Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jean H. Kawasoe"'
Autor:
James D. Friesen, K T Arndt, Jean H. Kawasoe, David B. Jansma, Jack Greenblatt, Jacques Archambault
Publikováno v:
Journal of Bacteriology. 180:2590-2598
Mutations that increase the low-level transcription of the Saccharomyces cerevisiae HIS4 gene, which results from deletion of the genes encoding transcription factors BAS1, BAS2, and GCN4, were isolated previously in SIT1 (also known as RPO21 , RPB1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4665506eb53617e26a1e93d2f84cd1f6
https://doi.org/10.1128/jb.180.10.2590-2598.1998
https://doi.org/10.1128/jb.180.10.2590-2598.1998
Autor:
Lindsay C. Burrage, Haifeng Shao, Sorana Pisano, Aga Gornicka, Sheila Ernest, Jean H. Kawasoe, Carrie A. Millward, David S. Sinasac, Annie E. Hill-Baskin, Chang-Wen Hsieh, Joseph H. Nadeau, Colleen M. Croniger
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 20(2)
Obesity is associated with increased susceptibility to dyslipidemia, insulin resistance, and hypertension, a combination of traits that comprise the traditional definition of the metabolic syndrome. Recent evidence suggests that obesity is also assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::777264082864b3472c35ba9003516f6b
https://pubmed.ncbi.nlm.nih.gov/19137372
https://pubmed.ncbi.nlm.nih.gov/19137372
Publikováno v:
Human molecular genetics. 16(18)
The genetic basis for susceptibility to testicular germ cell tumors (TGCTs) has been remarkably elusive. Although TGCTs are the most common cancer in young men and have an unusually strong familial risk, only one low-frequency susceptibility gene has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c19494f0ce8cb54d97cf6842dc0baddf
https://pubmed.ncbi.nlm.nih.gov/17616517
https://pubmed.ncbi.nlm.nih.gov/17616517
Autor:
Jean H. Kawasoe, Fumio Endo, Manoj Nanji, Koji Inui, T.T. Van Nguyen, Toshiharu Anezaki, Takashi Nakajima, Diane W. Cox
SummaryWilson disease (WD), an autosomal recessive disorder of copper transport, is characterized by impaired biliary excretion and by impaired incorporation of copper into cerulo-plasmin. Toxic accumulation of copper causes tissue damage, primarily
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd89871f4a58cea655983c0dd361c4d5
https://europepmc.org/articles/PMC1716137/
https://europepmc.org/articles/PMC1716137/
