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Archives of Surgery (Chicago, Ill. : 1960)|June 1, 1991
Sequential interleukin 2 and interleukin 2 receptor levels distinguish rejection from cyclosporine toxicity in liver allograft recipientsM A Simpson, T M Young-Fadok, P N Madras, et al.Liver Transplantation and Surgery : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|September 2, 1998
Combined liver-kidney transplantation in patients with cirrhosis and renal failure: effect of a positive cross-match and benefits of combined transplantationP E Morrissey, F Gordon, D Shaffer, et al.Molecular Human Reproduction|December 7, 2002
Expression and regulation of endothelin-1 and its receptors in human penile smooth muscle cellsS Granchi, G B Vannelli, L Vignozzi, et al.Journal of Endocrinological Investigation|April 14, 2010
Human prostatic urethra expresses vitamin D receptor and responds to vitamin D receptor ligationP Comeglio, A K Chavalmane, B Fibbi, et al.Plos Genetics|March 28, 2009
A common variant associated with dyslexia reduces expression of the KIAA0319 geneMegan Y Dennis, Silvia Paracchini, Thomas S Scerri, et al.Nature|July 3, 1986
Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal locationB Royer-Pokora, L M Kunkel, A P Monaco, et al.Cerebral Cortex (New York, N.Y. : 1991)|March 24, 2017
The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 SignalingFilipa Franquinho, Joana Nogueira-Rodrigues, Joana M Duarte, et al.European Journal of Human Genetics : EJHG|May 3, 2012
CNVs leading to fusion transcripts in individuals with autism spectrum disorderRichard Holt, Nuala H Sykes, Inês C Conceição, et al.Journal of Medical Genetics|February 4, 2005
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effectsJ A Lamb, G Barnby, E Bonora, et al.Cell|November 21, 1986
A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosomeG J van Ommen, J M Verkerk, M H Hofker, et al.Pageof 59