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Publications by Laryssa A. Huryn
Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome
American Journal of Human Genetics
Genetics
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Functional Analyses of Mutations in Receptor Tyrosine Kinase Genes in Non-Small Cell Lung Cancer: Double-Edged Sword of DDR2
Clinical Cancer Research
Cancer Research
Oncology
Germline-Activating RRAS2 Mutations Cause Noonan Syndrome
American Journal of Human Genetics
Genetics
Receptor Tyrosine Kinase (RTK); VEGF-A
Science-Business eXchange
Receptor Tyrosine Kinase–like Orphan Receptor 1 (ROR1)
Science-Business eXchange
AXL Receptor Tyrosine Kinase (AXL; UFO)
Science-Business eXchange
A Tyrosine Kinase-Activating Variant Asn666Ser in PDGFRB Causes a Progeria-Like Condition in the Severe End of Penttinen Syndrome
European Journal of Human Genetics
Genetics
The Activating C-Type Lectin-Like Receptor NKp65 Signals Through a Hemi-Immunoreceptor Tyrosine-Based Activation Motif (hemITAM) and Spleen Tyrosine Kinase (Syk)
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Tyrosine Kinase Signalling in Breast Cancer: ErbB Family Receptor Tyrosine Kinases
Breast Cancer Research
Cancer Research
Oncology
Clinical Outcomes of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Recurrent Adenosquamous Carcinoma of the Lung After Resection
OncoTargets and Therapy
Oncology
Pharmacology
