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Von Hippel-Lindau’s Disease
Qiao's Pathologyvon Hippel-Lindau syndrome (VHL) is a hereditary condition associated with tumors arising in multiple organs. Tumors in VHL include hemangioblastomas, which are blood vessel tumors of the brain, spinal cord, and eye. Here is the latest research.
Top 20 most recent papers
Genetic Profile of Indian Pheochromocytoma and Paraganglioma Patients - A Single Institutional Study
Indian Journal of Endocrinology and MetabolismNovember 20, 2019
Gaurav K AgarwalEesh Bhatia
Structure-Based Design of a Macrocyclic PROTAC
Angewandte ChemieNovember 19, 2019
Alessio CiulliJane E Wright
51
Intratumor Performance and Therapeutic Efficacy of PAMAM Dendrimers Carried by Clustered Nanoparticles
Nano LettersNovember 7, 2019
Hong-Jun LiJun Wang
Hypoxia on vhl-deficient cells to obtain hif related genes through bioinformatics analysis.
bioRxivDecember 3, 2019
Hua Lin, Hong-wei Liu
3
Mutations and Response to Rapalogs in Patients with Metastatic Renal Cell Carcinoma
Molecular Cancer TherapeuticsOctober 25, 2019
Amin H NassarDavid J. Kwiatkowski
19
Mutational profile and genotype/phenotype correlation of non-familial pheochromocytoma and paraganglioma
OncotargetOctober 15, 2019
Shatha AlbattalAli Matar Alzahrani
Discovery of Highly Potent and Efficient PROTAC Degraders of Androgen Receptor (AR) by Employing Weak Binding Affinity VHL E3 Ligase Ligands
Journal of Medicinal ChemistryDecember 5, 2019
Xin HanShaomeng J Wang
A novel strategy to block mitotic progression for targeted therapy
EBioMedicineOctober 25, 2019
Junlong Jack ChiYong Wan
8
Concurrent heterozygous Von-Hippel-Lindau and transmembrane-protein-127 gene mutation causing an erythropoietin-secreting pheochromocytoma in a normotensive patient with severe erythrocytosis
Journal of HypertensionSeptember 19, 2019
Aurelio NegroAderville Cabassi
HIF-independent synthetic lethality between CDK4/6 inhibition and VHL loss across species
Science SignalingOctober 1, 2019
Hilary E NicholsonWilliam G. Kaelin
128
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Location of the Positive Charges in Cationic Amphiphiles Modulates Their Mechanism of Action against Model Membranes
Langmuir : the ACS Journal of Surfaces and ColloidsOctober 8, 2019
Marcio M AlmeidaKarin A Riske
Central nervous system hemangioblastomas in the elderly (over 65 years): Clinical characteristics and outcome analysis
Clinical Neurology and NeurosurgeryNovember 25, 2019
Qiguang WangXu-hui Hui
Stabilization of myeloid-derived HIFs promotes vascular regeneration in retinal ischemia
AngiogenesisOctober 3, 2019
Pilar VillacampaJames W B Bainbridge
Growth characteristics and therapeutic decision markers in von Hippel-Lindau disease patients with renal cell carcinoma
Orphanet Journal of Rare DiseasesOctober 28, 2019
Patrick SchuhmacherStefan Zschiedrich
Rb1/Rbl1/Vhl loss induces mouse subretinal angiomatous proliferation and hemangioblastoma
JCI InsightOctober 16, 2019
Ran WeiDanian Chen
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1
Structure of maltotetraose-forming amylase from Pseudomonas saccharophila STB07 provides insights into its product specificity
International Journal of Biological MacromoleculesNovember 18, 2019
Ziqian ZhangZhao-Feng Li
2
The cause of melena in a female with Von Hippel-Lindau disease
GastroenterologySeptember 24, 2019
Peace EnehConor G Loftus
Hemangioblastoma Instead of Renal Cell Carcinoma Plays a Major Role in the Unfavorable Overall Survival of Von Hippel-Lindau Disease Patients
Frontiers in OncologyOctober 9, 2019
Bo-Wen ZhouKan Gong
3
Clinical and Biochemical Features of Pheochromocytoma Characteristic of Von Hippel-Lindau Syndrome
World Journal of SurgeryNovember 26, 2019
Shimena R LiLinwah Yip
Frequent Mutations of VHL Gene and the Clinical Phenotypes in the Largest Chinese Cohort With Von Hippel-Lindau Disease
Frontiers in GeneticsSeptember 18, 2019
Bao-An HongKan Gong
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