Deng HX - Search Results

1

Recent advances in the genetics of hereditary axonal sensory-motor neuropathies type 2.

Ajroud-Driss S, Deng HX, Siddique T. Ajroud-Driss S, et al. Among authors: deng hx. Curr Neurol Neurosci Rep. 2011 Jun;11(3):262-73. doi: 10.1007/s11910-011-0185-z. Curr Neurol Neurosci Rep. 2011. PMID: 21327736 Review.

2

Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4.

Deng HX, Klein CJ, Yan J, Shi Y, Wu Y, Fecto F, Yau HJ, Yang Y, Zhai H, Siddique N, Hedley-Whyte ET, Delong R, Martina M, Dyck PJ, Siddique T. Deng HX, et al. Nat Genet. 2010 Feb;42(2):165-9. doi: 10.1038/ng.509. Epub 2009 Dec 27. Nat Genet. 2010. PMID: 20037587 Free PMC article.

3

FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis.

Deng HX, Zhai H, Bigio EH, Yan J, Fecto F, Ajroud K, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T. Deng HX, et al. Ann Neurol. 2010 Jun;67(6):739-48. doi: 10.1002/ana.22051. Ann Neurol. 2010. PMID: 20517935 Free PMC article.

4

Mutant TRPV4-mediated toxicity is linked to increased constitutive function in axonal neuropathies.

Fecto F, Shi Y, Huda R, Martina M, Siddique T, Deng HX. Fecto F, et al. Among authors: deng hx. J Biol Chem. 2011 May 13;286(19):17281-91. doi: 10.1074/jbc.M111.237685. Epub 2011 Mar 21. J Biol Chem. 2011. PMID: 21454511 Free PMC article.

5

Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations.

Deng HX, Bigio EH, Zhai H, Fecto F, Ajroud K, Shi Y, Yan J, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T. Deng HX, et al. Arch Neurol. 2011 Aug;68(8):1057-61. doi: 10.1001/archneurol.2011.178. Arch Neurol. 2011. PMID: 21825243 Free PMC article.

6

SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis.

Fecto F, Yan J, Vemula SP, Liu E, Yang Y, Chen W, Zheng JG, Shi Y, Siddique N, Arrat H, Donkervoort S, Ajroud-Driss S, Sufit RL, Heller SL, Deng HX, Siddique T. Fecto F, et al. Among authors: deng hx. Arch Neurol. 2011 Nov;68(11):1440-6. doi: 10.1001/archneurol.2011.250. Arch Neurol. 2011. PMID: 22084127

7

Human Genetic Diseases.

Deng H, Riederer P, Deng HX, Le W, Xiong W, Guo Y. Deng H, et al. Among authors: deng hx. Biomed Res Int. 2015;2015:315216. doi: 10.1155/2015/315216. Epub 2015 May 20. Biomed Res Int. 2015. PMID: 26078946 Free PMC article. No abstract available.

8

Identification of TMEM230 mutations in familial Parkinson's disease.

Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, Xu Y, Chan P, Huang B, Gao XP, Song Z, Liu Z, Fecto F, Siddique N, Foroud T, Jankovic J, Ghetti B, Nicholson DA, Krainc D, Melen O, Vance JM, Pericak-Vance MA, Ma YC, Rajput AH, Siddique T. Deng HX, et al. Among authors: deng h, deng s. Nat Genet. 2016 Jul;48(7):733-9. doi: 10.1038/ng.3589. Epub 2016 Jun 6. Nat Genet. 2016. PMID: 27270108 Free PMC article.

9

Early Impairment of Synaptic and Intrinsic Excitability in Mice Expressing ALS/Dementia-Linked Mutant UBQLN2.

Radzicki D, Liu E, Deng HX, Siddique T, Martina M. Radzicki D, et al. Among authors: deng hx. Front Cell Neurosci. 2016 Sep 20;10:216. doi: 10.3389/fncel.2016.00216. eCollection 2016. Front Cell Neurosci. 2016. PMID: 27703430 Free PMC article.

10

Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot-Marie-Tooth Disease Type 2.

Deng S, Feely SME, Shi Y, Zhai H, Zhan L, Siddique T, Deng HX, Shy ME. Deng S, et al. Among authors: deng hx. Neuromolecular Med. 2020 Mar;22(1):68-72. doi: 10.1007/s12017-019-08564-4. Epub 2019 Aug 29. Neuromolecular Med. 2020. PMID: 31468327

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