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Publications by Taiki Abe
Germline-Activating RRAS2 Mutations Cause Noonan Syndrome
American Journal of Human Genetics
Genetics
Synthetic Study of Andrastins: Stereoselective Construction of the BCD-ring System
Journal of Antibiotics
Drug Discovery
Pharmacology
Related publications
Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome
American Journal of Human Genetics
Genetics
Corrigendum: Gain-Of-Function SOS1 Mutations Cause a Distinctive Form of Noonan Syndrome
Nature Genetics
Genetics
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis
American Journal of Human Genetics
Genetics
LRIG2 Mutations Cause Urofacial Syndrome
American Journal of Human Genetics
Genetics
Noonan Syndrome
Paediatrica Indonesiana
Neurofibromatosis-Noonan Syndrome
Mutations inRIT1cause Noonan Syndrome - Additional Functional Evidence and Expanding the Clinical Phenotype
Clinical Genetics
Genetics
NF1 Gene Mutations Are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome
Journal of Neurology & Stroke
NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome
American Journal of Human Genetics
Genetics