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 *

353 related articles for article (PubMed ID: 30650640)

  • 21. Genetic mutations and mechanisms in dilated cardiomyopathy.
    McNally EM; Golbus JR; Puckelwartz MJ
    J Clin Invest; 2013 Jan; 123(1):19-26. PubMed ID: 23281406
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Homozygous MYH7 R1820W mutation results in recessive myosin storage myopathy: scapuloperoneal and respiratory weakness with dilated cardiomyopathy.
    Yüceyar N; Ayhan Ö; Karasoy H; Tolun A
    Neuromuscul Disord; 2015 Apr; 25(4):340-4. PubMed ID: 25666907
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
    Merlo M; Sinagra G; Carniel E; Slavov D; Zhu X; Barbati G; Spezzacatene A; Ramani F; Salcedo E; Di Lenarda A; Mestroni L; Taylor MR;
    Clin Transl Sci; 2013 Dec; 6(6):424-8. PubMed ID: 24119082
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy.
    Carniel E; Taylor MR; Sinagra G; Di Lenarda A; Ku L; Fain PR; Boucek MM; Cavanaugh J; Miocic S; Slavov D; Graw SL; Feiger J; Zhu XZ; Dao D; Ferguson DA; Bristow MR; Mestroni L
    Circulation; 2005 Jul; 112(1):54-9. PubMed ID: 15998695
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Massive parallel sequencing questions the pathogenic role of missense variants in dilated cardiomyopathy.
    Dalin MG; Engström PG; Ivarsson EG; Unneberg P; Light S; Schaufelberger M; Gilljam T; Andersson B; Bergo MO
    Int J Cardiol; 2017 Feb; 228():742-748. PubMed ID: 27886618
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Distal myopathy with coexisting heterozygous TIA1 and MYH7 Variants.
    Brand P; Dyck PJ; Liu J; Berini S; Selcen D; Milone M
    Neuromuscul Disord; 2016 Aug; 26(8):511-5. PubMed ID: 27282841
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Young and early-onset dilated cardiomyopathy with malignant ventricular arrhythmia and sudden cardiac death induced by the heterozygous LDB3, MYH6, and SYNE1 missense mutations.
    Zhao T; Ma Y; Zhang Z; Xian J; Geng X; Wang F; Huang J; Yang Z; Luo Y; Lin Y
    Ann Noninvasive Electrocardiol; 2021 Jul; 26(4):e12840. PubMed ID: 33949037
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A PLN nonsense variant causes severe dilated cardiomyopathy in a novel autosomal recessive inheritance mode.
    Li Z; Chen P; Xu J; Yu B; Li X; Wang DW; Wang DW
    Int J Cardiol; 2019 Mar; 279():122-125. PubMed ID: 30638982
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients.
    Konno T; Shimizu M; Ino H; Matsuyama T; Yamaguchi M; Terai H; Hayashi K; Mabuchi T; Kiyama M; Sakata K; Hayashi T; Inoue M; Kaneda T; Mabuchi H
    J Am Coll Cardiol; 2003 Mar; 41(5):781-6. PubMed ID: 12628722
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Fetal Dilated Cardiomyopathy Associated With Variants of Uncertain Significance in MYH7 and DSG2 Genes: A Case Report and Review of the Literature.
    Kuo K; Speranza R; Hackmon R
    J Obstet Gynaecol Can; 2020 Sep; 42(9):1147-1150. PubMed ID: 32171501
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with dilated cardiomyopathy.
    Janin A; N'Guyen K; Habib G; Dauphin C; Chanavat V; Bouvagnet P; Eschalier R; Streichenberger N; Chevalier P; Millat G
    Clin Genet; 2017 Dec; 92(6):616-623. PubMed ID: 28436997
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.
    Ujfalusi Z; Vera CD; Mijailovich SM; Svicevic M; Yu EC; Kawana M; Ruppel KM; Spudich JA; Geeves MA; Leinwand LA
    J Biol Chem; 2018 Jun; 293(23):9017-9029. PubMed ID: 29666183
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy.
    van Spaendonck-Zwarts KY; Posafalvi A; van den Berg MP; Hilfiker-Kleiner D; Bollen IA; Sliwa K; Alders M; Almomani R; van Langen IM; van der Meer P; Sinke RJ; van der Velden J; Van Veldhuisen DJ; van Tintelen JP; Jongbloed JD
    Eur Heart J; 2014 Aug; 35(32):2165-73. PubMed ID: 24558114
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy.
    van Waning JI; Caliskan K; Michels M; Schinkel AFL; Hirsch A; Dalinghaus M; Hoedemaekers YM; Wessels MW; IJpma AS; Hofstra RMW; van Slegtenhorst MA; Majoor-Krakauer D
    J Am Coll Cardiol; 2019 Apr; 73(13):1601-1611. PubMed ID: 30947911
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Targeted Next-Generation Sequencing Reveals Hot Spots and Doubly Heterozygous Mutations in Chinese Patients with Familial Cardiomyopathy.
    Zhao Y; Feng Y; Zhang YM; Ding XX; Song YZ; Zhang AM; Liu L; Zhang H; Ding JH; Xia XS
    Biomed Res Int; 2015; 2015():561819. PubMed ID: 26199943
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The Phenotype and Outcome of Infantile Cardiomyopathy Caused by a Homozygous ELAC2 Mutation.
    Shinwari ZMA; Almesned A; Alakhfash A; Al-Rashdan AM; Faqeih E; Al-Humaidi Z; Alomrani A; Alghamdi M; Colak D; Alwadai A; Rababh M; Al-Fayyadh M; Al-Hassnan ZN
    Cardiology; 2017; 137(3):188-192. PubMed ID: 28441660
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies.
    Hoedemaekers YM; Caliskan K; Majoor-Krakauer D; van de Laar I; Michels M; Witsenburg M; ten Cate FJ; Simoons ML; Dooijes D
    Eur Heart J; 2007 Nov; 28(22):2732-7. PubMed ID: 17947214
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Impact of cardiac myosin light chain kinase gene mutation on development of dilated cardiomyopathy.
    Hodatsu A; Fujino N; Uyama Y; Tsukamoto O; Imai-Okazaki A; Yamazaki S; Seguchi O; Konno T; Hayashi K; Kawashiri MA; Asano Y; Kitakaze M; Takashima S; Yamagishi M
    ESC Heart Fail; 2019 Apr; 6(2):406-415. PubMed ID: 30690923
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Multigenic Disease and Bilineal Inheritance in Dilated Cardiomyopathy Is Illustrated in Nonsegregating LMNA Pedigrees.
    Cowan JR; Kinnamon DD; Morales A; Salyer L; Nickerson DA; Hershberger RE
    Circ Genom Precis Med; 2018 Jul; 11(7):e002038. PubMed ID: 30012837
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy.
    Kraoua L; Louati A; Ahmed SB; Abida N; Khemiri M; Menif K; Mrad R; Zaffran S; Jaouadi H
    Mol Genet Genomic Med; 2024 Jun; 12(6):e2486. PubMed ID: 38924380
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.