Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("TDP-43")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 126

  • Page / 6
Export

Selection :

  • and

Mutational analysis of TARDBP in neurodegenerative diseasesTICOZZI, Nicola; LECLERC, Ashley Lyn; VAN BLITTERSWIJK, Marka et al.Neurobiology of aging. 2011, Vol 32, Num 11, pp 2096-2099, issn 0197-4580, 4 p.Article

TDP-43 gene analysis in frontotemporal lobar degenerationROLLINSON, Sara; SNOWDEN, Julie S; NEARY, David et al.Neuroscience letters. 2007, Vol 419, Num 1, pp 1-4, issn 0304-3940, 4 p.Article

No association of TDP-43 with sporadic frontotemporal dementiaSCHUMACHER, Axel; FRIEDRICH, Patricia; DIEHL-SCHMID, Janine et al.Neurobiology of aging. 2009, Vol 30, Num 1, pp 157-159, issn 0197-4580, 3 p.Article

No association of PGRN 3'UTR rs5848 in frontotemporal lobar degenerationROLLINSON, Sara; ROHRER, Jonathan D; PICKERING-BROWN, Stuart M et al.Neurobiology of aging. 2011, Vol 32, Num 4, pp 754-755, issn 0197-4580, 2 p.Article

Endogenous TDP-43 localized to stress granules can subsequently form protein aggregatesPARKER, Sarah J; MEYEROWITZ, Jodi; JAMES, Janine L et al.Neurochemistry international. 2012, Vol 60, Num 4, pp 415-424, issn 0197-0186, 10 p.Article

Degradation of TDP-43 and its pathogenic form by autophagy and the ubiquitin-proteasome systemXIAOJU WANG; HUADONG FAN; ZHENG YING et al.Neuroscience letters. 2010, Vol 469, Num 1, pp 112-116, issn 0304-3940, 5 p.Article

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degenerationSEELAAR, Harro; KLIJNSMA, Kirsten Y; KONING, Inge De et al.Journal of neurology. 2010, Vol 257, Num 5, pp 747-753, issn 0340-5354, 7 p.Article

Progressive anterior operculum syndrome due to FTLD-TDP: a clinico-pathological investigationOTSUKI, Mika; NAKAGAWA, Yoshitsugu; WAKABAYASHI, Koichi et al.Journal of neurology. 2010, Vol 257, Num 7, pp 1148-1153, issn 0340-5354, 6 p.Article

A NEW CELLULAR MODEL OF PATHOLOGICAL TDP-43: THE NEUROTOXICITY OF STABLY EXPRESSED CTF25 OF TDP-43 DEPENDS ON THE PROTEASOMELIU, Y; DUAN, W; GUO, Y et al.Neuroscience. 2014, Vol 281, pp 88-98, issn 0306-4522, 11 p.Article

Nuclear import impairment causes cytoplasmic trans-activation response DNA-binding protein accumulation and is associated with frontotemporal lobar degenerationNISHIMURA, Agnes L; ZUPUNSKI, Vera; TROAKES, Claire et al.Brain. 2010, Vol 133, pp 1763-1771, issn 0006-8950, 9 p., 6Article

Arteriolosclerosis that affects multiple brain regions is linked to hippocampal sclerosis of ageingNELTNER, Janna H; ABNER, Erin L; VAN ELDIK, Linda J et al.Brain. 2014, Vol 137, pp 255-267, issn 0006-8950, 13 p., 1Article

Review: Recent progress in frontotemporal lobar degenerationPICKERING-BROWN, S. M.Neuropathology and applied neurobiology (Print). 2010, Vol 36, Num 1, pp 4-16, issn 0305-1846, 13 p.Article

Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degenerationROLLINSON, Sara; RIZZU, Patrizia; MEAD, Simon et al.Neurobiology of aging. 2009, Vol 30, Num 4, pp 656-665, issn 0197-4580, 10 p.Article

Abnormal hippocampal distribution of TDP-43 in patients with-late onset psychosisVELAKOULIS, Dennis; WALTERFANG, Mark; MOCELLIN, Ramon et al.Australian and New Zealand journal of psychiatry. 2009, Vol 43, Num 8, pp 739-745, issn 0004-8674, 7 p.Article

Colocalization of Transactivation-Responsive DNA-Binding Protein 43 and Huntingtin in Inclusions of Huntington DiseaseSCHWAB, Claudia; ARAI, Tetsuaki; HASEGAWA, Masato et al.Journal of neuropathology and experimental neurology. 2008, Vol 67, Num 12, pp 1159-1165, issn 0022-3069, 7 p.Article

Frontotemporal lobar degeneration: Diversity of FTLD lesionsSEILHEAN, D; BIELLE, F; PLU, I et al.Revue neurologique (Paris). 2013, Vol 169, Num 10, pp 786-792, issn 0035-3787, 7 p.Conference Paper

Molecular basis of amyotrophic lateral sclerosis : THE NEUROBIOLOGY OF NEURODEGENERATIVE DISORDER: FROM BASIC TO CLINICAL RESEARCHLISCIC, Rajka M; BRELJAK, Davorka.Progress in neuro-psychopharmacology & biological psychiatry. 2011, Vol 35, Num 2, pp 370-372, issn 0278-5846, 3 p.Article

Actualités dans la recherche fondamentale et clinique sur la sclérose latérale amyotrophique = Update on fundamental and clinical research in amyotrophic lateral sclerosisPRADAT, P.-F; CAMDESSANCHE, J.-P; VERSCHUEREN, A et al.Revue neurologique (Paris). 2009, Vol 165, Num 6-7, pp 532-541, issn 0035-3787, 10 p.Article

Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSGIJSELINCK, Ilse; SLEEGERS, Kristel; DE POOTER, Tim et al.Neurobiology of aging. 2009, Vol 30, Num 8, pp 1329-1331, issn 0197-4580, 3 p.Article

XBP1 depletion precedes ubiquitin aggregation and Golgi fragmentation in TDP-43 transgenic ratsJIANBIN TONG; CAO HUANG; FANGFANG BI et al.Journal of neurochemistry. 2012, Vol 123, Num 3-4, pp 406-416, issn 0022-3042, 11 p.Article

FUS-related proteinopathies: Lessons from animal modelsLANSON, Nicholas A; UDAI BHAN PANDEY.Brain research. 2012, Vol 1462, pp 44-60, issn 0006-8993, 17 p.Article

Increased expression of TDP-43 in the skin of amyotrophic lateral sclerosisSUZUKI, M; MIKAMI, H; WATANABE, T et al.Acta neurologica scandinavica. 2010, Vol 122, Num 5, pp 367-372, issn 0001-6314, 6 p.Article

Elucidating the genetics and pathology of Perry syndromeWIDER, Christian; DACHSEL, Justus C; FARRER, Matthew J et al.Journal of the neurological sciences. 2010, Vol 289, Num 1-2, pp 149-154, issn 0022-510X, 6 p.Conference Paper

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43 -negative neuronal inclusionsMACKENZIE, Ian R. A; FOTI, Dean; WOULFE, John et al.Brain. 2008, Vol 131, pp 1282-1293, issn 0006-8950, 12 p., 5Article

The evidence for altered RNA metabolism in amyotrophic lateral sclerosis (ALS)STRONG, Michael J.Journal of the neurological sciences. 2010, Vol 288, Num 1-2, pp 1-12, issn 0022-510X, 12 p.Article

  • Page / 6