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Evidence for the derivation of individual hair roots from three progenitor cells.

作者信息

Dancis J, Silvers D N, Balis M E, Cox R P, Schwartz M S

出版信息

Hum Genet. 1981;58(4):414-6. doi: 10.1007/BF00282826.

DOI:10.1007/BF00282826
PMID:7327563
Abstract
摘要

相似文献

1
Evidence for the derivation of individual hair roots from three progenitor cells.
Hum Genet. 1981;58(4):414-6. doi: 10.1007/BF00282826.
2
Mutation analysis and prenatal diagnosis in a Lesch-Nyhan family showing non-random X-inactivation interfering with carrier detection tests.对一个莱施-奈恩综合征家族进行的突变分析和产前诊断，该家族显示存在非随机X染色体失活现象，干扰了携带者检测试验。
Hum Genet. 1992 Jun;89(4):395-400. doi: 10.1007/BF00194310.
3
HPRT gene mutations in a female Lesch-Nyhan patient.
Adv Exp Med Biol. 1991;309B:109-12. doi: 10.1007/978-1-4615-7703-4_24.
4
Novel nonsense mutation in the hypoxanthine guanine phosphoribosyltransferase gene and nonrandom X-inactivation causing Lesch-Nyhan syndrome in a female patient.
Hum Mutat. 1996;7(1):52-8. doi: 10.1002/(SICI)1098-1004(1996)7:1<52::AID-HUMU7>3.0.CO;2-R.
5
Diagnosis of Lesch-Nyhan heterozygotes by peripheral blood.
Adv Exp Med Biol. 1986;195 Pt A:157-62. doi: 10.1007/978-1-4684-5104-7_24.
6
The diagnosis of the carrier state for the Lesch--Nyhan syndrome.
Q J Med. 1975 Apr;44(174):189-205.
7
Increased de novo purine synthesis in cultured skin fibroblasts from heterozygotes for the Lesch-Nyhan syndrome. A sensitive marker for carrier detection.莱施-奈恩综合征杂合子培养的皮肤成纤维细胞中嘌呤从头合成增加。一种用于携带者检测的敏感标志物。
Hum Hered. 1979;29(1):64-8. doi: 10.1159/000153018.
8
Prenatal diagnosis of HPRT mutant genes in Lesch-Nyhan syndrome.
Adv Exp Med Biol. 1998;431:211-4. doi: 10.1007/978-1-4615-5381-6_41.
9
An improved procedure for detection of hypoxanthine--guanine phosphoribosyl transferase heterozygotes.
Clin Chem. 1982 May;28(5):1181-4.
10
Comparison of surface differentiation antigens between HGPRT-positive and negative T-cells from two Lesch-Nyhan heterozygotes.
Adv Exp Med Biol. 1986;195 Pt A:281-5. doi: 10.1007/978-1-4684-5104-7_46.

引用本文的文献

1
Mosaic mutations of the FLN1 gene cause a mild phenotype in patients with periventricular heterotopia.FLN1基因的镶嵌突变在室周结节性异位患者中导致轻度表型。
Neurogenetics. 2004 Sep;5(3):191-6. doi: 10.1007/s10048-004-0187-y. Epub 2004 Jul 28.
2
Noninvasive test for fragile X syndrome, using hair root analysis.使用发根分析对脆性X综合征进行无创检测。
Am J Hum Genet. 1999 Jul;65(1):98-103. doi: 10.1086/302462.
3
Detection of the carrier state for an X-linked disorder, the Lesch-Nyhan syndrome, by the use of lymphocyte cloning.

本文引用的文献

1
SELECTION IN MAMMALIAN MOSAIC CELL POPULATIONS.哺乳动物嵌合细胞群体中的选择
Cold Spring Harb Symp Quant Biol. 1964;29:253-60. doi: 10.1101/sqb.1964.029.01.028.
2
Gene action in the X-chromosome of the mouse (Mus musculus L.).小鼠（小家鼠）X染色体上的基因作用。
Nature. 1961 Apr 22;190:372-3. doi: 10.1038/190372a0.
3
Absence of mosaicism in the lymphocyte in X-linked congenital hyperuricosuria.X连锁先天性高尿酸尿症患者淋巴细胞中不存在嵌合体现象。
通过淋巴细胞克隆检测X连锁疾病——莱施-尼汉综合征的携带者状态。
Hum Genet. 1983;64(3):288-90. doi: 10.1007/BF00279414.
4
Hair root analysis in X-linked ichthyosis.
J Inherit Metab Dis. 1983;6(4):173-7. doi: 10.1007/BF02310876.
Life Sci. 1968 Jun 15;7(12):587-91. doi: 10.1016/0024-3205(68)90079-9.
4
Lesch-Nyhan syndrome: rapid detection of heterozygotes by use of hair follicles.莱施-奈恩综合征：利用毛囊快速检测杂合子。
Science. 1971 May 7;172(3983):572-4. doi: 10.1126/science.172.3983.572.
5
Glucose-6 phosphate dehydrogenase mosaicism: utilization as a tracer in the study of the development of hair root cells.葡萄糖-6-磷酸脱氢酶嵌合体：作为追踪剂在毛根细胞发育研究中的应用。
Ann Hum Genet. 1969 Oct;33(2):171-6. doi: 10.1111/j.1469-1809.1969.tb01642.x.
6
Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome.莱施-奈恩综合征杂合子红细胞中葡萄糖-6-磷酸脱氢酶的半合子表达。
Proc Natl Acad Sci U S A. 1970 Jan;65(1):214-8. doi: 10.1073/pnas.65.1.214.
7
Detection of the heterozygote in Lesch-Nyhan disease by hair-root analysis.通过发根分析检测莱施-尼汉病杂合子。
N Engl J Med. 1972 Feb 24;286(8):390-5. doi: 10.1056/NEJM197202242860802.