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Proceedings of the National Academy of Sciences of the United States of America|March 15, 2001
p63 identifies keratinocyte stem cellsG Pellegrini, E Dellambra, O Golisano, et al.Cell|June 18, 1998
Intramolecular masking of nuclear import signal on NF-AT4 by casein kinase I and MEKK1J Zhu, F Shibasaki, R Price, et al.JBJS Reviews|March 1, 2022
Race, Utilization, and Outcomes in Total Hip and Knee Arthroplasty: A Systematic Review on Health-Care DisparitiesPaul M Alvarez, John F McKeon, Andrew I Spitzer, et al.Science (New York, N.Y.)|April 9, 1999
Ca2+-induced apoptosis through calcineurin dephosphorylation of BADH G Wang, N Pathan, I M Ethell, et al.Medical and Pediatric Oncology|July 24, 2001
Genetic analysis of p73 localized at chromosome 1p36.3 in primary neuroblastomasS Ichimiya, Y Nimura, H Kageyama, et al.Oncogene|February 19, 1999
p73 at chromosome 1p36.3 is lost in advanced stage neuroblastoma but its mutation is infrequentS Ichimiya, Y Nimura, H Kageyama, et al.Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|October 1, 1995
[Adjustable reconditioner for the treatment of patella fracture]A YangCell|October 27, 1999
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndromeJ Celli, P Duijf, B C Hamel, et al.Human Molecular Genetics|February 13, 2001
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63J A McGrath, P H Duijf, V Doetsch, et al.The Journal of the Acoustical Society of America|October 26, 2002
A boundary integral equation method using auxiliary interior surface approach for acoustic radiation and scattering in two dimensionsS A YangPageof 83