about
Tyr(612) and Tyr(632) in human insulin receptor substrate-1 are important for full activation of insulin-stimulated phosphatidylinositol 3-kinase activity and translocation of GLUT4 in adipose cellsTransitions at CpG dinucleotides, geographic clustering of TP53 mutations and food availability patterns in colorectal cancerEffects of PPARα inhibition in head and neck paraganglioma cellsIntegrative analysis of hereditary nonpolyposis colorectal cancer: the contribution of allele-specific expression and other assays to diagnostic algorithms.Insulin resistance due to mutations of the insulin receptor gene: an overview.Increased variance in germline allele-specific expression of APC associates with colorectal cancer.Low AMY1 Gene Copy Number Is Associated with Increased Body Mass Index in Prepubertal Boys.Analysis of adenomatous polyposis coli gene in thyroid tumoursCorrelation between mutations and mRNA expression of APC and MUTYH genes: new insight into hereditary colorectal polyposis predisposition.Microsatellite instability in thyroid tumours and tumour-like lesions.Analysis of extended genomic rearrangements in oncological research.Methods for routine diagnosis of genomic rearrangements: multiplex PCR-based methods and future perspectives.Integrative genetic, epigenetic and pathological analysis of paraganglioma reveals complex dysregulation of NOTCH signaling.Alterations of MEN1 and E-cadherin/β-catenin complex in sporadic pulmonary carcinoids.IRS1 G972R polymorphism and type 2 diabetes: a paradigm for the difficult ascertainment of the contribution to disease susceptibility of 'low-frequency-low-risk' variants.Overexpression of PY1289-HER3 in sporadic pulmonary carcinoid from patients bearing MEN1 gene variants.A novel T608R missense mutation in insulin receptor substrate-1 identified in a subject with type 2 diabetes impairs metabolic insulin signaling.Genetic evidence that juvenile nasopharyngeal angiofibroma is an integral FAP tumour.Association between rs12970134 Near MC4R and adiposity indexes in a homogenous population of Caucasian schoolchildren.Cytotoxic effect of a family of peroxisome proliferator-activated receptor antagonists in colorectal and pancreatic cancer cell lines.The CHEK2 c.1100delC mutation plays an irrelevant role in breast cancer predisposition in Italy.Variation of the insulin receptor substrate gene (IRS-1) in African Pygmies and Bantus.Paragangliomas arise through an autonomous vasculo-angio-neurogenic program inhibited by imatinib.The Anticancer Potential of Peroxisome Proliferator-Activated Receptor Antagonists.Absence of insulin receptor gene mutations in three insulin-resistant women with the polycystic ovary syndrome.Two mutant alleles of the insulin receptor gene in a family with a genetic form of insulin resistance: a 10 base pair deletion in exon 1 and a mutation substituting serine for asparagine-462.A novel deletion in exon 15 of the adenomatous polyposis coli gene in an Italian kindred.P53 mutations in colorectal cancer from northern Iran: Relationships with site of tumor origin, microsatellite instability and K-ras mutationsPatterns of K-ras mutation in colorectal carcinomas from Iran and Italy (a Gruppo Oncologico dell'Italia Meridionale study): influence of microsatellite instability status and country of originEffects of repurposed drug candidates nitroxoline and nelfinavir as single agents or in combination with erlotinib in pancreatic cancer cellsEffects of dichloroacetate as single agent or in combination with GW6471 and metformin in paraganglioma cellsCombined use of MLPA and nonfluorescent multiplex PCR analysis by high performance liquid chromatography for the detection of genomic rearrangementsHow Anesthetic, Analgesic and Other Non-Surgical Techniques During Cancer Surgery Might Affect Postoperative Oncologic Outcomes: A Summary of Current State of Evidence.Two unrelated patients with familial hyperproinsulinemia due to a mutation substituting histidine for arginine at position 65 in the proinsulin molecule: identification of the mutation by direct sequencing of genomic deoxyribonucleic acid amplifiedNormal coding sequence of insulin gene in Pima Indians and Nauruans, two groups with highest prevalence of type II diabetesA novel mutation at the splice junction of exon 9 of the APC gene in familial adenomatous polyposisMultiplex PCR analysis and genotype-phenotype correlations of frequent APC mutationsThyroid carcinoma usually occurs in patients with familial adenomatous polyposis in the absence of biallelic inactivation of the adenomatous polyposis coli geneBRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central ItalyTranscript dosage effect in familial adenomatous polyposis: model offered by two kindreds with exon 9 APC gene mutations
P50
Q24291346-BC054494-143B-47D7-936A-8A051EC511DFQ27342770-C474E9D0-328D-4620-990A-8F09B098B11FQ33779008-C4C02930-54EA-4242-A645-8393C4E114B9Q35053925-9DBDC3B4-509D-4C3C-82AD-853F549CDC03Q35198506-BAA35E19-EDD2-4133-A006-BB622F89A2AAQ35634864-9096FC08-50A2-4222-BFB7-60DE3A540B13Q36009799-3A448F82-535B-44AC-9CE8-9495479BE5DFQ36080630-E1AEADC9-00E8-4627-8572-DC691382D833Q36224094-43DAFE98-B823-454D-A4AE-5B0B547F8BF3Q36617401-49832754-EE5B-488C-9162-444E72C5D85FQ36860175-6CBC3635-6920-49B6-84CF-0A1D3DB5294DQ37035269-F5392CED-70F4-45E4-B7B8-E8E0BF841BEBQ37213634-CC440759-7F84-4C8F-A904-37EFA3A14B00Q41786175-701AE37E-3AB1-4301-B11C-D05D065FEFE0Q41809347-5E4CF17C-2E1A-4BEE-9A69-6CCDC3B218AAQ42721868-DC06195B-C257-4CBD-B1E0-5BC53CC18DDEQ42803390-5B270236-E74A-4629-A732-31310C388172Q43004309-283FB62D-444A-4729-BAD7-8D3DB50C29CAQ43746797-E15F50AC-ADFD-4D86-BDAA-9D1DBCC70C6FQ43974650-9DE86277-CC4F-4977-8E5B-EED8A17DE936Q44955073-91FE54CA-E6E1-4010-948D-7C67278E7F37Q46611593-5B77D3E2-862B-4F48-A7F9-A4CE53E55832Q47228308-C58661AE-2B0E-444E-AD2B-ECE2077409D5Q48350605-B078BA40-6DC4-4FEA-8142-FB4CCA97746CQ53814172-770CD059-DA60-4DEA-9055-E12C8BC945C2Q54180582-E7D16D90-6EB0-4D77-93B5-6A15AF51D81CQ54644852-698C1150-8E91-4A0C-9AE2-0C650514C394Q57157305-78C14B41-3207-40A9-AABA-8EFDF04D5FD9Q57157367-637D38A5-D927-48B9-A71B-F77677DC69F4Q58706536-87754C9D-E982-43C7-85C2-BFAD6EE1693EQ58751831-93FD6DF1-E30D-4F44-8C63-FEA73890598CQ61970275-F0350ED7-5CDF-4C90-ABEA-C0D634856FF9Q64933926-66966C4D-9BBE-451D-955A-0D80074780DCQ68526048-93753A0A-0774-4194-B7EA-3F3FB0FF1DCBQ70138980-1A9DD42C-9FA9-496C-B3D7-994B06A1CA3BQ72033689-0B482D30-1F2D-41F9-B12D-0C2C0B096022Q72234639-9994F3F0-82FB-4C90-A8FC-A5EDFBF64ECDQ73571175-40A93D7E-AC0E-4D9F-9933-5F5051494309Q73692286-F7E5A7E9-C151-4294-9202-91EDA8DA06B3Q74376868-418256A6-15DB-4849-B7C0-1A832DBBB50B
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Alessandro Cama
@ast
Alessandro Cama
@en
Alessandro Cama
@es
Alessandro Cama
@nl
type
label
Alessandro Cama
@ast
Alessandro Cama
@en
Alessandro Cama
@es
Alessandro Cama
@nl
altLabel
Alessandro CAMA
@en
prefLabel
Alessandro Cama
@ast
Alessandro Cama
@en
Alessandro Cama
@es
Alessandro Cama
@nl
P1053
J-3964-2018
P106
P1153
7004822238
P21
P31
P496
0000-0003-3647-1368