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

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

Mostrar outras versões (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...

ver descrição completa

Detalhes bibliográficos
Principais autores:	Caffrey, T, Joachim, C, Paracchini, S, Esiri, M, Wade-Martins, R
Formato:	Journal article
Idioma:	English
Publicado em:	Oxford University Press 2006
Assuntos:	Pharmacology Genetics (medical sciences) Neuropathology

Registros relacionados

Haplotype-specific expression of exon 10 at the human MAPT locus.
por: Caffrey, T, et al.
Publicado em: (2006)

Haplotype-specific expression of the N-terminal exons 2 and 3 at the human MAPT locus.
por: Caffrey, T, et al.
Publicado em: (2008)

Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders
por: Lai, M, et al.
Publicado em: (2017)

Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders
por: Mang Ching Lai, et al.
Publicado em: (2017-10-01)

APOE and MAPT Are Associated With Dementia in Neuropathologically Confirmed Parkinson's Disease
por: Jon-Anders Tunold, et al.
Publicado em: (2021-02-01)

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology.
por: Caffrey, T, et al.
Publicado em: (2007)

Functional MAPT haplotypes: Bridging the gap between genotype and neuropathology
por: Tara M. Caffrey, et al.
Publicado em: (2007-07-01)

P-selectin expression tracks cerebral atrophy in Mexican-Americans
por: Kochunov, P, et al.
Publicado em: (2012)

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

Association of MAPT (tau) haplotype with the pathology of Parkinson's disease
por: Parkkinen, L, et al.
Publicado em: (2013)

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

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

Different MAPT haplotypes influence expression of total MAPT in postmortem brain tissue
por: Christina V. Tauber, et al.
Publicado em: (2023-03-01)

Characterisation of pitch: an early onset model of sensorineural deafness
por: Carrott, L
Publicado em: (2014)

D-Amino acid oxidase (DAO) activity and expression are increased in schizophrenia
por: Burnet, P, et al.
Publicado em: (2008)

Haplotype-based association analysis of the MAPT locus in Late Onset Alzheimer's disease
por: Morris John C, et al.
Publicado em: (2007-01-01)

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

The role of MAPT sequence variation in mechanisms of disease susceptibility.
por: Caffrey, T, et al.
Publicado em: (2012)

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

Imaging neuroinflammatory processes with USPIO-MRI
por: Brown, AP
Publicado em: (2009)

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

Study of two mouse mutants to identify novel neurodegenerative pathways
por: Finelli, M, et al.
Publicado em: (2010)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
por: Paracchini, S, et al.
Publicado em: (2006)

Investigating circadian disruption in mouse models of neurological and metabolic disorders
por: Livieratos, A
Publicado em: (2013)

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

Macroscopic and Microscopic Cerebral Findings in Drug and Alcohol Abusers: The Point of View of the Forensic Pathologist
por: Angelo Montana, et al.
Publicado em: (2024-03-01)

Structural connectivity in schizophrenia and its impact on the dynamics of spontaneous functional networks.
por: Cabral, J, et al.
Publicado em: (2013)

Investigations of the potential schizophrenia susceptibility gene Kinase Interacting with Stathmin (KIS)
por: Bristow, G
Publicado em: (2010)

Editorial: Meeting new challenges in translationally relevant neurodegenerative disease research
por: Caitlin Shannon Latimer, et al.
Publicado em: (2024-08-01)

Accuracy of haplotype reconstruction from haplotype-tagging single-nucleotide polymorphisms
por: Forton, J, et al.
Publicado em: (2005)

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

A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia
por: Roneil Malkani, et al.
Publicado em: (2006-05-01)

MAPT haplotype-associated transcriptomic changes in progressive supranuclear palsy
por: Hadley W. Ressler, et al.
Publicado em: (2024-08-01)

The H2 MAPT haplotype is associated with familial frontotemporal dementia
por: Roberta Ghidoni, et al.
Publicado em: (2006-05-01)

The MAPT H1 Haplotype Is a Risk Factor for Alzheimer’s Disease in APOE ε4 Non-carriers
por: Pascual Sánchez-Juan, et al.
Publicado em: (2019-12-01)

An exploratory study on the mechanism of Huangqi Guizhi Wuwu Decoction in the treatment of neuropathic pain
por: Bo‐Yan Luo, et al.
Publicado em: (2022-06-01)

The neuropathology of the social cognitive network in autism
por: McKavanagh, R
Publicado em: (2014)

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

The behavioural and molecular characterisation of a novel LRRK2 BAC transgenic rat model of Parkinson’s disease
por: Sloan, M, et al.
Publicado em: (2014)

Neuroanatomical screening and analysis of transgenic and ENU induced mutagenised mice
por: Edwards, A
Publicado em: (2011)