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Genetics of human X-linked immunodeficiency diseases.

作者信息

Hendriks R W, Schuurman R K

机构信息

University Medical Center, Leiden, The Netherlands.

出版信息

Clin Exp Immunol. 1991 Aug;85(2):182-92. doi: 10.1111/j.1365-2249.1991.tb05702.x.

DOI:10.1111/j.1365-2249.1991.tb05702.x
PMID:1863997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1535742/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fa/1535742/3aa1d6de89e7/clinexpimmunol00059-0007-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fa/1535742/6c32a6b6c9bd/clinexpimmunol00059-0006-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fa/1535742/3aa1d6de89e7/clinexpimmunol00059-0007-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fa/1535742/6c32a6b6c9bd/clinexpimmunol00059-0006-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fa/1535742/3aa1d6de89e7/clinexpimmunol00059-0007-a.jpg

相似文献

1
Genetics of human X-linked immunodeficiency diseases.人类X连锁免疫缺陷疾病的遗传学
Clin Exp Immunol. 1991 Aug;85(2):182-92. doi: 10.1111/j.1365-2249.1991.tb05702.x.
2
Molecular genetic analysis of X-linked immunodeficiencies.
Year Immunol. 1993;7:162-7.
3
[Immunologic diseases with sex-linked heredity; current possibilities for prevention].
Ned Tijdschr Geneeskd. 1987 Oct 17;131(42):1849-53.
4
Experiments of nature: primary immune defects deciphered and defeated.自然实验：原发性免疫缺陷被破解与战胜。
Immunol Rev. 2000 Dec;178:5-7. doi: 10.1034/j.1600-065x.2000.17816.x.
5
Immunodeficiency syndromes. X-linked agammaglobulinemia, common variable immunodeficiency, Chédiak-Higashi syndrome, Wiskott-Aldrich syndrome, and X-linked lymphoproliferative disorder.
Dermatol Clin. 1995 Jan;13(1):65-71.
6
Carrier detection in X-linked immunodeficiencies. II: An X inactivation assay based on differential methylation of a line-1 repeat at the DXS255 locus.X连锁免疫缺陷的携带者检测。II：基于DXS255位点LINE-1重复序列差异甲基化的X染色体失活检测法。
Immunodeficiency. 1993;4(1-4):213-5.
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Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locus.X连锁免疫缺陷中的携带者检测。I：基于聚合酶链反应的MAOA基因座X染色体失活检测法。
Immunodeficiency. 1993;4(1-4):209-11.
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The primary immunodeficiencies.原发性免疫缺陷病
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X-linked immunodeficiencies.X连锁免疫缺陷病
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Molecular basis for X-linked immunodeficiencies.
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引用本文的文献

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Knockout of Results in a Sex Ratio Shift toward Males but Superovulation Cannot Compensate for the Reduced Litter Size.基因敲除导致性别比例向雄性偏移，但超数排卵无法弥补产仔数的减少。
Animals (Basel). 2023 Mar 17;13(6):1079. doi: 10.3390/ani13061079.
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Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoire.X连锁无丙种球蛋白血症中的骨髓细胞表达前B细胞特异性基因（λ样和V前B），并且免疫球蛋白V-D-J基因的使用强烈偏向于胎儿样谱系。
J Clin Invest. 1993 Apr;91(4):1616-29. doi: 10.1172/JCI116369.
3

本文引用的文献

1
Agammaglobulinemia.无丙种球蛋白血症
Pediatrics. 1952 Jun;9(6):722-8.
2
Recurrent bacterial infections and dysgamma-globulinemia: deficiency of 7S gamma-globulins in the presence of elevated 19S gamma-globulins. Report of two cases.复发性细菌感染与γ-球蛋白异常血症：19Sγ-球蛋白升高时7Sγ-球蛋白缺乏。两例报告。
Pediatrics. 1961 Aug;28:182-95.
3
Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea.系谱显示一种X连锁隐性疾病，其特征为耳漏、湿疹样皮炎和血性腹泻。
X chromosome inactivation analysis to distinguish sporadic cases of X-linked agammaglobulinaemia from common variable immunodeficiency.
Eur J Pediatr. 1993 Nov;152(11):900-4. doi: 10.1007/BF01957526.
4
Mapping of the X linked form of hyper IgM syndrome (HIGM1).X连锁型高IgM综合征（HIGM1）的定位
J Med Genet. 1993 Mar;30(3):202-5. doi: 10.1136/jmg.30.3.202.
5
Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locus.X染色体高变区DXS255位点两侧5'和3' CCGG位点的差异甲基化。
Hum Genet. 1991 Nov;88(1):105-11. doi: 10.1007/BF00204939.
Pediatrics. 1954 Feb;13(2):133-9.
4
Wiskott-Aldrich syndrome: cellular impairments and their implication for carrier detection.威斯科特-奥尔德里奇综合征：细胞损伤及其对携带者检测的意义。
Blood. 1980 Dec;56(6):1048-54.
5
Genes for growth hormone, chorionic somatommammotropin, and growth hormones-like gene on chromosome 17 in humans.人类17号染色体上的生长激素基因、绒毛膜促生长催乳素基因以及类生长激素基因。
Science. 1980 Jul 11;209(4453):289-92. doi: 10.1126/science.7384802.
6
The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979).
J Pediatr. 1980 Jul;97(1):72-8. doi: 10.1016/s0022-3476(80)80133-8.
7
X-linked hypogammaglobulinemia and isolated growth hormone deficiency.X连锁低丙种球蛋白血症与孤立性生长激素缺乏症。
N Engl J Med. 1980 Jun 26;302(26):1429-34. doi: 10.1056/NEJM198006263022601.
8
IgM-restricted production of immunoglobulin by lymphoid cell lines from patients with immunodeficiency with hyper IgM (dysgammaglobulinemia).来自高IgM免疫缺陷（异常丙种球蛋白血症）患者的淋巴细胞系对免疫球蛋白的IgM限制性产生。
Clin Immunol Immunopathol. 1981 Apr;19(1):91-7. doi: 10.1016/0090-1229(81)90050-7.
9
Polyclonal activation of human lymphocytes in vitro-II. Reappraisal of T and B cell-specific mitogens.人淋巴细胞的体外多克隆激活 - II。对T细胞和B细胞特异性有丝分裂原的重新评估。
J Immunol. 1980 Aug;125(2):827-32.
10
Differentiation of precursor T lymphocytes in man and delineation of the selective abnormalities in severe combined immune deficiency disease.人类前体T淋巴细胞的分化以及严重联合免疫缺陷病中选择性异常的描述。
Clin Immunol Immunopathol. 1982 Dec;25(3):303-15. doi: 10.1016/0090-1229(82)90195-7.