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 *

531 related articles for article (PubMed ID: 14999487)

  • 1. 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]  

  • 2. 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]  

  • 3. [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]  

  • 4. 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]  

  • 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. [X-linked recessive bulbospinal neuronopathy--Kennedy's syndrome].
    Andersen KV; Michler RP; Nilssen O; Tranebjaerg L; Aasly J
    Tidsskr Nor Laegeforen; 1999 Apr; 119(11):1591-4. PubMed ID: 10385801
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. Phenotypic differences in a large family with Kennedy's disease from the Middle Black Sea region of Turkey.
    Karaer H; Kaplan Y; Kurt S; Gundogdu A; Erdoğan B; Başak NA
    Amyotroph Lateral Scler; 2010; 11(1-2):148-53. PubMed ID: 20184516
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CAG repeat size correlates to electrophysiological motor and sensory phenotypes in SBMA.
    Suzuki K; Katsuno M; Banno H; Takeuchi Y; Atsuta N; Ito M; Watanabe H; Yamashita F; Hori N; Nakamura T; Hirayama M; Tanaka F; Sobue G
    Brain; 2008 Jan; 131(Pt 1):229-39. PubMed ID: 18056738
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A comparison of the lengths of androgen receptor triplet repeats in brain and blood in motor neuron diseases.
    Saunderson RB; Yu B; Trent RJ; Pamphlett R
    J Neurol Sci; 2008 Apr; 267(1-2):125-8. PubMed ID: 17997416
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy.
    La Spada AR; Roling DB; Harding AE; Warner CL; Spiegel R; Hausmanowa-Petrusewicz I; Yee WC; Fischbeck KH
    Nat Genet; 1992 Dec; 2(4):301-4. PubMed ID: 1303283
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Men with Kennedy disease have a reduced risk of androgenetic alopecia.
    Sinclair R; Greenland KJ; Egmond Sv; Hoedemaker C; Chapman A; Zajac JD
    Br J Dermatol; 2007 Aug; 157(2):290-4. PubMed ID: 17596176
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [DNA diagnosis of X-linked recessive bulbospinal muscular atrophy by androgen receptor gene mutations].
    Doyu M; Sobue G; Mukai E; Takahashi A; Mitsuma T
    Rinsho Shinkeigaku; 1992 Mar; 32(3):336-9. PubMed ID: 1628462
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A novel primer extension method to detect the number of CAG repeats in the androgen receptor gene in families with X-linked spinal and bulbar muscular atrophy].
    Sakoda S; Yamamoto Y
    Nihon Rinsho; 1993 Sep; 51(9):2414-9. PubMed ID: 8411722
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Androgen receptor mutation in Kennedy's disease.
    Fischbeck KH; Lieberman A; Bailey CK; Abel A; Merry DE
    Philos Trans R Soc Lond B Biol Sci; 1999 Jun; 354(1386):1075-8. PubMed ID: 10434308
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Elevated creatine kinase and transaminases in asymptomatic SBMA.
    Sorenson EJ; Klein CJ
    Amyotroph Lateral Scler; 2007 Feb; 8(1):62-4. PubMed ID: 17364438
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 27.