Search Results - "CHETTA, M."
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A Copernican revolution of multigenic analysis: A retrospective study on clinical exome sequencing in unclear genetic disorders
Published in Computational and structural biotechnology journal (01-12-2024)“…Despite the inevitable shift in medical practice towards a deeper understanding of disease etiology and progression through multigenic analysis, the profound…”
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2
ELOVL5 Is a Critical and Targetable Fatty Acid Elongase in Prostate Cancer
Published in Cancer research (Chicago, Ill.) (01-04-2021)“…The androgen receptor (AR) is the key oncogenic driver of prostate cancer, and despite implementation of novel AR targeting therapies, outcomes for metastatic…”
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3
Ductal adenocarcinoma of the prostate: A systematic review and meta‐analysis of incidence, presentation, prognosis, and management
Published in BJUI compass (01-01-2021)“…Context Ductal adenocarcinoma (DAC) is relatively rare, but is nonetheless the second most common subtype of prostate cancer. First described in 1967, opinion…”
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4
Polymorphic miRNA-mediated gene contribution to inhibitor development in haemophilia A
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-11-2012)“…Summary Development of inhibitory antibodies is perhaps the most serious complication of FVIII replacement therapy, precluding efficient clinical management of…”
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5
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-05-2010)“…One of the most severe and important complication in the treatment of patients with haemophilia A is the formation of neutralizing antibodies (FVIII…”
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6
Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-03-2012)Get full text
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7
A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome
Published in Cellular oncology (Dordrecht) (01-08-2014)“…Purpose The CDC73 gene, encoding parafibromin, has been identified as a tumour suppressor gene both in hyperparathyroidism-jaw tumour (HPT-JT) syndrome and in…”
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Severe outbreaks of polyarthritis in kids caused by Mycoplasma mycoides subspecies capri in Sicily
Published in Veterinary record (01-04-2012)“…Mycoplasmas isolated were from the all joints and milk on farm A and from the joints, ears, lung, brain, kidney, spleen and liver on farm B. The organisms were…”
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Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH
Published in American journal of medical genetics. Part A (01-07-2010)“…X;Y translocation is a relatively rare event in humans. Analyzed cytogenetically, the majority of these aberrations have breakpoints at Xp22 and Yq11. Females…”
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10
Spirocerca lupi isolated from gastric lesions in foxes (Vulpes vulpes) in Sicily (Italy)
Published in Polish journal of veterinary sciences (01-01-2010)“…Spirocerca lupi (Rudolphi 1809) is a cosmopolitan nematode of dogs and wild carnivores. In the past it has been reported in Italy, mainly in southern regions…”
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LY6G6D is a selectively expressed colorectal cancer antigen that can be used for targeting a therapeutic T-cell response by a T-cell engager
Published in Frontiers in immunology (08-09-2022)“…Colorectal cancer (CRC) is one of the most common cancers worldwide and demands more effective treatments. We sought to identify tumor selective CRC antigens…”
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12
Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridization
Published in Indian journal of human genetics (01-05-2008)“…Standard methods of mutation detection are time consuming in Hemophilia A (HA) rendering their application unavailable in some analysis such as prenatal…”
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A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin
Published in Blood (15-01-2005)“…Patients require different warfarin dosages to achieve the target therapeutic anticoagulation. The variability is largely genetically determined, and it can be…”
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14
Porous EH and EH-PEG Scaffolds as Gene Delivery Vehicles to Skeletal Muscle
Published in Pharmaceutical research (01-06-2011)“…ABSTRACT Purpose Synthetic biomaterials are widely used in an attempt to control the cellular behavior of regenerative tissues. This can be done by altering…”
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PO-0933: Prospective Evaulation Of Iort Boost In Women Undergoing Lumpectomy With Oncoplastic Reconstruction
Published in Radiotherapy and oncology (01-11-2020)Get full text
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16
Gene polymorphisms and sport attitude in Italian athletes
Published in Genetic testing and molecular biomarkers (01-04-2011)“…The aim of this study was to evaluate whether the distribution of polymorphisms in the ACE, ACTN3, NOS3, UCP2, and UCP3 genes, which has been reported to be…”
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Polymorphic mi RNA ‐mediated gene contribution to inhibitor development in haemophilia A
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-11-2012)“…Development of inhibitory antibodies is perhaps the most serious complication of FVIII replacement therapy, precluding efficient clinical management of…”
Get full text
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18
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin
Published in Haematologica (Roma) (01-12-2004)“…Istituto di Genetica Medica, Dipartimento di Scienze Biomediche, Universita di Foggia, Italy. BACKGROUND AND OBJECTIVES: There is very considerable…”
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Canine leptospirosis cases and molecular screening for Leptospira interrogans infection
Published in Pakistan veterinary journal (2016)“…A molecular survey for pathogenic Leptospira spp. in kenneled dogs in Sicily, Italy, showed up to 16% of positive results. A fatal leptospirosis case was…”
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MP67-19 DUCTAL ADENOCARCINOMA OF THE PROSTATE: A SYSTEMATIC REVIEW AND META-ANALYSIS OF INCIDENCE, PRESENTATION AND MANAGEMENT
Published in The Journal of urology (01-04-2020)Get full text
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