Showing results (841-850 of 978) with videos related to

Sort By:
Pageof 98
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.
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.
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.
The Journal of Biological Chemistry|August 7, 2026
p62/SQSTM1-KEAP1 complex prevents clearance of ubiquitinated Z alpha-1 antitrypsin and aggravates liver proteotoxicityNunzia Pastore, Sergio Attanasio, Francesco Annunziata, 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.
The Journal of Clinical Endocrinology and Metabolism|November 3, 2020
Clinical and Functional Consequences of C-Terminal Variants in MCT8: A Case SeriesFerdy S van Geest, Marcel E Meima, Kyra E Stuurman, et al.
Pageof 98