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International Journal of Molecular Sciences|December 24, 2021
Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman-Diamond Syndrome SubjectsAnnalisa Frattini, Simona Bolamperti, Roberto Valli, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 20, 2005
Polymorphisms of the CLCN7 gene are associated with BMD in womenUlrika Pettersson, Omar M E Albagha, Max Mirolo, et al.BMC Genomics|June 25, 2017
Genome-wide analysis of DNA methylation in hypothalamus and ovary of Capra hircusStefano Frattini, Emanuele Capra, Barbara Lazzari, et al.Neurogenetics|February 24, 2025
Axonal motor polyneuropathy in a 13 years old Girl with a de Novo variant in ADNPSara Scaccini, Carlo Alberto Cesaroni, Stefano Giuseppe Caraffi, et al.Brain Sciences|March 6, 2021
Manic and Depressive Symptoms in Children Diagnosed with Noonan SyndromePaolo Alfieri, Francesca Cumbo, Giulia Serra, et al.Tumori|May 24, 2014
Circulating free DNA in a screening program for early colorectal cancer detectionFederica Perrone, Andrea Lampis, Claudia Bertan, et al.Nature|August 21, 2020
Quantum error correction of a qubit encoded in grid states of an oscillatorP Campagne-Ibarcq, A Eickbusch, S Touzard, et al.American Journal of Medical Genetics. Part A|September 5, 2024
Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literatureChiara Brugnoli, Susanna Rizzi, Carlo Alberto Cesaroni, et al.Molecular Cytogenetics|November 25, 2021
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variationsAbdul Waheed Khan, Alyssa Kennedy, Elissa Furutani, et al.Genome Medicine|July 26, 2018
Single-cell transcriptome analysis of lineage diversity in high-grade gliomaJinzhou Yuan, Hanna Mendes Levitin, Veronique Frattini, et al.Pageof 80