BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 35491958)

  • 21. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.
    Mori AA; Castro LR; Bortolin RH; Bastos GM; Oliveira VF; Ferreira GM; Hirata TDC; Fajardo CM; Sampaio MF; Moreira DAR; Pachón-Mateos JC; Correia EB; Sousa AGMR; Brión M; Carracedo A; Hirata RDC; Hirata MH
    Forensic Sci Int Genet; 2021 May; 52():102478. PubMed ID: 33588347
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prevalence and Phenotypic Expression of Mutations in the MYH7, MYBPC3 and TNNT2 Genes in Families with Hypertrophic Cardiomyopathy in the South of Brazil: A Cross-Sectional Study.
    Mattos BP; Scolari FL; Torres MA; Simon L; Freitas VC; Giugliani R; Matte Ú
    Arq Bras Cardiol; 2016 Sep; 107(3):257-265. PubMed ID: 27737317
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family.
    Tu P; Sun H; Zhang X; Ran Q; He Y; Ran S
    BMC Med Genomics; 2022 Feb; 15(1):36. PubMed ID: 35209905
    [TBL] [Abstract][Full Text] [Related]  

  • 24. MYH7-related disorders in two Bulgarian families: Novel variants in the same region associated with different clinical manifestation and disease penetrance.
    Atemin S; Todorov T; Maver A; Chamova T; Georgieva B; Tincheva S; Pacheva I; Ivanov I; Taneva A; Zlatareva D; Tournev I; Guergueltcheva V; Gospodinova M; Chochkova L; Peterlin B; Mitev V; Todorova A
    Neuromuscul Disord; 2021 Jul; 31(7):633-641. PubMed ID: 34053846
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects.
    Granados-Riveron JT; Ghosh TK; Pope M; Bu'Lock F; Thornborough C; Eason J; Kirk EP; Fatkin D; Feneley MP; Harvey RP; Armour JA; David Brook J
    Hum Mol Genet; 2010 Oct; 19(20):4007-16. PubMed ID: 20656787
    [TBL] [Abstract][Full Text] [Related]  

  • 26. MYH7 in cardiomyopathy and skeletal muscle myopathy.
    Gao Y; Peng L; Zhao C
    Mol Cell Biochem; 2024 Feb; 479(2):393-417. PubMed ID: 37079208
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A Novel Missense Variant in Actin Binding Domain of
    Hesaraki M; Bora U; Pahlavan S; Salehi N; Mousavi SA; Barekat M; Rasouli SJ; Baharvand H; Ozhan G; Totonchi M
    Front Cardiovasc Med; 2022; 9():839862. PubMed ID: 35463789
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Variants in
    Chong JX; Childers MC; Marvin CT; Marcello AJ; Gonorazky H; Hazrati LN; Dowling JJ; Al Amrani F; Alanay Y; Nieto Y; Gabriel MÁM; Aylsworth AS; Buckingham KJ; Shively KM; Sommers O; Anderson K; ; ; Regnier M; Bamshad MJ
    HGG Adv; 2023 Jul; 4(3):100213. PubMed ID: 37457373
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic Profile of Left Ventricular Noncompaction Cardiomyopathy in Children-A Single Reference Center Experience.
    Piekutowska-Abramczuk D; Paszkowska A; Ciara E; Frączak K; Mirecka-Rola A; Wicher D; Pollak A; Rutkowska K; Sarnecki J; Ziółkowska L
    Genes (Basel); 2022 Jul; 13(8):. PubMed ID: 35893073
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Novel mutation in exon 14 of the sarcomere gene MYH7 in familial left ventricular noncompaction with bicuspid aortic valve.
    Basu R; Hazra S; Shanks M; Paterson DI; Oudit GY
    Circ Heart Fail; 2014 Nov; 7(6):1059-62. PubMed ID: 25415959
    [No Abstract]   [Full Text] [Related]  

  • 31. Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy.
    Petropoulou E; Soltani M; Firoozabadi AD; Namayandeh SM; Crockford J; Maroofian R; Jamshidi Y
    Eur J Med Genet; 2017 Sep; 60(9):485-488. PubMed ID: 28642161
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Multiplexed Functional Assessments of
    Friedman CE; Fayer S; Pendyala S; Chien WM; Loiben A; Tran L; Chao LS; McKinstry A; Ahmed D; Farris SD; Stempien-Otero A; Jonlin EC; Murry CE; Starita LM; Fowler DM; Yang KC
    Circ Genom Precis Med; 2024 Apr; 17(2):e004377. PubMed ID: 38362799
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy.
    Naderi N; Mohsen-Pour N; Nilipour Y; Pourirahim M; Maleki M; Kalayinia S
    BMC Cardiovasc Disord; 2023 Oct; 23(1):487. PubMed ID: 37794383
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Common pathogenic mechanism in patients with dropped head syndrome caused by different mutations in the MYH7 gene.
    Surikova Y; Filatova A; Polyak M; Skoblov M; Zaklyazminskaya E
    Gene; 2019 May; 697():159-164. PubMed ID: 30794915
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Role of
    Amor-Salamanca A; Santana Rodríguez A; Rasoul H; Rodríguez-Palomares JF; Moldovan O; Hey TM; Delgado MG; Cuenca DL; de Castro Campos D; Basurte-Elorz MT; Macías-Ruiz R; Fuentes Cañamero ME; Galvin J; Bilbao Quesada R; de la Higuera Romero L; Trujillo-Quintero JP; García-Cruz LM; Cárdenas-Reyes I; Jiménez-Jáimez J; García-Hernández S; Valverde-Gómez M; Gómez-Díaz I; Limeres Freire J; García-Pinilla JM; Gimeno-Blanes JR; Savattis K; García-Pavía P; Ochoa JP
    Circ Genom Precis Med; 2024 Apr; 17(2):e004404. PubMed ID: 38353104
    [TBL] [Abstract][Full Text] [Related]  

  • 37. New Genetic Variant in the
    Polyakova E; van Gils JM; Stöger JL; Kiès P; Egorova AD; Koopmann TT; van Dijk T; DeRuiter MC; Barge-Schaapveld DQCM; Jongbloed MRM
    Circ Genom Precis Med; 2023 Dec; 16(6):e004184. PubMed ID: 37818629
    [No Abstract]   [Full Text] [Related]  

  • 38. End-stage Hypertrophic Cardiomyopathy with Advanced Heart Failure in Patients Carrying MYH7 R453 Variants: A Case Series.
    Naito S; Higo S; Kameda S; Ogawa S; Tabata T; Akazawa Y; Nakamura D; Nakamoto K; Sera F; Kuramoto Y; Asano Y; Hikoso S; Miyagawa S; Sakata Y
    Intern Med; 2023 Nov; 62(21):3167-3173. PubMed ID: 36948619
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Low-frequency maternal novel MYH7 mosaicism mutation in recurrent fetal-onset severe left ventricular noncompaction: a case report.
    Kawamura H; Ikawa M; Hirono K; Kimura J; Okuno T; Kawatani M; Inai K; Hata Y; Nishida N; Yoshida Y
    Front Pediatr; 2023; 11():1195222. PubMed ID: 37360367
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Interpreting secondary cardiac disease variants in an exome cohort.
    Ng D; Johnston JJ; Teer JK; Singh LN; Peller LC; Wynter JS; Lewis KL; Cooper DN; Stenson PD; Mullikin JC; Biesecker LG;
    Circ Cardiovasc Genet; 2013 Aug; 6(4):337-46. PubMed ID: 23861362
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.