着色性干皮病互补组H被撤销，并重新归类为D组。 - Suppr

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超能文献

Xeroderma pigmentosum complementation group H is withdrawn and reassigned to group D.

作者信息

Robbins J H

出版信息

Hum Genet. 1991 Dec;88(2):242. doi: 10.1007/BF00206082.

DOI:10.1007/BF00206082

PMID:1757099

Abstract

摘要

相似文献

Xeroderma pigmentosum complementation group H is withdrawn and reassigned to group D.着色性干皮病互补组H被撤销，并重新归类为D组。

Hum Genet. 1991 Dec;88(2):242. doi: 10.1007/BF00206082.

Five complementation groups in xeroderma pigmentosum.着色性干皮病中的五个互补群。

Mutat Res. 1975 Dec;33(2-3):327-40. doi: 10.1016/0027-5107(75)90208-0.

Xeroderma pigmentosum complementation group H falls into complementation group D.着色性干皮病互补组H属于互补组D。

Mutat Res. 1991 Sep;255(2):201-8. doi: 10.1016/0921-8777(91)90054-s.

Studies on repair of adenovirus 2 by human fibroblasts using normal, xeroderma pigmentosum, and xeroderma pigmentosum heterozygous strains.利用正常人成纤维细胞、着色性干皮病患者成纤维细胞以及着色性干皮病杂合子菌株对腺病毒2进行修复的研究。

Cancer Res. 1974 Aug;34(8):1965-70.

A seventh complementation group in excision-deficient xeroderma pigmentosum.着色性干皮病切除缺陷型中的第七个互补群。

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The human gene for xeroderma pigmentosum complementation group G (XPG) maps to 13q33 by fluorescence in situ hybridization.通过荧光原位杂交技术，人类着色性干皮病G互补组（XPG）基因定位于13q33。

Genomics. 1994 May 1;21(1):283-5. doi: 10.1006/geno.1994.1261.

Complement analysis of xeroderma pigmentosum variants.着色性干皮病变异型的补体分析

Exp Cell Res. 1981 Nov;136(1):81-90. doi: 10.1016/0014-4827(81)90039-2.

Complementation of the DNA repair deficiency in human xeroderma pigmentosum group a and C cells by recombinant adenovirus-mediated gene transfer.重组腺病毒介导的基因转移对人类色素性干皮病 A 组和 C 组细胞中 DNA 修复缺陷的互补作用。

Hum Gene Ther. 2002 Oct 10;13(15):1833-44. doi: 10.1089/104303402760372936.

Complementation of the xeroderma pigmentosum DNA repair defect in cell-free extracts.无细胞提取物中着色性干皮病DNA修复缺陷的互补作用。

Cell. 1988 Apr 8;53(1):97-106. doi: 10.1016/0092-8674(88)90491-6.

A case of xeroderma pigmentosum complementation group F with neurological abnormalities.一例伴有神经异常的着色性干皮病F互补组病例。

Br J Dermatol. 1993 Jan;128(1):91-4. doi: 10.1111/j.1365-2133.1993.tb00154.x.

引用本文的文献

Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype.与着色性干皮病表型相关的科凯恩综合征互补组B

Hum Genet. 1996 Feb;97(2):176-9. doi: 10.1007/BF02265261.

UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I.UVs综合征是一种新的具有DNA修复缺陷的光敏性疾病类别，与着色性干皮病变异型和啮齿动物互补组I不同。

Am J Hum Genet. 1995 Jun;56(6):1267-76.

本文引用的文献

Assignment of two Japanese xeroderma pigmentosum patients to complementation group D and their characteristics.两名日本着色性干皮病患者被归入互补组D及其特征

Jpn J Cancer Res. 1985 Mar;76(3):162-6.

Delayed sensorineural deafness and skin carcinogenesis in a Japanese xeroderma pigmentosum group D patient.

Photodermatol. 1988 Apr;5(2):83-91.

No apparent neurologic defect in a patient with xeroderma pigmentosum complementation group D.

Arch Dermatol. 1988 Feb;124(2):256-60.

Lack of complementation between xeroderma pigmentosum complementation groups D and H.着色性干皮病互补组D和H之间缺乏互补作用。

Hum Genet. 1989 Feb;81(3):203-10. doi: 10.1007/BF00278989.

No lack of complementation for unscheduled DNA synthesis between xeroderma pigmentosum complementation groups D and H.着色性干皮病互补组D和H之间在非预定DNA合成方面不存在互补缺陷。

Hum Genet. 1989 Dec;84(1):99-101. doi: 10.1007/BF00210685.

Xeroderma pigmentosum complementation group H falls into complementation group D.着色性干皮病互补组H属于互补组D。

Mutat Res. 1991 Sep;255(2):201-8. doi: 10.1016/0921-8777(91)90054-s.

[Photosensitization and DNA repair. Possible nosologic relationship between Xeroderma pigmentosum and Cockayne's syndrome].[光敏作用与DNA修复。着色性干皮病和科凯恩综合征之间可能的疾病关系]

Arch Fr Pediatr. 1978 Dec;35(10 Suppl):65-74.

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