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Kidney International|March 13, 2003
Modeling study of human renal chloride channel (hCLC-5) mutations suggests a structural-functional relationshipFiona Wu, Philippe Roche, Paul T Christie, et al.Nature Clinical Practice. Endocrinology & Metabolism|December 18, 2007
Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 geneFadil M Hannan, M Andrew Nesbit, Paul T Christie, et al.Journal of Medical Genetics|December 1, 1998
Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27D Trump, P H Dixon, S Mumm, et al.Journal of Immunology (Baltimore, Md. : 1950)|February 6, 2008
CD44 is critically involved in infarct healing by regulating the inflammatory and fibrotic responsePeter Huebener, Tareq Abou-Khamis, Pawel Zymek, et al.Journal of Medical Genetics|December 24, 1998
Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomasC L Wu, N Thakker, W Neary, et al.Journal of the American Academy of Dermatology|January 9, 2025
Acral Lentiginous Melanoma. Part II. Staging, Surgical Management, The Role of Systemic Therapy, Shortcomings and Future DirectionsDaniella Jaguan, Sach Thakker, Micah Belzberg, et al.Clinical Therapeutics|December 13, 2006
Clinical assessment of pain, tolerability, and preference of an autoinjection pen versus a prefilled syringe for patient self-administration of the fully human, monoclonal antibody adalimumab: the TOUCH trialAlan Kivitz, Steven Cohen, James Edward Dowd, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1979
Differences in mutagenicity and cytotoxicity of (+)- and (-)-benzo[a]pyrene 4,5-oxide: a synergistic interaction of enantiomersR L Chang, A W Wood, W Levin, et al.Neuropharmacology|April 23, 2013
Adult siRNA-induced knockdown of mGlu7 receptors reduces anxiety in the mouseRichard M O'Connor, Deepak R Thakker, Markus Schmutz, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|September 4, 2013
Confirmation of oxidative stress and fatty acid disturbances in two further Papillon-Lefèvre syndrome families with identification of a new mutationP Bullón, J M Morillo, N Thakker, et al.Pageof 107