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Publications by Anne Camminady
HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1−/− Mice
American Journal of Human Genetics
Genetics
Related publications
A Novel Loss-Of-Function Mutation in HOXB1 Associated With Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family
Molecular Syndromology
Genetics
Cross-Regulation in the Mouse HoxB Complex: The Expression of Hoxb2 in Rhombomere 4 Is Regulated by Hoxb1.
Genes and Development
Genetics
Developmental Biology
Neuronal Defects in the Hindbrain of Hoxa1, Hoxb1 and Hoxb2 Mutants Reflect Regulatory Interactions Among These Hox Genes
Development (Cambridge)
Developmental Biology
Molecular Biology
Chick Lrrn2, a Novel Downstream Effector of Hoxb1 and Shh, Functions in the Selective Targeting of Rhombomere 4 Motor Neurons
Neural Development
Developmental Neuroscience
A Subset of Noradrenergic (NE) Neurons Defined by Developmental Expression of Hoxb1 Have a Distinct Role in Attenuating the Behavioral Response to Acute Stress
Molecular Psychiatry
Psychiatry
Molecular Neuroscience
Mental Health
Molecular Biology
Cellular
Generation and Phenotype of Mice Harboring a Nonsense Mutation in the V2 Vasopressin Receptor Gene
Journal of Clinical Investigation
Medicine
COL4A1 Mutation: Expansion of the Phenotype
Pediatric Research
Child Health
Pediatrics
Perinatology
The Phospholamban p.Arg14del Founder Mutation in Dutch Patients With Arrhythmogenic Cardiomyopathy
Netherlands Heart Journal
Cardiovascular Medicine
Cardiology
Inactivation of Lkb1 and Pten in Mice Recapitulates Human Lung SCC
Cancer Discovery
Oncology
