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Human Genetics|May 1, 1995
22q11 deletions in isolated and syndromic patients with tetralogy of FallotF Amati, A Mari, M C Digilio, et al.Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
The search for hemizygosity at 22qll in patients with isolated cleft palateR Mingarelli, M C Digilio, A Mari, et al.Critical Care Medicine|December 1, 1999
Ceramide concentrations in septic patients: a possible marker of multiple organ dysfunction syndromeG Delogu, G Famularo, F Amati, et al.The Analyst|November 5, 2014
Separation of small metabolites and lipids in spectra from biopsies by diffusion-weighted HR-MAS NMR: a feasibility studyG Diserens, M Vermathen, C Precht, et al.Molecular Human Reproduction|February 11, 2015
Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathwaysM Massimiani, L Vecchione, D Piccirilli, et al.American Journal of Medical Genetics|July 3, 1995
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): exclusion from the critical region on 8pF Amati, A Mari, R Mingarelli, et al.Diabetologia|February 18, 2011
Effects of weight loss and exercise on insulin resistance, and intramyocellular triacylglycerol, diacylglycerol and ceramideJ J Dubé, F Amati, F G S Toledo, et al.European Journal of Human Genetics : EJHG|December 22, 1999
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndromeF Amati, E Conti, A Novelli, et al.Clinical and Experimental Medicine|December 28, 2006
Gene expression profile study in CFTR mutated bronchial cell linesS Gambardella, M Biancolella, M R D'Apice, et al.Cytogenetics and Cell Genetics|July 4, 2001
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogasterA Ratti, F Amati, M Bozzali, et al.Pageof 4