Jonathan Crain

发表

Not by systems alone: identifying functional outliers in rare disease pedigrees

G. Lyon, J. Gillis, Sara Ballouz, 2017 .

Not by systems alone: replicability assessment of disease expression signals

G. Lyon, J. Gillis, Sara Ballouz, 2018 .

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations

Edward Yang, Laurence Faivre, Jillian S Parboosingh, 2015, American journal of human genetics.

Proteomic and genomic characterization of a yeast model for Ogden syndrome

G. Lyon, Jonathan Crain, Han Fang, 2016, bioRxiv.

Conformational Changes in Actinin-type Actin Binding Domains: Probing Actininduced Structural Dynamics in Dystrophin and Utrophin using EPR Spectroscopy

Jonathan Crain, 2014 .

Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway

Tae-Young Roh, T. Arnesen, G. Lyon, 2020, bioRxiv.

Naa 12 rescues embryonic lethality in Naa 10-Deficient Mice in the amino-1 terminal acetylation pathway 2 3

Ronen, Tae-Young Roh, T. Arnesen, 2020 .

Naa12 rescues embryonic lethality in Naa10-Deficient Mice in the amino-terminal acetylation pathway

Ronen, Tae-Young Roh, T. Arnesen, 2020 .

Mapping functional humoral correlates of protection against malaria challenge following RTS,S/AS01 vaccination

D. Lauffenburger, J. Weiner, Jishnu Das, 2020, Science Translational Medicine.

A human β-III-spectrin spinocerebellar ataxia type 5 mutation causes high-affinity F-actin binding

David D. Thomas, Jonathan Crain, T. Hays, 2016, Scientific Reports.