Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Bo I Li"'
Autor:
Chee Wai Chua, Nusrat J Epsi, Eva Y Leung, Shouhong Xuan, Ming Lei, Bo I Li, Sarah K Bergren, Hanina Hibshoosh, Antonina Mitrofanova, Michael M Shen
Publikováno v:
eLife, Vol 7 (2018)
Master regulatory genes of tissue specification play key roles in stem/progenitor cells and are often important in cancer. In the prostate, androgen receptor (AR) is a master regulator essential for development and tumorigenesis, but its specific fun
Externí odkaz:
https://doaj.org/article/cb375be9a2604443a71f9d6c7e3175fa
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0170724 (2017)
The morphology and severity of human congenital cataract varies even among individuals with the same mutation, suggesting that genetic background modifies phenotypic penetrance. The spontaneous mouse mutant, vacuolated lens (vl), arose on the C3H/HeS
Externí odkaz:
https://doaj.org/article/a4f4e03b91ab4258982dea5bfc724c27
Autor:
Michael M. Shen, Hanina Hibshoosh, Antonina Mitrofanova, Bo I. Li, Chee Wai Chua, Eva Leung, Nusrat J. Epsi, Ming Lei, Sarah K. Bergren, Shouhong Xuan
Publikováno v:
eLife, Vol 7 (2018)
eLife
eLife
Master regulatory genes of tissue specification play key roles in stem/progenitor cells and are often important in cancer. In the prostate, androgen receptor (AR) is a master regulator essential for development and tumorigenesis, but its specific fun
Autor:
Chee Wai Chua, Nusrat J Epsi, Eva Y Leung, Shouhong Xuan, Ming Lei, Bo I Li, Sarah K Bergren, Hanina Hibshoosh, Antonina Mitrofanova, Michael M Shen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdd75c029804daedd77890511be13e46
https://doi.org/10.7554/elife.28768.031
https://doi.org/10.7554/elife.28768.031
Autor:
Myka F. Ababon, Yong Lin, Bo I. Li, James H. Millonig, Tara C. Matise, Alejandro Q. Nato, Vikas Nanda, Paul G. Matteson
Publikováno v:
Developmental Biology. 402:17-31
The vacuolated lens (vl) mouse mutation arose on the C3H/HeSnJ background and results in lethality, neural tube defects (NTDs) and cataracts. The vl phenotypes are due to a deletion/frameshift mutation in the orphan GPCR, Gpr161. A recent study using
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0170724 (2017)
PLoS ONE
PLoS ONE
The morphology and severity of human congenital cataract varies even among individuals with the same mutation, suggesting that genetic background modifies phenotypic penetrance. The spontaneous mouse mutant, vacuolated lens (vl), arose on the C3H/HeS
Publikováno v:
Journal of Visualized Experiments : JoVE
Retinoic acid (RA) is an important developmental morphogen that coordinates anteroposterior and dorsoventral axis patterning, somitic differentiation, neurogenesis, patterning of the hindbrain and spinal cord, and the development of multiple organ sy
Autor:
Ming Gao Zhao, Guosong Liu, Arvind Govindarajan, Inna Slutsky, Xiang Zhao, Susumu Tonegawa, Bo I. Li, Ling Zhang, Min Zhuo, Chao Huang, Long Jun Wu, Nashat Abumaria
Publikováno v:
Neuron. 65(2):165-177
SUMMARY Learning and memory are fundamental brain functions affected by dietary and environmental factors. Here, we show that increasing brain magnesium using a newly developed magnesium compound (magnesium-L-threonate, MgT) leads to the enhancement
Autor:
Michelle L. Previtera, Gum Hwa Lee, Bo I. Li, Michael P. Moreau, Paul G. Matteson, Linda M. Brzustowicz, Norell M. Hadzimichalis, Anna M. Dulencin, James H. Millonig, Bonnie L. Firestein, Steven Buyske
Publikováno v:
Schizophrenia Research. 124:248-250
Dear Editors, Brzustowicz and colleagues (2004) identified significant linkage disequilibrium between schizophrenia and markers within the gene encoding nitric oxide synthase 1 (neuronal; NOS1) adaptor protein (NOS1AP; also termed carboxyl-terminal P
Autor:
Suzanne S.M. Karabin, Christina Botti, Elaine Lyon, Alison Millson, Susan Sklower Brooks, Sharon Anderson, James H. Millonig, Bo I. Li
Publikováno v:
American journal of medical genetics. Part A. (9)
In the follow-up of New Jersey newborn screens suggestive of medium chain acyl-CoA dehydrogenase deficiency (MCADD) during a 30-month period, we identified five patients of Hispanic American ethnicity. With information provided by the New Jersey Depa