Lattice_grid_med
Powered by LatticeGrid

Search Enter term and hit return. Use '*' for as a wildcard.

Publication Listing for the MeSH term Tuberous Sclerosis. Found 14 abstracts

Patel B, Patel J, Cho JH, Manne S, Bonala S, Henske E, Roegiers F, Markiewski M, Karbowniczek M. Exosomes mediate the acquisition of the disease phenotypes by cells with normal genome in tuberous sclerosis complex. Oncogene. 2016 Jun 09;35(23):3027-36.
Karbowniczek M, Zitserman D, Khabibullin D, Hartman T, Yu J, Morrison T, Nicolas E, Squillace R, Roegiers F, Henske EP. The evolutionarily conserved TSC/Rheb pathway activates Notch in tuberous sclerosis complex and Drosophila external sensory organ development. J Clin Invest. 2010 Jan;120(1):93-102.   PMCID: PMC2798691
Henske EP. Tuberous sclerosis and the kidney: from mesenchyme to epithelium, and beyond. Pediatric Nephrology. 2005 Jul;20(7):854-7.
Astrinidis A, Cash TP, Hunter DS, Walker CL, Chernoff J, Henske EP. Tuberin, the tuberous sclerosis complex 2 tumor suppressor gene product, regulates Rho activation, cell adhesion and migration. Oncogene. 2002 Dec 05;21(55):8470-6.
Duffy K, Al-Saleem T, Karbowniczek M, Ewalt D, Prowse AH, Henske EP. Mutational analysis of the von hippel lindau gene in clear cell renal carcinomas from tuberous sclerosis complex patients. Mod Pathol. 2002 Mar;15(3):205-10.
Khare L, Strizheva GD, Bailey JN, Au KS, Northrup H, Smith M, Smalley SL, Henske EP. A novel missense mutation in the GTPase activating protein homology region of TSC2 in two large families with tuberous sclerosis complex. J Med Genet. 2001 May;38(5):347-9.
Strizheva GD, Carsillo T, Kruger WD, Sullivan EJ, Ryu JH, Henske EP. The spectrum of mutations in TSC1 and TSC2 in women with tuberous sclerosis and lymphangiomyomatosis. Am J Respir Crit Care Med. 2001 Jan;163(1):253-8.
White R, Hua Y, Scheithauer B, Lynch DR, Henske EP, Crino PB. Selective alterations in glutamate and GABA receptor subunit mRNA expression in dysplastic neurons and giant cells of cortical tubers. Ann Neurol. 2001 Jan;49(1):67-78.
Yu J, Astrinidis A, Henske EP. Chromosome 16 loss of heterozygosity in tuberous sclerosis and sporadic lymphangiomyomatosis. Am J Respir Crit Care Med. 2001 Oct 15;164(8 Pt 1):1537-40.
Astrinidis A, Khare L, Carsillo T, Smolarek T, Au KS, Northrup H, Henske EP. Mutational analysis of the tuberous sclerosis gene TSC2 in patients with pulmonary lymphangioleiomyomatosis. J Med Genet. 2000 Jan;37(1):55-7.
Carsillo T, Astrinidis A, Henske EP. Mutations in the tuberous sclerosis complex gene TSC2 are a cause of sporadic pulmonary lymphangioleiomyomatosis. Proc Natl Acad Sci U S A. 2000 May 23;97(11):6085-90.
Henske EP, Thorner P, Patterson K, Zhuang Z, Bernstein J. Renal cell carcinoma in children with diffuse cystic hyperplasia of the kidneys. Pediatr Dev Pathol. 1999 May;2(3):270-4.
Henske EP, Ao X, Short MP, Greenberg R, Neumann HP, Kwiatkowski DJ, Russo I. Frequent progesterone receptor immunoreactivity in tuberous sclerosis-associated renal angiomyolipomas. Mod Pathol. 1998 Jul;11(7):665-8.
Yeung RS, Katsetos CD, Klein-Szanto A. Subependymal astrocytic hamartomas in the Eker rat model of tuberous sclerosis. Am J Pathol. 1997 Nov;151(5):1477-86.
The above publications are sorted by year, faculty last name, and first author. Click on any highlighted author listed to find all publications attributed to that individual. Click on the publication title to see the abstract. First authors who are faculty are highlighted like this. Last authors who are faculty are highlighted like this. Other authors who are faculty are highlighted like this.

MeSH cloud from publications including the MeSH term Tuberous Sclerosis

Tuberous Sclerosis genetics Human Non-US Gov't Support Repressor Proteins US Gov't Support-PHS Female pathology metabolism Male Loss of Heterozygosity Lymphangiomyomatosis Proteins Kidney Neoplasms Adult Middle Age Kidney Child Angiomyolipoma Exons Tumor Suppressor Genes Rats Signal Transduction physiology Hippel-Lindau Disease DNA Mutational Analysis Lung Neoplasms Mice chemistry Renal Cell Carcinoma Base Sequence Mutation Immunohistochemistry Animal complications Cell Adhesion Sequence Deletion Neurons Exosomes et [Etiology] Progesterone Receptors Mental Disorders Giant Cells Aged etiology Monomeric GTP-Binding Proteins Vitamin D-Dependent Calcium-Binding Protein Sense Organs analysis Myelin Basic Proteins Genome Neuropeptides physiopathology Microsatellite Repeats Neoplastic Gene Expression Regulation Hamartoma Adenocarcinoma Age Distribution Non-US Gov't Research Support Comparative Study ge [Genetics] co [Complications] Dogs GTPase-Activating Proteins me [Metabolism] Astrocytes Evolution Cell Cycle Proteins Tubulin Amino Acid Substitution Sequence Homology Smooth Muscle Adolescent Genetic Predisposition to Disease Human Chromosomes-Pair 16 Phenotype Notch Receptors Ligases Neoplasm DNA Hyperplasia GABA Receptors Drosophila Biopsy Ependyma SCID Mice Neurofilament Proteins Hereditary Neoplastic Syndromes Transfection Estrogen Receptors DNA Sequence Analysis Papillary Carcinoma Adolescence Case Report Brain Clear Cell Adenocarcinoma rho GTP-Binding Proteins Dominant Genes Drosophila Proteins Brain Diseases th [Therapy] Immunoenzyme Techniques Polymorphism (Genetics) Tumor Suppressor Proteins Preschool Child Cell Line Inbred F344 Rats Neoplasm Staging Point Mutation Neoplastic Cell Transformation Carcinoma embryology Glutamic Acid Cell Proliferation Cell Movement veterinary Glial Fibrillary Acidic Protein Single-Stranded Conformational Polymorphism Genotype Rodent Diseases Membrane Proteins Missense Mutation Animal Disease Models
Last updated on Saturday, July 11, 2020