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 *

154 related articles for article (PubMed ID: 37714561)

  • 1. Revisiting the role of ischaemia in familial cardiomyopathy: insights from an NRAP gene-related cardiomyopathy.
    AbdelMassih AF; Al Ali A; Musleh AS; Ramsi M
    BMJ Case Rep; 2023 Sep; 16(9):. PubMed ID: 37714561
    [No Abstract]   [Full Text] [Related]  

  • 2. Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy.
    Koskenvuo JW; Saarinen I; Ahonen S; Tommiska J; Weckström S; Seppälä EH; Tuupanen S; Kangas-Kontio T; Schleit J; Heliö K; Hathaway J; Gummesson A; Dahlberg P; Ojala TH; Vepsäläinen V; Kytölä V; Muona M; Sistonen J; Salmenperä P; Gentile M; Paananen J; Myllykangas S; Alastalo TP; Heliö T
    PLoS One; 2021; 16(2):e0245681. PubMed ID: 33534821
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathy.
    Truszkowska GT; Bilińska ZT; Muchowicz A; Pollak A; Biernacka A; Kozar-Kamińska K; Stawiński P; Gasperowicz P; Kosińska J; Zieliński T; Płoski R
    Sci Rep; 2017 Jun; 7(1):3362. PubMed ID: 28611399
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic Insights from Consanguineous Cardiomyopathy Families.
    Maurer C; Boleti O; Najarzadeh Torbati P; Norouzi F; Fowler ANR; Minaee S; Salih KH; Taherpour M; Birjandi H; Alizadeh B; Salih AF; Bijari M; Houlden H; Pittman AM; Maroofian R; Almashham YH; Karimiani EG; Kaski JP; Faqeih EA; Vakilian F; Jamshidi Y
    Genes (Basel); 2023 Jan; 14(1):. PubMed ID: 36672924
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Hereditary cardiomyopathies: a review. Mutation of structural proteins a common cause of hereditary cardiomyopathy].
    Sjöberg G; Kostareva A; Sejersen T
    Lakartidningen; 2005 Mar 14-20; 102(11):845-7, 850-3. PubMed ID: 15835520
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cardiac-specific NRAP overexpression causes right ventricular dysfunction in mice.
    Lu S; Crawford GL; Dore J; Anderson SA; Despres D; Horowits R
    Exp Cell Res; 2011 May; 317(8):1226-37. PubMed ID: 21276443
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel loss-of-function mutation in NRAP is associated with left ventricular non-compaction cardiomyopathy.
    Zhang Z; Xu K; Ji L; Zhang H; Yin J; Zhou M; Wang C; Yang S
    Front Cardiovasc Med; 2023; 10():1097957. PubMed ID: 36815016
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all.
    Callis TE; Jensen BC; Weck KE; Willis MS
    Expert Rev Mol Diagn; 2010 Apr; 10(3):329-51. PubMed ID: 20370590
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Contribution of genetics to cardiomyopathy].
    Komajda M
    Bull Acad Natl Med; 2002; 186(1):31-42; discussion 42-3. PubMed ID: 12146140
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional analysis of titin/connectin N2-B mutations found in cardiomyopathy.
    Matsumoto Y; Hayashi T; Inagaki N; Takahashi M; Hiroi S; Nakamura T; Arimura T; Nakamura K; Ashizawa N; Yasunami M; Ohe T; Yano K; Kimura A
    J Muscle Res Cell Motil; 2005; 26(6-8):367-74. PubMed ID: 16465475
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Genetics of inherited cardiomyopathies].
    Richard P; Fressart V; Charron P; Hainque B
    Pathol Biol (Paris); 2010 Oct; 58(5):343-52. PubMed ID: 19942368
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes.
    Xu Q; Dewey S; Nguyen S; Gomes AV
    J Mol Cell Cardiol; 2010 May; 48(5):899-909. PubMed ID: 20298698
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pregnancy, cardiomyopathies, and genetics.
    Van Tintelen JP; Pieper PG; Van Spaendonck-Zwarts KY; Van Den Berg MP
    Cardiovasc Res; 2014 Mar; 101(4):571-8. PubMed ID: 24451172
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The role of cytoskeletal proteins in cardiomyopathies.
    Towbin JA
    Curr Opin Cell Biol; 1998 Feb; 10(1):131-9. PubMed ID: 9484605
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ZBTB17 (MIZ1) Is Important for the Cardiac Stress Response and a Novel Candidate Gene for Cardiomyopathy and Heart Failure.
    Buyandelger B; Mansfield C; Kostin S; Choi O; Roberts AM; Ware JS; Mazzarotto F; Pesce F; Buchan R; Isaacson RL; Vouffo J; Gunkel S; Knöll G; McSweeney SJ; Wei H; Perrot A; Pfeiffer C; Toliat MR; Ilieva K; Krysztofinska E; López-Olañeta MM; Gómez-Salinero JM; Schmidt A; Ng KE; Teucher N; Chen J; Teichmann M; Eilers M; Haverkamp W; Regitz-Zagrosek V; Hasenfuss G; Braun T; Pennell DJ; Gould I; Barton PJ; Lara-Pezzi E; Schäfer S; Hübner N; Felkin LE; O'Regan DP; Brand T; Milting H; Nürnberg P; Schneider MD; Prasad S; Petretto E; Knöll R
    Circ Cardiovasc Genet; 2015 Oct; 8(5):643-52. PubMed ID: 26175529
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The genetic landscape of cardiomyopathy and its role in heart failure.
    McNally EM; Barefield DY; Puckelwartz MJ
    Cell Metab; 2015 Feb; 21(2):174-182. PubMed ID: 25651172
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Contiguous Gene Deletion of Chromosome 15q25.2q25.3 in Biallelic
    Grutters LA; Klein Wassink-Ruiter JS; Dijkhuizen T; Nijenhuis HP; Jongbloed JDH; Herkert JC
    Circ Genom Precis Med; 2023 Oct; 16(5):493-495. PubMed ID: 37671554
    [No Abstract]   [Full Text] [Related]  

  • 18. [Familial cardiomyopathy. Peripartum and primary congestive cardiomyopathy in a sister and brother].
    Strunge P
    Ugeskr Laeger; 1976 Oct; 138(42):2567-9. PubMed ID: 969012
    [No Abstract]   [Full Text] [Related]  

  • 19. Identification of the difference in the pathogenesis in heart failure arising from different etiologies using a microarray dataset.
    Yang G; Chen S; Ma A; Lu J; Wang T
    Clinics (Sao Paulo); 2017 Oct; 72(10):600-608. PubMed ID: 29160422
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MuRF2 regulates PPARγ1 activity to protect against diabetic cardiomyopathy and enhance weight gain induced by a high fat diet.
    He J; Quintana MT; Sullivan J; L Parry T; J Grevengoed T; Schisler JC; Hill JA; Yates CC; Mapanga RF; Essop MF; Stansfield WE; Bain JR; Newgard CB; Muehlbauer MJ; Han Y; Clarke BA; Willis MS
    Cardiovasc Diabetol; 2015 Aug; 14():97. PubMed ID: 26242235
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.