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Publications by N. Jabrane-Ferrat
Mutations in the Bare Lymphocyte Syndrome Define Critical Steps in the Assembly of the Regulatory Factor X Complex
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Related publications
Associations and Interactions Between Bare Lymphocyte Syndrome Factors
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Three Classes of Mutations in the a Subunit of the CCAAT-binding Factor CBF Delineate Functional Domains Involved in the Three-Step Assembly of the CBF-DNA Complex.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Self-Assembly and DNA Binding of the Blocking Factor in X Chromosome Inactivation
PLoS Computational Biology
Molecular Neuroscience
Evolution
Ecology
Genetics
Behavior
Molecular Biology
Systematics
Simulation
Cellular
Computational Theory
Mathematics
Modeling
Phosphomimetic Mutations Increase Phospholamban Oligomerization and Alter the Structure of Its Regulatory Complex
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Bare Lymphocyte Syndrome. Consequences of Absent Class II Major Histocompatibility Antigen Expression for B Lymphocyte Differentiation and Function.
Journal of Clinical Investigation
Medicine
Taking STEPs Forward to Understand Fragile X Syndrome
Results and Problems in Cell Differentiation
Developmental Biology
Cell Biology
Mutations in the Dynein Assembly Factor PF22 (DNAAF3) Cause Primary Ciliary Dyskinesia With Absent Dynein Arms
Cilia
Cell Biology
Mutations in the Wolfram Syndrome Type 1 Gene (WFS1) Define a Clinical Entity of Dominant Low-Frequency Sensorineural Hearing Loss
Archives of Otolaryngology–Head & Neck Surgery
Spectrum of Mutations in the OCRL1Gene in the Lowe Oculocerebrorenal Syndrome
American Journal of Human Genetics
Genetics
