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American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 12, 2013
TCR repertoire analysis by next generation sequencing allows complex differential diagnosis of T cell-related pathologyM Dziubianau, J Hecht, L Kuchenbecker, et al.Neurology|August 22, 2008
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre typeL Van Maldergem, M Yuksel-Apak, H Kayserili, et al.Angewandte Chemie (International Ed. in English)|January 1, 2023
Lithium-ion Mobility in Li6 B18 (Li3 N) and Li Vacancy Tuning in the Solid Solution Li6 B18 (Li3 N)1-x (Li2 O)xTassilo M F Restle, Lavinia Scherf, Jasmin V Dums, et al.The Journal of Clinical Endocrinology and Metabolism|January 26, 2006
Free fatty acids increase androgen precursors in vivoK Mai, T Bobbert, V Kullmann, et al.Cell|May 30, 1997
Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone developmentF Otto, A P Thornell, T Crompton, et al.Diabetologia|July 29, 2011
Identification of an intracellular metabolic signature impairing beta cell function in the rat beta cell line INS-1E and human isletsI Goehring, N S Sauter, G Catchpole, et al.Diabetologia|January 13, 2019
Correction to: Identification of an intracellular metabolic signature impairing beta cell function in the rat beta cell line INS-1E and human isletsI Goehring, N S Sauter, G Catchpole, et al.Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractF R Goodman, S Mundlos, Y Muragaki, et al.American Journal of Human Genetics|July 11, 2006
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromeC G Woods, S Stricker, P Seemann, et al.Cell|May 30, 1997
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasiaS Mundlos, F Otto, C Mundlos, et al.Pageof 23