Search details
1.
Feline chimerism revealed by DNA profiling.
Anim Genet
; 51(4): 631-633, 2020 Aug.
Article
in English
| MEDLINE | ID: mdl-32452546
2.
Genetic Evidence That Captured Retroviral Envelope syncytins Contribute to Myoblast Fusion and Muscle Sexual Dimorphism in Mice.
PLoS Genet
; 12(9): e1006289, 2016 09.
Article
in English
| MEDLINE | ID: mdl-27589388
3.
Progressive Structural Defects in Canine Centronuclear Myopathy Indicate a Role for HACD1 in Maintaining Skeletal Muscle Membrane Systems.
Am J Pathol
; 187(2): 441-456, 2017 Feb.
Article
in English
| MEDLINE | ID: mdl-27939133
4.
Feline low-grade alimentary lymphoma: an emerging entity and a potential animal model for human disease.
BMC Vet Res
; 14(1): 306, 2018 Oct 11.
Article
in English
| MEDLINE | ID: mdl-30305106
5.
Myod and H19-Igf2 locus interactions are required for diaphragm formation in the mouse.
Development
; 140(6): 1231-9, 2013 Mar.
Article
in English
| MEDLINE | ID: mdl-23406902
6.
Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy.
PLoS Genet
; 9(6): e1003430, 2013 Jun.
Article
in English
| MEDLINE | ID: mdl-23754947
7.
A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeys.
Genet Sel Evol
; 47: 28, 2015 Apr 08.
Article
in English
| MEDLINE | ID: mdl-25887951
8.
Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys.
Genet Sel Evol
; 46: 65, 2014 Sep 25.
Article
in English
| MEDLINE | ID: mdl-25927731
9.
MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers.
Proc Natl Acad Sci U S A
; 107(33): 14697-702, 2010 Aug 17.
Article
in English
| MEDLINE | ID: mdl-20682747
10.
A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis.
Proc Natl Acad Sci U S A
; 107(33): 14775-80, 2010 Aug 17.
Article
in English
| MEDLINE | ID: mdl-20679209
11.
Hacd2 deficiency in mice leads to an early and lethal mitochondrial disease.
Mol Metab
; 69: 101677, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36693621
12.
Receptor interacting protein kinase-3 mediates both myopathy and cardiomyopathy in preclinical animal models of Duchenne muscular dystrophy.
J Cachexia Sarcopenia Muscle
; 14(6): 2520-2531, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-37909859
13.
Thyroid-stimulating hormone receptor signaling restores skeletal muscle stem cell regeneration in rats with muscular dystrophy.
Sci Transl Med
; 15(685): eadd5275, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36857434
14.
Allelic heterogeneity of albinism in the domestic cat.
Anim Genet
; 48(1): 127-128, 2017 Feb.
Article
in English
| MEDLINE | ID: mdl-27634063
15.
A dog model for centronuclear myopathy carrying the most common DNM2 mutation.
Dis Model Mech
; 15(4)2022 04 01.
Article
in English
| MEDLINE | ID: mdl-35244154
16.
Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis.
Acta Neuropathol Commun
; 10(1): 60, 2022 04 25.
Article
in English
| MEDLINE | ID: mdl-35468843
17.
Isolation and Phospholipid Enrichment of Muscle Mitochondria and Mitoplasts.
Bio Protoc
; 11(20): e4201, 2021 Oct 20.
Article
in English
| MEDLINE | ID: mdl-34761073
18.
Cardiolipin content controls mitochondrial coupling and energetic efficiency in muscle.
Sci Adv
; 7(1)2021 01.
Article
in English
| MEDLINE | ID: mdl-33523852
19.
Absence of SARS-CoV-2 infection in cats and dogs in close contact with a cluster of COVID-19 patients in a veterinary campus.
One Health
; 10: 100164, 2020 Dec.
Article
in English
| MEDLINE | ID: mdl-32904469
20.
Genetic heterogeneity of polydactyly in Maine Coon cats.
J Feline Med Surg
; 22(12): 1103-1113, 2020 12.
Article
in English
| MEDLINE | ID: mdl-32067556