Haplotype-specific expression of exon 10 at the human MAPT locus

Haplotype-specific expression of exon 10 at the human MAPT locus

Pokaż inne wersje (1)

Neurofibrillary tangles composed of exon 10+ microtubule associated protein tau (MAPT) deposits are the characteristic feature of the neurodegenerative diseases progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD). PSP, CBD and more recently Alzheimer's disease and Parkinson...

Szczegółowa specyfikacja

Opis bibliograficzny
Główni autorzy:	Caffrey, T, Joachim, C, Paracchini, S, Esiri, M, Wade-Martins, R
Format:	Journal article
Język:	English
Wydane:	Oxford University Press 2006
Hasła przedmiotowe:	Pharmacology Genetics (medical sciences) Neuropathology

Podobne zapisy

Haplotype-specific expression of exon 10 at the human MAPT locus.
od: Caffrey, T, i wsp.
Wydane: (2006)

Haplotype-specific expression of the N-terminal exons 2 and 3 at the human MAPT locus.
od: Caffrey, T, i wsp.
Wydane: (2008)

Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders
od: Lai, M, i wsp.
Wydane: (2017)

Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders
od: Mang Ching Lai, i wsp.
Wydane: (2017-10-01)

APOE and MAPT Are Associated With Dementia in Neuropathologically Confirmed Parkinson's Disease
od: Jon-Anders Tunold, i wsp.
Wydane: (2021-02-01)

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology.
od: Caffrey, T, i wsp.
Wydane: (2007)

Functional MAPT haplotypes: Bridging the gap between genotype and neuropathology
od: Tara M. Caffrey, i wsp.
Wydane: (2007-07-01)

P-selectin expression tracks cerebral atrophy in Mexican-Americans
od: Kochunov, P, i wsp.
Wydane: (2012)

NMDA Receptors Subunits, Medical Conditions Involved in, and Their Roles as Drug Targets
od: Mohamed Omer
Wydane: (2020-07-01)

Association of MAPT (tau) haplotype with the pathology of Parkinson's disease
od: Parkkinen, L, i wsp.
Wydane: (2013)

The influence of selected sulphur containing compounds on retinal cell death: neuroprotective effects of hydrogen sulphide in a glaucoma model
od: Abdul Majid, A
Wydane: (2011)

A molecular, anatomical and developmental account of copine-6 protein expression in the rodent brain
od: Faram, R
Wydane: (2013)

Different MAPT haplotypes influence expression of total MAPT in postmortem brain tissue
od: Christina V. Tauber, i wsp.
Wydane: (2023-03-01)

Characterisation of pitch: an early onset model of sensorineural deafness
od: Carrott, L
Wydane: (2014)

D-Amino acid oxidase (DAO) activity and expression are increased in schizophrenia
od: Burnet, P, i wsp.
Wydane: (2008)

Haplotype-based association analysis of the MAPT locus in Late Onset Alzheimer's disease
od: Morris John C, i wsp.
Wydane: (2007-01-01)

Genetics: The MAPT locus-a genetic paradigm in disease susceptibility.
od: Wade-Martins, R
Wydane: (2012)

The role of MAPT sequence variation in mechanisms of disease susceptibility.
od: Caffrey, T, i wsp.
Wydane: (2012)

Elucidating the role of GBA in the pathology of Parkinson's disease using patient derived dopaminergic neurons differentiated from induced pluripotent stem cells.
od: Ribeiro Fernandes, HJ
Wydane: (2014)

Imaging neuroinflammatory processes with USPIO-MRI
od: Brown, AP
Wydane: (2009)

D-amino acid oxidase, D-serine and the dopamine system: their interactions and implications for schizophrenia
od: Betts, J
Wydane: (2012)

Study of two mouse mutants to identify novel neurodegenerative pathways
od: Finelli, M, i wsp.
Wydane: (2010)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
od: Paracchini, S, i wsp.
Wydane: (2006)

Investigating circadian disruption in mouse models of neurological and metabolic disorders
od: Livieratos, A
Wydane: (2013)

Using fast-scan cyclic voltammetry to investigate monoamine release in BAC transgenic rodent models of Parkinson's Disease
od: Potgieter, D
Wydane: (2014)

Macroscopic and Microscopic Cerebral Findings in Drug and Alcohol Abusers: The Point of View of the Forensic Pathologist
od: Angelo Montana, i wsp.
Wydane: (2024-03-01)

Structural connectivity in schizophrenia and its impact on the dynamics of spontaneous functional networks.
od: Cabral, J, i wsp.
Wydane: (2013)

Investigations of the potential schizophrenia susceptibility gene Kinase Interacting with Stathmin (KIS)
od: Bristow, G
Wydane: (2010)

Editorial: Meeting new challenges in translationally relevant neurodegenerative disease research
od: Caitlin Shannon Latimer, i wsp.
Wydane: (2024-08-01)

Accuracy of haplotype reconstruction from haplotype-tagging single-nucleotide polymorphisms
od: Forton, J, i wsp.
Wydane: (2005)

Using neuroimaging and histology to understand hyperexcitability and atypical connectivity in autism spectrum disorder
od: Ravishankar, M
Wydane: (2015)

A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia
od: Roneil Malkani, i wsp.
Wydane: (2006-05-01)

MAPT haplotype-associated transcriptomic changes in progressive supranuclear palsy
od: Hadley W. Ressler, i wsp.
Wydane: (2024-08-01)

The H2 MAPT haplotype is associated with familial frontotemporal dementia
od: Roberta Ghidoni, i wsp.
Wydane: (2006-05-01)

The MAPT H1 Haplotype Is a Risk Factor for Alzheimer’s Disease in APOE ε4 Non-carriers
od: Pascual Sánchez-Juan, i wsp.
Wydane: (2019-12-01)

An exploratory study on the mechanism of Huangqi Guizhi Wuwu Decoction in the treatment of neuropathic pain
od: Bo‐Yan Luo, i wsp.
Wydane: (2022-06-01)

The neuropathology of the social cognitive network in autism
od: McKavanagh, R
Wydane: (2014)

Investigations of the role of d-amino acid oxidase and serine racemase in schizophrenia
od: Verrall, L
Wydane: (2008)

The behavioural and molecular characterisation of a novel LRRK2 BAC transgenic rat model of Parkinson’s disease
od: Sloan, M, i wsp.
Wydane: (2014)

Neuroanatomical screening and analysis of transgenic and ENU induced mutagenised mice
od: Edwards, A
Wydane: (2011)