Amanote Research

Amanote Research

    RegisterSign In

Discover open access scientific publications

Search, annotate, share and cite publications


Publications by Taiki Abe

Germline-Activating RRAS2 Mutations Cause Noonan Syndrome

American Journal of Human Genetics
Genetics
2019English

Synthetic Study of Andrastins: Stereoselective Construction of the BCD-ring System

Journal of Antibiotics
Drug DiscoveryPharmacology
2019English

Related publications

Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome

American Journal of Human Genetics
Genetics
2019English

Corrigendum: Gain-Of-Function SOS1 Mutations Cause a Distinctive Form of Noonan Syndrome

Nature Genetics
Genetics
2007English

Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis

American Journal of Human Genetics
Genetics
2016English

LRIG2 Mutations Cause Urofacial Syndrome

American Journal of Human Genetics
Genetics
2013English

Noonan Syndrome

Paediatrica Indonesiana
2018English

Neurofibromatosis-Noonan Syndrome

2020English

Mutations inRIT1cause Noonan Syndrome - Additional Functional Evidence and Expanding the Clinical Phenotype

Clinical Genetics
Genetics
2015English

NF1 Gene Mutations Are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome

Journal of Neurology & Stroke
2017English

NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome

American Journal of Human Genetics
Genetics
2005English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy