W. Giblin

发表

rearrangements due to a hypomorphic RAG1 mutation Leaky severe combined immunodeficiency and aberrant DNA

F. Alt, D. Schatz, D. Ferguson, 2009 .

The deacylase SIRT5 supports melanoma viability by regulating chromatin dynamics

Erika L. Varner, M. Rivera, Ho-Joon Lee, 2020, bioRxiv.

Sirtuin 6 Builds a Wall Against Inflammation, Trumping Diabetes

D. Lombard, W. Giblin, 2017, Diabetes.

Leaky SCID and aberrant DNA rearrangements due to a hypomorphic RAG1 mutation

F. Alt, D. Ferguson, Hwei-Ling Cheng, 2008 .

Cutaneous lesions of hemophagocytic syndrome in a patient with T-cell lymphoma and active Epstein-Barr infection.

K. Smith, H. Skelton, W. James, 1991, Journal of the American Academy of Dermatology.

A Recurrent Loss‐of‐Function Alanyl‐tRNA Synthetase (AARS) Mutation in Patients with Charcot‐Marie‐Tooth Disease Type 2N (CMT2N)

J. Lupski, Yi-Chung Lee, S. Züchner, 2014 .

Sirtuins: guardians of mammalian healthspan.

D. Lombard, M. Skinner, W. Giblin, 2014, Trends in genetics : TIG.

Sirtuins, healthspan, and longevity in mammals

D. Lombard, W. Giblin, 2021, Handbook of the Biology of Aging.

A Role for Sirtuins in Maintaining Mammalian Lifespan and Healthspan

W. Giblin, 2017 .

The deacylase SIRT5 supports melanoma viability by influencing chromatin dynamics.

Erika L. Varner, M. Rivera, Ho-Joon Lee, 2021, The Journal of clinical investigation.

Leaky severe combined immunodeficiency and aberrant DNA rearrangements due to a hypomorphic RAG1 mutation.

F. Alt, D. Schatz, D. Ferguson, 2009, Blood.

A hypomorphic Artemis human disease allele causes aberrant chromosomal rearrangements and tumorigenesis.

Tehmina Masud, Gerwin H. Westfield, J. Sekiguchi, 2011, Human molecular genetics.

Impact of a hypomorphic Artemis disease allele on lymphocyte development, DNA end processing, and genome stability

Gerwin H. Westfield, J. Sekiguchi, W. Giblin, 2009, The Journal of experimental medicine.

A Recurrent loss‐of‐function alanyl‐tRNA synthetase (AARS ) mutation in patients with charcot‐marie‐tooth disease type 2N (CMT2N)

J. Lupski, Yi-Chung Lee, S. Züchner, 2012, Human mutation.

The deacylase sirtuin 5 reduces malonylation in nonmitochondrial metabolic pathways in diabetic kidney disease

V. Nair, J. Hodgin, M. Kretzler, 2023, The Journal of biological chemistry.

Diverse Roles for SIRT6 in Mammalian Healthspan and Longevity

D. Lombard, Bernadette M. M. Zwaans, W. Giblin, 2016 .