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Biorxiv : the Preprint Server for Biology
|
February 20, 2025
DNA methylation as a contributor to dysregulation of <i>STX6</i> and other frontotemporal lobar degeneration genetic risk-associated loci
Naiomi Rambarack, Katherine Fodder, Megha Murthy, et al.
Acta Neuropathologica Communications
|
July 5, 2025
DNA methylation as a contributor to dysregulation of STX6 and other frontotemporal Lobar degeneration genetic risk-associated loci
Naiomi Rambarack, Katherine Fodder, Megha Murthy, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 3, 2025
Mapping genetic effects on splicing in ten thousand post-mortem brain samples reveals novel mediators of neurological disease risk
Aline Réal, Kailash Bp, Winston H Dredge, et al.
Biorxiv : the Preprint Server for Biology
|
April 1, 2025
Cytosine-to-uracil RNA editing is upregulated by pro-inflammatory stimulation of myeloid cells
Hyomin Seo, Winston H Cuddleston, Ting Fu, et al.
Acta Neuropathologica
|
May 7, 2023
Brain DNA methylomic analysis of frontotemporal lobar degeneration reveals OTUD4 in shared dysregulated signatures across pathological subtypes
Katherine Fodder, Megha Murthy, Patrizia Rizzu, et al.
Acta Neuropathologica Communications
|
August 17, 2024
MAPT haplotype-associated transcriptomic changes in progressive supranuclear palsy
Hadley W Ressler, Jack Humphrey, Ricardo A Vialle, et al.
Brain Communications
|
June 22, 2026
Transcriptomic and pathological analysis of the hnRNP network reveals glial involvement in frontotemporal lobar degeneration pathological subtypes
Ariana Gatt, Yazead Buhidma, Katherine Fodder, et al.
Biorxiv : the Preprint Server for Biology
|
December 3, 2025
Sensitivity to TDP-43 loss and degradation resistance determine cryptic exon biomarker potential
Anna-Leigh Brown, Matteo Zanovello, Alla Mikheenko, et al.
Acta Neuropathologica
|
July 18, 2021
HnRNP K mislocalisation is a novel protein pathology of frontotemporal lobar degeneration and ageing and leads to cryptic splicing
Alexander Bampton, Ariana Gatt, Jack Humphrey, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 19, 2025
Meta-analysis of genetic regulation of RNA editing in the human brain identifies new genes underlying neurological disease
Winston H Dredge, Kailash Bp, Aline Réal, et al.
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Showing results (11-20 of 67) with videos related to
Sort By:
Page
of 7
Biorxiv : the Preprint Server for Biology
|
February 20, 2025
DNA methylation as a contributor to dysregulation of <i>STX6</i> and other frontotemporal lobar degeneration genetic risk-associated loci
Naiomi Rambarack, Katherine Fodder, Megha Murthy, et al.
Acta Neuropathologica Communications
|
July 5, 2025
DNA methylation as a contributor to dysregulation of STX6 and other frontotemporal Lobar degeneration genetic risk-associated loci
Naiomi Rambarack, Katherine Fodder, Megha Murthy, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 3, 2025
Mapping genetic effects on splicing in ten thousand post-mortem brain samples reveals novel mediators of neurological disease risk
Aline Réal, Kailash Bp, Winston H Dredge, et al.
Biorxiv : the Preprint Server for Biology
|
April 1, 2025
Cytosine-to-uracil RNA editing is upregulated by pro-inflammatory stimulation of myeloid cells
Hyomin Seo, Winston H Cuddleston, Ting Fu, et al.
Acta Neuropathologica
|
May 7, 2023
Brain DNA methylomic analysis of frontotemporal lobar degeneration reveals OTUD4 in shared dysregulated signatures across pathological subtypes
Katherine Fodder, Megha Murthy, Patrizia Rizzu, et al.
Acta Neuropathologica Communications
|
August 17, 2024
MAPT haplotype-associated transcriptomic changes in progressive supranuclear palsy
Hadley W Ressler, Jack Humphrey, Ricardo A Vialle, et al.
Brain Communications
|
June 22, 2026
Transcriptomic and pathological analysis of the hnRNP network reveals glial involvement in frontotemporal lobar degeneration pathological subtypes
Ariana Gatt, Yazead Buhidma, Katherine Fodder, et al.
Biorxiv : the Preprint Server for Biology
|
December 3, 2025
Sensitivity to TDP-43 loss and degradation resistance determine cryptic exon biomarker potential
Anna-Leigh Brown, Matteo Zanovello, Alla Mikheenko, et al.
Acta Neuropathologica
|
July 18, 2021
HnRNP K mislocalisation is a novel protein pathology of frontotemporal lobar degeneration and ageing and leads to cryptic splicing
Alexander Bampton, Ariana Gatt, Jack Humphrey, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 19, 2025
Meta-analysis of genetic regulation of RNA editing in the human brain identifies new genes underlying neurological disease
Winston H Dredge, Kailash Bp, Aline Réal, et al.
Page
of 7