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Journal Article
Familial Cancer, ISSN 1389-9600, 1/2019, Volume 18, Issue 1, pp. 91 - 95
Hemangioblastomas are rare vascularized central nervous system tumors, which can occur sporadically or be associated with von Hippel Lindau Syndrome. The... 
Human Genetics | Biomedicine, general | Biomedicine | Hypoxia Inducible Factor alpha (HIFα) | Von Hippel Lindau Syndrome (VHL) | Cancer Research | Epidemiology | Hemangioblastoma | Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome (HLRCC) | Hypoxia Inducible Factor alpha (HIF) | ONCOLOGY | GENETICS & HEREDITY | FUMARATE-HYDRATASE | MUTATIONS | EXPRESSION | Neoplastic Syndromes, Hereditary - pathology | Uterine Neoplasms - pathology | Humans | Middle Aged | Male | von Hippel-Lindau Disease - diagnosis | von Hippel-Lindau Disease - pathology | Leiomyomatosis - diagnosis | Skin Neoplasms - diagnosis | Leiomyomatosis - pathology | Neoplastic Syndromes, Hereditary - genetics | Uterine Neoplasms - diagnosis | Chromosomes, Human, Pair 1 - genetics | Skin - pathology | Chromosome Deletion | Skin Neoplasms - pathology | Uterine Neoplasms - genetics | Autism Spectrum Disorder - genetics | Hypoxia-Inducible Factor 1, alpha Subunit - genetics | Neoplastic Syndromes, Hereditary - diagnosis | Hemangioblastoma - diagnosis | von Hippel-Lindau Disease - genetics | Phenotype | Hemangioblastoma - pathology | Hemangioblastoma - genetics | Pedigree | Skin Neoplasms - genetics | Leiomyomatosis - genetics | Genetic Carrier Screening | Tricarboxylic acid cycle | Kidneys | Central nervous system | Fumarate hydratase | Kidney cancer | Hypoxia | VHL protein | Tumorigenesis | Mutation | Clear cell-type renal cell carcinoma | Kidney transplantation | Tumors | Cancer | Index Medicus
Journal Article
American Journal of Medical Genetics, Part A, ISSN 1552-4825, 10/2009, Volume 149, Issue 10, pp. 2147 - 2151
Journal Article
Neuropathology, ISSN 0919-6544, 02/2017, Volume 37, Issue 1, pp. 3 - 11
Hemangioblastoma (HB) is mainly located in the brain and the spinal cord. The tumor is composed of two major components, namely neoplastic stromal cells and... 
VEGF/VEGFR2 | hemangioblastoma | SDF1α/CXCR4 | angiogenesis | EphrinB2/EphB4 | Dll4/Notch | VEGFR2 | VEGF | CXCR4 EXPRESSION | Notch | TUMOR-SUPPRESSOR GENE | CXCR4 | CELL-PROLIFERATION | PATHOLOGY | FACTOR RECEPTOR | NEUROSCIENCES | CLINICAL NEUROLOGY | EphB4 | HYPOXIA-INDUCIBLE FACTORS | Dll4 | EphrinB2 | BREAST-CANCER | SDF1 | CENTRAL-NERVOUS-SYSTEM | UP-REGULATION | PRIMARY GLIOBLASTOMA | ENDOTHELIAL GROWTH-FACTOR | Hemangioblastoma - metabolism | Up-Regulation | Receptors, Notch - metabolism | Spinal Neoplasms - pathology | Cranial Fossa, Posterior - pathology | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Male | Receptors, Notch - genetics | Vascular Endothelial Growth Factor A - metabolism | Cranial Fossa, Posterior - metabolism | Vascular Endothelial Growth Factor A - genetics | Neovascularization, Pathologic - pathology | Vascular Endothelial Growth Factor Receptor-2 - genetics | Receptor, EphB4 - genetics | Young Adult | Chemokine CXCL12 - genetics | Skull Base Neoplasms - genetics | Adult | Female | Receptors, CXCR4 - genetics | Endothelial Cells - metabolism | Vascular Endothelial Growth Factor Receptor-2 - metabolism | Ephrin-B2 - metabolism | Receptor, EphB4 - metabolism | Receptors, CXCR4 - metabolism | Ephrin-B2 - genetics | Chemokine CXCL12 - metabolism | Hemangioblastoma - pathology | Hemangioblastoma - genetics | Spinal Neoplasms - genetics | Adolescent | Spinal Neoplasms - metabolism | Neovascularization, Pathologic - genetics | Signal Transduction - physiology | Skull Base Neoplasms - pathology | Aged | Neovascularization, Pathologic - metabolism | Endothelial Cells - pathology | Skull Base Neoplasms - metabolism | Endothelial growth factors | RNA | Epigenetic inheritance | Localization | Rodents | Index Medicus
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 04/2005, Volume 25, Issue 8, pp. 3163 - 3172
Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... 
HYPOXIA-INDUCIBLE FACTOR | OVEREXPRESSING ERYTHROPOIETIN | UBIQUITIN LIGASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENE-EXPRESSION | FACTOR (HIF)-1-ALPHA | HEPATIC HEMANGIOBLASTOMA | UP-REGULATION | RENAL-CELL CARCINOMA | ENDOTHELIAL GROWTH-FACTOR | TRANSGENIC MICE | CELL BIOLOGY | Polycythemia - genetics | Liver - pathology | Hemangioma, Cavernous - metabolism | Vascular Endothelial Growth Factor A - metabolism | Hepatocytes - metabolism | Ubiquitin-Protein Ligases - physiology | Vascular Endothelial Growth Factor A - genetics | Hypoxia-Inducible Factor 1, alpha Subunit | Aryl Hydrocarbon Receptor Nuclear Translocator | Gene Deletion | Tumor Suppressor Proteins - genetics | Erythropoietin - metabolism | Genes, Tumor Suppressor | DNA-Binding Proteins - physiology | Gene Expression | Transcription Factors - physiology | Liver Neoplasms - genetics | Gene Silencing | Receptors, Aryl Hydrocarbon - genetics | Phosphotransferases (Alcohol Group Acceptor) - genetics | Transcription Factors - genetics | von Hippel-Lindau Disease - genetics | DNA-Binding Proteins - genetics | Receptors, Aryl Hydrocarbon - physiology | Mice, Knockout | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Erythropoietin - genetics | Tumor Suppressor Proteins - physiology | Liver - blood supply | Animals | von Hippel-Lindau Disease - metabolism | Liver Neoplasms - metabolism | Polycythemia - metabolism | Mice | Von Hippel-Lindau Tumor Suppressor Protein | Ubiquitin-Protein Ligases - genetics | Hemangioma, Cavernous - genetics | Index Medicus
Journal Article
Familial Cancer, ISSN 1389-9600, 10/2016, Volume 15, Issue 4, pp. 607 - 616
Journal Article
Journal Article
Oncogene, ISSN 0950-9232, 09/2015, Volume 34, Issue 37, pp. 4855 - 4866
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 11/2018, Volume 19, Issue 1, pp. 204 - 204
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 6/2014, Volume 35, Issue 2, pp. 91 - 106
Abstract Purpose: To investigate genotype-phenotype correlation and to analyze functional and structural changes in the retina of patients with von... 
VHL disease | Genotype-phenotype correlation | retinal function and structure | Retinal function and structure | VHL GENE | PROTEIN | TUMOR-SUPPRESSOR GENE | RENAL-CELL CARCINOMA | GERM-LINE MUTATIONS | PHEOCHROMOCYTOMA | ANGIOMATOSIS | MOLECULAR PATHOLOGY | HEMANGIOBLASTOMA | GENETICS & HEREDITY | OPHTHALMOLOGY | EXPRESSION | Adrenal Gland Neoplasms - surgery | Hemangioblastoma - surgery | Kidney Neoplasms - genetics | Humans | Middle Aged | Carcinoma, Renal Cell - genetics | Carcinoma, Renal Cell - surgery | Male | Mutation, Missense | Pheochromocytoma - physiopathology | Young Adult | Kidney Neoplasms - surgery | Carcinoma, Renal Cell - physiopathology | Kidney Neoplasms - physiopathology | DNA Mutational Analysis | Retinal Neoplasms - physiopathology | Adult | Female | Von Hippel-Lindau Tumor Suppressor Protein - genetics | Cerebellar Neoplasms - physiopathology | Electroretinography | Genetic Association Studies | Tomography, Optical Coherence | Retina - physiopathology | Cerebellar Neoplasms - genetics | von Hippel-Lindau Disease - genetics | von Hippel-Lindau Disease - physiopathology | Hemangioblastoma - physiopathology | Adrenal Gland Neoplasms - physiopathology | Hemangioblastoma - genetics | Pedigree | Adolescent | Pheochromocytoma - genetics | Aged | Pheochromocytoma - surgery | Retinal Neoplasms - surgery | Cerebellar Neoplasms - surgery | Adrenal Gland Neoplasms - genetics | Retinal Neoplasms - genetics | Index Medicus | Carcinoma | pedigree analysis | retinal thickness | structure analysis | B wave | optic nerve tumor | VHL gene | central nervous system tumor | Oftalmologi | Tomography | neuroendocrine tumor | Ophthalmology | female | A wave | Retinal Neoplasms | Kidney Neoplasms | Goldenhar syndrome | Optical Coherence | gene | pheochromocytoma | article | genetic analysis | Cerebellar Neoplasms | electroretinogram | functional assessment | Adrenal Gland Neoplasms | Mutation | adult | Missense | male | optical coherence tomography | clinical examination | hemangioblastoma | electroretinography | missense mutation | Renal Cell | clinical article | retina | priority journal | human | phenotype | genotype phenotype correlation | gene mutation | von Hippel Lindau disease | aged | visual acuity | von Hippel-Lindau Disease | eye examination | controlled study | mutational analysis | exon
Journal Article