Zobrazeno 1 - 10
of 1 080
pro vyhledávání: '"L J, Russell"'
Autor:
Kemeny, John G.
Publikováno v:
The Journal of Symbolic Logic, 1956 Jun 01. 21(2), 207-207.
Externí odkaz:
https://www.jstor.org/stable/2268781
Autor:
John G. Kemeny
Publikováno v:
Journal of Symbolic Logic. 21:207-207
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b743223c5be790386d9241c70bc9e77
https://doi.org/10.2307/2268781
https://doi.org/10.2307/2268781
Autor:
James Thomson
Publikováno v:
Journal of Symbolic Logic. 29:197-197
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e1340aac2361f1b1e2912411d17a283
https://doi.org/10.2307/2270378
https://doi.org/10.2307/2270378
Autor:
Benson Mates
Publikováno v:
Journal of Symbolic Logic. 35:306-306
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6539263dad7f8ffc48e6690945ecfb7c
https://doi.org/10.1017/s0022481200091489
https://doi.org/10.1017/s0022481200091489
Publikováno v:
Nature; November 1950, Vol. 166 Issue: 4228 p811-811, 1p
Autor:
Trinh, Hoa Thi1 (AUTHOR), Pham, Tuan Anh1 (AUTHOR) anhpt@utt.edu.vn, Tho, Vu Dinh1 (AUTHOR), Nguyen, Duy Hung1 (AUTHOR)
Publikováno v:
PLoS ONE. 11/27/2024, Vol. 19 Issue 11, p1-17. 17p.
Autor:
A Graham, L J Russell
Publikováno v:
Biochemical Journal. 298:579-584
Epidermal growth factor (EGF), a potent mitogenic polypeptide, stimulated the uptake and degradation of [3H]sucrose-labelled low-density lipoprotein (LDL) by HepG2 cells. The increase in LDL uptake was prevented by the presence of the tyrosine kinase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04edc3e6c95a442479293669e1506f4c
https://doi.org/10.1042/bj2980579
https://doi.org/10.1042/bj2980579
Publikováno v:
ACS Symposium Series ISBN: 9780841239487
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::209c229bc55866531798c7c3718fcfc0
https://doi.org/10.1021/bk-2006-0922.ch019
https://doi.org/10.1021/bk-2006-0922.ch019
Autor:
S, Beiraghi, A, Miller-Chisholm, W J, Kimberling, C E, Sun, Y F, Wang, L J, Russell, M, Khoshnevisan, A L, Storm, R E, Long, P D, Witt, M, Mazaheri, S R, Diehl
Publikováno v:
Journal of craniofacial genetics and developmental biology. 19(3)
Van der Woude syndrome (VWS) is an autosomal dominant craniofacial disorder with high penetrance and variable expression. Its clinical features are variably expressed, but include cleft lip and/or cleft palate, lip pits and hypodontia. All VWS famili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b9c79962e9dd8177c9505834e07fb2cc
https://pubmed.ncbi.nlm.nih.gov/10589394
https://pubmed.ncbi.nlm.nih.gov/10589394
Publikováno v:
The Journal of the Kentucky Medical Association. 92(4)
The presence of genetic disorders in a high percentage of adolescents with significant visual impairments emphasizes the important role that genetic counseling can play in this population. However, its intended goals have been controversial. Response
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac544e84e5d3da387cde0c1d78020bff
https://pubmed.ncbi.nlm.nih.gov/8006502
https://pubmed.ncbi.nlm.nih.gov/8006502