Teisha Y. Bradshaw

Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension

Talat Nasim, Takeshi Ogo, Mohammad Ejaz Ahmed et al. · Human Mutation · 2011 · 185 citations

Genetics, Pulmonary Hypertension, Molecular Genetics +18

Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies

Laura Southgate, Rajiv D. Machado, Katie Snape et al. · The American Journal of Human Genetics · 2011 · 117 citations · Full text

Limb Anomalies, Signal Transduction, Signaling Pathway +7

Altered organization of the intermediate filament cytoskeleton and relocalization of proteostasis modulators in cells lacking the ataxia protein sacsin

Emma J. Duncan, Roxanne Larivière, Teisha Y. Bradshaw et al. · Human Molecular Genetics · 2017 · 65 citations · Full text

A reduction in Drp1-mediated fission compromises mitochondrial health in autosomal recessive spastic ataxia of Charlevoix Saguenay

Teisha Y. Bradshaw, Lisa E. L. Romano, Emma J. Duncan et al. · Human Molecular Genetics · 2016 · 61 citations · Full text

Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction

Avinaash Maharaj, Jack Williams, Teisha Y. Bradshaw et al. · The Journal of Steroid Biochemistry and Molecular Biology · 2020 · 26 citations · Full text

Hela Cell Lines, Mitophagy, Biochemistry +12