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 *

122 related articles for article (PubMed ID: 34606642)

  • 1. Prevalence of the E321G MYH1 variant in Brazilian Quarter Horses.
    de Albuquerque AL; Zanzarini Delfiol DJ; Andrade DGA; Albertino LG; Sonne L; Borges AS; Valberg SJ; Finno CJ; Oliveira-Filho JP
    Equine Vet J; 2022 Sep; 54(5):952-957. PubMed ID: 34606642
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prevalence of the E321G MYH1 variant for immune-mediated myositis and nonexertional rhabdomyolysis in performance subgroups of American Quarter Horses.
    Gianino GM; Valberg SJ; Perumbakkam S; Henry ML; Gardner K; Penedo C; Finno CJ
    J Vet Intern Med; 2019 Mar; 33(2):897-901. PubMed ID: 30623495
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An E321G MYH1 mutation is strongly associated with nonexertional rhabdomyolysis in Quarter Horses.
    Valberg SJ; Henry ML; Perumbakkam S; Gardner KL; Finno CJ
    J Vet Intern Med; 2018 Sep; 32(5):1718-1725. PubMed ID: 30079499
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prevalence of clinical signs and factors impacting expression of myosin heavy chain myopathy in Quarter Horse-related breeds with the MYH1
    Valberg SJ; Schultz AE; Finno CJ; Bellone RR; Hughes SS
    J Vet Intern Med; 2022 May; 36(3):1152-1159. PubMed ID: 35426178
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A missense mutation in MYH1 is associated with susceptibility to immune-mediated myositis in Quarter Horses.
    Finno CJ; Gianino G; Perumbakkam S; Williams ZJ; Bordbari MH; Gardner KL; Burns E; Peng S; Durward-Akhurst SA; Valberg SJ
    Skelet Muscle; 2018 Mar; 8(1):7. PubMed ID: 29510741
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Myofibre Hyper-Contractility in Horses Expressing the Myosin Heavy Chain Myopathy Mutation,
    Ochala J; Finno CJ; Valberg SJ
    Cells; 2021 Dec; 10(12):. PubMed ID: 34943936
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Allele frequency of muscular genetic disorders in bull-catching (vaquejada) quarter horses.
    Sperandio LMS; Lago GR; Albertino LG; Araújo CET; Ferreira C; Borges AS; Oliveira-Filho JP
    J Equine Vet Sci; 2024 May; 136():105052. PubMed ID: 38531516
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Myosin heavy-chain myopathy in 2 American quarter horses.
    Faccin M; Landsgaard KA; Milliron SM; Jennings AH; Keith Chaffin M; Giaretta PR; Rech RR
    Vet Pathol; 2024 May; 61(3):462-467. PubMed ID: 37818977
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prevalence of Genetic Mutations in Horses With Muscle Disease From a Neuromuscular Disease Laboratory.
    Aleman M; Scalco R; Malvick J; Grahn RA; True A; Bellone RR
    J Equine Vet Sci; 2022 Nov; 118():104129. PubMed ID: 36150530
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The American Quarter Horse: population structure and relationship to the thoroughbred.
    Petersen JL; Mickelson JR; Cleary KD; McCue ME
    J Hered; 2014; 105(2):148-62. PubMed ID: 24293614
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Absence of myofibrillar myopathy in Quarter Horses with a histopathological diagnosis of type 2 polysaccharide storage myopathy and lack of association with commercial genetic tests.
    Valberg SJ; Henry ML; Herrick KL; Velez-Irizarry D; Finno CJ; Petersen JL
    Equine Vet J; 2023 Mar; 55(2):230-238. PubMed ID: 35288976
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Type 2 polysaccharide storage myopathy in Quarter Horses is a novel glycogen storage disease causing exertional rhabdomyolysis.
    Valberg SJ; Williams ZJ; Finno CJ; Schultz A; Velez-Irizarry D; Henry ML; Gardner K; Petersen JL
    Equine Vet J; 2023 Jul; 55(4):618-631. PubMed ID: 36102343
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evaluation of allele frequencies of inherited disease genes in subgroups of American Quarter Horses.
    Tryon RC; Penedo MC; McCue ME; Valberg SJ; Mickelson JR; Famula TR; Wagner ML; Jackson M; Hamilton MJ; Nooteboom S; Bannasch DL
    J Am Vet Med Assoc; 2009 Jan; 234(1):120-5. PubMed ID: 19119976
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characteristics of Thoroughbred and Quarter Horse racehorses that sustained a complete scapular fracture.
    Vallance SA; Case JT; Entwistle RC; Kinde H; Barr BC; Moore J; Anderson ML; Arthur RM; Stover SM
    Equine Vet J; 2012 Jul; 44(4):425-31. PubMed ID: 21950466
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic polymorphisms in vitamin E transport genes as determinants for risk of equine neuroaxonal dystrophy.
    Ma Y; Peng S; Donnelly CG; Ghosh S; Miller AD; Woolard K; Finno CJ
    J Vet Intern Med; 2024; 38(1):417-423. PubMed ID: 37937700
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Case-control study of high-speed exercise history of Thoroughbred and Quarter Horse racehorses that died related to a complete scapular fracture.
    Vallance SA; Entwistle RC; Hitchens PL; Gardner IA; Stover SM
    Equine Vet J; 2013 May; 45(3):284-92. PubMed ID: 23240828
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinicopathological and pedigree investigation of a novel spinocerebellar neurological disease in juvenile Quarter Horses in North America.
    Willis AT; Dahlgren AR; Woolard KD; Ghosh S; Donnelly CG; de la Concha-Bermejillo A; Pacheco A; Watson KD; Berryhill E; Aleman M; Wensley F; Humphreys S; Whitehead AE; Goldsmith D; Chesen B; Ragsdale J; Tompkins JE; Nash R; Plunkett AH; Qualls HJ; Rodriguez K; Hochanadel D; Miller AD; Finno CJ
    J Vet Intern Med; 2024; 38(3):1808-1814. PubMed ID: 38669583
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Electrophysiological studies in American Quarter horses with neuroaxonal dystrophy.
    Finno CJ; Aleman M; Ofri R; Hollingsworth SR; Madigan JE; Winfield L; Bannasch DL
    Vet Ophthalmol; 2012 Sep; 15 Suppl 2():3-7. PubMed ID: 22432889
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pedigree analysis and exclusion of alpha-tocopherol transfer protein (TTPA) as a candidate gene for neuroaxonal dystrophy in the American Quarter Horse.
    Finno CJ; Famula T; Aleman M; Higgins RJ; Madigan JE; Bannasch DL
    J Vet Intern Med; 2013; 27(1):177-85. PubMed ID: 23186252
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evidence for origin of lavender foal syndrome among Egyptian Arabian horses in Egypt.
    AbouEl Ela NH; El Araby IE; Saleh AA; Abd El-Fattah AH; Hagag NM; Brooks SA; Radwan MA; Kalbfleisch T
    Equine Vet J; 2023 May; 55(3):487-493. PubMed ID: 35665534
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.