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Genes|January 12, 2021
Comparative Genomics Provides Insights into the Taxonomy of Azoarcus and Reveals Separate Origins of Nif Genes in the Proposed Azoarcus and Aromatoleum GeneraRoberto Tadeu Raittz, Camilla Reginatto De Pierri, Marta Maluk, et al.
Chest|July 22, 2021
Neonatal Lung Ultrasound and Surfactant Administration: A Pragmatic, Multicenter StudyFrancesco Raimondi, Fiorella Migliaro, Iuri Corsini, et al.
Archives of Oral Biology|June 25, 2013
Genes expressed in dental enamel development are associated with molar-incisor hypomineralizationFabiano Jeremias, Mine Koruyucu, Erika C Küchler, et al.
Oncology Letters|August 7, 2012
Therapy of Hodgkin's lymphoma in clinical practice: A retrospective long-term follow-up analysisSara Aquino, Marino Clavio, Edoardo Rossi, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|February 28, 2013
Next-generation sequencing for disorders of low and high bone mineral densityG Sule, P M Campeau, V W Zhang, et al.
American Journal of Medical Genetics. Part A|February 14, 2013
Maternal vitamin K deficient embryopathy: association with hyperemesis gravidarum and Crohn diseaseHelga V Toriello, Miriam Erick, Jean-Luc Alessandri, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 13, 2015
APO866 Increases Antitumor Activity of Cyclosporin-A by Inducing Mitochondrial and Endoplasmic Reticulum Stress in Leukemia CellsAntonia Cagnetta, Irene Caffa, Chirag Acharya, et al.
Genes|July 2, 2021
The TNFRSF13C H159Y Variant Is Associated with Severe COVID-19: A Retrospective Study of 500 Patients from Southern ItalyRoberta Russo, Immacolata Andolfo, Vito Alessandro Lasorsa, et al.
Iscience|March 22, 2021
Common variants at 21q22.3 locus influence MX1 and TMPRSS2 gene expression and susceptibility to severe COVID-19Immacolata Andolfo, Roberta Russo, Vito Alessandro Lasorsa, et al.
The Journal of Clinical Investigation|November 9, 2023
Hypomorphic variants of SEL1L-HRD1 ER-associated degradation are associated with neurodevelopmental disordersHuilun H Wang, Liangguang L Lin, Zexin J Li, et al.
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