John C. Fyfe

Michigan State University — United States

Medicine · Health Sciences

28h-index3.7kcitations59works0.02yr avg
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Research Topics

Folate and B Vitamins Research(11), Glycogen Storage Diseases and Myoclonus(11), Porphyrin Metabolism and Disorders(8), Thyroid Disorders and Treatments(7), Neurogenetic and Muscular Disorders Research(7)

Publications59 total

Non-Syndromic Cleft Palate and Transverse Limb Deficiency Segregating in a Family of Dogs
Research Square (Research Square)·2021· 1 citedOpen Access
PRESUMPTIVE CONGENITAL HYPOTHYROIDISM IN RED PANDAS (AILURUS FULGENS FULGENS) FROM FOUR SUCCESSIVE LITTERS
Journal of Zoo and Wildlife Medicine·2021· 1 cited
Blood and bone marrow findings in two pups with mucopolysaccharidosis type VII
Veterinary Clinical Pathology·2021
Secondary Palate Development in the Dog ( <i>Canis lupus familiaris</i> )
The Cleft Palate-Craniofacial Journal·2020· 5 cited
Inherited selective cobalamin malabsorption in Komondor dogs associated with a CUBN splice site variant
BMC Veterinary Research·2018· 10 citedOpen Access
Congenital dyshormonogenic hypothyroidism with goiter caused by a sodium/iodide symporter (SLC5A5) mutation in a family of Shih-Tzu dogs
Domestic Animal Endocrinology·2018· 8 cited
Natural Progression of Canine Glycogen Storage Disease Type IIIa.
PubMed·2016· 21 citedOpen Access
Molecular Genetic Characterization of Thyroid Dyshormonogenesis in a French Bulldog
Journal of Veterinary Internal Medicine·2015· 8 citedOpen Access
Failure to thrive and life-threatening complications due to inherited selective cobalamin malabsorption effectively managed in a juvenile Australian shepherd dog.
PubMed·2015· 19 citedOpen Access
Correction of glycogen storage disease type III with rapamycin in a canine model
Journal of Molecular Medicine·2014· 44 cited
Selective Intestinal Cobalamin Malabsorption with Proteinuria (Imerslund-Gräsbeck Syndrome) in Juvenile Beagles
Journal of Veterinary Internal Medicine·2014· 29 citedOpen Access
scAAV9 Intracisternal Delivery Results in Efficient Gene Transfer to the Central Nervous System of a Feline Model of Motor Neuron Disease
Human Gene Therapy·2013· 41 cited
An exon 53 frameshift mutation in CUBN abrogates cubam function and causes Imerslund-Gräsbeck syndrome in dogs
Molecular Genetics and Metabolism·2013· 26 citedOpen Access
A thyroid peroxidase (TPO) mutation in dogs reveals a canid-specific gene structure
Mammalian Genome·2012· 9 cited
Congenital Hypothyroidism with Goiter in Tenterfield Terriers
Journal of Veterinary Internal Medicine·2012· 19 cited
Morphometric Characterization Of The Pulmonary Hypoplasia Phenotype In A Canine Model Of Fetal Neuroaxonal Dystrophy
2012
Characterization of a canine model of glycogen storage disease type IIIa
Disease Models & Mechanisms·2012· 40 citedOpen Access
55 PROPAGATION OF MULTIPLE CAT HEREDITARY DISEASE MODELS FOLLOWING ASSISTED REPRODUCTION WITH FROZEN SEMEN AND EMBRYOS
Reproduction Fertility and Development·2011· 2 cited
Failure of lower motor neuron radial outgrowth precedes retrograde degeneration in a feline model of spinal muscular atrophy
The Journal of Comparative Neurology·2011· 4 cited
Corrigendum to “A complex rearrangement in GBE1 causes both perinatal hypoglycemic collapse and late-juvenile-onset neuromuscular degeneration in glycogen storage disease type IV of Norwegian forest cats” [Mol. Genet. Metab. 90 (2007) 383–392]
Molecular Genetics and Metabolism·2011
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Frequent Co-authors

Urs Giger(10), Donald F. Patterson(10), Søren K. Moestrup(6), Paula S. Henthorn(6), Mark E. Haskins(6), Christian Jacobsen(5), P Verroust(5), Erik Christensen(5), Qianchuan He(5), Thomas E. Willnow(4), Renata Kozyraki(4), Peter F. Jezyk(4), Shelby L. Hemker(4), Béatrice Joussemet(3), Philippe Moullier(3), Martine Barkats(3), Albert de la Chapelle(3), John H. Wolfe(3), Thomas J. Van Winkle(3), Danbin Xu(3)