Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hirva Bakeri"'
Publikováno v:
Diabetes Spectr
AIM To measure cost and length of stay in patients with and without a diagnosis of diabetes admitted with cardiovascular, pulmonary, or cerebrovascular disease. METHODS Retrospective study used International Classification of Diseases, 10th Revision,
Publikováno v:
Endocrinology, Diabetes and Obesity. 1
Autor:
Oleg V. Bulgakov, Anand Swaroop, Lijin Dong, Pinghu Liu, Chen Lin, Jingqi Lei, D. Thad Whitaker, Chunqiao Liu, Hirva Bakeri, Tiansen Li
Publikováno v:
Human Molecular Genetics. 22:2234-2246
Development of axons and dendrites constitutes a critical event in neuronal maturation and seems to require signaling through the planar cell polarity (PCP) pathway. Mutations in components of the PCP pathway lead to a spectrum of neurological phenot
Publikováno v:
American Journal of Gastroenterology. 111:S662-S663
Autor:
Hirva Bakeri, Carl Cirino, Larissa Krüger Gomes, Edgar Naut, Sana Siddiqui, Alyssa M. Austria
Publikováno v:
American Journal of Gastroenterology. 111:S945-S946
Publikováno v:
Human molecular genetics. 21(8)
Nineteen Wnt ligands and 10 Frizzled (Fz) receptors mediate multiple distinct cellular events during neuronal development. However, their precise roles in cell-type specification and organogenesis are poorly delineated because of overlapping function
Autor:
Daniel S. Krauth, Cécilia Maubaret, Kecia L. Feathers, Chunqiao Liu, R.E. Hurd, George E. Thomas, Robert K. Koenekoop, Irma Lopez, Maria M Campos, Matthew Brooks, John R. Heckenlively, Andrew R. Webster, Naushin Waseem, Hirva Bakeri, Ignacio R. Rodriguez, Manessa Shaw, Bo Chang, Anand Swaroop, James S. Friedman, Shomi S. Bhattacharya, Kari Branham, Debra A. Thompson
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 107(35)
Retinal degenerative diseases, such as retinitis pigmentosa and Leber congenital amaurosis, are a leading cause of untreatable blindness with substantive impact on the quality of life of affected individuals and their families. Mouse mutants with ret