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Publications by Adolfo Cavalié
Plasma Cell Deficiency in Humans With Heterozygous Mutations in SEC61A1
Journal of Allergy and Clinical Immunology
Allergy
Immunology
TRP4 (CCE1) Protein Is Part of Native Calcium Release-Activated Ca2+-Like Channels in Adrenal Cells
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Related publications
Cortisone-Reductase Deficiency Associated With Heterozygous Mutations in 11 -Hydroxysteroid Dehydrogenase Type 1
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Heterozygous Mylk3 Knockout Mice Partially Recapitulate Human DCM With Heterozygous MYLK3 Mutations
Frontiers in Physiology
Physiology
B-Cell Activating Factor Receptor Deficiency Is Associated With an Adult-Onset Antibody Deficiency Syndrome in Humans
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Pyogenic Bacterial Infections in Humans With MyD88 Deficiency
Pediatrics
Child Health
Pediatrics
Perinatology
Molecular and Phenotypic Abnormalities in Individuals With Germline Heterozygous PTEN Mutations and Autism
Molecular Psychiatry
Psychiatry
Molecular Neuroscience
Mental Health
Molecular Biology
Cellular
Lineage Tracing in Humans Enabled by Mitochondrial Mutations and Single-Cell Genomics
Cell
Biochemistry
Genetics
Molecular Biology
Novel Heterozygous Mutations in JAG1 and NOTCH2 Genes in a Neonatal Patient With Alagille Syndrome
Case Reports in Pediatrics
Transcobalamin II Deficiency in Four Cases With Novel Mutations
Turkish Journal of Haematology
Hematology
APC Mutations in Colorectal Tumors With Mismatch Repair Deficiency.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary