156 related articles for article (PubMed ID: 10428170)
21. Gonadal structures in a fetus with complete androgen insensitivity syndrome and persistent Müllerian derivatives: comparison with normal fetal development.
Corbetta S; Muzza M; Avagliano L; Bulfamante G; Gaetti L; Eller-Vainicher C; Beck-Peccoz P; Spada A
Fertil Steril; 2011 Mar; 95(3):1119.e9-14. PubMed ID: 20971460
[TBL] [Abstract][Full Text] [Related]
22. Ala 586 Asp mutation in androgen receptor disrupts transactivation function without affecting androgen binding.
Rajender S; Gupta NJ; Chakrabarty B; Singh L; Thangaraj K
Fertil Steril; 2009 Mar; 91(3):933.e23-8. PubMed ID: 19062009
[TBL] [Abstract][Full Text] [Related]
23. Tumors of dysgenetic gonads in Swyer syndrome.
Zieliñska D; Zajaczek S; Rzepka-Górska I
J Pediatr Surg; 2007 Oct; 42(10):1721-4. PubMed ID: 17923202
[TBL] [Abstract][Full Text] [Related]
24. 46 XY pure gonadal dysgenesis with gonadoblastoma and dysgerminoma.
Ben Temime R; Chachial A; Attial L; Ghodbanel I; Makhloufl T; Koubaal A; Kourda N; Ben Jilani S; Dammak T; El May A; Rahal K
Tunis Med; 2008 Jul; 86(7):710-3. PubMed ID: 19472738
[TBL] [Abstract][Full Text] [Related]
25. [Complete form of androgen insensitivity syndrome in Brazilian patients due to P766A mutation in the androgen receptor].
Corrêa RV; Wey JC; Billerbeck AE; Melo KF; Mendonça BB; Wey MV; Arnhold IJ
Arq Bras Endocrinol Metabol; 2005 Feb; 49(1):98-102. PubMed ID: 16544040
[TBL] [Abstract][Full Text] [Related]
26. [Identification of a novel frameshift mutation of human androgen receptor gene in a patient featuring complete androgen insensitivity syndrome].
Xie JH; Qu JH; Xiao QZ; Zhou YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):99-101. PubMed ID: 23450491
[TBL] [Abstract][Full Text] [Related]
27. Frame-shift mutation in hormone binding domain of human androgen receptor gene causes complete androgen insensitivity.
Chung HW; Kim SC; Kim HL
Mol Cells; 1998 Dec; 8(6):741-5. PubMed ID: 9895128
[TBL] [Abstract][Full Text] [Related]
28. Point mutations detected in the androgen receptor gene of three men with partial androgen insensitivity syndrome.
Saunders PT; Padayachi T; Tincello DG; Shalet SM; Wu FC
Clin Endocrinol (Oxf); 1992 Sep; 37(3):214-20. PubMed ID: 1424203
[TBL] [Abstract][Full Text] [Related]
29. A large deletion/insertion-induced frameshift mutation of the androgen receptor gene in a family with a familial complete androgen insensitivity syndrome.
Cong P; Ye Y; Wang Y; Lu L; Yong J; Yu P; Joseph KK; Jin F; Qi M
Gene; 2012 Jun; 500(2):220-3. PubMed ID: 22487869
[TBL] [Abstract][Full Text] [Related]
30. 46,XY pure gonadal dysgenesis with gonadoblastoma.
Ikarashi T; Sudo N; Arakawa O; Furuya M; Kato M; Hirasawa H; Kato M; Kaneko H
Nihon Sanka Fujinka Gakkai Zasshi; 1989 Nov; 41(11):1831-5. PubMed ID: 2592807
[TBL] [Abstract][Full Text] [Related]
31. Identification of a novel mutation in exon 1 of androgen receptor gene in an azoospermic patient with mild androgen insensitivity syndrome: case report and literature review.
Goglia U; Vinanzi C; Zuccarello D; Malpassi D; Ameri P; Casu M; Minuto F; Foresta C; Ferone D
Fertil Steril; 2011 Nov; 96(5):1165-9. PubMed ID: 21962961
[TBL] [Abstract][Full Text] [Related]
32. A novel Arg615Ser mutation of androgen receptor DNA-binding domain in three 46,XY sisters with complete androgen insensitivity syndrome and bilateral inguinal hernia.
Sharma V; Singh R; Thangaraj K; Jyothy A
Fertil Steril; 2011 Feb; 95(2):804.e19-21. PubMed ID: 20888558
[TBL] [Abstract][Full Text] [Related]
33. Primary amenorrhea in a young Polish woman with complete androgen insensitivity syndrome and Sertoli-Leydig cell tumor: identification of a new androgen receptor gene mutation and evidence of aromatase hyperactivity and apoptosis dysregulation within the tumor.
Jarzabek K; Philibert P; Koda M; Sulkowski S; Kotula-Balak M; Bilinska B; Kottler ML; Wolczynski S; Sultan C
Gynecol Endocrinol; 2007 Sep; 23(9):499-504. PubMed ID: 17852420
[TBL] [Abstract][Full Text] [Related]
34. Gonadoblastoma arising in undifferentiated gonadal tissue within dysgenetic gonads.
Cools M; Stoop H; Kersemaekers AM; Drop SL; Wolffenbuttel KP; Bourguignon JP; Slowikowska-Hilczer J; Kula K; Faradz SM; Oosterhuis JW; Looijenga LH
J Clin Endocrinol Metab; 2006 Jun; 91(6):2404-13. PubMed ID: 16608895
[TBL] [Abstract][Full Text] [Related]
35. A frame-shift mutation of the androgen receptor gene in a patient with receptor-negative complete testicular feminization: comparison with a single base substitution in a receptor-reduced incomplete form.
Imai A; Ohno T; Iida K; Ohsuye K; Okano Y; Tamaya T
Ann Clin Biochem; 1995 Sep; 32 ( Pt 5)():482-6. PubMed ID: 8830623
[TBL] [Abstract][Full Text] [Related]
36. Germ cells and ova in dysgenetic gonads of a 46-XY female dizygotic twin.
Cussen LJ; MacMahon RA
Am J Dis Child; 1979 Apr; 133(4):373-5. PubMed ID: 433851
[TBL] [Abstract][Full Text] [Related]
37. A case of complete testicular feminization: laparoscopic orchiectomy and analysis of androgen receptor gene mutation.
Kanayama H; Naroda T; Inoue Y; Kurokawa Y; Kagawa S
Int J Urol; 1999 Jun; 6(6):327-30. PubMed ID: 10404311
[TBL] [Abstract][Full Text] [Related]
38. Neoplasia arising in dysgenetic gonads.
Troche V; Hernandez E
Obstet Gynecol Surv; 1986 Feb; 41(2):74-9. PubMed ID: 3005934
[TBL] [Abstract][Full Text] [Related]
39. Case report of dysgerminoma in a patient with 46,XX pure gonadal dysgenesis.
Maeyama M; Kagami T; Miyakawa I; Tooya T; Kawasaki N; Iwamasa T
Gynecol Oncol; 1983 Dec; 16(3):405-13. PubMed ID: 6654183
[TBL] [Abstract][Full Text] [Related]
40. Removal of gonads in Y-chromosome-bearing gonadal dysgenesis and in androgen insensitivity syndrome by laparoscopic surgery.
Ulrich U; Keckstein J; Buck G
Surg Endosc; 1996 Apr; 10(4):422-5. PubMed ID: 8661793
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]