BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 29909144)

  • 1. PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population.
    Fan TS; Wu RM; Lin HI; Cheng C; Lin CH
    Neurobiol Aging; 2018 Nov; 71():265.e15-265.e16. PubMed ID: 29909144
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical findings of autosomal-dominant striatal degeneration and PDE8B mutation screening in parkinsonism and related disorders.
    Ni J; Yi X; Liu Z; Sun W; Yuan Y; Yang J; Jiang H; Shen L; Tang B; Liu Y; Wang J
    Parkinsonism Relat Disord; 2019 Dec; 69():94-98. PubMed ID: 31726290
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel mutation of PDE8B Gene in a Japanese family with autosomal-dominant striatal degeneration.
    Azuma R; Ishikawa K; Hirata K; Hashimoto Y; Takahashi M; Ishii K; Inaba A; Yokota T; Orimo S
    Mov Disord; 2015 Dec; 30(14):1964-7. PubMed ID: 26769607
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene.
    Appenzeller S; Schirmacher A; Halfter H; Bäumer S; Pendziwiat M; Timmerman V; De Jonghe P; Fekete K; Stögbauer F; Lüdemann P; Hund M; Quabius ES; Ringelstein EB; Kuhlenbäumer G
    Am J Hum Genet; 2010 Jan; 86(1):83-7. PubMed ID: 20085714
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort.
    Lin HH; Wu RM; Lin HI; Chen ML; Tai CH; Lin CH
    Neurobiol Aging; 2017 Feb; 50():169.e3-169.e4. PubMed ID: 27838047
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lack of PTRHD1 mutation in patients with young-onset and familial Parkinson's disease in a Taiwanese population.
    Chen SJ; Ho CH; Lin HY; Lin CH; Wu RM
    Neurobiol Aging; 2021 Apr; 100():118.e15-118.e16. PubMed ID: 33004232
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Haplotype analysis of the promoter region of phosphodiesterase type 8B (PDE8B) in correlation with inactivating PDE8B mutation and the serum thyroid-stimulating hormone levels.
    Horvath A; Faucz F; Finkielstain GP; Nikita ME; Rothenbuhler A; Almeida M; Mericq V; Stratakis CA
    Thyroid; 2010 Apr; 20(4):363-7. PubMed ID: 20373981
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex.
    Horvath A; Giatzakis C; Tsang K; Greene E; Osorio P; Boikos S; Libè R; Patronas Y; Robinson-White A; Remmers E; Bertherat J; Nesterova M; Stratakis CA
    Eur J Hum Genet; 2008 Oct; 16(10):1245-53. PubMed ID: 18431404
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Association analysis of PDE8B gene polymorphisms with the susceptibility to Hyperthyroxinemia in Chinese Han population].
    Zhan M; Zhao SX; Gu ZH; Guo CC; Song ZY; Song HD
    Zhonghua Yi Xue Za Zhi; 2012 Mar; 92(12):801-5. PubMed ID: 22781450
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic analysis of PODXL gene in patients with familial and young-onset Parkinson's disease in a Taiwanese population.
    Chen SJ; Wu RM; Ho CH; Cheng J; Lin HY; Lin CH
    Neurobiol Aging; 2019 Dec; 84():235.e9-235.e10. PubMed ID: 31564376
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population.
    Chen KH; Wu RM; Lin HI; Tai CH; Lin CH
    Neurobiol Aging; 2015 Oct; 36(10):2905.e7-8. PubMed ID: 26149920
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours.
    Rothenbuhler A; Horvath A; Libé R; Faucz FR; Fratticci A; Raffin Sanson ML; Vezzosi D; Azevedo M; Levy I; Almeida MQ; Lodish M; Nesterova M; Bertherat J; Stratakis CA
    Clin Endocrinol (Oxf); 2012 Aug; 77(2):195-9. PubMed ID: 22335482
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phosphodiesterase 8B gene polymorphism in women with recurrent miscarriage: a retrospective case control study.
    Granfors M; Karypidis H; Hosseini F; Skjöldebrand-Sparre L; Stavreus-Evers A; Bremme K; Landgren BM; Sundström-Poromaa I; Wikström AK; Åkerud H
    BMC Med Genet; 2012 Dec; 13():121. PubMed ID: 23237535
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Impact of phosphodiesterase 8B gene rs4704397 variation on thyroid homeostasis in childhood obesity.
    Grandone A; Perrone L; Cirillo G; Di Sessa A; Corona AM; Amato A; Cresta N; Romano T; Miraglia del Giudice E
    Eur J Endocrinol; 2012 Feb; 166(2):255-60. PubMed ID: 22084153
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Contribution of glucocerebrosidase mutation in a large cohort of sporadic Parkinson's disease in Taiwan.
    Huang CL; Wu-Chou YH; Lai SC; Chang HC; Yeh TH; Weng YH; Chen RS; Huang YZ; Lu CS
    Eur J Neurol; 2011 Oct; 18(10):1227-32. PubMed ID: 21338444
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population.
    Fan TS; Lin CH; Lin HI; Chen ML; Wu RM
    Am J Med Genet B Neuropsychiatr Genet; 2017 Oct; 174(7):751-756. PubMed ID: 28766910
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism.
    Agretti P; De Marco G; Di Cosmo C; Bagattini B; Ferrarini E; Montanelli L; Vitti P; Tonacchera M
    J Endocrinol Invest; 2014 Feb; 37(2):189-94. PubMed ID: 24497218
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A meta-analysis of the associations between common variation in the PDE8B gene and thyroid hormone parameters, including assessment of longitudinal stability of associations over time and effect of thyroid hormone replacement.
    Taylor PN; Panicker V; Sayers A; Shields B; Iqbal A; Bremner AP; Beilby JP; Leedman PJ; Hattersley AT; Vaidya B; Frayling T; Evans J; Tobias JH; Timpson NJ; Walsh JP; Dayan CM
    Eur J Endocrinol; 2011 May; 164(5):773-80. PubMed ID: 21317282
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function.
    Arnaud-Lopez L; Usala G; Ceresini G; Mitchell BD; Pilia MG; Piras MG; Sestu N; Maschio A; Busonero F; Albai G; Dei M; Lai S; Mulas A; Crisponi L; Tanaka T; Bandinelli S; Guralnik JM; Loi A; Balaci L; Sole G; Prinzis A; Mariotti S; Shuldiner AR; Cao A; Schlessinger D; Uda M; Abecasis GR; Nagaraja R; Sanna S; Naitza S
    Am J Hum Genet; 2008 Jun; 82(6):1270-80. PubMed ID: 18514160
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tremor without parkinsonism: A new phenotype of autosomal-dominant striatal degeneration.
    Sun YM; Li HQ; Zhang Y
    Parkinsonism Relat Disord; 2021 Jun; 87():122-123. PubMed ID: 34022587
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.