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The Journal of Biological Chemistry|April 23, 1999
Role of the copper-binding domain in the copper transport function of ATP7B, the P-type ATPase defective in Wilson diseaseJ R Forbes, G Hsi, D W CoxClinical Genetics|November 18, 2003
Genetic variation in the promoter and 5' UTR of the copper transporter, ATP7B, in patients with Wilson diseaseL M Cullen, L Prat, D W CoxThe American Review of Respiratory Disease|May 1, 1976
Protease inhibitors in patients with chronic obstructive pulmonary disease: the alpha-antitrypsin heterozygote controversyD W Cox, V H Hoeppner, H LevisonMammalian Genome : Official Journal of the International Mammalian Genome Society|July 27, 2001
ATP6H, a subunit of vacuolar ATPase involved in metal transport: evaluation in canine copper toxicosisM Nanji, V A Coronado, D W CoxGenomics|September 15, 1994
A linkage map of human chromosome 14, including 13 gene lociD W Cox, G Billingsley, V T NguyenAmerican Journal of Medical Genetics|January 1, 1985
X;14 translocation:an exception to the critical region hypothesis on the human X-chromosomeV D Markovic, D W Cox, J WilkinsonSubstance Abuse Treatment, Prevention, and Policy|September 1, 2023
Development of an addiction recovery patient-reported outcome measure: Response to Addiction Recovery (R2AR)Elisabeth Okrant, Sharon Reif, Constance M HorganExperimental Cell Research|April 23, 2003
Examining the mechanism of Erk nuclear translocation using green fluorescent proteinAngela M Horgan, Philip J S StorkHuman Molecular Genetics|October 1, 1996
The toxic milk mouse is a murine model of Wilson diseaseM B Theophilos, D W Cox, J F MercerThe Biochemical Journal|October 15, 1988
Kinetic analysis of the cerebral creatine kinase reaction under hypoxic and hypoglycaemic conditions in vitro. A 31P-n.m.r. studyD W Cox, P G Morris, H S BachelardPageof 37