A SQSTM1 POLYMORPHISM CONFERS RISK FOR SPORADIC INCLUSION BODY MYOSITIS DISEASE EXPRESSION

被引：0

作者：

Pytte, Julia ^{[1
,3
]}

Van Loenhout, Maria ^{[3
]}

Mastaglia, Frank ^{[2
]}

James, Ian ^{[3
]}

Flynn, Loren L. ^{[2
,3
]}

MacDougall, Gabriella ^{[1
]}

Beer, Kelly ^{[3
]}

Coudert, Jerome ^{[3
]}

Sooda, Anu ^{[3
]}

Akkari, P. Anthony ^{[1
,2
,3
,4
,5
]}

Needham, Merilee ^{[3
]}

机构：

[1] UWA, Crawley, Australia

[2] Perron Inst, Nedlands, WA, Australia

[3] Murdoch Univ, Murdoch, WA, Australia

[4] Duke Univ, Durham, NC USA

[5] Black Swan Pharmaceut, Durham, NC USA

来源：

CLINICAL AND EXPERIMENTAL RHEUMATOLOGY | 2023年 / 41卷 / 02期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

P-8

引用

页码：438 / 438

页数：1

共 50 条

[41] Sporadic ALS with compound heterozygous mutations in the SQSTM1 gene
Hiroshi Shimizu
Yasuko Toyoshima
Atsushi Shiga
Akio Yokoseki
Keiko Arakawa
Yumi Sekine
Takayoshi Shimohata
Takeshi Ikeuchi
Masatoyo Nishizawa
Akiyoshi Kakita
Osamu Onodera
Hitoshi Takahashi
Acta Neuropathologica, 2013, 126 : 453 - 459
[42] SQSTM1 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
Fecto, Faisal
Yan, Jianhua
Vemula, S. Pavan
Liu, Erdong
Yang, Yi
Chen, Wenjie
Zheng, Jian Guo
Shi, Yong
Siddique, Nailah
Arrat, Hasan
Donkervoort, Sandra
Ajroud-Driss, Senda
Sufit, Robert L.
Heller, Scott L.
Deng, Han-Xiang
Siddique, Teepu
ARCHIVES OF NEUROLOGY, 2011, 68 (11) : 1440 - 1446
[43] Sporadic ALS with compound heterozygous mutations in the SQSTM1 gene
Shimizu, Hiroshi
Toyoshima, Yasuko
Shiga, Atsushi
Yokoseki, Akio
Arakawa, Keiko
Sekine, Yumi
Shimohata, Takayoshi
Ikeuchi, Takeshi
Nishizawa, Masatoyo
Kakita, Akiyoshi
Onodera, Osamu
Takahashi, Hitoshi
ACTA NEUROPATHOLOGICA, 2013, 126 (03) : 453 - 459
[44] TREX1 mutations are not associated with sporadic inclusion body myositis
Cox, F. M.
Boon, E. M. J.
van der Lans, C. A. C.
Bakker, E.
Verschuuren, J. J. G. M.
Badrising, U. A.
EUROPEAN JOURNAL OF NEUROLOGY, 2010, 17 (08) : 1108 - 1109
[45] CN-1A AUTOANTIBODIES ARE SPECIFIC FOR SPORADIC INCLUSION BODY MYOSITIS
Diederichsen, Louise Pyndt
Korsholm, Sine Sondergaard
Iversen, Line Vinderslev
Nielsen, Christoffer Tandrup
Hermansen, Marie-Louise From
Jacobsen, Soren
Witting, Nanna
Krogager, Markus E.
Friis, Tina
ANNALS OF THE RHEUMATIC DISEASES, 2019, 78 : 841 - 842
[46] Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms
Mastaglia, F. L.
Rojana-udomsart, A.
James, I.
Needham, M.
Day, T. J.
Kiers, L.
Corbett, J. A.
Saunders, A. M.
Lutz, M. W.
Roses, A. D.
NEUROMUSCULAR DISORDERS, 2013, 23 (12) : 969 - 974
[47] Association study reveals novel risk loci for sporadic inclusion body myositis
Johari, M.
Arumilli, M.
Palmio, J.
Savarese, M.
Tasca, G.
Mirabella, M.
Sandholm, N.
Lohi, H.
Hackman, P.
Udd, B.
EUROPEAN JOURNAL OF NEUROLOGY, 2017, 24 (04) : 572 - 577
[48] Quadriceps strength is a sensitive marker of disease progression in sporadic inclusion body myositis
Allenbach, Yves
Benveniste, Olivier
Decostre, Valerie
Canal, Aurelie
Eymard, Bruno
Herson, Serge
Bloch-Queyrat, Coralie
Hogrel, Jean-Yves
NEUROMUSCULAR DISORDERS, 2012, 22 (11) : 980 - 986
[49] Sporadic inclusion body myositis correlates with increased expression and cross-linking by transglutaminases 1 and 2
Choi, YC
Park, GT
Kim, TS
Sunwoo, IN
Steinert, PM
Kim, SY
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) : 8703 - 8710
[50] The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis
Gang, Qiang
Bettencourt, Conceicao
Machado, Pedro M.
Fox, Zoe
Brady, Stefen
Healy, Estelle
Parton, Matt
Holton, Janice L.
Hilton-Jones, David
Shieh, Perry B.
Zanoteli, Edmar
De Paepe, Boel
De Bleecker, Jan
Shaibani, Aziz
Ripolone, Michela
Violano, Raffaella
Moggio, Maurizio
Barohn, Richard J.
Dimachkie, Mazen M.
Mora, Marina
Mantegazza, Renato
Zanotti, Simona
Hanna, Michael G.
Houlden, Henry
NEUROBIOLOGY OF AGING, 2015, 36 (04) : 1766.e1 - 1766.e3

← 1 2 3 4 5 →