Works matching AU Sher, Roger B.

Results: 13

Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease.

Published in:

PLoS ONE, 2022, v. 17, n. 9, p. 1, doi. 10.1371/journal.pone.0274615

By:

Alexander, Guillermo M.;
Heiman-Patterson, Terry D.;
Bearoff, Frank;
Sher, Roger B.;
Hennessy, Laura;
Terek, Shannon;
Caccavo, Nicole;
Cox, Gregory A.;
Philip, Vivek M.;
Blankenhorn, Elizabeth A.

Publication type:

Article

A major QTL on mouse chromosome 17 resulting in lifespan variability in SOD1-G93A transgenic mouse models of amyotrophic lateral sclerosis.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2014, v. 15, n. 7/8, p. 588, doi. 10.3109/21678421.2014.932381

By:

Sher, Roger B.;
Heiman-Patterson, Terry D.;
Blankenhorn, Elizabeth A.;
Jiang, Juliann;
Alexander, Guillermo;
Deitch, Jeffrey S.;
Cox, Gregory A.

Publication type:

Article

Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 19, p. 2801, doi. 10.1093/hmg/ddi313

By:

Huebsch, Kimberly A.;
Kudryashova, Elena;
Wooley, Christine M.;
Sher, Roger B.;
Seburn, Kevin L.;
Spencer, Melissa J.;
Cox, Gregory A.

Publication type:

Article

Embryonic Exposure to the Environmental Neurotoxin BMAA Negatively Impacts Early Neuronal Development and Progression of Neurodegeneration in the Sod1-G93R Zebrafish Model of Amyotrophic Lateral Sclerosis.

Published in:

Toxicological Sciences, 2017, v. 157, n. 1, p. 129, doi. 10.1093/toxsci/kfx020

By:

Powers, Samantha;
Kwok, Samantha;
Lovejoy, Emily;
Lavin, Tom;
Sher, Roger B.

Publication type:

Article

The SATB1‐MIR22‐GBA axis mediates glucocerebroside accumulation inducing a cellular senescence‐like phenotype in dopaminergic neurons.

Published in:

Aging Cell, 2024, v. 23, n. 4, p. 1, doi. 10.1111/acel.14077

By:

Russo, Taylor;
Kolisnyk, Benjamin;
B. S., Aswathy;
Plessis‐Belair, Jonathan;
Kim, Tae Wan;
Martin, Jacqueline;
Ni, Jason;
Pearson, Jordan A.;
Park, Emily J.;
Sher, Roger B.;
Studer, Lorenz;
Riessland, Markus

Publication type:

Article

Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.

Published in:

2020

By:

Martin, Paige B.;
Kigoshi-Tansho, Yu;
Sher, Roger B.;
Ravenscroft, Gianina;
Stauffer, Jennifer E.;
Kumar, Rajesh;
Yonashiro, Ryo;
Müller, Tina;
Griffith, Christopher;
Allen, William;
Pehlivan, Davut;
Harel, Tamar;
Zenker, Martin;
Howting, Denise;
Schanze, Denny;
Faqeih, Eissa A.;
Almontashiri, Naif A. M.;
Maroofian, Reza;
Houlden, Henry;
Mazaheri, Neda

Publication type:

Correction Notice

NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.

Published in:

Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18327-6

By:

Martin, Paige B.;
Kigoshi-Tansho, Yu;
Sher, Roger B.;
Ravenscroft, Gianina;
Stauffer, Jennifer E.;
Kumar, Rajesh;
Yonashiro, Ryo;
Müller, Tina;
Griffith, Christopher;
Allen, William;
Pehlivan, Davut;
Harel, Tamar;
Zenker, Martin;
Howting, Denise;
Schanze, Denny;
Faqeih, Eissa A.;
Almontashiri, Naif A. M.;
Maroofian, Reza;
Houlden, Henry;
Mazaheri, Neda

Publication type:

Article

NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.

Published in:

Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18327-6

By:

Martin, Paige B.;
Kigoshi-Tansho, Yu;
Sher, Roger B.;
Ravenscroft, Gianina;
Stauffer, Jennifer E.;
Kumar, Rajesh;
Yonashiro, Ryo;
Müller, Tina;
Griffith, Christopher;
Allen, William;
Pehlivan, Davut;
Haral, Tamar;
Zenker, Martin;
Howting, Denise;
Schanze, Denny;
Faqeih, Eissa A.;
Almontashiri, Naif A. M.;
Maroofian, Reza;
Houlden, Henry;
Mazaheri, Neda

Publication type:

Article

Genetic Background Effects on Disease Onset and Lifespan of the Mutant Dynactin p150<sup>Glued</sup> Mouse Model of Motor Neuron Disease.

Published in:

PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0117848

By:

Heiman-Patterson, Terry D.;
Blankenhorn, Elizabeth P.;
Sher, Roger B.;
Jiang, Juliann;
Welsh, Priscilla;
Dixon, Meredith C.;
Jeffrey, Jeremy I.;
Wong, Philip;
Cox, Gregory A.;
Alexander, Guillermo M.

Publication type:

Article

Rhabdomyosarcomas in Aging A/J Mice.

Published in:

PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023498

By:

Sher, Roger B.;
Cox, Gregory A.;
Mills, Kevin D.;
Sundberg, John P.

Publication type:

Article

NEMF mutations in mice illustrate how Importin-β specific nuclear transport defects recapitulate neurodegenerative disease hallmarks.

Published in:

PLoS Genetics, 2024, v. 20, n. 9, p. 1, doi. 10.1371/journal.pgen.1011411

By:

Plessis-Belair, Jonathan;
Ravano, Kathryn;
Han, Ellen;
Janniello, Aubrey;
Molina, Catalina;
Sher, Roger B.

Publication type:

Article

Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy.

Published in:

Human Molecular Genetics, 2019, v. 28, n. 16, p. 2635, doi. 10.1093/hmg/ddz068

By:

Sayed-Zahid, Ambreen A;
Sher, Roger B;
Rizzo, Stacey J Sukoff;
Anderson, Laura C;
Patenaude, Kathryn E;
Cox, Gregory A

Publication type:

Article

Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy.

Published in:

Human Molecular Genetics, 2011, v. 20, n. 19, p. 3841, doi. 10.1093/hmg/ddr305

By:

Mitsuhashi, Satomi;
Hatakeyama, Hideyuki;
Karahashi, Minako;
Koumura, Tomoko;
Nonaka, Ikuya;
Hayashi, Yukiko K.;
Noguchi, Satoru;
Sher, Roger B.;
Nakagawa, Yasuhito;
Manfredi, Giovanni;
Goto, Yu-ichi;
Cox, Gregory A.;
Nishino, Ichizo

Publication type:

Article