Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Elaine Louie"'
Autor:
James German, Elaine Louie
Publikováno v:
Clinical Genetics. 19:71-74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3795f0dbbe2bd33133b0dd231229f09c
https://doi.org/10.1111/j.1399-0004.1981.tb00671.x
https://doi.org/10.1111/j.1399-0004.1981.tb00671.x
Autor:
Elaine Louie
In The Occasional Vegetarian, Elaine Louie provides pieces from her popular New York Times column,'The Temporary Vegetarian,'which features recipes from a wide variety of chefs who reveal the vegetarian dishes they like to cook at their restaurants a
Autor:
Lawrence R. Finger, Elaine Louie, Jaiyu Pu, L G Billips, Robert Wasserman, Richard R. Hardy, Rajeev Vibhakar, Peter D. Burrows
Publikováno v:
Gene. 197:177-187
We report the complete cDNA sequence and the genomic structure of the human PD-1 homologue. An analysis of the expression pattern of the human PD-1 gene (hPD-1) and the murine PD-1 gene (mPD-1) in developing bone marrow B-lineage cells was also under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c33589640cac8f16feb635c79c77ad24
https://doi.org/10.1016/s0378-1119(97)00260-6
https://doi.org/10.1016/s0378-1119(97)00260-6
Autor:
Daniel Tsun-Yee Chiu, Elaine Louie, Bertram H. Lubin, Chuan-Su Du, Lin Zuo, Lotung Chao, Ellson Y. Chen, Tsan Z. Liu
Publikováno v:
Biochemical and Biophysical Research Communications. 180:988-993
Using a direct PCR sequencing technique, we have identified two DNA base substitutions in 8 different biochemical G6PD variants of Chinese origin. Neither one of these abnormalities has been reported in other ethnic groups. An abnormality (C1) of G t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aba6cfe1c910057b1348380ca9846606
https://doi.org/10.1016/s0006-291x(05)81163-5
https://doi.org/10.1016/s0006-291x(05)81163-5
Publikováno v:
Human genetics. 89(2)
Cystic fibrosis (CF) is an autosomal recessive disease caused by different mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The frequency of the major mutation (delta F508) in the Hungarian population is 64%. To ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c4118363a64b7f84cb3692a25508902
https://pubmed.ncbi.nlm.nih.gov/1375186
https://pubmed.ncbi.nlm.nih.gov/1375186
Publikováno v:
Human Genetics. 87
Hungarian cystic fibrosis (CF) families (n = 33) including 114 family members have been analysed for the presence of the delta F508 mutation within the cystic fibrosis transmembrane conductance regulator (CFTR) gene, and have been haplotyped with pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::527e742dedc0c1832f98a01c263dc059
https://doi.org/10.1007/bf00197180
https://doi.org/10.1007/bf00197180
Autor:
Chuan-Su Du, Daniel T. Y. Chiu, Bertram H. Lubin, Elaine Louie, Lotung Chao, Ellson Y. Chen, Lin Zuo
Publikováno v:
Nucleic Acids Research. 19:6056-6056
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed8fdeb1f8c70edbbb87819c005d5c2a
https://doi.org/10.1093/nar/19.21.6056
https://doi.org/10.1093/nar/19.21.6056
Publikováno v:
Teratogenesis, Carcinogenesis, and Mutagenesis. 6:555-562
According to the embryonic stress hypothesis of teratogenesis, anatomical malformation can be the consequence of the induction of a heat-shock response (HSR) in the embryo at some critical stage during the determination or differentiation of organs.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5bc5515bb5b9ff02157d71346272db8
https://doi.org/10.1002/tcm.1770060609
https://doi.org/10.1002/tcm.1770060609
Autor:
Yoshihide Tsujimoto, Abbas Ar-Rushdi, Carlo M. Croce, Elaine Louie, Kay Huebner, Lalitha Nagarajan
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 83(8)
The human homolog, hpim, of the murine pim-1 gene, which is activated in murine T-cell lymphomas by insertion of retrovirus proviral genomes in the pim-1 region, has been molecularly cloned; the cloned probe has been used to map the hpim locus to hum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b48d2ad82f60dd9bfd3a3465a4fcb512
https://pubmed.ncbi.nlm.nih.gov/3458216
https://pubmed.ncbi.nlm.nih.gov/3458216
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 84(8)
Experimental hybridization of cultured cells was employed to determine whether the strikingly elevated rates of sister-chromatid exchange (SCE) exhibited by Bloom's syndrome (BS) and hamster cell line EM9 have the same or different bases. Seventeen c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a1886d483bed487a9f187b7129cb54a
https://pubmed.ncbi.nlm.nih.gov/3470802
https://pubmed.ncbi.nlm.nih.gov/3470802