Showing results (31-40 of 90) with videos related to

Sort By:
Pageof 9
International Journal of Immunogenetics|November 30, 2005
Variability in TRBV haplotype frequency and composition in Caucasian, African American, Western African and Chinese populationsJ L Brzezinski, R Deka, A G Menon, et al.
Neurogenetics|March 25, 2000
Genomic structure of human anion exchanger 3 and its potential role in hereditary neurological diseaseD D Einum, J Zhang, P J Arneson, et al.
Kidney International|August 1, 2000
Expression of renal aquaporins 1, 2, and 3 in a rat model of cisplatin-induced polyuriaB K Kishore, C M Krane, D Di Iulio, et al.
Cancer Genetics and Cytogenetics|November 24, 1999
hREC2, a RAD51-like gene, is disrupted by t(12;14) (q15;q24.1) in a uterine leiomyomaS E Ingraham, R A Lynch, S Kathiresan, et al.
Genomics|February 12, 1998
DNA sequence, chromosomal localization, and tissue expression of the mouse proteasome subunit lmp10 (Psmb10) geneM Cruz, L A Elenich, T A Smolarek, et al.
Diagnostic Microbiology and Infectious Disease|December 1, 1994
Development of a polymerase chain reaction assay to detect the presence of Streptococcus pneumoniae DNAL R Friedland, A G Menon, S F Reising, et al.
Mediators of Inflammation|April 26, 2018
Systemic Inflammatory Cytokines Predict the Infectious Complications but Not Prolonged Postoperative Ileus after Colorectal SurgeryG S A Boersema, Z Wu, A G Menon, et al.
Genes, Chromosomes & Cancer|August 1, 1996
Role of genomic instability in meningioma progressionM Simon, A J Kokkino, R E Warnick, et al.
Progress in Clinical and Biological Research|January 1, 1985
Structural organization of the alpha and beta globin loci of the goatJ B Lingrel, T M Townes, S G Shapiro, et al.
American Journal of Human Genetics|June 13, 1998
Evidence that lymphangiomyomatosis is caused by TSC2 mutations: chromosome 16p13 loss of heterozygosity in angiomyolipomas and lymph nodes from women with lymphangiomyomatosisT A Smolarek, L L Wessner, F X McCormack, et al.
Pageof 9