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 *

139 related articles for article (PubMed ID: 37029485)

  • 1. Novel insights on GTPBP3-associated hypertrophic cardiomyopathy.
    Angelova P; Velchev V; Stoyanov N; Atemin S; Todorov T; Tourtourikov I; Mitev V; Todorova A
    Am J Med Genet A; 2023 Jul; 191(7):1804-1813. PubMed ID: 37029485
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pathogenicity Analysis of a Novel Variant in
    Zhang Q; Ouyang Q; Xiang J; Li H; Lv H; An Y
    Genes (Basel); 2023 Feb; 14(3):. PubMed ID: 36980825
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel
    Tong W; Liu W; Guo H; Wang J; Yu S; Zhang J; Liu C; Chen J; Zhao X
    Cardiol Young; 2020 Jan; 30(1):100-106. PubMed ID: 31747981
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole-exome sequencing reveals a likely pathogenic LMNA variant causing hypertrophic cardiomyopathy.
    Mahdavi M; Mohsen-Pour N; Maleki M; Ghasemi S; Tabib A; Houshmand G; Naderi N; Masoumi T; Pouraliakbar H; Kalayinia S
    Lab Med; 2024 Jan; 55(1):62-70. PubMed ID: 37246508
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel pathogenic variant of MYBPC3 responsible for hypertrophic cardiomyopathy.
    Yang X; Li Z; Wang Q; Zhang Y; Zhao C
    Cardiol Young; 2022 Apr; 32(4):539-544. PubMed ID: 34180388
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy.
    Kopajtich R; Nicholls TJ; Rorbach J; Metodiev MD; Freisinger P; Mandel H; Vanlander A; Ghezzi D; Carrozzo R; Taylor RW; Marquard K; Murayama K; Wieland T; Schwarzmayr T; Mayr JA; Pearce SF; Powell CA; Saada A; Ohtake A; Invernizzi F; Lamantea E; Sommerville EW; Pyle A; Chinnery PF; Crushell E; Okazaki Y; Kohda M; Kishita Y; Tokuzawa Y; Assouline Z; Rio M; Feillet F; Mousson de Camaret B; Chretien D; Munnich A; Menten B; Sante T; Smet J; Régal L; Lorber A; Khoury A; Zeviani M; Strom TM; Meitinger T; Bertini ES; Van Coster R; Klopstock T; Rötig A; Haack TB; Minczuk M; Prokisch H
    Am J Hum Genet; 2014 Dec; 95(6):708-20. PubMed ID: 25434004
    [TBL] [Abstract][Full Text] [Related]  

  • 7.
    Çağlayan AO; Sezer RG; Kaymakçalan H; Ulgen E; Yavuz T; Baranoski JF; Bozaykut A; Harmanci AS; Yalcin Y; Youngblood MW; Yasuno K; Bilgüvar K; Gunel M
    Cold Spring Harb Mol Case Stud; 2017 Sep; 3(5):. PubMed ID: 28630369
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole-exome sequencing identifies rare compound heterozygous mutations in the MYBPC3 gene associated with severe familial hypertrophic cardiomyopathy.
    Zhou N; Qin S; Liu Y; Tang L; Zhao W; Pan C; Qiu Z; Wang X; Shu X
    Eur J Med Genet; 2018 Aug; 61(8):434-441. PubMed ID: 29524613
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Potential digenic inheritance of familial hypertrophic cardiomyopathy identified by whole-exome sequencing.
    Ren MB; Chai XR; Li L; Wang X; Yin C
    Mol Genet Genomic Med; 2020 Mar; 8(3):e1150. PubMed ID: 31960626
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion of Gtpbp3 in zebrafish revealed the hypertrophic cardiomyopathy manifested by aberrant mitochondrial tRNA metabolism.
    Chen D; Zhang Z; Chen C; Yao S; Yang Q; Li F; He X; Ai C; Wang M; Guan MX
    Nucleic Acids Res; 2019 Jun; 47(10):5341-5355. PubMed ID: 30916346
    [TBL] [Abstract][Full Text] [Related]  

  • 11. FLNC and MYLK2 Gene Mutations in a Chinese Family with Different Phenotypes of Cardiomyopathy.
    Qin X; Li P; Qu HQ; Liu Y; Xia Y; Chen S; Yang Y; Huang S; Wen P; Zhou X; Li X; Wang Y; Tian L; Hakonarson H; Wu Y; Zhuang J
    Int Heart J; 2021 Jan; 62(1):127-134. PubMed ID: 33455984
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Potential Oligogenic Etiology of Hypertrophic Cardiomyopathy: A Classic Single-Gene Disorder.
    Li L; Bainbridge MN; Tan Y; Willerson JT; Marian AJ
    Circ Res; 2017 Mar; 120(7):1084-1090. PubMed ID: 28223422
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome sequencing identifies a FHOD3 p.S527del mutation in a Chinese family with hypertrophic cardiomyopathy.
    Huang S; Pu T; Wei W; Xu R; Wu Y
    J Gene Med; 2020 Mar; 22(3):e3146. PubMed ID: 31742804
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities.
    Bukaeva A; Myasnikov R; Kulikova O; Meshkov A; Kiseleva A; Petukhova A; Zotova E; Sparber P; Ershova A; Sotnikova E; Kudryavtseva M; Zharikova A; Koretskiy S; Mershina E; Ramensky V; Zaicenoka M; Vyatkin Y; Muraveva A; Abisheva A; Nikityuk T; Sinitsyn V; Divashuk M; Dadali E; Pokrovskaya M; Drapkina O
    Int J Mol Sci; 2024 Jul; 25(14):. PubMed ID: 39062799
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy.
    Bagnall RD; Ingles J; Dinger ME; Cowley MJ; Ross SB; Minoche AE; Lal S; Turner C; Colley A; Rajagopalan S; Berman Y; Ronan A; Fatkin D; Semsarian C
    J Am Coll Cardiol; 2018 Jul; 72(4):419-429. PubMed ID: 30025578
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CSRP3, p.Arg122*, is responsible for hypertrophic cardiomyopathy in a Chinese family.
    Huang H; Chen Y; Jin J; Du R; Tang K; Fan L; Xiang R
    J Gene Med; 2022 Jan; 24(1):e3390. PubMed ID: 34558151
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features.
    Jolfayi AG; Naderi N; Ghasemi S; Salmanipour A; Adimi S; Maleki M; Kalayinia S
    BMC Cardiovasc Disord; 2024 Jan; 24(1):1. PubMed ID: 38166572
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Ups and Downs of Genetic Diagnosis of Hypertrophic Cardiomyopathy.
    Gómez J; Reguero JR; Coto E
    Rev Esp Cardiol (Engl Ed); 2016 Jan; 69(1):61-8. PubMed ID: 26654849
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.
    Waldmüller S; Schroeder C; Sturm M; Scheffold T; Imbrich K; Junker S; Frische C; Hofbeck M; Bauer P; Bonin M; Gawaz M; Gramlich M
    Mol Cell Probes; 2015 Oct; 29(5):308-14. PubMed ID: 25979592
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Controversial molecular functions of CBS versus non-CBS domain variants of PRKAG2 in arrhythmia and cardiomyopathy: A case report and literature review.
    Gong X; Yu P; Wu T; He Y; Zhou K; Hua Y; Lin S; Wang T; Huang H; Li Y
    Mol Genet Genomic Med; 2022 Jul; 10(7):e1962. PubMed ID: 35588295
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.