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Toxicology|May 27, 2026
The respiratory sensitizer methylene diphenyl diisocyanate (MDI) reprograms human cells of the alveolar tractBrunhilde Blömeke, Jutta Lichter, Anna Weßendorf, et al.Biochemistry|April 19, 1988
Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase geneU Lichter-Konecki, D S Konecki, A G DiLella, et al.Stem Cell Reports|April 30, 2015
Kinome-wide shRNA screen identifies the receptor tyrosine kinase AXL as a key regulator for mesenchymal glioblastoma stem-like cellsPeng Cheng, Emma Phillips, Sung-Hak Kim, et al.Journal of Neuropathology and Experimental Neurology|May 26, 1998
Primitive neuroectodermal tumors of the cerebral hemispheres in two siblings with TP53 germline mutationJ Reifenberger, G Janssen, R G Weber, et al.The American Journal of Pathology|July 17, 1998
Recurrent chromosomal imbalances detected in biopsy material from oral premalignant and malignant lesions by combined tissue microdissection, universal DNA amplification, and comparative genomic hybridizationR G Weber, M Scheer, I A Born, et al.Journal of Critical Care|July 6, 2025
Response to furosemide and the receipt of kidney replacement therapy in critically ill patientsAmir Gal Oz, Ron Wald, Dekel Stavi, et al.Translational Vision Science & Technology|October 19, 2021
Demographic, Comorbid, and Clinical Variables Associated With Pointwise Visual Field Damage in Glaucoma: Data From the AGIS and CIGTS Clinical TrialsBrenda W Gillespie, Leslie M Niziol, Joshua R Ehrlich, et al.International Journal of Cancer|November 22, 2012
Protein phosphatase 1, regulatory subunit 15B is a survival factor for ERα-positive breast cancerMaria Shahmoradgoli, Yasser Riazalhosseini, Daniel Haag, et al.Cancer Genetics and Cytogenetics|December 7, 2000
Low grade fibromyxoid sarcoma. a further low-grade soft tissue malignancy characterized by a ring chromosomeA Mezzelani, G Sozzi, M Nessling, et al.The American Journal of Pathology|August 1, 1997
High-level DNA amplifications are common genetic aberrations in B-cell neoplasmsC A Werner, H Döhner, S Joos, et al.Pageof 134