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European Journal of Medical Genetics|November 14, 2015
Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a familyLinh T T Duong, Louise K Hoeffding, Kirsten B Petersen, et al.
Circulation. Cardiovascular Imaging|November 17, 2017
Cerebral Oxygenation Measurements by Magnetic Resonance Imaging in Fetuses With and Without Heart DefectsMette H Lauridsen, Niels Uldbjerg, Tine B Henriksen, et al.
Journal of Medical Genetics|December 5, 2006
A novel locus on 19q13 associated with autosomal-dominant macular dystrophy in a large Greek familyZ Yang, G Kitsos, Z Tong, et al.
Age (Dordrecht, Netherlands)|May 9, 2009
Evidence of DNA damage in Alzheimer disease: phosphorylation of histone H2AX in astrocytesNa-Hye Myung, Xiongwei Zhu, Inna I Kruman, et al.
Neuromuscular Disorders : NMD|April 19, 2020
No effect of oral sucrose or IV glucose during exercise in phosphorylase b kinase deficiencyA G Andersen, M C Ørngreen, D E T Raaschou-Pedersen, et al.
International Journal of Biological Macromolecules|July 7, 2020
Copper and iron ions accelerate the prion-like propagation of α-synuclein: A vicious cycle in Parkinson's diseaseYang Li, Chen Yang, Shilin Wang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 19, 2023
Prenatal detection of orofacial clefts in Denmark from 2009 to 2018F H Sander, D S Jørgensen, L P Jakobsen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 18, 2026
Photoexcitation induces translocation of a common fluorescent pH and proton-transfer probe confined in reverse micellesGerardo A Virgen, Sulejman Skoko, Ashley M Stingel, et al.
Medical Physics|September 8, 2018
Theoretical and experimental analysis of photon counting detector CT for proton stopping power predictionVicki T Taasti, David C Hansen, Gregory J Michalak, et al.
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