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Bare-patches, a new sex-linked gene in the mouse, associated with a high production of XO females. I. A preliminary report of breeding experiments.

作者信息

Phillips R J, Hawker S G, Moseley H J

出版信息

Genet Res. 1973 Aug;22(1):91-9.

PMID:4588955
Abstract
摘要

相似文献

1
Bare-patches, a new sex-linked gene in the mouse, associated with a high production of XO females. I. A preliminary report of breeding experiments.
Genet Res. 1973 Aug;22(1):91-9.
2
Bare-patches, a new sex-linked gene in the mouse, associated with a high production of XO females. I. A preliminary report of breeding experiments.
J Chem Soc Perkin 1. 1974;1:91-9.
3
Bare-patches, a new sex-linked gene in the mouse, associated with a high production of XO females. II. Investigations into the nature and mechanism of the XO production.
Genet Res. 1974 Aug;24(1):27-41. doi: 10.1017/s0016672300015056.
4
Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.com.褴褛小鼠和X连锁显性点状软骨发育不良中δ8-δ7甾醇异构酶的突变。jderry@immunex.com。
Nat Genet. 1999 Jul;22(3):286-90. doi: 10.1038/10350.
5
[Factors affecting complementation in compounds of the T-locus lethal haplotypes of the house mouse].
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[Analysis of dominant and recessive sex-linked lethal mutations induced by low radiation doses in genetically different strains of Drosophila melanogaster w and MS].[对黑腹果蝇w和MS不同遗传品系中低辐射剂量诱导的显性和隐性性连锁致死突变的分析]
Genetika. 1994 Sep;30(9):1220-3.
7
[A family with Steinert's myotomic dystrophy affecting only the females].一个仅女性受斯坦纳特型肌强直性营养不良影响的家族
J Genet Hum. 1975 Oct;23 SUPPL:180.
8
[Effect of the female genotype on the yield of dominant lethal mutations induced by thiophosphamide in mature mouse spermia].
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Variation in recombination frequencies in Schizophyllum commune and its genetic control.裂褶菌重组频率的变异及其遗传控制。
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Genetics analysis of mouse mutations Abnormal feet and tail and rough coat, which cause developmental abnormalities and alopecia.小鼠突变的遗传学分析 足部和尾巴异常以及被毛粗糙，会导致发育异常和脱发。
Mamm Genome. 2002 Dec;13(12):675-9. doi: 10.1007/s00335-002-2191-6.

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Developmental expression pattern of the cholesterogenic enzyme NSDHL and negative selection of NSDHL-deficient cells in the heterozygous Bpa(1H)/+ mouse.胆固醇生成酶 NSDHL 的发育表达模式及杂合 Bpa(1H)/+ 小鼠中 NSDHL 缺陷细胞的负选择。
Mol Genet Metab. 2009 Dec;98(4):356-66. doi: 10.1016/j.ymgme.2009.06.016. Epub 2009 Jul 4.
3
Meiotic exchange and segregation in female mice heterozygous for paracentric inversions.
雌性小鼠臂内倒位杂合子时的减数分裂交换与分离
Genetics. 2004 Mar;166(3):1199-214. doi: 10.1534/genetics.166.3.1199.
4
Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.
Mamm Genome. 1993;4(3):171-6. doi: 10.1007/BF00352233.
5
Genetic and physical mapping of the biglycan gene on the mouse X chromosome.
Mamm Genome. 1993;4(1):33-6. doi: 10.1007/BF00364660.
6
Homologous genes for X-linked chondrodysplasia punctata in man and mouse.人类和小鼠中X连锁点状软骨发育不良的同源基因。
Hum Genet. 1983;63(1):24-7. doi: 10.1007/BF00285392.
7
Oocyte development in XO foetuses of man and mouse: the possible role of heterologous X-chromosome pairing in germ cell survival.人类和小鼠XO胎儿中的卵母细胞发育：异源X染色体配对在生殖细胞存活中的可能作用。
Chromosoma. 1986;94(2):115-24. doi: 10.1007/BF00286989.
8
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation.
Hum Genet. 1992 Aug;89(6):659-65. doi: 10.1007/BF00221958.
9
Human male infertility, probably genetically determined, due to defective meiosis and spermatogenic arrest.人类男性不育症，可能由基因决定，是由于减数分裂缺陷和生精停滞所致。
Am J Hum Genet. 1979 Sep;31(5):634-41.
10
X-linked dominant chondrodysplasia punctata. Review of literature and report of a case.X连锁显性点状软骨发育不良。文献综述及一例报告
Hum Genet. 1979;53(1):65-73. doi: 10.1007/BF00289453.