Showing results (31-40 of 112) with videos related to
Sort By:
Pageof 12
Cancer Research|February 6, 2008
A functional role for KLF6-SV1 in lung adenocarcinoma prognosis and chemotherapy responseAnalisa DiFeo, Lauren Feld, Estefania Rodriguez, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 9, 2012
Shaking the family tree: identification of novel and biologically active alternatively spliced isoforms across the KLF family of transcription factorsOlga Camacho-Vanegas, Jacob Till, Irene Miranda-Lorenzo, et al.Molecular & Cellular Proteomics : MCP|June 23, 2019
Insights into Impact of DNA Copy Number Alteration and Methylation on the Proteogenomic Landscape of Human Ovarian Cancer via a Multi-omics Integrative AnalysisXiaoyu Song, Jiayi Ji, Kevin J Gleason, et al.Annals of Medicine|November 26, 1999
Immunological findings in thymoma and thymoma-related syndromesA M Masci, G Palmieri, F Perna, et al.American Journal of Medical Genetics|June 22, 2000
Inherited multicentric osteolysis with arthritis: a variant resembling Torg syndrome in a Saudi familyA Al Aqeel, W Al Sewairi, B Edress, et al.American Journal of Human Genetics|March 3, 1999
Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22J A Martignetti, R J Desnick, E Aliprandis, et al.Human Mutation|February 5, 2009
Systemic hyalinosis mutations in the CMG2 ectodomain leading to loss of function through retention in the endoplasmic reticulumJulie Deuquet, Laurence Abrami, Analisa Difeo, et al.Journal of Ovarian Research|October 25, 2011
Decreased levels of serum glutathione peroxidase 3 are associated with papillary serous ovarian cancer and disease progressionDeep Agnani, Olga Camacho-Vanegas, Catalina Camacho, et al.American Journal of Human Genetics|March 31, 2000
The gene for May-Hegglin anomaly localizes to a <1-Mb region on chromosome 22q12.3-13.1J A Martignetti, K E Heath, J Harris, et al.American Journal of Medical Genetics|May 26, 1999
Type 1 Gaucher disease presenting with extensive mandibular lytic lesions: identification and expression of a novel acid beta-glucosidase mutationM P Wasserstein, J A Martignetti, R Zeitlin, et al.Pageof 12