Results 231 to 238 of about 23,999 (238)

Functional assessment of variants in the TSC1 and TSC2 genes identified in individuals with Tuberous Sclerosis Complex

Human Mutation, 2011
Marianne Hoogeveen-Westerveld, Rosemary Ekong, Sue Povey   +2 more
exaly  

Variants WithinTSC2Exons 25 and 31 Are Very Unlikely to Cause Clinically Diagnosable Tuberous Sclerosis

Human Mutation, 2016
Rosemary Ekong, Mark Nellist, Marianne Hoogeveen-Westerveld   +2 more
exaly  

Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype – phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex

European Journal of Human Genetics, 2005
Mark Nellist, Peter Elfferich, S Verhoef   +2 more
exaly  

The TSC1–TSC2 Complex

2010
openaire   +1 more source

Mutation in TSC2 and activation of mammalian target of rapamycin signalling pathway in renal angiomyolipoma

Lancet, The, 2003
Hongbing Zhang, Elizabeth P Henske, David J Kwiatkowski   +2 more
exaly  

Repression of TSC1/TSC2 mediated by MeCP2 regulates human embryo lung fibroblast cell differentiation and proliferation

International Journal of Biological Macromolecules, 2017
Er-Bao Bian, Cheng Huang, Xiongwen Lv
exaly  

Distribution of Tsc2 protein in various normal rat tissues and renal tumours of Tsc2 mutant (Eker) rat detected by immunohistochemistry

Virchows Archiv Fur Pathologische Anatomie Und Physiologie Und Fur Klinische Medizin, 1999
Tomokazu Fukuda, Toshiyuki Kobayashi, Okio Hino   +2 more
exaly  

TSC1, TSC2, and Tuberous Sclerosis

2016
openaire   +1 more source