M. Gitcho

发表

Potentiation of insulin-stimulated glucose transport by the AMP-activated protein kinase.

J. Ju, M. Gitcho, C. Casmaer, 2007, American journal of physiology. Cell physiology.

TDP‐43 A315T mutation in familial motor neuron disease

J. Morris, A. Pestronk, A. Goate, 2008, Annals of neurology.

Pathogenic cysteine mutations affect progranulin function and production of mature granulins

A. Goate, Jane Y. Wu, C. Cruchaga, 2010, Journal of neurochemistry.

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

L. Petrucelli, J. Mathis, Jeffrey A. Johnson, 2013, Molecular therapy : the journal of the American Society of Gene Therapy.

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

A. Goate, N. Cairns, M. Forman, 2009, Journal of Biological Chemistry.

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

N. Cairns, M. Gitcho, Stephani A. Davis, 2018, Neuroscience Letters.

Selective forelimb impairment in rats expressing a pathological TDP-43 25 kDa C-terminal fragment to mimic amyotrophic lateral sclerosis.

L. Petrucelli, J. Mathis, Jeffrey A. Johnson, 2013, Molecular therapy : the journal of the American Society of Gene Therapy.

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

J. Morris, M. Mesulam, A. Goate, 2009, Acta Neuropathologica.

FUS Immunogold Labeling TEM Analysis of the Neuronal Cytoplasmic Inclusions of Neuronal Intermediate Filament Inclusion Disease: A Frontotemporal Lobar Degeneration with FUS Proteinopathy

A. Goate, N. Cairns, E. Bigio, 2011, Journal of Molecular Neuroscience.

TDP‐43 proteinopathy in familial motor neurone disease with TARDBP A315T mutation: a case report

N. Cairns, R. Perrin, J. Morris, 2010, Neuropathology and applied neurobiology.

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

N. Cairns, C. Ferris, M. Gitcho, 2021, Neuroscience Letters.

Effects of inhaled cannabis high in Δ9-THC or CBD on the aging brain: A translational MRI and behavioral study

M. Febo, P. Kulkarni, C. Ferris, 2023, Frontiers in Aging Neuroscience.

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions.

J. Morris, J. Trojanowski, V. Lee, 2007, The American journal of pathology.

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

B. Kraemer, M. Gitcho, R. Klein, 2011, The European journal of neuroscience.

Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia

J. Morris, A. Goate, N. Cairns, 2008, Human mutation.

ALS and FTLD: two faces of TDP‐43 proteinopathy

N. Cairns, L. Grinberg, J. Zidar, 2008, European journal of neurology.

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulin

J. Morris, A. Goate, N. Cairns, 2006, Annals of neurology.

TDP-43 expression influences amyloidβ plaque deposition and tau aggregation

N. Cairns, M. Gitcho, Stephani A. Davis, 2017, Neurobiology of Disease.

Neuropathologic Heterogeneity in HDDD1: A Familial Frontotemporal Lobar Degeneration With Ubiquitin-positive Inclusions and Progranulin Mutation

J. Morris, A. Goate, N. Cairns, 2007, Alzheimer disease and associated disorders.

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

J. Mathis, M. Gitcho, K. Baker, 2015, Journal of medical primatology.