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Human Molecular Genetics|May 16, 1998
The UTX gene escapes X inactivation in mice and humansA Greenfield, L Carrel, D Pennisi, et al.The Journal of Investigative Dermatology|February 14, 2002
Hailey-Hailey disease: molecular and clinical characterization of novel mutations in the ATP2C1 geneCarol Dobson-Stone, Rebecca Fairclough, Eimear Dunne, et al.Human Molecular Genetics|November 6, 2010
PCSK6 is associated with handedness in individuals with dyslexiaThomas S Scerri, William M Brandler, Silvia Paracchini, et al.Nature Genetics|May 1, 1996
A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndromeE Maestrini, A P Monaco, J A McGrath, et al.Oncogene|May 1, 1994
The t(X;18)(p11.2;q11.2) translocation found in human synovial sarcomas involves two distinct loci on the X chromosomeJ M Shipley, J Clark, A J Crew, et al.American Journal of Human Genetics|January 23, 1999
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexiaS E Fisher, A J Marlow, J Lamb, et al.Transplantation|January 1, 1991
Successful treatment of diabetes with the biohybrid artificial pancreas in dogsT Maki, C S Ubhi, H Sanchez-Farpon, et al.Proceedings of the National Academy of Sciences of the United States of America|August 15, 1992
Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissuesJ P Hugnot, H Gilgenkrantz, N Vincent, et al.American Journal of Human Genetics|June 1, 1996
Mutations and phenotype in isolated glycerol kinase deficiencyA P Walker, F Muscatelli, A N Stafford, et al.Molecular Human Reproduction|November 14, 2003
Effects of hypoxia on endothelin-1 sensitivity in the corpus cavernosumS Filippi, M Marini, G B Vannelli, et al.Pageof 59