메뉴 건너뛰기




Volumn 17, Issue 12, 2001, Pages 697-701

A high density of X-linked genes for general cognitive ability: A run-away process shaping human evolution?

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOME; BONE DYSPLASIA; CLEFT PALATE; COGNITION; DISEASE ASSOCIATION; EVOLUTION; GENE MAPPING; GROWTH RETARDATION; HAPLOTYPE; INFERTILITY; MENTAL DEFICIENCY; MORBIDITY; NONHUMAN; NUTRITION; POLYDACTYLY; PRIORITY JOURNAL; REVIEW; X CHROMOSOME;

EID: 0035577350     PISSN: 01689525     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-9525(01)02446-5     Document Type: Review
Times cited : (213)

References (34)
  • 9
    • 0030253109 scopus 로고    scopus 로고
    • Comparative genome organization of vertebrates
    • (1996) Mamm. Genome , vol.7 , pp. 717-734
  • 13
    • 0001688073 scopus 로고
    • Evolution of postmating reproductive isolation: The composite nature of Haldane's rule and its genetic bases
    • (1993) Am. Nat. , vol.142 , pp. 187-212
    • Wu, C.I.1    Davis, A.W.2
  • 18
    • 0027715424 scopus 로고
    • Enhanced expression of the murine FMR1 gene during germ cell proliferation suggests a special function in both the male and the female gonad
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 2043-2050
    • Baechner, D.1
  • 21
    • 0029007354 scopus 로고
    • Sex differences in mental test scores, variability, and numbers of high-scoring individuals
    • (1995) Science , vol.269 , pp. 41-45
    • Hedges, L.V.1    Nowell, A.2
  • 23
    • 0030137717 scopus 로고    scopus 로고
    • Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators
    • (1996) Nat. Genet. , vol.13 , pp. 105-108
    • Gécz, J.1
  • 24
    • 17344369362 scopus 로고    scopus 로고
    • Mutations in GDI1 are responsible for X-linked non-specific mental retardation
    • (1998) Nat. Genet. , vol.19 , pp. 134-139
    • D'Adamo, P.1
  • 25
    • 0032580161 scopus 로고    scopus 로고
    • Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation
    • (1998) Nature , vol.392 , pp. 923-926
    • Billuart, P.1
  • 26
    • 0031710557 scopus 로고    scopus 로고
    • PAK3 mutation in nonsyndromic X-linked mental retardation
    • (1998) Nat. Genet. , vol.20 , pp. 25-30
    • Allen, K.M.1
  • 27
    • 0029832136 scopus 로고    scopus 로고
    • Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome
    • (1996) Nature , vol.384 , pp. 567-570
    • Trivier, E.1
  • 28
    • 0032819848 scopus 로고    scopus 로고
    • A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation
    • (1999) Nat. Genet. , vol.23 , pp. 25-31
    • Carrié, A.1
  • 29
    • 0033968407 scopus 로고    scopus 로고
    • A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation
    • (2000) Nat. Genet. , vol.24 , pp. 167-171
    • Zemni, R.1
  • 30
    • 0033775672 scopus 로고    scopus 로고
    • Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation
    • (2000) Nat. Genet. , vol.26 , pp. 247-250
    • Kutsche, K.1
  • 31
    • 0033572435 scopus 로고    scopus 로고
    • A novel risosomal S6-kinase (RSK4; RPS6KA6) is commonly deleted in patients with complex X-linked mental retardation
    • (1999) Genomics , vol.62 , pp. 332-343
    • Yntema, H.G.1
  • 32
    • 0032872234 scopus 로고    scopus 로고
    • Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 1833-1838
    • Chelly, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.