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Volumn 62, Issue 6, 1998, Pages 1555-1557

Familial skewed X inactivation and X-linked mutations: Unbalanced X inactivation is a powerfulmeans to ascertain X-linked genes that affect cell proliferation [7] (multiple letters)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROLIFERATION; CHROMOSOME INACTIVATION; DISOMY; FAMILIAL DISEASE; GENE DELETION; GENE MUTATION; GENETIC LINKAGE; HUMAN; LETTER; PEDIGREE; PRIORITY JOURNAL; X CHROMOSOME LINKAGE;

EID: 0031749799     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301858     Document Type: Letter
Times cited : (22)

References (14)
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    • Genetic control of X inactivation and processes leading to X-inactivation skewing
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    • Belmont, JW1
  • 3
    • 0024443514 scopus 로고
    • Studies of X-chromosome inactivation in trisomies
    • PA Jacobs BR Migeon Studies of X-chromosome inactivation in trisomies Cytogenet Cell Genet 50 1989 75 77
    • (1989) Cytogenet Cell Genet , vol.50 , pp. 75-77
    • Jacobs, PA1    Migeon, BR2
  • 4
    • 0030895047 scopus 로고    scopus 로고
    • Long-range cis effects of ectopic X- inactivation centres on a mouse autosome
    • JT Lee R Jaenisch Long-range cis effects of ectopic X- inactivation centres on a mouse autosome Nature 386 1997 275 279
    • (1997) Nature , vol.386 , pp. 275-279
    • Lee, JT1    Jaenisch, R2
  • 5
    • 0030581152 scopus 로고    scopus 로고
    • A 450 kb transgene displays properties of the mammalian X-inactivation center
    • JT Lee WM Strauss JA Dausman R Jaenisch A 450 kb transgene displays properties of the mammalian X-inactivation center Cell 86 1996 83 94
    • (1996) Cell , vol.86 , pp. 83-94
    • Lee, JT1    Strauss, WM2    Dausman, JA3    Jaenisch, R4
  • 6
    • 0019496026 scopus 로고
    • Structural anomalies of the X chromosome and inactivation center
    • MG Mattei JF Mattei I Vidal F Giraud Structural anomalies of the X chromosome and inactivation center Hum Genet 56 1981 401 408
    • (1981) Hum Genet , vol.56 , pp. 401-408
    • Mattei, MG1    Mattei, JF2    Vidal, I3    Giraud, F4
  • 7
    • 0027467322 scopus 로고
    • The postulated X-inactivation center at Xq27 is most reasonably explained by ascertainment bias: heterozygous expression of recessive mutations is a powerful means of detecting unbalanced X inactivation
    • BR Migeon The postulated X-inactivation center at Xq27 is most reasonably explained by ascertainment bias: heterozygous expression of recessive mutations is a powerful means of detecting unbalanced X inactivation Am J Hum Genet 52 1993 431 432
    • (1993) Am J Hum Genet , vol.52 , pp. 431-432
    • Migeon, BR1
  • 9
    • 0343558600 scopus 로고
    • Adrenoleukodystrophy: evidence for X-linkage, inactivation and selection favoring the mutant allele in heterozygous cells
    • BR Migeon HW Moser AB Moser JA Sprenkle D Sillence RA Norum Adrenoleukodystrophy: evidence for X-linkage, inactivation and selection favoring the mutant allele in heterozygous cells Proc Natl Acad Sci USA 78 1981 5066 5070
    • (1981) Proc Natl Acad Sci USA , vol.78 , pp. 5066-5070
    • Migeon, BR1    Moser, HW2    Moser, AB3    Sprenkle, JA4    Sillence, D5    Norum, RA6
  • 10
    • 0029846444 scopus 로고    scopus 로고
    • Selection against mutant alleles in blood leukocytes is a consistent feature in incontinentia pigmenti type 2
    • JE Parrish AE Scheuerle RA Lewis ML Levy DL Nelson Selection against mutant alleles in blood leukocytes is a consistent feature in incontinentia pigmenti type 2 Hum Mol Genet 5 1996 1777 1783
    • (1996) Hum Mol Genet , vol.5 , pp. 1777-1783
    • Parrish, JE1    Scheuerle, AE2    Lewis, RA3    Levy, ML4    Nelson, DL5
  • 11
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    • Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28
    • E Pegoraro J Whitaker P Mowery-Rushton U Surti M Lanasa EP Hoffman Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28 Am J Hum Genet 61 1997 160 170
    • (1997) Am J Hum Genet , vol.61 , pp. 160-170
    • Pegoraro, E1    Whitaker, J2    Mowery-Rushton, P3    Surti, U4    Lanasa, M5    Hoffman, EP6
  • 12
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    • A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation
    • RM Plenge BD Hendrich C Schwartz F Arena A Naumova C Sapienza R Winter A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation Nat Genet 17 1997 353 356
    • (1997) Nat Genet , vol.17 , pp. 353-356
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  • 13
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    • Choroideremia, congenital deafness and mental retardation in a family with an X chromosomal deletion
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    • (1987) Ophthalmic Paediatr Genet , vol.8 , pp. 139-143
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.