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 *

163 related articles for article (PubMed ID: 34460321)

  • 41. Genetic screening for hypertrophic cardiomyopathy in large, asymptomatic military cohorts.
    Brough J; Jain M; Jerves T; Kruszka P; McGuffey E
    Am J Med Genet C Semin Med Genet; 2020 Mar; 184(1):124-128. PubMed ID: 32030882
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy.
    Chida A; Inai K; Sato H; Shimada E; Nishizawa T; Shimada M; Furutani M; Furutani Y; Kawamura Y; Sugimoto M; Ishihara J; Fujiwara M; Soga T; Kawana M; Fuji S; Tateno S; Kuraishi K; Kogaki S; Nishimura M; Ayusawa M; Ichida F; Yamazawa H; Matsuoka R; Nonoyama S; Nakanishi T
    Heart Vessels; 2017 Jun; 32(6):700-707. PubMed ID: 27885498
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Mutation-specific pathology and treatment of hypertrophic cardiomyopathy in patients, mouse models and human engineered heart tissue.
    Wijnker PJM; van der Velden J
    Biochim Biophys Acta Mol Basis Dis; 2020 Aug; 1866(8):165774. PubMed ID: 32217077
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Recommendations for gene assays for cardiomyopathy in children].
    Subspecialty Group of Cardiology, The Society of Pediatrics, Chinese Medical Association The Editorial Board, Chinese Journal of Pediatrics
    Zhonghua Er Ke Za Zhi; 2013 Aug; 51(8):595-7. PubMed ID: 24225290
    [No Abstract]   [Full Text] [Related]  

  • 45. A new missense mutation, p.Arg719Leu, of the beta-myosin heavy chain gene in a patient with familial hypertrophic cardiomyopathy.
    Gawor M; Bilińska ZT; Franaszczyk M; Michalak E; Rafał P; Grzybowski J
    Minerva Cardioangiol; 2017 Feb; 65(1):96-102. PubMed ID: 27910300
    [No Abstract]   [Full Text] [Related]  

  • 46. Gene symbol: MYH7.
    Iascone MR; Marchetti D; Ferrazzi P
    Hum Genet; 2007 Feb; 120(6):915. PubMed ID: 17438618
    [No Abstract]   [Full Text] [Related]  

  • 47. Targeted next-generation sequencing (NGS) of nine candidate genes with custom AmpliSeq in patients and a cardiomyopathy risk group.
    Glotov AS; Kazakov SV; Zhukova EA; Alexandrov AV; Glotov OS; Pakin VS; Danilova MM; Poliakova IV; Niyazova SS; Chakova NN; Komissarova SM; Kurnikova EA; Sarana AM; Sherbak SG; Sergushichev AA; Shalyto AA; Baranov VS
    Clin Chim Acta; 2015 Jun; 446():132-40. PubMed ID: 25892673
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy].
    Laredo R; Monserrat L; Hermida-Prieto M; Fernández X; Rodríguez I; Cazón L; Alvariño I; Dumont C; Piñón P; Peteiro J; Bouzas B; Castro-Beiras A
    Rev Esp Cardiol; 2006 Oct; 59(10):1008-18. PubMed ID: 17125710
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Gene symbol: MYH7.
    Iascone MR; Marchetti D; Ferrazzi P
    Hum Genet; 2007 Feb; 120(6):916. PubMed ID: 17438619
    [No Abstract]   [Full Text] [Related]  

  • 50. Structural effects of the slow/b-cardiac myosin heavy chain R453C mutation in cardiac and skeletal muscle.
    Tajsharghi H; Fyhr IM
    Scand Cardiovasc J; 2008 Apr; 42(2):153-6. PubMed ID: 18365899
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.
    Lu C; Wu W; Liu F; Yang K; Li J; Liu Y; Wang R; Si N; Gao P; Liu Y; Zhang S; Zhang X
    J Transl Med; 2018 Aug; 16(1):241. PubMed ID: 30165862
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Cardiac Myosin Inhibitors for Obstructive Hypertrophic Cardiomyopathy: Where Are We on the Hype Cycle?
    Ommen SR
    J Am Coll Cardiol; 2022 Jul; 80(2):109-110. PubMed ID: 35798444
    [No Abstract]   [Full Text] [Related]  

  • 53. Cranial, axial and proximal myopathy and hypertrophic cardiomyopathy caused by a mutation in the globular head region of the MYH7 gene.
    Díaz-Manera J; Alejaldre A; Llauger J; Mirabet S; Rojas-García R; Ramos-Fransi A; Gallardo E; Illa I
    Eur J Neurol; 2014 Jun; 21(6):e51-2. PubMed ID: 24805292
    [No Abstract]   [Full Text] [Related]  

  • 54. Confirmation of cause and manner of death via a comprehensive cardiac autopsy including whole exome next-generation sequencing.
    Loporcaro CG; Tester DJ; Maleszewski JJ; Kruisselbrink T; Ackerman MJ
    Arch Pathol Lab Med; 2014 Aug; 138(8):1083-9. PubMed ID: 24298987
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Cardiac myosin inhibitors for hypertrophic cardiomyopathy: shedding light on their clinical potential.
    Rao SJ; Forst B; Kanwal AK; Kanwal A; Aronow WS; Naidu SS
    Expert Opin Investig Drugs; 2023 Jan; 32(1):1-4. PubMed ID: 36625220
    [No Abstract]   [Full Text] [Related]  

  • 56. High resolution melting: improvements in the genetic diagnosis of hypertrophic cardiomyopathy in a Portuguese cohort.
    Santos S; Marques V; Pires M; Silveira L; Oliveira H; Lança V; Brito D; Madeira H; Esteves JF; Freitas A; Carreira IM; Gaspar IM; Monteiro C; Fernandes AR
    BMC Med Genet; 2012 Mar; 13():17. PubMed ID: 22429680
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy.
    De Bortoli M; Calore C; Lorenzon A; Calore M; Poloni G; Mazzotti E; Rigato I; Marra MP; Melacini P; Iliceto S; Thiene G; Basso C; Daliento L; Corrado D; Rampazzo A; Bauce B
    Eur J Hum Genet; 2017 Oct; 25(10):1165-1169. PubMed ID: 28699631
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.
    Ishikawa T; Jou CJ; Nogami A; Kowase S; Arrington CB; Barnett SM; Harrell DT; Arimura T; Tsuji Y; Kimura A; Makita N
    Circ Arrhythm Electrophysiol; 2015 Apr; 8(2):400-8. PubMed ID: 25717017
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Exome sequencing identifies a novel MYH7 p.G407C mutation responsible for familial hypertrophic cardiomyopathy.
    Guo Q; Xu Y; Wang X; Guo Y; Xu R; Sun K; Chen S
    DNA Cell Biol; 2014 Oct; 33(10):699-704. PubMed ID: 24963656
    [TBL] [Abstract][Full Text] [Related]  

  • 60. β-Cardiac myosin hypertrophic cardiomyopathy mutations release sequestered heads and increase enzymatic activity.
    Adhikari AS; Trivedi DV; Sarkar SS; Song D; Kooiker KB; Bernstein D; Spudich JA; Ruppel KM
    Nat Commun; 2019 Jun; 10(1):2685. PubMed ID: 31213605
    [TBL] [Abstract][Full Text] [Related]  

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