BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

354 related articles for article (PubMed ID: 22334387)

  • 21. [Pathogenesis of androgen insensitivity syndrome].
    Okabe T; Nawata H
    Nihon Rinsho; 1998 Jul; 56(7):1881-6. PubMed ID: 9702070
    [TBL] [Abstract][Full Text] [Related]  

  • 22. G708E mutation in the androgen receptor results in complete loss of androgen function.
    Rajender S; Pooja S; Gupta NJ; Chakrabarty B; Singh L; Thangaraj K
    J Androl; 2011; 32(2):193-8. PubMed ID: 20671138
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Development of NIPBL locus-specific database using LOVD: from novel mutations to further genotype-phenotype correlations in Cornelia de Lange Syndrome.
    Oliveira J; Dias C; Redeker E; Costa E; Silva J; Reis Lima M; den Dunnen JT; Santos R
    Hum Mutat; 2010 Nov; 31(11):1216-22. PubMed ID: 20824775
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular cell biology of androgen receptor signalling.
    Bennett NC; Gardiner RA; Hooper JD; Johnson DW; Gobe GC
    Int J Biochem Cell Biol; 2010 Jun; 42(6):813-27. PubMed ID: 19931639
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Androgen insensitivity syndrome. Clinical features and molecular genetics].
    Sólyom J; Scheiber D; Fekete G
    Orv Hetil; 2001 Aug; 142(31):1659-65. PubMed ID: 11556259
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Role of the androgen receptor CAG repeat polymorphism in prostate cancer, and spinal and bulbar muscular atrophy.
    Kumar R; Atamna H; Zakharov MN; Bhasin S; Khan SH; Jasuja R
    Life Sci; 2011 Mar; 88(13-14):565-71. PubMed ID: 21284948
    [TBL] [Abstract][Full Text] [Related]  

  • 27. L859F mutation in androgen receptor gene results in complete loss of androgen binding to the receptor.
    Rajender S; Singh L; Thangaraj K
    J Androl; 2007; 28(5):772-6. PubMed ID: 17522416
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The androgen receptor gene mutations database.
    Gottlieb B; Trifiro M; Lumbroso R; Pinsky L
    Nucleic Acids Res; 1997 Jan; 25(1):158-62. PubMed ID: 9016528
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Promoter-dependent activity on androgen receptor N-terminal domain mutations in androgen insensitivity syndrome.
    Tadokoro-Cuccaro R; Davies J; Mongan NP; Bunch T; Brown RS; Audi L; Watt K; McEwan IJ; Hughes IA
    Sex Dev; 2014; 8(6):339-49. PubMed ID: 25500996
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Impaired helix 12 dynamics due to proline 892 substitutions in the androgen receptor are associated with complete androgen insensitivity.
    Elhaji YA; Stoica I; Dennis S; Purisima EO; Lumbroso R; Beitel LK; Trifiro MA
    Hum Mol Genet; 2006 Mar; 15(6):921-31. PubMed ID: 16449235
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Two percent of Finnish prostate cancer patients have a germ-line mutation in the hormone-binding domain of the androgen receptor gene.
    Mononen N; Syrjäkoski K; Matikainen M; Tammela TL; Schleutker J; Kallioniemi OP; Trapman J; Koivisto PA
    Cancer Res; 2000 Nov; 60(22):6479-81. PubMed ID: 11103816
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Loss of endogenous androgen receptor protein accelerates motor neuron degeneration and accentuates androgen insensitivity in a mouse model of X-linked spinal and bulbar muscular atrophy.
    Thomas PS; Fraley GS; Damian V; Woodke LB; Zapata F; Sopher BL; Plymate SR; La Spada AR
    Hum Mol Genet; 2006 Jul; 15(14):2225-38. PubMed ID: 16772330
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical and molecular aspects of androgen receptor defects.
    Wieacker PF; Knoke I; Jakubiczka S
    Exp Clin Endocrinol Diabetes; 1998; 106(6):446-53. PubMed ID: 10079022
    [TBL] [Abstract][Full Text] [Related]  

  • 34. LOVD v.2.0: the next generation in gene variant databases.
    Fokkema IF; Taschner PE; Schaafsma GC; Celli J; Laros JF; den Dunnen JT
    Hum Mutat; 2011 May; 32(5):557-63. PubMed ID: 21520333
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The androgen receptor gene mutations database.
    Patterson MN; Hughes IA; Gottlieb B; Pinsky L
    Nucleic Acids Res; 1994 Sep; 22(17):3560-2. PubMed ID: 7937057
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Computational analysis of androgen receptor (AR) variants to decipher the relationship between protein stability and related-diseases.
    Chen F; Chen X; Jiang F; Leng F; Liu W; Gui Y; Yu J
    Sci Rep; 2020 Jul; 10(1):12101. PubMed ID: 32694570
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Androgen insensitivity syndrome and co-activator disease].
    Tanaka K; Nomura M; Nawata H
    Nihon Rinsho; 2004 Feb; 62(2):344-50. PubMed ID: 14968543
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Long-term followup and comparison between genotype and phenotype in 29 cases of complete androgen insensitivity syndrome.
    Cheikhelard A; Morel Y; Thibaud E; Lortat-Jacob S; Jaubert F; Polak M; Nihoul-Fekete C
    J Urol; 2008 Oct; 180(4):1496-501. PubMed ID: 18710728
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene.
    Lim DH; Rehal PK; Nahorski MS; Macdonald F; Claessens T; Van Geel M; Gijezen L; Gille JJ; Giraud S; Richard S; van Steensel M; Menko FH; Maher ER
    Hum Mutat; 2010 Jan; 31(1):E1043-51. PubMed ID: 19802896
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The human FOXL2 mutation database.
    Beysen D; Vandesompele J; Messiaen L; De Paepe A; De Baere E
    Hum Mutat; 2004 Sep; 24(3):189-93. PubMed ID: 15300845
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.