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Biochemistry. Biokhimiia|May 6, 2014
Kinase mTOR: regulation and role in maintenance of cellular homeostasis, tumor development, and agingA A Parkhitko, O O Favorova, D I Khabibullin, et al.The American Journal of Surgical Pathology|March 21, 1998
Apparent renal cell carcinomas in tuberous sclerosis are heterogeneous: the identification of malignant epithelioid angiomyolipomaM Pea, F Bonetti, G Martignoni, et al.Journal of Medical Genetics|January 14, 2000
Mutational analysis of the tuberous sclerosis gene TSC2 in patients with pulmonary lymphangioleiomyomatosisA Astrinidis, L Khare, T Carsillo, et al.American Journal of Respiratory and Critical Care Medicine|February 24, 2001
The spectrum of mutations in TSC1 and TSC2 in women with tuberous sclerosis and lymphangiomyomatosisG D Strizheva, T Carsillo, W D Kruger, et al.Annals of Human Genetics|July 1, 1997
Cloning and evaluation of RALGDS as a candidate for the tuberous sclerosis gene TSC1D Humphrey, J Kwiatkowska, E P Henske, et al.Genes, Chromosomes & Cancer|August 1, 1995
Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band 16p13 occurs in sporadic as well as TSC-associated renal angiomyolipomasE P Henske, H P Neumann, B W Scheithauer, et al.Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|August 4, 1998
Frequent progesterone receptor immunoreactivity in tuberous sclerosis-associated renal angiomyolipomasE P Henske, X Ao, M P Short, et al.American Journal of Human Genetics|June 13, 1998
Evidence that lymphangiomyomatosis is caused by TSC2 mutations: chromosome 16p13 loss of heterozygosity in angiomyolipomas and lymph nodes from women with lymphangiomyomatosisT A Smolarek, L L Wessner, F X McCormack, et al.Annals of Human Genetics|January 1, 1995
Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1E P Henske, M P Short, S Jozwiak, et al.Oncogene|October 20, 2009
Differential requirement of CAAX-mediated posttranslational processing for Rheb localization and signalingA B Hanker, N Mitin, R S Wilder, et al.Pageof 5