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Bioinformatics (Oxford, England)|April 12, 2011
Performance assessment of copy number microarray platforms using a spike-in experimentEitan Halper-Stromberg, Laurence Frelin, Ingo Ruczinski, et al.
Cell|October 22, 2003
Nitric oxide regulates exocytosis by S-nitrosylation of N-ethylmaleimide-sensitive factorKenji Matsushita, Craig N Morrell, Beatrice Cambien, et al.
Stroke|September 25, 2023
mTORC1 Inhibitor Rapamycin Inhibits Growth of Cerebral Cavernous Malformation in Adult MiceLun Li, Aileen A Ren, Siqi Gao, et al.
Scientific Reports|June 10, 2018
Wireless control of cellular function by activation of a novel protein responsive to electromagnetic fieldsVijai Krishnan, Sarah A Park, Samuel S Shin, et al.
Pediatric Neurology|April 4, 2021
Multicenter Research Data of Epilepsy Management in Patients With Sturge-Weber SyndromeLindsay F Smegal, Alison J Sebold, Adrienne M Hammill, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 15, 2014
Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutationsRobert Shenkar, Changbin Shi, Tania Rebeiz, et al.
Psychosomatic Medicine|December 26, 2007
Childhood socioeconomic status and serotonin transporter gene polymorphism enhance cardiovascular reactivity to mental stressRedford B Williams, Douglas A Marchuk, Ilene C Siegler, et al.
American Journal of Human Genetics|November 19, 2003
Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformationsChristina L Liquori, Michel J Berg, Adrian M Siegel, et al.
JAMA|November 17, 2005
Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposisKevin Sweet, Joseph Willis, Xiao-Ping Zhou, et al.
Pediatric Neurology|December 12, 2022
Cannabidiol Treatment for Neurological, Cognitive, and Psychiatric Symptoms in Sturge-Weber SyndromeLindsay F Smegal, Pooja Vedmurthy, Matthew Ryan, et al.
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