Zobrazeno 1 - 10
of 98
pro vyhledávání: '"D F, PATTERSON"'
Autor:
A. Sanchez Londoño, J. A. Nadeau, Sarah A Reed, A. S. Schauer, D. F. Patterson, A. K. Jones, E. K. LaVigne
Publikováno v:
Journal of Animal Science. 93:5672-5680
Success as equine athletes requires proper muscle growth in young horses. Muscle hypertrophy occurs through protein synthesis and the contribution of muscle satellite cells, which can be stimulated or inhibited by cytokines and growth factors present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::149679ef6a967c5cd30f265484e718d3
https://doi.org/10.2527/jas.2015-9634
https://doi.org/10.2527/jas.2015-9634
Autor:
D. F. Patterson, D. K. Detweiler
Publikováno v:
Zentralblatt für Veterinärmedizin Reihe A. 10:121-132
ummary Splitting of the second heart sound is best detected in the pulmonary and aortic valve areas. Splitting of the second sound in the dog must be differentiated from other extra sounds such as systolic clicks and protodiastolic gallop sounds. Alt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0878afd3f0312f5c548de35a1c12372a
https://doi.org/10.1111/j.1439-0442.1963.tb00010.x
https://doi.org/10.1111/j.1439-0442.1963.tb00010.x
Publikováno v:
Zentralblatt für Veterinärmedizin Reihe A. 10:195-202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffc2b420966bf3c91a38b8c16d9cfebb
https://doi.org/10.1111/j.1439-0442.1963.tb00018.x
https://doi.org/10.1111/j.1439-0442.1963.tb00018.x
Autor:
E K, LaVigne, A K, Jones, A Sanchez, Londoño, A S, Schauer, D F, Patterson, J A, Nadeau, S A, Reed
Publikováno v:
Journal of animal science. 93(12)
Success as equine athletes requires proper muscle growth in young horses. Muscle hypertrophy occurs through protein synthesis and the contribution of muscle satellite cells, which can be stimulated or inhibited by cytokines and growth factors present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::403bc1d8ac881e119e46d339e1c5c4ea
https://pubmed.ncbi.nlm.nih.gov/26641176
https://pubmed.ncbi.nlm.nih.gov/26641176
Autor:
D. F. Patterson, D. K. Detweiler
Publikováno v:
Annals of the New York Academy of Sciences. 127:322-340
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d28bc6dec4f9a628bc3eda8cc0a4c92
https://doi.org/10.1111/j.1749-6632.1965.tb49409.x
https://doi.org/10.1111/j.1749-6632.1965.tb49409.x
Publikováno v:
Annals of the New York Academy of Sciences. 127:242-305
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2a91cf921639bb04502d8b6f166bb5b
https://doi.org/10.1111/j.1749-6632.1965.tb49407.x
https://doi.org/10.1111/j.1749-6632.1965.tb49407.x
Autor:
Donna M. Dambach, Paula S. Henthorn, D. F. Patterson, P. F. Jezyk, T. Meister, Margret L. Casal
Publikováno v:
Veterinary Pathology. 41:319-325
Glomerular disease was diagnosed by histopathologic examination in 11 related Bullmastiff dogs, and clinical and laboratory data were collected retrospectively. Four female and seven male dogs between the ages of 2.5 and 11 years were affected. Clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c39ee0585f230e64e376c65aff7fdac5
https://doi.org/10.1354/vp.41-4-319
https://doi.org/10.1354/vp.41-4-319
Autor:
D F, PATTERSON
Publikováno v:
A listing of research in the cardiovascular field. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3b65ea083bef47f3396b90fd2cc8dd8a
https://pubmed.ncbi.nlm.nih.gov/24547413
https://pubmed.ncbi.nlm.nih.gov/24547413
Publikováno v:
Journal of Heredity. 90:494-497
Conotruncal defects (CTDs) of the heart are a frequent component of DiGeorge, velocardiofacial, or other syndromes caused by deletions of the human chromosome 22q11 region (HSA22q11). In addition, some human patients with isolated nonsyndromic CTDs h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c6a4c3c47b665db537108884ed0be20
https://doi.org/10.1093/jhered/90.4.494
https://doi.org/10.1093/jhered/90.4.494
Autor:
Marie T. Vanier, Paola Luzi, David A. Wenger, Teresa Victoria, Mohammad A. Rafi, D F Patterson, M H Haskins, Charles H. Vite
Publikováno v:
Journal of Heredity. 90:138-142
Krabbe disease or globoid cell leukodystrophy (GLD) is an autosomal recessive disorder resulting from the defective lysosomal hydrolysis of specific galactolipids found primarily in myelin. This leads to severe neurological symptoms including seizure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::245e586c4227b3eefe33791d50319eb5
https://doi.org/10.1093/jhered/90.1.138
https://doi.org/10.1093/jhered/90.1.138