BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 28717081)

  • 1. Severe Glomerular Endothelial Injury Associated with a Short D4Z4 Repeat on Chromosome 4q35.
    Hibino S; Takeda A; Nishino I; Iwata N; Nakano M; Tanaka K; Yamakawa S; Nagai T; Uemura O
    Intern Med; 2017; 56(14):1849-1853. PubMed ID: 28717081
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues.
    Tsien F; Sun B; Hopkins NE; Vedanarayanan V; Figlewicz D; Winokur S; Ehrlich M
    Mol Genet Metab; 2001 Nov; 74(3):322-31. PubMed ID: 11708861
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy.
    Goto K; Nishino I; Hayashi YK
    Neuromuscul Disord; 2006 Apr; 16(4):256-61. PubMed ID: 16545566
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical Application of Optical Genome Mapping for Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy.
    Shim Y; Seo J; Lee ST; Choi JR; Choi YC; Shin S; Park HJ
    Ann Lab Med; 2024 Sep; 44(5):437-445. PubMed ID: 38724225
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Polymorphism of the D4Z4 locus associated with facioscapulohumeral muscular dystrophy 1A in Shanghai population.
    Zhang YZ; Sun SC; Wu HC; Fan QS; Song YJ; Yu W; Jeanpierre M; Urtizberea JA
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):380-2. PubMed ID: 16086272
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical features.
    Dorobek M; van der Maarel SM; Lemmers RJ; Ryniewicz B; Kabzińska D; Frants RR; Gawel M; Walecki J; Hausmanowa-Petrusewicz I
    J Child Neurol; 2015 Apr; 30(5):580-7. PubMed ID: 24717985
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Facioscapulohumeral muscular dystrophy. Phenotype-genotype correlation in patients with borderline D4Z4 repeat numbers.
    Butz M; Koch MC; Müller-Felber W; Lemmers RJ; van der Maarel SM; Schreiber H
    J Neurol; 2003 Aug; 250(8):932-7. PubMed ID: 12928911
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Facioscapulohumeral Muscular Dystrophy.
    DeSimone AM; Pakula A; Lek A; Emerson CP
    Compr Physiol; 2017 Sep; 7(4):1229-1279. PubMed ID: 28915324
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hybridization analysis of D4Z4 repeat arrays linked to FSHD.
    Ehrlich M; Jackson K; Tsumagari K; Camaño P; Lemmers RJ
    Chromosoma; 2007 Apr; 116(2):107-16. PubMed ID: 17131163
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Clinical and genetical features of Japanese early-onset facioscapulohumeral muscular dystrophy].
    Yamanaka G; Goto K; Hayashi YK; Miyajima T; Hoshika A; Arahata K
    No To Hattatsu; 2002 Jul; 34(4):318-24. PubMed ID: 12134683
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular combing compared to Southern blot for measuring D4Z4 contractions in FSHD.
    Vasale J; Boyar F; Jocson M; Sulcova V; Chan P; Liaquat K; Hoffman C; Meservey M; Chang I; Tsao D; Hensley K; Liu Y; Owen R; Braastad C; Sun W; Walrafen P; Komatsu J; Wang JC; Bensimon A; Anguiano A; Jaremko M; Wang Z; Batish S; Strom C; Higgins J
    Neuromuscul Disord; 2015 Dec; 25(12):945-51. PubMed ID: 26420234
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
    Deak KL; Lemmers RJ; Stajich JM; Klooster R; Tawil R; Frants RR; Speer MC; van der Maarel SM; Gilbert JR
    Neurology; 2007 Feb; 68(8):578-82. PubMed ID: 17229919
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Facioscapulohumeral muscular dystrophy.
    Tawil R; Van Der Maarel SM
    Muscle Nerve; 2006 Jul; 34(1):1-15. PubMed ID: 16508966
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Translocation between chromosomes 4q35 and 10q26 in facioscapulohumeral muscular dystrophy].
    Su QX; Zhang C; Zeng Y; Lu XL; Liu XR; Wang ZH; Zhu YZ
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Oct; 25(5):581-4. PubMed ID: 14650163
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q.
    Jiang G; Yang F; van Overveld PG; Vedanarayanan V; van der Maarel S; Ehrlich M
    Hum Mol Genet; 2003 Nov; 12(22):2909-21. PubMed ID: 14506132
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophy.
    Buzhov BT; Lemmers RJ; Tournev I; van der Wielen MJ; Ishpekova B; Petkov R; Petrova J; Frants RR; Padberg GW; van der Maarel SM
    Neuromuscul Disord; 2005 Jul; 15(7):471-5. PubMed ID: 15935668
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
    Osborne RJ; Welle S; Venance SL; Thornton CA; Tawil R
    Neurology; 2007 Feb; 68(8):569-77. PubMed ID: 17151338
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Recent advances in facioscapulohumeral muscular dystrophy].
    Hayashi YK; Goto K; Nishio I
    Rinsho Shinkeigaku; 2012; 52(11):1154-7. PubMed ID: 23196547
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tongue atrophy in facioscapulohumeral muscular dystrophy.
    Yamanaka G; Goto K; Matsumura T; Funakoshi M; Komori T; Hayashi YK; Arahata K
    Neurology; 2001 Aug; 57(4):733-5. PubMed ID: 11524495
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Facioscapulohumeral muscular dystrophy. The spectrum of clinical manifestations and molecular genetic changes].
    Krasnianski M; Neudecker S; Eger K; Schulte-Mattler W; Zierz S
    Nervenarzt; 2003 Feb; 74(2):151-8. PubMed ID: 12596016
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.