Differential Allelic Expression of SOS1 and Hyperexpression of the Activating SOS1 C.755C Variant in a Noonan Syndrome Family

European Journal of Human Genetics - United Kingdom
doi 10.1038/ejhg.2015.20
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

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

Nature Genetics
Genetics
2007English

Loss of Halophytism by Interference With SOS1 Expression

Plant Physiology
Plant ScienceGeneticsPhysiology
2009English

Cytogenetic Analysis and Examination of SOS1 Gene Mutation in a Turkish Family With Hereditary Gingival Fibromatosis

Journal of Hard Tissue Biology
Sports MedicineCell BiologyBiochemistryOrthopedicsBiomaterialsDentistryMedicine
2009English

Direct Inhibition of Oncogenic KRAS by Hydrocarbon-Stapled SOS1 Helices

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2015English

Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome

American Journal of Human Genetics
Genetics
2019English

Structure Based Search for Multiple Binding Sites of SOS1 PR Domain Recognizes an Uncovered Motif Favoring GRB2-SOS1 Association

Biophysical Journal
Biophysics
2019English

Germline-Activating RRAS2 Mutations Cause Noonan Syndrome

American Journal of Human Genetics
Genetics
2019English

Characterization of GRB2 and SOS1 Binding Downstream of TCR Activation

English

miR-124 Inhibits the Growth of Glioblastoma Through the Downregulation of SOS1

Molecular Medicine Reports
OncologyGeneticsMolecular BiologyBiochemistryCancer ResearchMolecular Medicine
2013English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy