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Neurogenetics|March 29, 2000
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosisT Siddique, M A Pericak-Vance, J Caliendo, et al.Cancer Gene Therapy|April 28, 2012
IL15 combined with Caspy2 provides enhanced therapeutic efficiency against murine malignant neoplasm growth and metastasisY Yang, X-M Zhang, N Zhang, et al.Neoplasma|February 5, 2013
Regulation of epidermal growth factor receptor signaling by plasmid-based microRNA-7 inhibits human malignant gliomas growth and metastasis in vivoW Wang, L X Dai, S Zhang, et al.Mucosal Immunology|May 30, 2020
Intestinal epithelium-derived BATF3 promotes colitis-associated colon cancer through facilitating CXCL5-mediated neutrophils recruitmentY Lin, L Cheng, Y Liu, et al.Human Molecular Genetics|November 18, 1998
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factorA Al-Chalabi, P M Andersen, B Chioza, et al.JAMA|October 4, 2000
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22B A Hosler, T Siddique, P C Sapp, et al.The Journal of Investigative Dermatology|June 9, 2000
Identification of a locus for disseminated superficial actinic porokeratosis at chromosome 12q23.2-24.1J H Xia, Y F Yang, H Deng, et al.Neurology|August 3, 1999
Neurodegenerative diseases of Guam: analysis of TAUJ Pérez-Tur, L Buée, H R Morris, et al.Journal of Medical Genetics|April 17, 2008
Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotypeD Lambrechts, K Poesen, R Fernández-Santiago, et al.Science (New York, N.Y.)|March 3, 2009
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisT J Kwiatkowski, D A Bosco, A L Leclerc, et al.Pageof 11