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Human Mutation|June 20, 2003
Severe hypophosphatasia: characterization of fifteen novel mutations in the ALPL geneM Spentchian, Y Merrien, M Herasse, et al.Nature Genetics|February 12, 2008
Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)David Geneviève, Valérie Proulle, Bertrand Isidor, et al.Cancer Immunology, Immunotherapy : CII|July 14, 2018
Interactions among myeloid regulatory cells in cancerViktor Umansky, Gosse J Adema, Jaroslaw Baran, et al.Nature Cell Biology|February 12, 2024
Biomolecular condensation orchestrates clathrin-mediated endocytosis in plantsJonathan Michael Dragwidge, Yanning Wang, Lysiane Brocard, et al.Nature Genetics|May 20, 2003
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosinEtgar Levy-Nissenbaum, Regina C Betz, Moshe Frydman, et al.Journal of the American College of Emergency Physicians Open|January 26, 2022
Temporal trends in reperfusion therapy for patients with acute ischemic strokeCarlos El Khoury, Corine Aboa-Eboule, Laurie Fraticelli, et al.American Journal of Human Genetics|March 31, 2009
TMEM126A, encoding a mitochondrial protein, is mutated in autosomal-recessive nonsyndromic optic atrophySylvain Hanein, Isabelle Perrault, Olivier Roche, et al.Bulletin Du Cancer|April 12, 2023
[Treatments for rare ovarian tumors: What's new?]Coriolan Lebreton, Stanislas Quesada, Marta Bini, et al.Journal of Adolescent and Young Adult Oncology|July 14, 2025
The UNI-AJA Project: A Feasibility Study Based on Real-World Data in French Adolescents and Young Adults with CancerEmmanuel Desandes, Alizée Diatchenko, Hugo Crochet, et al.Advanced Materials (Deerfield Beach, Fla.)|July 21, 2015
Design of hydrophilic metal organic framework water adsorbents for heat reallocationAmandine Cadiau, Ji Sun Lee, Daiane Damasceno Borges, et al.Pageof 185