Zobrazeno 1 - 10
of 342
pro vyhledávání: '"J. Winand"'
Autor:
José P. Oliveira-Filho, Peres R. Badial, Paulo Henrique J. Cunha, Ana Paula Bordon, João P. Araujo Jr, Thomas J. Divers, Nena J. Winand, Alexandre S. Borges
Publikováno v:
Pesquisa Veterinária Brasileira, Vol 34, Iss 1, Pp 51-56 (2014)
Hypoferremia observed during systemic inflammatory disorders is regulated by hepcidin. Hepcidin up-regulation is particularly important during acute inflammation, as it restricts the availability of iron, which is necessary for pathogenic microorgani
Externí odkaz:
https://doaj.org/article/17486ccd83c4469f97c499701ba18ba8
Akademický článek
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Akademický článek
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Autor:
Nena J. Winand, Alexandre Secorun Borges, Peres Ramos Badial, Lissandro Gonçalves Conceição, José P. Oliveira-Filho, Robson M. Liboreiro
Publikováno v:
LOCUS Repositório Institucional da UFV
Universidade Federal de Viçosa (UFV)
instacron:UFV
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Universidade Federal de Viçosa (UFV)
instacron:UFV
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2018-12-11T16:49:59Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-10-01 The Ehlers-Danlos syndrome in horses is a group of genetic connective tissue disorders clinically characterized by skin fragility and hyperex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3980a7971ecc31a5d07016c25a64c97d
http://www.locus.ufv.br/handle/123456789/23144
http://www.locus.ufv.br/handle/123456789/23144
Publikováno v:
Journal of the American Animal Hospital Association. 50:130-135
This report describes a case of feline dystrophin-deficient muscular dystrophy (DDMD) with an atypical clinical presentation. A novel gene mutation is reported to be responsible for dystrophin-deficient hypertrophic muscular dystrophy. In an emergenc
Autor:
Alexandre Secorun Borges, Paulo Henrique Jorge da Cunha, Peres Ramos Badial, Thomas J. Divers, José P. Oliveira-Filho, Nena J. Winand, João Pessoa Araújo, Ana Paula Bordon
Publikováno v:
Pesquisa Veterinária Brasileira, Volume: 34, Issue: 1, Pages: 51-56, Published: JAN 2014
Pesquisa Veterinária Brasileira, Vol 34, Iss 1, Pp 51-56 (2014)
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Pesquisa Veterinária Brasileira v.34 n.1 2014
Pesquisa Veterinária Brasileira
Colégio Brasileiro de Patologia Animal (CBPA)
instacron:EMBRAPA
Pesquisa Veterinária Brasileira, Vol 34, Iss 1, Pp 51-56 (2014)
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Pesquisa Veterinária Brasileira v.34 n.1 2014
Pesquisa Veterinária Brasileira
Colégio Brasileiro de Patologia Animal (CBPA)
instacron:EMBRAPA
Made available in DSpace on 2014-10-01T13:08:41Z (GMT). No. of bitstreams: 0 Previous issue date: 2014-01-01Bitstream added on 2014-10-01T14:03:54Z : No. of bitstreams: 1 S0100-736X2014000100009.pdf: 659682 bytes, checksum: 4bf40c1af2c43a561b912e0562
Akademický článek
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Autor:
Rogério Martins Amorim, José Fernando Garcia, Thaís de Lima Carvalho, Luiz Antonio de Lima Resende, Nena J. Winand, Alexandre Secorun Borges, José P. Oliveira-Filho, José Diomedes Barbosa, Jorge Estefano S. Souza, Lígia Souza Lima Silveira da Mota, Carlos Magno Chaves Oliveira
Publikováno v:
Neuromuscular Disorders. 23:206-213
Hereditary myotonia caused by mutations in CLCN1 has been previously described in humans, goats, dogs, mice and horses. The goal of this study was to characterize the clinical, morphological and genetic features of hereditary myotonia in Murrah buffa
Autor:
Hans Peter Bächinger, Keith D. Zientek, Kazuhiro Nagata, Kazunori Mizuno, Ann M. Rashmir-Raven, Janice A. Vranka, Yoshihiro Ishikawa, Elena Pokidysheva, Nena J. Winand, Douglas R. Keene, Sergei P. Boudko
Publikováno v:
Journal of Biological Chemistry. 287:22253-22265
The rate-limiting step of folding of the collagen triple helix is catalyzed by cyclophilin B (CypB). The G6R mutation in cyclophilin B found in the American Quarter Horse leads to autosomal recessive hyperelastosis cutis, also known as hereditary equ
Autor:
João Pessoa Araújo, Nena J. Winand, José P. Oliveira-Filho, Peres Ramos Badial, Alexandre Secorun Borges, Thomas J. Divers, Juliana Regina Peiró, Paulo Henrique Jorge da Cunha
Publikováno v:
Veterinary Immunology and Immunopathology. 141:157-161
Hepcidin is a highly conserved disulfide-bonded peptide that plays a central role in iron homeostasis. During systemic inflammation, hepcidin up-regulation is responsible for hypoferremia. This study aimed to analyze the influence of the inflammatory