Rhabdomyosarcomas in Aging A/J Mice

por Sher, Roger B., Cox, Gregory A., Mills, Kevin D., Sundberg, John P.
Publicado 2011

Complex Seizure Disorder Caused by Brunol4 Deficiency in Mice

por Yang, Yan, Mahaffey, Connie L, Bérubé, Nathalie, Maddatu, Terry P, Cox, Gregory A, Frankel, Wayne N
Publicado 2007

Development-on-chip: in vitro neural tube patterning with a microfluidic device

por Demers, Christopher J., Soundararajan, Prabakaran, Chennampally, Phaneendra, Cox, Gregory A., Briscoe, James, Collins, Scott D., Smith, Rosemary L.
Publicado 2016

A microfluidic approach to rescue ALS motor neuron degeneration using rapamycin

por Chennampally, Phaneendra, Sayed-Zahid, Ambreen, Soundararajan, Prabakaran, Sharp, Jocelyn, Cox, Gregory A., Collins, Scott D., Smith, Rosemary L.
Publicado 2021

Author Correction: A microfluidic approach to rescue ALS motor neuron degeneration using rapamycin

por Chennampally, Phaneendra, Sayed-Zahid, Ambreen, Soundararajan, Prabakaran, Sharp, Jocelyn, Cox, Gregory A., Collins, Scott D., Smith, Rosemary L.
Publicado 2021

Hyperactive Somatostatin Interneurons Contribute to Excitotoxicity in Neurodegenerative Disorders

por Zhang, Wen, Zhang, Lifeng, Liang, Bo, Schroeder, David, Zhang, Zhong-wei, Cox, Gregory A., Li, Yun, Lin, Da-Ting
Publicado 2016

Corticospinal Motor Neurons Are Susceptible to Increased ER Stress and Display Profound Degeneration in the Absence of UCHL1 Function

por Jara, Javier H., Genç, Barış, Cox, Gregory A., Bohn, Martha C., Roos, Raymond P., Macklis, Jeffrey D., Ulupınar, Emel, Özdinler, P. Hande
Publicado 2015

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

por 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.
Publicado 2022

Genetic Background Effects on Disease Onset and Lifespan of the Mutant Dynactin p150(Glued) Mouse Model of Motor Neuron Disease

por 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.
Publicado 2015

Retrotransposon Insertion in the T-cell Acute Lymphocytic Leukemia 1 (Tal1) Gene Is Associated with Severe Renal Disease and Patchy Alopecia in Hairpatches (Hpt) Mice

por Hosur, Vishnu, Cox, Melissa L., Burzenski, Lisa M., Riding, Rebecca L., Alley, Lynn, Lyons, Bonnie L., Kavirayani, Anoop, Martin, Kimberly A., Cox, Gregory A., Johnson, Kenneth R., Shultz, Leonard D.
Publicado 2013

Absence of UCHL 1 function leads to selective motor neuropathy

por Genç, Barış, Jara, Javier H., Schultz, Megan C., Manuel, Marin, Stanford, Macdonell J., Gautam, Mukesh, Klessner, Jodi L., Sekerkova, Gabriella, Heller, Daniel B., Cox, Gregory A., Heckman, Charles J., DiDonato, Christine J., Özdinler, P. Hande
Publicado 2016

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

por 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, Galehdari, Hamid, Douglas, Ganka, Posey, Jennifer E., Ryan, Monique, Lupski, James R., Laing, Nigel G., Joazeiro, Claudio A. P., Cox, Gregory A.
Publicado 2020

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

por 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, Galehdari, Hamid, Douglas, Ganka, Posey, Jennifer E., Ryan, Monique, Lupski, James R., Laing, Nigel G., Joazeiro, Claudio A. P., Cox, Gregory A.
Publicado 2020

Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders

por Fairfield, Heather, Srivastava, Anuj, Ananda, Guruprasad, Liu, Rangjiao, Kircher, Martin, Lakshminarayana, Anuradha, Harris, Belinda S., Karst, Son Yong, Dionne, Louise A., Kane, Coleen C., Curtain, Michelle, Berry, Melissa L., Ward-Bailey, Patricia F., Greenstein, Ian, Byers, Candice, Czechanski, Anne, Sharp, Jocelyn, Palmer, Kristina, Gudis, Polyxeni, Martin, Whitney, Tadenev, Abby, Bogdanik, Laurent, Pratt, C. Herbert, Chang, Bo, Schroeder, David G., Cox, Gregory A., Cliften, Paul, Milbrandt, Jeffrey, Murray, Stephen, Burgess, Robert, Bergstrom, David E., Donahue, Leah Rae, Hamamy, Hanan, Masri, Amira, Santoni, Federico A., Makrythanasis, Periklis, Antonarakis, Stylianos E., Shendure, Jay, Reinholdt, Laura G.
Publicado 2015