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Publications by K. Mesbah
Mutation in the Trap /Ssr1 Gene, Encoding Translocon-Associated Protein , Results in Outflow Tract Morphogenetic Defects
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Related publications
Homozygous Missense N629D hERG (KCNH2) Potassium Channel Mutation Causes Developmental Defects in the Right Ventricle and Its Outflow Tract and Embryonic Lethality
Circulation Research
Cardiovascular Medicine
Physiology
Cardiology
The Mouse Bone Morphogenetic Protein-4 Gene
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Hereditary Spastic Paraplegia SPG13 Is Associated With a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60
American Journal of Human Genetics
Genetics
A Gene Trap Knockout of the Tiam-1 Protein Results in Malformation of the Early Embryonic Brain
Molecules and Cells
Medicine
Cell Biology
Molecular Biology
Role of the DLGAP2 Gene Encoding the SAP90/PSD-95-Associated Protein 2 in Schizophrenia
PLoS ONE
Multidisciplinary
deaD, a New Escherichia Coli Gene Encoding a Presumed ATP-dependent RNA Helicase, Can Suppress a Mutation in rpsB, the Gene Encoding Ribosomal Protein S2.
Journal of Bacteriology
Microbiology
Molecular Biology
Long Distance Lipid: Protein Coupling in the Protein Translocon
Biophysical Journal
Biophysics
Benign Neoplasms in the Right Ventricular Outflow Tract
Baylor University Medical Center Proceedings
Medicine
Biallelic Mutations in LRRC56, Encoding a Protein Associated With Intraflagellar Transport, Cause Mucociliary Clearance and Laterality Defects
American Journal of Human Genetics
Genetics
