BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 9544375)

  • 21. Point mutation in the steroid-binding domain of the androgen receptor gene in a family with complete androgen insensitivity syndrome (CAIS).
    Jakubiczka S; Werder EA; Wieacker P
    Hum Genet; 1992 Nov; 90(3):311-2. PubMed ID: 1487249
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Response to treatment in patients with partial androgen insensitivity due to mutations in the DNA-binding domain of the androgen receptor.
    Lundberg Giwercman Y; Nikoshkov A; Lindsten K; Byström B; Pousette A; Knudtzon J; Alm J; Wedell A
    Horm Res; 2000; 53(2):83-8. PubMed ID: 10971094
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. A novel nonsense mutation in the androgen receptor gene causes the complete androgen insensitivity syndrome.
    Liu X; Fu J; Cai Z; Sun L; Zhang X; Li Z; Diao R; Wang Z; Yu G; Cai Z; Gui Y
    J Androl; 2012; 33(3):357-60. PubMed ID: 21757511
    [TBL] [Abstract][Full Text] [Related]  

  • 25. An androgen receptor mutation in the direct vicinity of the proposed C-terminal alpha-helix of the ligand binding domain containing the AF-2 transcriptional activating function core is associated with complete androgen insensitivity.
    Peters I; Weidemann W; Romalo G; Knorr D; Schweikert HU; Spindler KD
    Mol Cell Endocrinol; 1999 Feb; 148(1-2):47-53. PubMed ID: 10221770
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel Mutations Segregating with Complete Androgen Insensitivity Syndrome and their Molecular Characteristics.
    Malcher A; Jedrzejczak P; Stokowy T; Monem S; Nowicka-Bauer K; Zimna A; Czyzyk A; Maciejewska-Jeske M; Meczekalski B; Bednarek-Rajewska K; Wozniak A; Rozwadowska N; Kurpisz M
    Int J Mol Sci; 2019 Oct; 20(21):. PubMed ID: 31671693
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel substitution (Leu707Arg) in exon 4 of the androgen receptor gene causes complete androgen resistance.
    Lumbroso S; Lobaccaro JM; Georget V; Leger J; Poujol N; Térouanne B; Evain-Brion D; Czernichow P; Sultan C
    J Clin Endocrinol Metab; 1996 May; 81(5):1984-8. PubMed ID: 8626869
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Complete androgen insensitivity syndrome and discordant Müllerian remnants: two cases with novel mutation in the androgen receptor.
    Güven A; Dursun F; Özkanlı S; Güçlüer B; Kuru Lİ
    J Pediatr Endocrinol Metab; 2013; 26(9-10):909-14. PubMed ID: 23729616
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Novel and recurrent mutations in patients with androgen insensitivity syndromes.
    Ledig S; Jakubiczka S; Neulen J; Aulepp U; Burck-Lehmann U; Mohnike K; Thiele H; Zierler H; Brewer C; Wieacker P
    Horm Res; 2005; 63(6):263-9. PubMed ID: 15925895
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. A novel point mutation in the hormone binding domain of the androgen receptor associated with partial and minimal androgen insensitivity syndrome.
    Galli-Tsinopoulou A; Hiort O; Schuster T; Messer G; Kuhnle U
    J Pediatr Endocrinol Metab; 2003 Feb; 16(2):149-54. PubMed ID: 12713250
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular basis of androgen insensitivity.
    Brinkmann A; Jenster G; Ris-Stalpers C; van der Korput H; Brüggenwirth H; Boehmer A; Trapman J
    Steroids; 1996 Apr; 61(4):172-5. PubMed ID: 8732995
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Single nucleotide substitution of the androgen receptor gene in a case with receptor-positive androgen insensitivity syndrome (complete form).
    Kasumi H; Komori S; Yamasaki N; Shima H; Isojima S
    Acta Endocrinol (Copenh); 1993 Apr; 128(4):355-60. PubMed ID: 8498155
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Mutation analysis of the androgen receptor gene in a complete androgen insensitivity syndrome family].
    Wu W; Luo F; Geng Q; Hao Y; Chen W; Cai J; Xie J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):606-9. PubMed ID: 19953479
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel androgen receptor gene mutations in Australian patients with complete androgen insensitivity syndrome.
    MacLean HE; Ball EM; Rekaris G; Warne GL; Zajac JD
    Hum Mutat; 2004 Mar; 23(3):287. PubMed ID: 14974091
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Partial androgen insensitivity and correlations with the predicted three dimensional structure of the androgen receptor ligand-binding domain.
    Yong EL; Tut TG; Ghadessy FJ; Prins G; Ratnam SS
    Mol Cell Endocrinol; 1998 Feb; 137(1):41-50. PubMed ID: 9607727
    [TBL] [Abstract][Full Text] [Related]  

  • 37. One additional mutation at exon A amplifies thermolability of androgen receptor in a case with complete androgen insensitivity syndrome.
    Tanaka H; Komori S; Sakata K; Shima H; Koyama K
    Gynecol Endocrinol; 1998 Apr; 12(2):75-82. PubMed ID: 9610419
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Five novel androgen receptor gene mutations associated with complete androgen insensitivity syndrome.
    Jääskeläinen J; Mongan NP; Harland S; Hughes IA
    Hum Mutat; 2006 Mar; 27(3):291. PubMed ID: 16470553
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutations.
    Holterhus PM; Werner R; Hoppe U; Bassler J; Korsch E; Ranke MB; Dörr HG; Hiort O
    J Mol Med (Berl); 2005 Dec; 83(12):1005-13. PubMed ID: 16283146
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome].
    Soriano Guillén L; Muñoz Calvo MT; Martinez Pérez J; Pozo Román J; Martín Sobrino MA; González Medeiro I; Argente Oliver J
    An Esp Pediatr; 2002 Apr; 56(4):347-52. PubMed ID: 11927080
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.