These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 8749704)

  • 1. Kennedy's disease: clinical and molecular study of two Italian families.
    Pareyson D; Castellotti B; Botti S; Defanti CA; Gellera C; Taroni F; Sghirlanzoni A
    Ital J Neurol Sci; 1995 Oct; 16(7):467-71. PubMed ID: 8749704
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular analysis of the androgen receptor gene in Kennedy's disease. Report of two families and review of the literature.
    Lumbroso S; Lobaccaro JM; Vial C; Sassolas G; Ollagnon B; Belon C; Pouget J; Sultan C
    Horm Res; 1997; 47(1):23-9. PubMed ID: 9010714
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Polymorphic CAG repeat length in the androgen receptor gene and association with neurodegeneration in a heterozygous female carrier of Kennedy's disease.
    Greenland KJ; Beilin J; Castro J; Varghese PN; Zajac JD
    J Neurol; 2004 Jan; 251(1):35-41. PubMed ID: 14999487
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CAG-repeat expansion in androgen receptor in Kennedy's disease is not a loss of function mutation.
    Neuschmid-Kaspar F; Gast A; Peterziel H; Schneikert J; Muigg A; Ransmayr G; Klocker H; Bartsch G; Cato AC
    Mol Cell Endocrinol; 1996 Mar; 117(2):149-56. PubMed ID: 8737374
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spinal and bulbar muscular atrophy: androgen receptor dysfunction caused by a trinucleotide repeat expansion.
    MacLean HE; Warne GL; Zajac JD
    J Neurol Sci; 1996 Feb; 135(2):149-57. PubMed ID: 8867071
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical manifestations and AR gene mutations in Kennedy's disease.
    Liu X; Zhu M; Li X; Tang J
    Funct Integr Genomics; 2019 May; 19(3):533-539. PubMed ID: 30612224
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy.
    Belsham DD; Yee WC; Greenberg CR; Wrogemann K
    J Neurol Sci; 1992 Oct; 112(1-2):133-8. PubMed ID: 1469423
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Kennedy's disease (spinal and bulbar muscular atrophy): a clinically oriented review of a rare disease.
    Breza M; Koutsis G
    J Neurol; 2019 Mar; 266(3):565-573. PubMed ID: 30006721
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [From gene to disease; androgen receptor gene, androgen insensitivity syndrome, and spinal and bulbar muscle atrophy].
    Boehmer AL; Brinkmann AO; Niermeijer MF; Halley DJ; Drop SL
    Ned Tijdschr Geneeskd; 2001 Dec; 145(48):2326-8. PubMed ID: 11766302
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor gene.
    Amato AA; Prior TW; Barohn RJ; Snyder P; Papp A; Mendell JR
    Neurology; 1993 Apr; 43(4):791-4. PubMed ID: 8469342
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Kennedy's disease: genetic diagnosis of an inherited form of motor neuron disease.
    Choi WT; MacLean HE; Chu S; Warne GL; Zajac JD
    Aust N Z J Med; 1993 Apr; 23(2):187-92. PubMed ID: 8517843
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Abnormal androgen receptor binding affinity in subjects with Kennedy's disease (spinal and bulbar muscular atrophy).
    MacLean HE; Choi WT; Rekaris G; Warne GL; Zajac JD
    J Clin Endocrinol Metab; 1995 Feb; 80(2):508-16. PubMed ID: 7852512
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Kennedy's disease: expansion of the CAG trinucleotide].
    Domitrz I; Jedrzejowska M; Lipowska M; Siddique T; KwieciƄski H
    Neurol Neurochir Pol; 2001; 35(1 Suppl):107-14. PubMed ID: 11732276
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Kennedy's disease: pathogenesis and clinical approaches.
    Greenland KJ; Zajac JD
    Intern Med J; 2004 May; 34(5):279-86. PubMed ID: 15151675
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CAG repeat length variation in sperm from a patient with Kennedy's disease.
    Zhang L; Fischbeck KH; Arnheim N
    Hum Mol Genet; 1995 Feb; 4(2):303-5. PubMed ID: 7757084
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.
    La Spada AR; Wilson EM; Lubahn DB; Harding AE; Fischbeck KH
    Nature; 1991 Jul; 352(6330):77-9. PubMed ID: 2062380
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Somatic stability of the expanded CAG trinucleotide repeat in X-linked spinal and bulbar muscular atrophy.
    Spiegel R; La Spada AR; Kress W; Fischbeck KH; Schmid W
    Hum Mutat; 1996; 8(1):32-7. PubMed ID: 8807333
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [The DNA diagnosis of a familial case of Kennedy's spinal and bulbar amyotrophy].
    Petrukhin AS; Zavadenko NN; Petrukhin AA; Evgrafov OV
    Zh Nevrol Psikhiatr Im S S Korsakova; 1997; 97(3):45-8. PubMed ID: 9157759
    [TBL] [Abstract][Full Text] [Related]  

  • 20. ["Jaw drop" as an atypical manifestation of Kennedy's disease].
    Larsen K; Smith TA
    Ugeskr Laeger; 2005 Aug; 167(35):3310-1. PubMed ID: 16138977
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.