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Human Molecular Genetics|February 4, 2010
Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15George W Nelson, Barry I Freedman, Donald W Bowden, et al.
Plos Pathogens|June 26, 2007
Regulatory polymorphisms in the cyclophilin A gene, PPIA, accelerate progression to AIDSPing An, Li Hua Wang, Holli Hutcheson-Dilks, et al.
Scientific Reports|October 12, 2019
Interactive spatial scale effects on species distribution modeling: The case of the giant pandaThomas Connor, Andrés Viña, Julie A Winkler, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 11, 2012
F8 haplotype and inhibitor risk: results from the Hemophilia Inhibitor Genetics Study (HIGS) Combined CohortJ Schwarz, J Astermark, E D Menius, et al.
Journal of Neurosurgery|September 6, 2024
A taxonomy for cerebellar cavernous malformations: subtypes of cerebellar lesionsLea Scherschinski, Adam T Eberle, Satvir Saggi, et al.
Journal of Electrocardiology|April 28, 2019
Association of sickle cell trait with atrial fibrillation: The REGARDS cohortDaniel R Douce, Elsayed Z Soliman, Rakhi Naik, et al.
American Journal of Physiology. Renal Physiology|August 9, 2013
Focal segmental glomerulosclerosis is associated with a PDSS2 haplotype and, independently, with a decreased content of coenzyme Q10David L Gasser, Cheryl A Winkler, Min Peng, et al.
European Journal of Pediatrics|July 24, 2025
A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiencySung Kweon Cho, Guenter Schwarz, Velibor Tasic, et al.
Clinical Case Reports|September 6, 2021
Genotypical glioblastoma of the frontal lobe mimicking ganglioglioma: A case report and review of the literatureTheo F J Kraus, Johannes Pöppe, Lukas Machegger, et al.
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