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Publications by Karl Martin Klein
A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy
American Journal of Human Genetics
Genetics
Burden-Of-Illness and Cost-Driving Factors in Dravet Syndrome Patients and Carers: A Prospective, Multicenter Study From Germany
European Journal of Paediatric Neurology
Medicine
Child Health
Neurology
Pediatrics
Perinatology
Related publications
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis
American Journal of Human Genetics
Genetics
Phosphoinositide Regulation of Clathrin-Mediated Endocytosis
Biochemical Society Transactions
Biochemistry
Clathrin-Mediated Endocytosis Is Inhibited During Mitosis
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Cargo- And Adaptor-Specific Mechanisms Regulate Clathrin-Mediated Endocytosis
Journal of Cell Biology
Medicine
Cell Biology
Mechanoregulation of Clathrin-Mediated Endocytosis in Isolated Cells and Developing Tissues
Biophysical Journal
Biophysics
A Functional GFP Fusion for Imaging Clathrin-Mediated Endocytosis
Traffic
Biochemistry
Genetics
Cell Biology
Molecular Biology
Structural Biology
Ikarugamycin: A Natural Product Inhibitor of Clathrin-Mediated Endocytosis
Traffic
Biochemistry
Genetics
Cell Biology
Molecular Biology
Structural Biology
Rapid and Efficient Clathrin-Mediated Endocytosis Revealed in Genome-Edited Mammalian Cells
Nature Cell Biology
Cell Biology
Control of Clathrin-Mediated Endocytosis by NIMA Family Kinases
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
