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Results 1 to 25 of 54

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Hamartin and tuberin modulate gene transcription via β-cateninJOZWIAK, Jaroslaw; WLODARSKI, Pawel.Journal of neuro-oncology. 2006, Vol 79, Num 3, pp 229-234, issn 0167-594X, 6 p.Article

Differential localization of hamartin and tuberin and increased S6 phosphorylation in a tuberJANSEN, F. E; NOTENBOOM, R. G. E; NELLIST, M et al.Neurology. 2004, Vol 63, Num 7, pp 1293-1295, issn 0028-3878, 3 p.Article

Hamartin Variants That Are Frequent in Focal Dysplasias and Cortical Tubers Have Reduced Tuberin Binding and Aberrant Subcellular Distribution In VitroLUGNIER, Céline; MAJORES, Michael; FASSUNKE, Jana et al.Journal of neuropathology and experimental neurology. 2009, Vol 68, Num 10, pp 1136-1146, issn 0022-3069, 11 p.Article

The tuberous sclerosis gene products hamartin and tuberin are multifunctional proteins with a wide spectrum of interacting partnersROSNER, Margit; HANNEDER, Michaela; SIEGEL, Nicol et al.Mutation research. Reviews in mutation research. 2008, Vol 658, Num 3, pp 234-246, issn 1383-5742, 13 p.Article

Akt regulates nuclear/cytoplasmic localization of tuberinROSNER, M; FREILINGER, A; HENGSTSCHLÄGER, M et al.Oncogene (Basingstoke). 2007, Vol 26, Num 4, pp 521-531, issn 0950-9232, 11 p.Article

The tuberous sclerosis genes, TSC1 and TSC2, trigger different gene expression responsesROSNER, Margit; FREILINGER, Angelika; LUBEC, Gert et al.International journal of oncology. 2005, Vol 27, Num 5, pp 1411-1424, issn 1019-6439, 14 p.Article

The cellular response to ectopic overexpression of the tuberous sclerosis genes, TSC1 and TSC2 : A proteomic approachHENGSTSCHLÄGER, Markus; ROSNER, Margit; FOUNTOULAKIS, Michael et al.International journal of oncology. 2005, Vol 27, Num 3, pp 831-838, issn 1019-6439, 8 p.Article

Graded loss of tuberin in an allelic series of brain models of TSC correlates with survival, and biochemical, histological and behavioral featuresYUAN, Elizabeth; TSAI, Peter T; GREENE-COLOZZI, Emily et al.Human molecular genetics (Print). 2012, Vol 21, Num 19, pp 4286-4300, issn 0964-6906, 15 p.Article

Dissociate expression of tuberous sclerosis complex 1 product hamartin in a skin and pulmonary lesion of a tuberous sclerosis complexWATAYA-KANEDA, Mari; KATAYAMA, Ichiro.Human pathology. 2009, Vol 40, Num 3, pp 430-434, issn 0046-8177, 5 p.Article

Hamartin and tuberin : Working together for tumour suppressionJOZWIAK, Jaroslaw.International journal of cancer. 2006, Vol 118, Num 1, pp 1-5, issn 0020-7136, 5 p.Article

Tuberin and p27 expression in breast cancer patients with or without BRCA germline mutationsDRESSLER, Anne Catharina; HUDELIST, Gernot; FINK-RETTER, Anneliese et al.Journal of cancer research and clinical oncology. 2013, Vol 139, Num 8, pp 1349-1355, issn 0171-5216, 7 p.Article

Tuberous sclerosis complex genes: from flies to human geneticsHENGSTSCHLÄGER, Markus.Archives of dermatological research (Print). 2001, Vol 293, Num 8, pp 383-386, issn 0340-3696Article

Rapl activity is elevated in malignant astrocytomas independent of tuberous sclerosis complex-2 gene expressionLAU, Nelson; UHLMANN, Erik J; VON LINTIG, Friederike C et al.International journal of oncology. 2002, Vol 22, Num 1, pp 195-200, issn 1019-6439, 6 p.Article

Loss of tuberin, the tuberous-sclerosis-complex-2 gene product is associated with angiogenesisNGUYEN-YU, Phuong-Anh; FACKLER, Ingrid; RUST, Adelheid et al.Journal of cutaneous pathology. 2001, Vol 28, Num 9, pp 470-475, issn 0303-6987Article

Simultaneous loss of hamartin and tuberin from the cerebrum, kidney and heart with tuberous sclerosisMIZUGUCHI, M; IKEDA, K; TAKASHIMA, S et al.Acta neuropathologica. 2000, Vol 99, Num 5, pp 503-510, issn 0001-6322Article

Heterozygosity for the tuberous sclerosis complex (TSC) gene products results in increased astrocyte numbers and decreased p27-Kip1 expression in TSC2+/- cellsUHLMANN, Erik J; APICELLI, Anthony J; BALDWIN, Rebecca L et al.Oncogene (Basingstoke). 2002, Vol 21, Num 25, pp 4050-4059, issn 0950-9232, 10 p.Article

Tuberous sclerosis complex: Genetics to pathogenesisNARAYANAN, Vinodh.Pediatric neurology. 2003, Vol 29, Num 5, pp 404-409, issn 0887-8994, 6 p.Article

The role of tuberous sclerosis gene products, tuberin and hamartin, in cell cycle regulation and cell proliferationWATAYA-KANEDA, Mari; YOSHIKAWA, Kunihiko; ITAMI, Satoshi et al.Recent research developments in biophysics and biochemistry vol. 3 - 2003 Part II. Recent research developments in biophysics and biochemistry. 2003, pp 703-710, isbn 81-271-0014-5, 8 p.Book Chapter

Identification of the coding sequences responsible for tsc2-mediated tumor suppression using a transgenic rat systemMOMOSE, Shuji; KOBAYASHI, Toshiyuki; MITANI, Hiroaki et al.Human molecular genetics (Print). 2002, Vol 11, Num 24, pp 2997-3006, issn 0964-6906, 10 p.Article

The Tuberin/mTOR Pathway Promotes Apoptosis of Tubular Epithelial Cells in DiabetesVELAGAPUDI, Chakradhar; BHANDARI, Basant S; ABBOUD-WERNER, Sherry et al.Journal of the American Society of Nephrology. 2011, Vol 22, Num 2, pp 262-273, issn 1046-6673, 12 p.Article

Hamartin and tuberin interaction with the G2/M cyclin-dependent kinase CDK1 and its regulatory cyclins A and BCATANIA, Michael G; MISCHEL, Paul S; VINTERS, Harry V et al.Journal of neuropathology and experimental neurology. 2001, Vol 60, Num 7, pp 711-723, issn 0022-3069Article

Expression profile of the tumorigenic factors associated with tumor size and sex steroid hormone status in uterine leiomyomataWEI, Jian-Jun; CHIRIBOGA, Luis; MITTAL, Khush et al.Fertility and sterility. 2005, Vol 84, Num 2, pp 474-484, issn 0015-0282, 11 p.Article

SYNTHESIS OF TUBERIN AND RELATED-N-STYRYLFORMAMIDES.MASSEY IJ; HARRISON IT.1977; CHEM. AND INDUSTRY; G.B.; DA. 1977; NO 22; PP. 920; BIBL. 2 REF.Article

Novel mechanism of regulation of the DNA repair enzyme OGG1 in tuberin-deficient cellsHABIB, Samy L; BHANDARI, Besant K; SADEK, Nahed et al.Carcinogenesis (New York. Print). 2010, Vol 31, Num 11, pp 2022-2030, issn 0143-3334, 9 p.Article

Neuropathology of tuberous sclerosisMIZUGUCHI, Masashi; TAKASHIMA, Sachio.Brain & development (Tokyo. 1979). 2001, Vol 23, Num 7, pp 508-515, issn 0387-7604Conference Paper

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