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Cytogenetics and Cell Genetics|January 1, 1991
Regional assignment of the human gene coding for a multifunctional polypeptide (P4HB) acting as the beta-subunit of prolyl 4-hydroxylase and the enzyme protein disulfide isomerase to 17q25L Pajunen, T A Jones, A Goddard, et al.European Journal of Immunology|December 1, 1983
Chromosome assignment of monoclonal antibody-defined determinants on human leukemic cellsF Katz, S Povey, M Parkar, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1985
Chromosomal assignments of the genes coding for human types II, III, and IV collagen: a dispersed gene familyE Solomon, L R Hiorns, N Spurr, et al.The Journal of Surgical Research|February 1, 1993
Increased circulating cholecystokinin in obstruction-induced acute pancreatitis. II. Pancreatic duct obstruction with and without bile duct obstructionY Toriumi, I Samuel, D P Wilcockson, et al.The Journal of the American Osteopathic Association|May 29, 2019
Relationship Between Elevated Automatic Blood Pressure Readings and Manual Blood Pressure Readings in Adult Patients With Normal and High Body Mass IndexMunif M Hussain, Ian E Solomon, Vanessa Pazdernik, et al.American Journal of Human Genetics|December 1, 1989
Assignment of the gene coding for the alpha-subunit of prolyl 4-hydroxylase to human chromosome region 10q21.3-23.1L Pajunen, T A Jones, T Helaakoski, et al.Journal of Extracellular Vesicles|January 9, 2024
Novel method for collecting hippocampal interstitial fluid extracellular vesicles (EVISF ) reveals sex-dependent changes in microglial EV proteome in response to Aβ pathologyMorgan C Pait, Sarah D Kaye, Yixin Su, et al.Somatic Cell Genetics|March 1, 1976
Human gene mapping using an X/autosome translocationE Solomon, M Bobrow, P N Goodfellow, et al.Oncogene|June 20, 1996
The 5' end of the BRCA1 gene lies within a duplicated region of human chromosome 17q21M A Brown, C F Xu, H Nicolai, et al.Cancer Genetics and Cytogenetics|May 1, 1994
A case of acute monocytic leukemia with t(11;17) involving a rearrangement of MLL-1 and a region proximal to the RARA geneB R Reeves, H Kempski, K Jani, et al.Pageof 46