIA; BARDET BIEDL SYNDROME; BLOOM SYNDROME; CAENORHABDITIS ELEGANS; CYSTIC FIBROSIS; DROSOPHILA; ELLIPTOCYTOSIS; FACIOGENITAL DYSPLASIA; GENE DELETION; HUMAN; HYPOMAGNESEMIA; KALLMANN SYNDROME; KARTAGENER SYNDROME; MALE INFERTILITY; MALE STERILITY; MOUSE; MYOTONIC DYSTROPHY; NONHUMAN; OLIGOSPERMIA; OPITZ SYNDROME; PHENOTYPE; PLEIOTROPY; POPULATION GENETICS; PRIORITY JOURNAL; RECESSIVE GENE; REVIEW; SERTOLI CELL ONLY SYNDROME; SPECIES DIFFERENCE; TERATOSPERMIA; USHER SYNDROME; Y CHROMOSOME; YEAST;

EID: 0034564094     PISSN: 01689525     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-9525(00)02140-5     Document Type: Note
Times cited : (90)

References (57)
  • 1
    • 0001456033 scopus 로고
    • Relative incidence of etiological disorders in male infertility
    • Santen R.J., Swerdloff R.S. (Eds.), Male Reproductive Dysfunction. Diagnosis and Management of Hypogonadism, Infertility, and Impotence, Marcel Dekker
    • (1986) , pp. 341-372
    • Baker H.W.G., et, al.1
  • 2
    • 0007225234 scopus 로고    scopus 로고
    • World Health Organization (1987) Towards more objectivity in diagnosis and management of male infertility. Int. J. Androl. (Suppl. 7), 1-53
  • 4
    • 0030833888 scopus 로고    scopus 로고
    • Estimating familial and genetic contributions to variability in human testicular function: a pilot twin study
    • (1997) Int. J. Androl. , vol.20 , pp. 215-221
    • Handelsman, D.J.1
  • 6
  • 7
    • 0017119580 scopus 로고
    • Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm
    • (1976) Hum. Genet. , vol.34 , pp. 119-124
    • Tiepolo, L.1    Zuffardi, O.2
  • 10
    • 9044223283 scopus 로고    scopus 로고
    • Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching
    • (1996) Nat. Genet. , vol.13 , pp. 167-174
    • Banfi S., et, al.1
  • 11
    • 1842415403 scopus 로고    scopus 로고
    • Genome cross-referencing and XREFdb: implications for the identification and analysis of genes mutated in human disease
    • (1997) Nat. Genet. , vol.15 , pp. 339-344
    • Bassett D.E., et, al.1
  • 12
    • 0030986495 scopus 로고    scopus 로고
    • Evolutionary origins and maintenance of redundant gene expression during development
    • (1997) Trends Genet. , vol.13 , pp. 360-364
    • Cooke J., et, al.1
  • 13
    • 0007160779 scopus 로고    scopus 로고
    • The C. elegans sequencing consortium (1998) Genome sequence of the nematode C. elegans. A platform for investigating biology. Science 282, 2012-2018
  • 17
    • 0032493878 scopus 로고    scopus 로고
    • Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis
    • (1998) Cell , vol.94 , pp. 387-398
    • Dernburg A.F., et, al.1
  • 19
    • 0014920801 scopus 로고
    • A gross reduction in chiasma formation during meiotic prophase and a defective DNA repair mechanism associated with a case of human male infertility
    • (1970) Cytogenetics , vol.9 , pp. 460-467
    • Pearson P.L., et, al.1
  • 25
    • 0000808485 scopus 로고    scopus 로고
    • Spermatogenesis
    • Riddle D.L., et al. (Eds.), C. elegans II,, Cold Spring Harbor Laboratory Press
    • (1997) , pp. 271-294
    • L'Hernault, S.W.1
  • 34
    • 0028901601 scopus 로고
    • The paternal inheritance of the centrosome, the cell's microtubule-organizing center, in humans, and the implications for infertility
    • (1995) Nat. Med. , vol.1 , pp. 47-52
    • Simerly C., et, al.1
  • 36
    • 0029863453 scopus 로고    scopus 로고
    • Coordinate developmental control of the meiotic cell cycle and spermatid differentiation in Drosophila males
    • (1996) Development , vol.122 , pp. 1331-1341
    • Lin T.Y., et, al.1
  • 38
    • 0007226146 scopus 로고
    • Drosophila. A Laboratory Handbook, Cold Spring Harbor Laboratory Press
    • (1989)
    • Ashburner, M.1
  • 41
    • 0007292094 scopus 로고    scopus 로고
    • The FlyBase Consortium (1999) The FlyBase database of the Drosophila genome projects and community literature. Nucleic Acids Res. 27, 74-78
  • 44
    • 0028915583 scopus 로고
    • The making of a spermatozoon: a molecular perspective
    • (1995) Dev. Genet. , vol.16 , pp. 95-103
    • Hecht, N.B.1
  • 46
    • 0025158110 scopus 로고
    • A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome
    • (1990) Cell , vol.62 , pp. 777-791
    • Weeda G., et, al.1
  • 47
  • 48
    • 0007299791 scopus 로고    scopus 로고
    • Mounkes, L.C., et al. (1992) A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3 a human excision repair gene. 71, 925-937.
  • 51
    • 0019170931 scopus 로고
    • The genetics of Drosophila subobscura populations. XIII. A study of lethal allelism
    • (1980) Genetica , vol.54 , pp. 197-207
    • Loukas M., et, al.1
  • 53
    • 0007159523 scopus 로고    scopus 로고
    • Guillaume, E. et al. (2000) Proteome analysis of spermatogonia: identification of a first set of 53 proteins. Proteome 10. 1007/s102160000003 ()
  • 54
    • 0027444586 scopus 로고
    • Toward a molecular genetic analysis of spermatogenesis in Drosophila melanogaster: characterization of male-sterile mutants generated by single element mutagenesis
    • (1993) Genetics , vol.135 , pp. 489-505
    • Castrillon D.H., et, al.1
  • 56
  • 57
    • 0031857749 scopus 로고    scopus 로고
    • The Y chromosomal fertility factor Threads in Drosophila hydei harbors a functional gene encoding an axonemal dynein b heavy chain protein
    • (1998) Genetics , vol.149 , pp. 1363-1376
    • Kurek R., et, al.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.