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 *

134 related articles for article (PubMed ID: 9761394)

  • 61. Exclusion of the expansion of CAG/CTG repeats at thirteen loci on chromosome 12 as a candidate genetic mutation in scapuloperoneal spinal muscular atrophy with anticipation.
    Isozumi K; DeLong R; Kaplan J; Hung WY; Siddique T
    Hum Genet; 1997 Jun; 99(6):701-3. PubMed ID: 9187660
    [TBL] [Abstract][Full Text] [Related]  

  • 62. 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]  

  • 63. [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]  

  • 64. The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy.
    Rosenbohm A; Hirsch S; Volk AE; Grehl T; Grosskreutz J; Hanisch F; Herrmann A; Kollewe K; Kress W; Meyer T; Petri S; Prudlo J; Wessig C; Müller HP; Dreyhaupt J; Weishaupt J; Kubisch C; Kassubek J; Weydt P; Ludolph AC
    J Neurol; 2018 May; 265(5):1026-1036. PubMed ID: 29464380
    [TBL] [Abstract][Full Text] [Related]  

  • 65. In vivo expansion of trinucleotide repeats yields plasmid and YAC constructs for targeting and transgenesis.
    Sopher BL; Myrick SB; Hong JY; Smith AC; La Spada AR
    Gene; 2000 Dec; 261(2):383-90. PubMed ID: 11167027
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Pathogenesis-targeting therapeutics for spinal and bulbar muscular atrophy (SBMA).
    Suzuki K; Kastuno M; Banno H; Sobue G
    Neuropathology; 2009 Aug; 29(4):509-16. PubMed ID: 19486304
    [TBL] [Abstract][Full Text] [Related]  

  • 67. 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]  

  • 68. Association of spinal and bulbar muscular atrophy with myotonic dystrophy type 1.
    Jinnai K; Nishimoto K; Itoh K; Hashimoto K; Takahashi K
    Muscle Nerve; 2004 May; 29(5):729-33. PubMed ID: 15116379
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Transcriptional activation by the androgen receptor in X-linked spinal and bulbar muscular atrophy.
    Nakajima H; Kimura F; Nakagawa T; Furutama D; Shinoda K; Shimizu A; Ohsawa N
    J Neurol Sci; 1996 Oct; 142(1-2):12-6. PubMed ID: 8902713
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Prevalence of metabolic syndrome and non-alcoholic fatty liver disease in a cohort of italian patients with spinal-bulbar muscular atrophy.
    Francini-Pesenti F; Querin G; Martini C; Mareso S; Sacerdoti D
    Acta Myol; 2018 Sep; 37(3):204-209. PubMed ID: 30838350
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Convenient diagnosis of spinal and bulbar muscular atrophy using a microchip electrophoresis system.
    Maruyama H; Morino H; Izumi Y; Noda K; Kawakami H
    Am J Neurodegener Dis; 2013; 2(1):35-9. PubMed ID: 23515294
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Founder effect in spinal and bulbar muscular atrophy (SBMA).
    Tanaka F; Doyu M; Ito Y; Matsumoto M; Mitsuma T; Abe K; Aoki M; Itoyama Y; Fischbeck KH; Sobue G
    Hum Mol Genet; 1996 Sep; 5(9):1253-7. PubMed ID: 8872464
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Pathogenesis, animal models and therapeutics in spinal and bulbar muscular atrophy (SBMA).
    Katsuno M; Adachi H; Waza M; Banno H; Suzuki K; Tanaka F; Doyu M; Sobue G
    Exp Neurol; 2006 Jul; 200(1):8-18. PubMed ID: 16513111
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Mutant androgen receptor accumulation in spinal and bulbar muscular atrophy scrotal skin: a pathogenic marker.
    Banno H; Adachi H; Katsuno M; Suzuki K; Atsuta N; Watanabe H; Tanaka F; Doyu M; Sobue G
    Ann Neurol; 2006 Mar; 59(3):520-6. PubMed ID: 16358333
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Gene expression analysis reveals early dysregulation of disease pathways and links Chmp7 to pathogenesis of spinal and bulbar muscular atrophy.
    Malik B; Devine H; Patani R; La Spada AR; Hanna MG; Greensmith L
    Sci Rep; 2019 Mar; 9(1):3539. PubMed ID: 30837566
    [TBL] [Abstract][Full Text] [Related]  

  • 76. X-linked spinal and bulbar muscular atrophy without proximal atrophy.
    Boz C; Sahin N; Kalay E; Velioglu S; Ozmenoglu M
    Clin Neurol Neurosurg; 2002 Dec; 105(1):14-7. PubMed ID: 12445917
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Wide range of reduced penetrance alleles in spinal and bulbar muscular atrophy: a model-based approach.
    Laskaratos A; Breza M; Karadima G; Koutsis G
    J Med Genet; 2021 Jun; 58(6):385-391. PubMed ID: 32571900
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice.
    Bingham PM; Scott MO; Wang S; McPhaul MJ; Wilson EM; Garbern JY; Merry DE; Fischbeck KH
    Nat Genet; 1995 Feb; 9(2):191-6. PubMed ID: 7719348
    [TBL] [Abstract][Full Text] [Related]  

  • 79. [SBMA: a rare disease but a classic ALS mimic syndrome].
    Pradat PF
    Presse Med; 2014 May; 43(5):580-6. PubMed ID: 24785145
    [TBL] [Abstract][Full Text] [Related]  

  • 80. [Dynamic mutations in hereditary neurodegenerative disorders].
    Nilssen O
    Tidsskr Nor Laegeforen; 1999 Aug; 119(20):3021-7. PubMed ID: 10504853
    [TBL] [Abstract][Full Text] [Related]  

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