173 related articles for article (PubMed ID: 37071642)
1. Presence of known feline ALMS1 and MYBPC3 variants in a diverse cohort of cats with hypertrophic cardiomyopathy in Japan.
Akiyama N; Suzuki R; Saito T; Yuchi Y; Ukawa H; Matsumoto Y
PLoS One; 2023; 18(4):e0283433. PubMed ID: 37071642
[TBL] [Abstract][Full Text] [Related]
2. Absence of known feline MYH7 and MYBPC3 variants in a diverse cohort of cats with hypertrophic cardiomyopathy.
O'Donnell K; Adin D; Atkins CE; DeFrancesco T; Keene BW; Tou S; Meurs KM
Anim Genet; 2021 Aug; 52(4):542-544. PubMed ID: 33970514
[TBL] [Abstract][Full Text] [Related]
3. Myosin-binding protein C DNA variants in domestic cats (A31P, A74T, R820W) and their association with hypertrophic cardiomyopathy.
Longeri M; Ferrari P; Knafelz P; Mezzelani A; Marabotti A; Milanesi L; Pertica G; Polli M; Brambilla PG; Kittleson M; Lyons LA; Porciello F
J Vet Intern Med; 2013; 27(2):275-85. PubMed ID: 23323744
[TBL] [Abstract][Full Text] [Related]
4. Analysis of 8 sarcomeric candidate genes for feline hypertrophic cardiomyopathy mutations in cats with hypertrophic cardiomyopathy.
Meurs KM; Norgard MM; Kuan M; Haggstrom J; Kittleson M
J Vet Intern Med; 2009; 23(4):840-3. PubMed ID: 19566849
[TBL] [Abstract][Full Text] [Related]
5. Association of A31P and A74T polymorphisms in the myosin binding protein C3 gene and hypertrophic cardiomyopathy in Maine Coon and other breed cats.
Wess G; Schinner C; Weber K; Küchenhoff H; Hartmann K
J Vet Intern Med; 2010; 24(3):527-32. PubMed ID: 20412438
[TBL] [Abstract][Full Text] [Related]
6. Precision medicine validation: identifying the
Ontiveros ES; Ueda Y; Harris SP; Stern JA;
J Feline Med Surg; 2019 Dec; 21(12):1086-1093. PubMed ID: 30558461
[TBL] [Abstract][Full Text] [Related]
7. Prevalence of cardiac myosin-binding protein C3 mutations in Maine Coon cats with hypertrophic cardiomyopathy.
Sukumolanan P; Petchdee S
Vet World; 2022 Feb; 15(2):502-508. PubMed ID: 35400937
[TBL] [Abstract][Full Text] [Related]
8. A feline orthologue of the human MYH7 c.5647G>A (p.(Glu1883Lys)) variant causes hypertrophic cardiomyopathy in a Domestic Shorthair cat.
Schipper T; Van Poucke M; Sonck L; Smets P; Ducatelle R; Broeckx BJG; Peelman LJ
Eur J Hum Genet; 2019 Nov; 27(11):1724-1730. PubMed ID: 31164718
[TBL] [Abstract][Full Text] [Related]
9. HCM-associated ALMS1 variant: Allele drop-out and frequency in Italian Sphynx cats.
Turba ME; Ferrari P; Milanesi R; Gentilini F; Longeri M
Anim Genet; 2023 Oct; 54(5):643-646. PubMed ID: 37345275
[TBL] [Abstract][Full Text] [Related]
10. The genetic basis of hypertrophic cardiomyopathy in cats and humans.
Kittleson MD; Meurs KM; Harris SP
J Vet Cardiol; 2015 Dec; 17 Suppl 1(Suppl 1):S53-73. PubMed ID: 26776594
[TBL] [Abstract][Full Text] [Related]
11. Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats: a longitudinal study.
Granström S; Godiksen MT; Christiansen M; Pipper CB; Martinussen T; Møgelvang R; Søgaard P; Willesen JL; Koch J
J Vet Cardiol; 2015 Dec; 17 Suppl 1():S268-81. PubMed ID: 26776585
[TBL] [Abstract][Full Text] [Related]
12. Prevalence of the MYBPC3-A31P mutation in a large European feline population and association with hypertrophic cardiomyopathy in the Maine Coon breed.
Mary J; Chetboul V; Sampedrano CC; Abitbol M; Gouni V; Trehiou-Sechi E; Tissier R; Queney G; Pouchelon JL; Thomas A
J Vet Cardiol; 2010 Dec; 12(3):155-61. PubMed ID: 21051304
[TBL] [Abstract][Full Text] [Related]
13. Association of the myosin binding protein C3 mutation (MYBPC3 R820W) with cardiac death in a survey of 236 Ragdoll cats.
Borgeat K; Casamian-Sorrosal D; Helps C; Luis Fuentes V; Connolly DJ
J Vet Cardiol; 2014 Jun; 16(2):73-80. PubMed ID: 24906243
[TBL] [Abstract][Full Text] [Related]
14. A deleterious mutation in the ALMS1 gene in a naturally occurring model of hypertrophic cardiomyopathy in the Sphynx cat.
Meurs KM; Williams BG; DeProspero D; Friedenberg SG; Malarkey DE; Ezzell JA; Keene BW; Adin DB; DeFrancesco TC; Tou S
Orphanet J Rare Dis; 2021 Feb; 16(1):108. PubMed ID: 33639992
[TBL] [Abstract][Full Text] [Related]
15. The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans.
Ripoll Vera T; Monserrat Iglesias L; Hermida Prieto M; Ortiz M; Rodriguez Garcia I; Govea Callizo N; Gómez Navarro C; Rosell Andreo J; Gámez Martínez JM; Pons Lladó G; Cremer Luengos D; Torres Marqués J
Int J Cardiol; 2010 Nov; 145(2):405-407. PubMed ID: 20542340
[TBL] [Abstract][Full Text] [Related]
16. Heat shock proteins and small nucleolar RNAs are dysregulated in a Drosophila model for feline hypertrophic cardiomyopathy.
Tallo CA; Duncan LH; Yamamoto AH; Slaydon JD; Arya GH; Turlapati L; Mackay TFC; Carbone MA
G3 (Bethesda); 2021 Jan; 11(1):. PubMed ID: 33561224
[TBL] [Abstract][Full Text] [Related]
17. A genome-first approach to rare variants in hypertrophic cardiomyopathy genes MYBPC3 and MYH7 in a medical biobank.
Park J; Packard EA; Levin MG; Judy RL; ; Damrauer SM; Day SM; Ritchie MD; Rader DJ
Hum Mol Genet; 2022 Mar; 31(5):827-837. PubMed ID: 34542152
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Genetics of feline hypertrophic cardiomyopathy.
Gil-Ortuño C; Sebastián-Marcos P; Sabater-Molina M; Nicolas-Rocamora E; Gimeno-Blanes JR; Fernández Del Palacio MJ
Clin Genet; 2020 Sep; 98(3):203-214. PubMed ID: 32215921
[TBL] [Abstract][Full Text] [Related]
20. A Novel Homozygous Intronic Variant in TNNT2 Associates With Feline Cardiomyopathy.
McNamara JW; Schuckman M; Becker RC; Sadayappan S
Front Physiol; 2020; 11():608473. PubMed ID: 33304277
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
