A. R. Duncan

发表

RAPGEF5 regulates nuclear translocation of β-catenin

M. Khokha, Woong Y. Hwang, John N. Griffin, 2017, bioRxiv.

RAPGEF 5 Regulates Nuclear Translocation of b-Catenin Graphical Abstract Highlights

M. Khokha, Woong Y. Hwang, John N. Griffin, 2017 .

RAPGEF5 regulates nuclear translocation of β-catenin

M. Khokha, John N. Griffin, Karen J. Liu, 2017, bioRxiv.

COVID-19: neonatal–perinatal perspectives

Emily M. Herzberg, K. Leeman, Ravikiran M. Raju, 2020, Journal of Perinatology.

Ontogeny and the effects of exogenous and endogenous glucocorticoids on tight junction protein expression in ovine cerebral cortices

A. R. Duncan, B. Stonestreet, G. Sadowska, 2009, Brain Research.

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.

P. Grant, N. Brunetti‐Pierri, D. Calame, 2022, American journal of human genetics.

Homozygous nonsense mutation in SGCA is a common cause of limb‐girdle muscular dystrophy in Assiut, Egypt

M. Lek, D. Macarthur, L. Kunkel, 2016, Muscle & nerve.

De novo variants in MPP5 cause global developmental delay and behavioral changes.

Seonhee Kim, P. Grant, D. Harris, 2020, Human molecular genetics.

Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects.

C. Lelliott, B. Yalcin, P. Grant, 2020, American journal of human genetics.

Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores

L. Kunkel, J. Mendell, C. Bönnemann, 2012, neurogenetics.

Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE

L. Kunkel, P. Kang, H. Lidov, 2011, BMC Medical Genetics.

Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy.

M. Khokha, A. R. Duncan, 2016, Seminars in cell & developmental biology.

The Heterotaxy Candidate Gene, Tmem195, Regulates Nuclear Localization Of Beta-Catenin

A. R. Duncan, 2015 .

Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders.

Jill A. Madden, P. Grant, A. O’Donnell-Luria, 2021, American journal of human genetics.

Alkylglycerol monooxygenase, a heterotaxy candidate gene, regulates left-right patterning via Wnt signaling.

M. Khokha, F. del Viso, A. R. Duncan, 2019, Developmental biology.

Efficient identification of novel mutations in patients with limb girdle muscular dystrophy

L. Kunkel, P. Kang, R. R. Bennett, 2010, neurogenetics.

Homozygous nonsense mutation in SGCA is a common cause of limb‐girdle muscular dystrophy in Assiut, Egypt

M. Lek, D. Macarthur, L. Kunkel, 2016, Muscle & nerve.