Sfoglia per Rivista GENES
Azathioprine Biotransformation in Young Patients with Inflammatory Bowel Disease: Contribution of Glutathione-S Transferase M1 and A1 Variants
2019-01-01 Lucafo, M.; Stocco, G.; Martelossi, S.; Favretto, D.; Franca, R.; Malusa, N.; Lora, A.; Bramuzzo, M.; Naviglio, S.; Cecchin, E.; Toffoli, G.; Ventura, A.; Decorti, G.
The Baron Pasquale Revoltella's Will in the Forensic Genetics Era
2023-01-01 Fattorini, Paolo; Previderè, Carlo; Bonin, Serena; Sorçaburu Ciglieri, Solange; Grignani, Pierangela; Pitacco, Paola; Concato, Monica; Bertoglio, Barbara; Zupanič Pajnič, Irena
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures
2022-01-01 Spedicati, Beatrice; Morgan, Anna; Pianigiani, Giulia; Musante, Luciana; Rubinato, Elisa; Santin, Aurora; Nardone, Giuseppe Giovanni; Faletra, Flavio; Girotto, Giorgia
The Contribution of Genetics to Muscle Disuse, Retraining, and Aging
2022-01-01 Sirago, Giuseppe; Picca, Anna; Giacomello, Emiliana; Marzetti, Emanuele; Toniolo, Luana
Development and Validation of MPS-Based System for Human Appearance Prediction in Challenging Forensic Samples
2022-01-01 Melchionda, Filomena; Silvestrini, Beatrice; Robino, Carlo; Bini, Carla; Fattorini, Paolo; Martinez-Labarga, Cristina; De Angelis, Flavio; Tagliabracci, Adriano; Turchi, Chiara
Eye and Hair Color Prediction of Ancient and Second World War Skeletal Remains Using a Forensic PCR-MPS Approach
2022-01-01 Zupanič Pajnič, Irena Zupanič; Zupanc, Tomaž; Leskovar, Tamara; Črešnar, Matija; Fattorini, Paolo
The Genetic Diagnosis of Ultrarare DEEs: An Ongoing Challenge
2022-01-01 Musante, Luciana; Costa, Paola; Zanus, Caterina; Faletra, Flavio; Murru, Flora M.; Bianco, Anna M.; La Bianca, Martina; Ragusa, Giulia; Athanasakis, Emmanouil; D’Adamo, Adamo P.; Carrozzi, Marco; Gasparini, Paolo
Genetic dissection of temperament personality traits in Italian isolates
2022-01-01 Concas, M. P.; Minelli, A.; Aere, S.; Morgan, A.; Tesolin, P.; Gasparini, P.; Gennarelli, M.; Girotto, G.
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders
2023-01-01 Di Stazio, Mariateresa; Zanus, Caterina; Faletra, Flavio; Pesaresi, Alessia; Ziccardi, Ilaria; Morgan, Anna; Girotto, Giorgia; Costa, Paola; Carrozzi, Marco; D’Adamo, Adamo P.; Musante, Luciana
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability
2021-01-01 Concas, Maria Pina; Morgan, Anna; Serra, Fabrizio; Nagtegaal, Andries Paul; Oosterloo, Berthe C.; Seshadri, Sudha; Heard-Costa, Nancy; Van Camp, Guy; Fransen, Erik; Francescatto, Margherita; Logroscino, Giancarlo; Sardone, Rodolfo; Quaranta, Nicola; Gasparini, Paolo; Girotto, Giorgia
Lights and shadows in the genetics of syndromic and non-syndromic hearing loss in the Italian population
2020-01-01 Morgan, A.; Lenarduzzi, S.; Spedicati, B.; Cattaruzzi, E.; Murru, F. M.; Pelliccione, G.; Mazza, D.; Zollino, M.; Graziano, C.; Ambrosetti, U.; Seri, M.; Faletra, F.; Girotto, G.
Non-syndromic autosomal dominant hearing loss: The first italian family carrying a mutation in the NCOA3 gene
2021-01-01 Tesolin, P.; Morgan, A.; Notarangelo, M.; Ortore, R. P.; Concas, M. P.; Notarangelo, A.; Girotto, G.
Ophthalmologic Manifestations of Primary Sjögren’s Syndrome
2021-01-01 Maria Roszkowska, Anna; William Oliverio, Giovanni; Aragona, Emanuela; Inferrera, Leandro; Antonella Severo, Alice; Alessandrello, Federica; Spinella, Rosaria; Imelde Postorino, Elisa; Aragona, Pasquale
Pendred syndrome, or not pendred syndrome? That is the question
2021-01-01 Tesolin, P.; Fiorino, S.; Lenarduzzi, S.; Rubinato, E.; Cattaruzzi, E.; Ammar, L.; Castro, V.; Orzan, E.; Granata, C.; Dell'Orco, D.; Morgan, A.; Girotto, G.
Pharmacogenomics and personalized medicine
2020-01-01 Cecchin, E.; Stocco, G.
The role of knockout olfactory receptor genes in odor discrimination
2021-01-01 Concas, M. P.; Cocca, M.; Francescatto, M.; Battistuzzi, T.; Spedicati, B.; Feresin, A.; Morgan, A.; Gasparini, P.; Girotto, G.
SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome
2022-01-01 Migliore, C.; Vendramin, A.; Mckee, S.; Prontera, P.; Faravelli, F.; Sachdev, R.; Dias, P.; Mascaro, M.; Licastro, D.; Meroni, G.
Transient Receptor Potential Ankyrin 1 (TRPA1) Methylation and Chronic Pain: A Systematic Review
2023-01-01 Celsi, Fulvio; Peri, Francesca; Cavasin, Julia; Zupin, Luisa; Cozzi, Giorgio; Barbi, Egidio; Crovella, Sergio
Unraveling the Epigenetic Tapestry: Decoding the Impact of Epigenetic Modifications in Hidradenitis Suppurativa Pathogenesis
2023-01-01 Nardacchione, Elena Maria; Tricarico, Paola Maura; Moura, Ronald; D’Adamo, Adamo Pio; Thasneem, Ayshath; Suleman, Muhammad; Marzano, Angelo Valerio; Crovella, Sergio; Moltrasio, Chiara
Unveiling the Impact of Gene Presence/Absence Variation in Driving Inter-Individual Sequence Diversity within the CRP-I Gene Family in Mytilus spp
2023-01-01 Gualandi, Nicolò; Fracarossi, Davide; Riommi, Damiano; Sollitto, Marco; Greco, Samuele; Mardirossian, Mario; Pacor, Sabrina; Hori, Tiago; Pallavicini, Alberto; Gerdol, Marco
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