Noonan Syndrome News and Research

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Noonan Syndrome (NS) is a relatively common congenital genetic condition that affects both males and females equally.
Study finds promising new treatment for infants with Noonan Syndrome

Study finds promising new treatment for infants with Noonan Syndrome

Research reviews role of protein tyrosine phosphatase in molecular biology

Research reviews role of protein tyrosine phosphatase in molecular biology

Study uncovers new mechanism controlling the master cancer regulator

Study uncovers new mechanism controlling the master cancer regulator

Researchers identify LZTR1 as evolutionarily conserved component of RAS pathway

Researchers identify LZTR1 as evolutionarily conserved component of RAS pathway

Protein researchers identify several new potential targets for cancer

Protein researchers identify several new potential targets for cancer

Alex’s experiences of living with rare genetic disease

Alex’s experiences of living with rare genetic disease

NHGRI researchers use facial recognition software to diagnose rare genetic disease

NHGRI researchers use facial recognition software to diagnose rare genetic disease

New stem-cell model of heart tissue unravels mechanisms linked to hypertrophic cardiomyopathy

New stem-cell model of heart tissue unravels mechanisms linked to hypertrophic cardiomyopathy

Study identifies genetic mutations responsible for development of cardiac hypertrophy in adults

Study identifies genetic mutations responsible for development of cardiac hypertrophy in adults

Study shows inhibition of SHP-2 enzyme can diminish lupus symptoms

Study shows inhibition of SHP-2 enzyme can diminish lupus symptoms

UAB lab to offer new tests for genetic diseases using next-generation sequencing

UAB lab to offer new tests for genetic diseases using next-generation sequencing

Scientists engineer stem cells to better understand mechanisms behind leukemia

Scientists engineer stem cells to better understand mechanisms behind leukemia

Researchers develop mouse model that reproduces most typical features of Noonan syndrome

Researchers develop mouse model that reproduces most typical features of Noonan syndrome

Medical geneticists diagnose genetic syndromes, improve children’s quality of life

Medical geneticists diagnose genetic syndromes, improve children’s quality of life

Researchers find new drug compound that treats laboratory mice with congenital heart disease

Researchers find new drug compound that treats laboratory mice with congenital heart disease

USC scientists unlock mystery of why new cases of Noonan Syndrome are so common

USC scientists unlock mystery of why new cases of Noonan Syndrome are so common

Excessive ERK activation underlies lymphatic defects in RASopathies

Excessive ERK activation underlies lymphatic defects in RASopathies

Researchers discover alternative mechanism for Ras protein activation

Researchers discover alternative mechanism for Ras protein activation

PD0325901 drug may hold potential to prevent neurofibromatosis 1 in children

PD0325901 drug may hold potential to prevent neurofibromatosis 1 in children

Researchers discover how SHP-2 genetic defect may result in heart malformation

Researchers discover how SHP-2 genetic defect may result in heart malformation