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Publications by Katja Kloth
Activating Mutations in PAK1, Encoding P21-Activated Kinase 1, Cause a Neurodevelopmental Disorder
American Journal of Human Genetics
Genetics
Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome
American Journal of Human Genetics
Genetics
Related publications
P21 Protein (Cdc42 Rac)-Activated Kinase 1 (PAK1)
Science-Business eXchange
LKB1 Suppresses P21-Activated Kinase-1 (PAK1) by Phosphorylation of Thr109in the P21-Binding Domain
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
The Role of the Pleckstrin Homology Domain-Containing Protein CKIP-1 in Activation of P21-Activated Kinase 1 (PAK1)
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Inhibition or Ablation of P21-Activated Kinase (PAK1) Disrupts Glucose Homeostatic Mechanismsin Vivo
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Mutations in LNPK , Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental Syndrome
American Journal of Human Genetics
Genetics
The P21-Activated Kinase PAK3 Forms Heterodimers With PAK1 in Brain Implementing Trans-Regulation of PAK3 Activity
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder
American Journal of Human Genetics
Genetics
P21-Activated Kinase 1: PAK’ed With Potential
Oncotarget
Oncology
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder
American Journal of Human Genetics
Genetics
