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Physical Review Letters|January 22, 2002
Calculation of a deuterium double shock Hugoniot from ab initio simulationsB Militzer, D M Ceperley, J D Kress, et al.Klinische Padiatrie|September 1, 1995
[X-chromosome recessive lymphoproliferative disease (XLP): molecular genetic studies]V Schuster, T Grimm, W Kress, et al.Journal of Molecular Biology|September 15, 1983
Changes in the X-ray reflections from contracting muscle during rapid mechanical transients and their structural implicationsH E Huxley, R M Simmons, A R Faruqi, et al.Glia|September 7, 2012
Astrocytic CX43 hemichannels and gap junctions play a crucial role in development of chronic neuropathic pain following spinal cord injuryMichael J Chen, Benjamin Kress, Xiaoning Han, et al.International Journal of Molecular Sciences|October 13, 2021
Reduced Endothelial Leptin Signaling Increases Vascular Adrenergic Reactivity in a Mouse Model of Congenital Generalized LipodystrophyThiago Bruder-Nascimento, Taylor C Kress, Matthew Pearson, et al.Molecular Cell|October 13, 1999
A Xenopus protein related to hnRNP I has a role in cytoplasmic RNA localizationC A Cote, D Gautreau, J M Denegre, et al.The Journal of Biological Chemistry|September 10, 1981
Properties of N-acetyl-beta-D-hexosaminidase from isolated normal and I-cell lysosomesA L Miller, B C Kress, R Stein, et al.Cell|February 23, 1996
Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndromeM Pontoglio, J Barra, M Hadchouel, et al.Nucleic Acids Research|November 1, 2018
OrthoInspector 3.0: open portal for comparative genomicsYannis Nevers, Arnaud Kress, Audrey Defosset, et al.American Journal of Medical Genetics. Part A|March 19, 2008
Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophyBirgit Zirn, Wolfram Kress, Tiemo Grimm, et al.Pageof 255