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 *

198 related articles for article (PubMed ID: 18632251)

  • 41. Zebrafish as a model for caveolin-associated muscle disease; caveolin-3 is required for myofibril organization and muscle cell patterning.
    Nixon SJ; Wegner J; Ferguson C; Méry PF; Hancock JF; Currie PD; Key B; Westerfield M; Parton RG
    Hum Mol Genet; 2005 Jul; 14(13):1727-43. PubMed ID: 15888488
    [TBL] [Abstract][Full Text] [Related]  

  • 42. A limb-girdle muscular dystrophy 2I model of muscular dystrophy identifies corrective drug compounds for dystroglycanopathies.
    Serafini PR; Feyder MJ; Hightower RM; Garcia-Perez D; Vieira NM; Lek A; Gibbs DE; Moukha-Chafiq O; Augelli-Szafran CE; Kawahara G; Widrick JJ; Kunkel LM; Alexander MS
    JCI Insight; 2018 Sep; 3(18):. PubMed ID: 30232282
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Cascade effect of cardiac myogenesis gene expression during cardiac looping in tbx5 knockdown zebrafish embryos.
    Lu JH; Lu JK; Choo SL; Li YC; Yeh HW; Shiue JF; Yeh VC
    J Biomed Sci; 2008 Nov; 15(6):779-87. PubMed ID: 18661250
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Fukutin-Related Protein: From Pathology to Treatments.
    Ortiz-Cordero C; Azzag K; Perlingeiro RCR
    Trends Cell Biol; 2021 Mar; 31(3):197-210. PubMed ID: 33272829
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Molecular cloning and expression of phospholipase C epsilon 1 in zebrafish.
    Zhou W; Hildebrandt F
    Gene Expr Patterns; 2009 Jun; 9(5):282-8. PubMed ID: 19332147
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Spatiotemporal expression of smooth muscle markers in developing zebrafish gut.
    Georgijevic S; Subramanian Y; Rollins EL; Starovic-Subota O; Tang AC; Childs SJ
    Dev Dyn; 2007 Jun; 236(6):1623-32. PubMed ID: 17474123
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Abnormal glycosylation of the alpha-dystroglycan: deficient sugars are no good.
    Topaloglu H
    Neurology; 2009 May; 72(21):1798-9. PubMed ID: 19321844
    [No Abstract]   [Full Text] [Related]  

  • 48. A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum.
    Van Reeuwijk J; Olderode-Berends MJ; Van den Elzen C; Brouwer OF; Roscioli T; Van Pampus MG; Scheffer H; Brunner HG; Van Bokhoven H; Hol FA
    Clin Genet; 2010 Sep; 78(3):275-81. PubMed ID: 20236121
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Diagnosis and etiology of congenital muscular dystrophy.
    Peat RA; Smith JM; Compton AG; Baker NL; Pace RA; Burkin DJ; Kaufman SJ; Lamandé SR; North KN
    Neurology; 2008 Jul; 71(5):312-21. PubMed ID: 18160674
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Basement membrane fragility underlies embryonic lethality in fukutin-null mice.
    Kurahashi H; Taniguchi M; Meno C; Taniguchi Y; Takeda S; Horie M; Otani H; Toda T
    Neurobiol Dis; 2005; 19(1-2):208-17. PubMed ID: 15837576
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Loss of selenoprotein N function causes disruption of muscle architecture in the zebrafish embryo.
    Deniziak M; Thisse C; Rederstorff M; Hindelang C; Thisse B; Lescure A
    Exp Cell Res; 2007 Jan; 313(1):156-67. PubMed ID: 17123513
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Mutation in the delta-subunit of the nAChR suppresses the muscle defects caused by lack of Dystrophin.
    Etard C; Behra M; Ertzer R; Fischer N; Jesuthasan S; Blader P; Geisler R; Strähle U
    Dev Dyn; 2005 Dec; 234(4):1016-25. PubMed ID: 16245342
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Protein O-mannosyltransferase activities in lymphoblasts from patients with alpha-dystroglycanopathies.
    Manya H; Bouchet C; Yanagisawa A; Vuillaumier-Barrot S; Quijano-Roy S; Suzuki Y; Maugenre S; Richard P; Inazu T; Merlini L; Romero NB; Leturcq F; Bezier I; Topaloglu H; Estournet B; Seta N; Endo T; Guicheney P
    Neuromuscul Disord; 2008 Jan; 18(1):45-51. PubMed ID: 17869517
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Dystroglycanopathies: coming into focus.
    Godfrey C; Foley AR; Clement E; Muntoni F
    Curr Opin Genet Dev; 2011 Jun; 21(3):278-85. PubMed ID: 21397493
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Restoration of Functional Glycosylation of α-Dystroglycan in FKRP Mutant Mice Is Associated with Muscle Regeneration.
    Awano H; Blaeser A; Keramaris E; Xu L; Tucker J; Wu B; Lu P; Lu QL
    Am J Pathol; 2015 Jul; 185(7):2025-37. PubMed ID: 25976249
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Muscular dystrophies due to glycosylation defects.
    Muntoni F; Torelli S; Brockington M
    Neurotherapeutics; 2008 Oct; 5(4):627-32. PubMed ID: 19019316
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Altered glycosylation of alpha-dystroglycan in neurons of Fukuyama congenital muscular dystrophy brains.
    Saito Y; Yamamoto T; Mizuguchi M; Kobayashi M; Saito K; Ohno K; Osawa M
    Brain Res; 2006 Feb; 1075(1):223-8. PubMed ID: 16466646
    [TBL] [Abstract][Full Text] [Related]  

  • 58. POMT2, a key enzyme in Walker-Warburg syndrome: somatic sPOMT2, but not testis-specific tPOMT2, is crucial for mannosyltransferase activity in vivo.
    Lommel M; Willer T; Strahl S
    Glycobiology; 2008 Aug; 18(8):615-25. PubMed ID: 18490429
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Expression of protocadherin 18 in the CNS and pharyngeal arches of zebrafish embryos.
    Kubota F; Murakami T; Tajika Y; Yorifuji H
    Int J Dev Biol; 2008; 52(4):397-405. PubMed ID: 18415941
    [TBL] [Abstract][Full Text] [Related]  

  • 60. FKRP-dependent glycosylation of fibronectin regulates muscle pathology in muscular dystrophy.
    Wood AJ; Lin CH; Li M; Nishtala K; Alaei S; Rossello F; Sonntag C; Hersey L; Miles LB; Krisp C; Dudczig S; Fulcher AJ; Gibertini S; Conroy PJ; Siegel A; Mora M; Jusuf P; Packer NH; Currie PD
    Nat Commun; 2021 May; 12(1):2951. PubMed ID: 34012031
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.