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1
Male pseudohermaphroditism presumably due to target organ unresponsiveness to androgens. Deficient 5alpha-dihydrotestosterone binding in cultured skin fibroblasts.男性假两性畸形可能是由于靶器官对雄激素无反应。培养的皮肤成纤维细胞中5α-二氢睾酮结合不足。
J Clin Invest. 1976 Aug;58(2):345-50. doi: 10.1172/JCI108478.
2
5alpha-reductase activity of genital and nongenital skin fibroblasts from patients with 5alpha-reductase deficiency, androgen insensitivity, or unknown forms of male pseudohermaphroditism.5α-还原酶缺乏症、雄激素不敏感或不明形式男性假两性畸形患者生殖器及非生殖器皮肤成纤维细胞的5α-还原酶活性。
Am J Med Genet. 1978;1(4):407-16. doi: 10.1002/ajmg.1320010404.
3
Dihydrotestosterone binding by cultured human fibroblasts. Comparison of cells from control subjects and from patients with hereditary male pseudohermaphroditism due to androgen resistance.培养的人成纤维细胞对双氢睾酮的结合。对照受试者与雄激素抵抗所致遗传性男性假两性畸形患者细胞的比较。
J Clin Invest. 1976 May;57(5):1342-51. doi: 10.1172/JCI108402.
4
Male pseudohermaphroditism: diagnosis in cell culture.男性假两性畸形:细胞培养中的诊断
Can Med Assoc J. 1977 Jun 4;116(11):1274-5, 1277.
5
Complete androgen insensitivity with a normal amount of 5 alpha-dihydrotestosterone-binding activity in labium majus skin fibroblasts.大阴唇皮肤成纤维细胞中5α - 双氢睾酮结合活性正常的完全雄激素不敏感症
Am J Med Genet. 1979;4(4):401-11. doi: 10.1002/ajmg.1320040410.
6
Expression of androgen-responsive properties in human skin fibroblast strains of genital and nongenital origin.来自生殖器和非生殖器部位的人皮肤成纤维细胞株中雄激素反应特性的表达。
Somatic Cell Genet. 1977 Jan;3(1):17-25. doi: 10.1007/BF01550984.
7
Reduced affinity of the androgen receptor for 5 alpha-dihydrotestosterone but not methyltrienolone in a form of partial androgen resistance. Studies on cultured genital skin fibroblasts.在一种部分雄激素抵抗形式中,雄激素受体对5α - 双氢睾酮的亲和力降低,但对甲基三烯olone的亲和力未降低。对培养的生殖器皮肤成纤维细胞的研究。
J Clin Invest. 1985 Apr;75(4):1291-6. doi: 10.1172/JCI111829.
8
Testicular feminization associated with a thermolabile androgen receptor in culutred human fibroblasts.培养的人成纤维细胞中与热不稳定雄激素受体相关的睾丸女性化
J Clin Invest. 1979 Dec;64(6):1624-31. doi: 10.1172/JCI109624.
9
Specific 5alpha-dihydrotestosterone binding in labial skin fibroblasts cultured from patients.with male pseudohermaphroditism.从男性假两性畸形患者培养的阴唇皮肤成纤维细胞中特异性5α-二氢睾酮结合
Clin Genet. 1976 Jun;9(6):567-74. doi: 10.1111/j.1399-0004.1976.tb01614.x.
10
Androgen binding in cultured human fibroblasts from patients with idiopathic hypospadias.特发性尿道下裂患者培养的人成纤维细胞中的雄激素结合
Horm Metab Res. 1987 Oct;19(10):497-501. doi: 10.1055/s-2007-1011862.

引用本文的文献

1
Management of disorders of sex development.性发育障碍的管理。
Nat Rev Endocrinol. 2014 Sep;10(9):520-9. doi: 10.1038/nrendo.2014.108. Epub 2014 Jul 15.
2
Substitution of arginine-839 by cysteine or histidine in the androgen receptor causes different receptor phenotypes in cultured cells and coordinate degrees of clinical androgen resistance.雄激素受体中第839位精氨酸被半胱氨酸或组氨酸取代,会在培养细胞中导致不同的受体表型以及不同程度的临床雄激素抵抗。
J Clin Invest. 1994 Aug;94(2):546-54. doi: 10.1172/JCI117368.
3
The presence of androgen-binding receptors in genital and nongenital skin fibroblasts.雄激素结合受体在生殖器和非生殖器皮肤成纤维细胞中的存在。
Hum Genet. 1980 Feb;53(2):271-3. doi: 10.1007/BF00273510.
4
DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminisation).培养的人成纤维细胞中的双氢睾酮受体:对一个雄激素不敏感(完全性睾丸女性化)家族的结合研究
J Med Genet. 1982 Oct;19(5):349-53. doi: 10.1136/jmg.19.5.349.
5
Cultured human skin fibroblasts: a model for the study of androgen action.培养的人皮肤成纤维细胞:雄激素作用研究的模型。
Mol Cell Biochem. 1981 Apr 13;36(1):3-22. doi: 10.1007/BF02354827.
6
Familial incomplete male pseudohermaphroditism associated with impaired nuclear androgen retention. Studies in cultured skin fibroblasts.与核雄激素保留受损相关的家族性不完全男性假两性畸形。对培养的皮肤成纤维细胞的研究。
J Clin Invest. 1983 Apr;71(4):850-8. doi: 10.1172/jci110839.
7
Carrier detection in the testicular feminisation syndrome: deficient 5 alpha-dihydrotestosterone binding in cultured skin fibroblasts from the mothers of patients with complete androgen insensitivity.睾丸女性化综合征的携带者检测:完全雄激素不敏感患者母亲的培养皮肤成纤维细胞中5α-双氢睾酮结合缺陷
J Med Genet. 1984 Jun;21(3):178-81. doi: 10.1136/jmg.21.3.178.
8
Deletion of the steroid-binding domain of the human androgen receptor gene in one family with complete androgen insensitivity syndrome: evidence for further genetic heterogeneity in this syndrome.在一个患有完全性雄激素不敏感综合征的家族中,人类雄激素受体基因类固醇结合结构域的缺失:该综合征存在进一步遗传异质性的证据。
Proc Natl Acad Sci U S A. 1988 Nov;85(21):8151-5. doi: 10.1073/pnas.85.21.8151.
9
An exonic point mutation of the androgen receptor gene in a family with complete androgen insensitivity.一个患有完全性雄激素不敏感综合征的家族中雄激素受体基因的外显子点突变。
Am J Hum Genet. 1990 Jun;46(6):1095-100.
10
Replacement of arginine 773 by cysteine or histidine in the human androgen receptor causes complete androgen insensitivity with different receptor phenotypes.人类雄激素受体中精氨酸773被半胱氨酸或组氨酸取代会导致完全性雄激素不敏感,并伴有不同的受体表型。
Am J Hum Genet. 1992 Jul;51(1):143-55.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
THE LIMITED IN VITRO LIFETIME OF HUMAN DIPLOID CELL STRAINS.人二倍体细胞株的体外寿命有限。
Exp Cell Res. 1965 Mar;37:614-36. doi: 10.1016/0014-4827(65)90211-9.
3
FURTHER OBSERVATIONS ON THE SYNDROME, "TESTICULAR FEMINIZATION".关于“睾丸女性化”综合征的进一步观察
Am J Obstet Gynecol. 1963 Nov 15;87:731-48.
4
Lack of stereospecificity of glucose binding to human erythrocyte membrane protein upon reduction with sodium borohydride.用硼氢化钠还原后葡萄糖与人红细胞膜蛋白结合缺乏立体特异性。
Biochem Biophys Res Commun. 1969 Aug 15;36(4):690-5. doi: 10.1016/0006-291x(69)90361-1.
5
Absence of response to dihydrotestosterone in the syndrome of testicular feminization.睾丸女性化综合征中对双氢睾酮无反应
J Clin Endocrinol Metab. 1969 Sep;29(9):1284-6. doi: 10.1210/jcem-29-9-1284.
6
Familial syndrome of streak gonads and normal male karyotype in five phenotypic females.五名表型女性的条索状性腺和正常男性核型的家族综合征。
N Engl J Med. 1970 Jul 2;283(1):6-11. doi: 10.1056/NEJM197007022830102.
7
Testosterone metabolism by serially subcultured fibroblasts from genital and nongenital skin of individual human donors.来自个体人类供体生殖器和非生殖器皮肤的连续传代培养成纤维细胞的睾酮代谢。
Biochem Biophys Res Commun. 1972 Jan 31;46(2):364-9. doi: 10.1016/s0006-291x(72)80147-5.
8
A new male pseudo-hermaphroditism associated with hypertension due to a block of 17 -hydroxylation.一种与17α-羟化受阻所致高血压相关的新型男性假两性畸形。
J Clin Endocrinol Metab. 1972 Jul;35(1):67-72. doi: 10.1210/jcem-35-1-67.
9
Metabolism of 4- 14 C-testosterone by serially subcultured human skin fibroblasts.经连续传代培养的人皮肤成纤维细胞对4-¹⁴C-睾酮的代谢
J Clin Endocrinol Metab. 1972 Jan;34(1):133-43. doi: 10.1210/jcem-34-1-133.
10
Syndrome of androgen insensitivity in man: absence of 5 alpha-dihydrotestosterone binding protein in skin fibroblasts.男性雄激素不敏感综合征:皮肤成纤维细胞中缺乏5α-二氢睾酮结合蛋白。
J Clin Endocrinol Metab. 1974 Jun;38(6):1143-6. doi: 10.1210/jcem-38-6-1143.

男性假两性畸形可能是由于靶器官对雄激素无反应。培养的皮肤成纤维细胞中5α-二氢睾酮结合不足。

Male pseudohermaphroditism presumably due to target organ unresponsiveness to androgens. Deficient 5alpha-dihydrotestosterone binding in cultured skin fibroblasts.

作者信息

Kaufman M, Straisfeld C, Pinsky L

出版信息

J Clin Invest. 1976 Aug;58(2):345-50. doi: 10.1172/JCI108478.

DOI:10.1172/JCI108478
PMID:182718
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC333189/
Abstract

Maximum specific 5alpha-dihydrotestosterone (DHT) binding activity (Bmax) had been measured in intact confluent monolayers representing fibroblast strains derived form nongenital and genital (labium majus) skin of normal individuals and of 11 patients fulfilling the clinicogenetic criteria of complete testicular feminization (TF). Nine labium majus strains from adult females had a mean Bmax value three times greater than that of seven nongenital strains from adult females (33 vs. 11 fmol/mg cell protein). The Bmax results for 13 adult nongenital strains varied from 5.6 to 23.3 fmol/mg protein; the values for males and females had very similar means and ranges. The variation could not be correlated with the chronologic age of adult skin explant donors or with the in vitro age (mean population doubling level) of the cultures assayed. The Bmax activities of three nongenital strains from normal infants (two male, one female) did not exceed 5 fmol/mg protein. Seven of eight nongenital TF strains had Bmax values below 2 fmol/mg protein; the value for the eighth coincided with the lower limit of normal adults. The lower limit of DHT binding in normal labium majus strains was 15 fmol/mg protein. Three of five labial strains from patients with TF had Bmax values close to zero; the other two fell between 10 and 15 fmol/mg protein. It is apparant that labial skin fibroblast strains from clinically homogeneous patients with TF had highly variable degrees of DHT binding deficiency, and that they permit a more reliable diagnosis of severe and intermediate degrees of DHT binding deficiency than do strains of nongenital skin fibroblasts.

摘要

已在完整的汇合单层细胞中测量了最大特异性5α - 双氢睾酮(DHT)结合活性(Bmax),这些单层细胞代表了源自正常个体以及11例符合完全睾丸女性化(TF)临床遗传学标准患者的非生殖器和生殖器(大阴唇)皮肤的成纤维细胞系。来自成年女性的9个大阴唇细胞系的平均Bmax值比来自成年女性的7个非生殖器细胞系的平均Bmax值大三倍(33对11 fmol/mg细胞蛋白)。13个成年非生殖器细胞系的Bmax结果在5.6至23.3 fmol/mg蛋白之间;男性和女性的值具有非常相似的均值和范围。这种变化与成年皮肤外植体供体的实际年龄或所检测培养物的体外年龄(平均群体倍增水平)无关。来自正常婴儿(2例男性,1例女性)的3个非生殖器细胞系的Bmax活性不超过5 fmol/mg蛋白。8个非生殖器TF细胞系中有7个的Bmax值低于2 fmol/mg蛋白;第8个的值与正常成年人的下限一致。正常大阴唇细胞系中DHT结合的下限为15 fmol/mg蛋白。来自TF患者的5个阴唇细胞系中有3个的Bmax值接近零;另外2个介于10至15 fmol/mg蛋白之间。显然,来自临床同质的TF患者的阴唇皮肤成纤维细胞系具有高度可变的DHT结合缺陷程度,并且与非生殖器皮肤成纤维细胞系相比,它们能更可靠地诊断严重和中度的DHT结合缺陷。