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International Journal of Molecular Sciences|April 3, 2021
Subunits of the PBAP Chromatin Remodeler Are Capable of Mediating Enhancer-Driven Transcription in DrosophilaYulii V Shidlovskii, Oleg V Bylino, Alexander V Shaposhnikov, et al.
Biomolecules|May 27, 2023
Deep Intronic LINE-1 Insertions in NF1: Expanding the Spectrum of Neurofibromatosis Type 1-Associated RearrangementsViola Alesi, Silvia Genovese, Francesca Romana Lepri, et al.
Scientific Reports|June 16, 2023
Analysis of gut microbiota in patients with Williams-Beuren Syndrome reveals dysbiosis linked to clinical manifestationsFederica Del Chierico, Valeria Marzano, Matteo Scanu, et al.
Molecular Plant-Microbe Interactions : MPMI|May 31, 2013
Tomato below ground-above ground interactions: Trichoderma longibrachiatum affects the performance of Macrosiphum euphorbiae and its natural antagonistsDonatella Battaglia, Simone Bossi, Pasquale Cascone, et al.
Genes, Brain, and Behavior|April 6, 2017
Visual perception skills: a comparison between patients with Noonan syndrome and 22q11.2 deletion syndromeG Piccini, D Menghini, A D'Andrea, et al.
Clinical Genetics|October 2, 2009
Mild ring 17 syndrome shares common phenotypic features irrespective of the chromosomal breakpoints locationC Surace, S Piazzolla, P Sirleto, et al.
The Journal of Biological Chemistry|June 6, 2003
SAMP14, a novel, acrosomal membrane-associated, glycosylphosphatidylinositol-anchored member of the Ly-6/urokinase-type plasminogen activator receptor superfamily with a role in sperm-egg interactionJagathpala Shetty, Michael J Wolkowicz, Laura C Digilio, et al.
Neurogenetics|April 13, 2011
FGF17, a gene involved in cerebellar development, is downregulated in a patient with Dandy-Walker malformation carrying a de novo 8p deletionGinevra Zanni, Sabina Barresi, Lorena Travaglini, et al.
American Journal of Medical Genetics. Part A|October 24, 2020
Atypical 7q11.23 deletions excluding ELN gene result in Williams-Beuren syndrome craniofacial features and neurocognitive profileViola Alesi, Sara Loddo, Valeria Orlando, et al.
American Journal of Medical Genetics. Part A|September 30, 2014
Identification of TBX5 mutations in a series of 94 patients with Tetralogy of FallotAnwar Baban, Alex Vincent Postma, Monica Marini, et al.
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