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Publications by Nicholas Katsanis
Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome That Expands the Phenotypic Spectrum of Condensinopathies
American Journal of Human Genetics
Genetics
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction
Gastroenterology
Hepatology
Gastroenterology
Endoglin Mediates Fibronectin/Α5β1 Integrin and TGF-β Pathway Crosstalk in Endothelial Cells
EMBO Journal
Immunology
Molecular Biology
Biochemistry
Microbiology
Neuroscience
Medicine
Genetics
Functional Modules, Mutational Load and Human Genetic Disease
Trends in Genetics
Genetics
Ciliopathy Proteins Regulate Paracrine Signaling by Modulating Proteasomal Degradation of Mediators
Journal of Clinical Investigation
Medicine
Dissecting Intraflagellar Transport, One Molecule at a Time
Developmental Cell
Biochemistry
Developmental Biology
Genetics
Cell Biology
Molecular Biology
Zebrafish Assays of Ciliopathies
Methods in Cell Biology
Cell Biology
The Meckel Syndrome- Associated Protein MKS1 Functionally Interacts With Components of the BBSome and IFT Complexes to Mediate Ciliary Trafficking and Hedgehog Signaling
PLoS ONE
Multidisciplinary
Loss of Function Mutations inNNTAre Associated With Left Ventricular NoncompactionCLINICAL PERSPECTIVE
Circulation: Cardiovascular Genetics
The Vertebrate Primary Cilium in Development, Homeostasis, and Disease
Cell
Biochemistry
Genetics
Molecular Biology
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