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American Journal of Physiology. Gastrointestinal and Liver Physiology|May 17, 2014
Experimental evidence and mathematical modeling of thermal effects on human colonic smooth muscle contractilityA Altomare, A Gizzi, M P L Guarino, et al.Genomics|March 1, 1997
A gene-based genetic linkage and comparative map of the rat X chromosomeI Y Millwood, M T Bihoreau, D Gauguier, et al.American Journal of Human Genetics|April 15, 2005
Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABATGabrielle Barnby, Aaron Abbott, Nuala Sykes, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 3, 2003
Chorea-acanthocytosis: clinical and genetic findings in three families from the Arabian peninsulaSaeed Bohlega, Adel Al-Jishi, Carol Dobson-Stone, et al.International Journal of Cancer|March 15, 1975
Activation of C-type viruses during skin graft rejection in the mouse. Interrelationships between immunostimulation and immunosuppressionM S Hirsch, D A Ellis, A P Kelly, et al.Journal of Medical Genetics|March 1, 1994
X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphismsS Cochrane, J Bergoffen, N D Fairweather, et al.The American Journal of Medicine|September 26, 2017
Infection and Malignancy Outweigh Cardiovascular Mortality in Kidney Transplant Recipients: Post Hoc Analysis of the FAVORIT TrialLarry A Weinrauch, John A D'Elia, Matthew R Weir, et al.Genomics|January 27, 1998
Two members of the human MAGEB gene family located in Xp21.3 are expressed in tumors of various histological originsC Lurquin, C De Smet, F Brasseur, et al.American Journal of Medical Genetics|September 22, 1999
Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism ConsortiumE Maestrini, C Lai, A Marlow, et al.The Journal of Bone and Joint Surgery. British Volume|September 28, 2004
Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype studyD E Porter, L Lonie, M Fraser, et al.Pageof 59