Effect of the Histone Deacetylase Inhibitor FRM-0334 on Progranulin Levels in Patients With Progranulin Gene Haploinsufficiency
暂无分享,去创建一个
G. Frisoni | B. Boeve | F. Pasquier | M. Grossman | C. Mummery | M. Onofrj | R. Vandenberghe | S. McGinnis | K. Marek | D. Hannequin | A. Boxer | D. Hilt | J. V. van Swieten | B. Borroni | I. Goodman | R. La Joie | I. Le Ber | S. Auriacombe | G. Wisniewski | H. Riordan | J. Hesterman | H. Moebius | L. Iaccarino | L. Edwards | P. Ljubenkov | J. Rojas | H. Patzke | M. Koestler | G. Koenig | Baruch Harris | Beth Ann Haynes | Peter A. Ljubenkov | M. Grossman
[1] David T. Jones,et al. Use of the CDR® plus NACC FTLD in mild FTLD: Data from the ARTFL/LEFFTDS consortium , 2019, Alzheimer's & Dementia.
[2] A. Fagan,et al. Cerebrospinal fluid biomarkers predict frontotemporal dementia trajectory , 2018, Annals of clinical and translational neurology.
[3] Jesse A. Brown,et al. An 8-week, open-label, dose-finding study of nimodipine for the treatment of progranulin insufficiency from GRN gene mutations , 2017, Alzheimer's & dementia.
[4] Z. Modrušan,et al. Progranulin deficiency causes impairment of autophagy and TDP-43 accumulation , 2017, The Journal of experimental medicine.
[5] Param Priya Singh,et al. Progranulin, lysosomal regulation and neurodegenerative disease , 2017, Nature Reviews Neuroscience.
[6] Y. Pijnenburg,et al. Progranulin Levels in Plasma and Cerebrospinal Fluid in Granulin Mutation Carriers , 2016, Dementia and Geriatric Cognitive Disorders Extra.
[7] S. Ourselin,et al. Neurofilament light chain: a biomarker for genetic frontotemporal dementia , 2016, Annals of clinical and translational neurology.
[8] Vrishabhsagar Ruikar,et al. Interactive Voice/Web Response System in clinical research , 2016, Perspectives in clinical research.
[9] Aditya Kumar Bubna,et al. Vorinostat—An Overview , 2015, Indian journal of dermatology.
[10] A. L. Munain,et al. Increasing progranulin levels and blockade of the ERK1/2 pathway: Upstream and downstream strategies for the treatment of progranulin deficient frontotemporal dementia , 2015, European Neuropsychopharmacology.
[11] L. Grinberg,et al. Cerebrospinal fluid neurofilament concentration reflects disease severity in frontotemporal degeneration , 2014, Annals of neurology.
[12] V. Sossi,et al. Anterior brain glucose hypometabolism predates dementia in progranulin mutation carriers , 2013, Neurology.
[13] Min Jae Lee,et al. Tau degradation: The ubiquitin–proteasome system versus the autophagy-lysosome system , 2013, Progress in Neurobiology.
[14] Pierre J Magistretti,et al. Brain energy metabolism: focus on astrocyte-neuron metabolic cooperation. , 2011, Cell metabolism.
[15] Barbara Stanley,et al. The Columbia-Suicide Severity Rating Scale: initial validity and internal consistency findings from three multisite studies with adolescents and adults. , 2011, The American journal of psychiatry.
[16] Robert V Farese,et al. Suberoylanilide Hydroxamic Acid (Vorinostat) Up-regulates Progranulin Transcription , 2011, The Journal of Biological Chemistry.
[17] N. Bresolin,et al. Cerebrospinal fluid biomarkers in Progranulin mutations carriers. , 2011, Journal of Alzheimer's disease : JAD.
[18] M. Hornberger,et al. Clinical Staging and Disease Progression in Frontotemporal Dementia Supplemental Data at Www.neurology.org , 2022 .
[19] R. Petersen,et al. Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members , 2009, Brain : a journal of neurology.
[20] Nathaniel Mercaldo,et al. Development of methodology for conducting clinical trials in frontotemporal lobar degeneration. , 2008, Brain : a journal of neurology.
[21] C. Haass,et al. Missense Mutations in the Progranulin Gene Linked to Frontotemporal Lobar Degeneration with Ubiquitin-immunoreactive Inclusions Reduce Progranulin Production and Secretion* , 2008, Journal of Biological Chemistry.
[22] S. Targum,et al. The clinical global impressions scale: applying a research tool in clinical practice. , 2007, Psychiatry (Edgmont (Pa. : Township)).
[23] P. Pietrini,et al. Clinicopathologic features of frontotemporal dementia with Progranulin sequence variation , 2007, Neurology.
[24] S. Melquist,et al. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. , 2006, Human molecular genetics.
[25] S. Melquist,et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 , 2006, Nature.
[26] A. Petzold. Neurofilament phosphoforms: Surrogate markers for axonal injury, degeneration and loss , 2005, Journal of the Neurological Sciences.
[27] A. Bateman,et al. The complementary deoxyribonucleic acid sequence, tissue distribution, and cellular localization of the rat granulin precursor. , 1993, Endocrinology.