Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Aaron M Feliciano"'
Autor:
Jason J. Bisaillon, Legairre A. Radden II, Eric T. Szabo, Samantha R. Hughes, Aaron M. Feliciano, Alex V. Nesta, Belinda Petrovic, Kenneth M. Palanza, Dainius Lancinskas, Theodore A. Szmurlo, David C. Artus, Martin A. Kapper, James P. Mulrooney, Thomas R. King
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 378-390 (2014)
Because of the similar phenotypes they generate and their proximate reported locations on Chromosome 7, we tested the recessive retarded hair growth (rhg) and frizzy (fr) mouse mutations for allelism, but found instead that these defects complement.
Externí odkaz:
https://doaj.org/article/9efcf5e7a54343e2a3afd8cd858106f1
Autor:
Belinda Petrovic, David C. Artus, Dainius Lancinskas, Samantha R. Hughes, Legairre A. Radden, Eric T. Szabo, Martin A. Kapper, Jason J. Bisaillon, James P. Mulrooney, Aaron M Feliciano, Alex V. Nesta, Kenneth M. Palanza, Theodore A. Szmurlo, Thomas R. King
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 378-390 (2014)
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 378-390 (2014)
Because of the similar phenotypes they generate and their proximate reported locations on Chromosome 7, we tested the recessive retarded hair growth (rhg) and frizzy (fr) mouse mutations for allelism, but found instead that these defects complement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f334028ffb8f2ea62c01d6201ca5398
Autor:
Aaron M Feliciano, Damek V Spacek, Francisco Ramirez, Elisabeth B Adkins, Nelson Vila-Santana, José M Horák, Legairre A. Radden, Kevin M Child, Alexis Salas, Samantha R. Hughes, Thomas R. King
Publikováno v:
BMC Genetics
Background Mice homozygous for the juvenile alopecia mutation (jal) display patches of hair loss that appear as soon as hair develops in the neonatal period and persist throughout life. Although a report initially describing this mouse variant sugges
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10e4334d1d625f857f7902ed8a485d41
http://europepmc.org/articles/PMC3656803
http://europepmc.org/articles/PMC3656803
Autor:
Kevin M Child, Damek V Spacek, Thomas R. King, Aaron M Feliciano, Legairre A. Radden, Elisabeth B Adkins
Publikováno v:
BMC Research Notes
Background Mice homozygous for the spontaneous wooly mutation (abbreviated wly) are recognized as early as 3–4 weeks of age by the rough or matted appearance of their coats. Previous genetic analysis has placed wly in a 5.9 Mb interval on Chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55b43ba91d47ec69813b86a1b809fd06