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Genomics|July 1, 1995
A 5.4-Mb continuous pulsed-field gel electrophoresis map of human 9q34.1 between ABL and D9S114, including the tuberous sclerosis (TSC1) regionE P Henske, D J KwiatkowskiNeurology|October 26, 1999
New developments in the neurobiology of the tuberous sclerosis complexP B Crino, E P HenskeThe Journal of Clinical Investigation|January 15, 1997
Loss of the polycystic kidney disease (PKD1) region of chromosome 16p13 in renal cyst cells supports a loss-of-function model for cyst pathogenesisJ L Brasier, E P HenskeProceedings of the National Academy of Sciences of the United States of America|May 24, 2000
Mutations in the tuberous sclerosis complex gene TSC2 are a cause of sporadic pulmonary lymphangioleiomyomatosisT Carsillo, A Astrinidis, E P HenskeAmerican Journal of Respiratory and Critical Care Medicine|November 13, 2001
Chromosome 16 loss of heterozygosity in tuberous sclerosis and sporadic lymphangiomyomatosisJ Yu, A Astrinidis, E P HenskeSeminars in Pediatric Neurology|January 6, 1999
Renal angiomyolipomas, cysts, and cancer in tuberous sclerosis complexH P Neumann, G Schwarzkopf, E P HenskeBiochemistry. Biokhimiia|April 18, 2013
Autophagy: mechanisms, regulation, and its role in tumorigenesisA A Parkhitko, O O Favorova, E P HenskeChest|January 13, 2000
Frequent estrogen and progesterone receptor immunoreactivity in renal angiomyolipomas from women with pulmonary lymphangioleiomyomatosisH Logginidou, X Ao, I Russo, et al.Cancer Research|November 11, 1998
Hamartin, the product of the tuberous sclerosis 1 (TSC1) gene, interacts with tuberin and appears to be localized to cytoplasmic vesiclesT L Plank, R S Yeung, E P HenskePediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 7, 1999
Renal cell carcinoma in children with diffuse cystic hyperplasia of the kidneysE P Henske, P Thorner, K Patterson, et al.Pageof 5