Works matching AU Sher, Roger B.

Results: 13

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
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
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
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
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
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
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
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
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
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
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