Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Elisabeth B Adkins"'
Autor:
Thomas J Sproule, Jason A Bubier, Fiorella C Grandi, Victor Z Sun, Vivek M Philip, Caroline G McPhee, Elisabeth B Adkins, John P Sundberg, Derry C Roopenian
Publikováno v:
PLoS Genetics, Vol 10, Iss 2, p e1004068 (2014)
Epidermolysis Bullosa (EB) encompasses a spectrum of mechanobullous disorders caused by rare mutations that result in structural weakening of the skin and mucous membranes. While gene mutated and types of mutations present are broadly predictive of t
Externí odkaz:
https://doaj.org/article/84d04d093961450db79237a9c92f19a8
Autor:
Tomomi Sakai, Herbert C. Morse, Alina Nicolae, Derry C. Roopenian, Caroline M. Leeth, Jing Chen, Dong-Mi Shin, Jerold E. Rehg, Shweta Jain, Elaine S. Jaffe, Mark Raffeld, Alexander L. Kovalchuk, Elisabeth B Adkins, Thomas A. Waldmann, Jerrold M. Ward, Hongsheng Wang, Thomas J. Sproule
Publikováno v:
The American journal of pathology. 185(11)
SJL/J mice exhibit a high incidence of mature B-cell lymphomas that require CD4(+) T cells for their development. We found that their spleens and lymph nodes contained increased numbers of germinal centers and T follicular helper (TFH) cells. Microar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef376c9186acfafa68c9bb85166af256
https://pubmed.ncbi.nlm.nih.gov/26363366
https://pubmed.ncbi.nlm.nih.gov/26363366
Autor:
Derry C. Roopenian, Elisabeth B Adkins, Caroline G. McPhee, Victor Z. Sun, Jason A. Bubier, Vivek M. Philip, Fiorella C. Grandi, John P. Sundberg, Thomas J. Sproule
Publikováno v:
PLoS Genetics, Vol 10, Iss 2, p e1004068 (2014)
PLoS Genetics
PLoS Genetics
Epidermolysis Bullosa (EB) encompasses a spectrum of mechanobullous disorders caused by rare mutations that result in structural weakening of the skin and mucous membranes. While gene mutated and types of mutations present are broadly predictive of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8c70da02e6ab2f6a195f3d3c9910a1b
http://europepmc.org/articles/PMC3923665?pdf=render
http://europepmc.org/articles/PMC3923665?pdf=render
Autor:
Elisabeth B Adkins, Xulong Wang, Thomas J Sproule, Gregory G Christianson, Giljun Park, Sarah-Kate Lane-Reiticker, Shweta Jain, Gregory W Carter, Herbert C Morse, Derry C Roopenian
Publikováno v:
The Journal of Immunology. 196:204.11-204.11
T follicular helper cells (TFH) localize to B cell follicles and secrete Interleukin 21 (IL21), a cytokine that is vital for driving the proliferation of antigen-stimulated B cells within germinal centers and their subsequent differentiation into mem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0966f3c2db1103cb17f8ebc3897eb748
https://doi.org/10.4049/jimmunol.196.supp.204.11
https://doi.org/10.4049/jimmunol.196.supp.204.11
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