Genetic strategies to study TDP-43 in rodents and to develop preclinical therapeutics for amyotrophic lateral sclerosis

Yazar: Wang, David B., Gitcho, Michael A., Kraemer, Brian C., Klein, Ronald L.
Baskı/Yayın Bilgisi 2011

TDP-43 expression influences amyloid β plaque deposition and tau aggregation

Yazar: Davis, Stephani A., Gan, Kok Ann, Dowell, James A., Cairns, Nigel J., Gitcho, Michael A.
Yayımlandı Neurobiol Dis (2017)

VCP Mutations Causing Frontotemporal Lobar Degeneration Disrupt Localization of TDP-43 and Induce Cell Death

Yazar: Gitcho, Michael A., Strider, Jeffrey, Carter, Deborah, Taylor-Reinwald, Lisa, Forman, Mark S., Goate, Alison M., Cairns, Nigel J.
Baskı/Yayın Bilgisi 2009

POTENTIATION OF INSULIN-STIMULATED GLUCOSE TRANSPORT BY THE AMP-ACTIVATED PROTEIN KINASE

Yazar: Ju, Jeong-Sun, Gitcho, Michael A., Casmaer, Carter A., Patil, Pankaj B., Han, Dae-Gyue, Spencer, Susan A., Fisher, Jonathan S.
Baskı/Yayın Bilgisi 2006

Hippocampal neurobiology and function in an aged mouse model of TDP-43 proteinopathy in an APP/PSEN1 background

Yazar: Arezoumandan, Sanaz, Cai, Xuezhu, Kalkarni, Praveen, Davis, Stephani A., Wilson, Katherine, Ferris, Craig F., Cairns, Nigel J., Gitcho, Michael A.
Yayımlandı Neurosci Lett (2021)

TDP-43 interacts with mitochondrial proteins critical for mitophagy and mitochondrial dynamics

Yazar: Davis, Stephani A., Itaman, Sheed, Khalid-Janney, Christopher M., Sherard, Justin A., Dowell, James A., Cairns, Nigel J., Gitcho, Michael A.
Yayımlandı Neurosci Lett (2018)

Pathogenic Cysteine Mutations Affect Progranulin Function and Production of Mature Granulins

Yazar: Wang, Jun, Van Damme, Philip, Cruchaga, Carlos, Gitcho, Michael A., Vidal, Jose Manuel, Seijo-Martínez, Manuel, Wang, Lei, Wu, Jane Y., Robberecht, Wim, Goate, Alison
Baskı/Yayın Bilgisi 2009

TARDBP 3′-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

Yazar: Gitcho, Michael A., Bigio, Eileen H., Mishra, Manjari, Johnson, Nancy, Weintraub, Sandra, Mesulam, Marsel, Rademakers, Rosa, Chakraverty, Sumi, Cruchaga, Carlos, Morris, John C., Goate, Alison M., Cairns, Nigel J.
Baskı/Yayın Bilgisi 2009

FUS immunogold labelling TEM analysis of the neuronal cytoplasmic inclusions of neuronal intermediate filament inclusion disease: a frontotemporal lobar degeneration with FUS prote...

Yazar: Page, Tristan, Gitcho, Michael A., Mosaheb, Sabrina, Carter, Deborah, Chakraverty, Sumi, Perry, Robert H., Bigio, Eileen H., Gearing, Marla, Ferrer, Isidre, Goate, Alison M., Cairns, Nigel J., Thorpe, Julian R.
Baskı/Yayın Bilgisi 2011

Selective Forelimb Impairment in Rats Expressing a Pathological TDP-43 25 kDa C-terminal Fragment to Mimic Amyotrophic Lateral Sclerosis

Yazar: Dayton, Robert D, Gitcho, Michael A, Orchard, Elysse A, Wilson, Jon D, Wang, David B, Cain, Cooper D, Johnson, Jeffrey A, Zhang, Yong-Jie, Petrucelli, Leonard, Mathis, J Michael, Klein, Ronald L
Baskı/Yayın Bilgisi 2013

Initial gene vector dosing for studying symptomatology of amyotrophic lateral sclerosis in non-human primates

Yazar: Jackson, Kasey L., Dayton, Robert D., Fisher-Perkins, Jeanne M., Didier, Peter J., Baker, Kate C., Weimer, Maria, Gutierrez, Amparo, Cain, Cooper D., Mathis, J. Michael, Gitcho, Michael A., Bunnell, Bruce A., Klein, Ronald L.
Yayımlandı J Med Primatol (2015)

Molecular Characterization of Novel Progranulin (GRN) Mutations in Frontotemporal Dementia

Yazar: Mukherjee, Odity, Wang, Jun, Gitcho, Michael, Chakraverty, Sumi, Taylor-Reinwald, Lisa, Shears, Shantia, Kauwe, John S.K., Norton, Joanne, Levitch, Denise, Bigio, Eileen H., Hatanpaa, Kimmo J., White, Charles L., Morris, John C., Cairns, Nigel J., Goate, Alison
Baskı/Yayın Bilgisi 2008

TDP-43 A315T Mutation in Familial Motor Neuron Disease

Yazar: Gitcho, Michael A., Baloh, Robert H., Chakraverty, Sumi, Mayo, Kevin, Norton, Joanne B., Levitch, Denise, Hatanpaa, Kimmo J., White, Charles L., Bigio, Eileen H., Caselli, Richard, Baker, Matt, Al-Lozi, Muhammad T., Morris, John C., Pestronk, Alan, Rademakers, Rosa, Goate, Alison M., Cairns, Nigel J.
Baskı/Yayın Bilgisi 2008

HDDD2 Is a Familial Frontotemporal Lobar Degeneration with Ubiquitin-Positive, Tau-Negative Inclusions Caused by a Missense Mutation in the Signal Peptide of Progranulin

Yazar: Mukherjee, Odity, Pastor, Pau, Cairns, Nigel J., Chakraverty, Sumi, Kauwe, John S. K., Shears, Shantia, Behrens, Maria I., Budde, John, Hinrichs, Anthony L., Norton, Joanne, Levitch, Denise, Taylor-Reinwald, Lisa, Gitcho, Michael, Tu, P.-H., Grinberg, Lea Tenenholz, Liscic, Rajka M., Armendariz, Javier, Morris, John C., Goate, Alison M.
Baskı/Yayın Bilgisi 2006

TDP-43 in Familial and Sporadic Frontotemporal Lobar Degeneration with Ubiquitin Inclusions

Yazar: Cairns, Nigel J., Neumann, Manuela, Bigio, Eileen H., Holm, Ida E., Troost, Dirk, Hatanpaa, Kimmo J., Foong, Chan, White, Charles L., Schneider, Julie A., Kretzschmar, Hans A., Carter, Deborah, Taylor-Reinwald, Lisa, Paulsmeyer, Katherine, Strider, Jeffrey, Gitcho, Michael, Goate, Alison M., Morris, John C., Mishra, Manjari, Kwong, Linda K., Stieber, Anna, Xu, Yan, Forman, Mark S., Trojanowski, John Q., Lee, Virginia M.-Y., Mackenzie, Ian R.A.
Baskı/Yayın Bilgisi 2007