Deng HX - Search Results

1

A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosis.

Aksoy H, Dean G, Elian M, Deng HX, Deng G, Juneja T, Storey E, McKinlay Gardner RJ, Jacob RL, Laing NG, Siddique T. Aksoy H, et al. Among authors: deng hx, deng g. Neuroepidemiology. 2003 Jul-Aug;22(4):235-8. doi: 10.1159/000070564. Neuroepidemiology. 2003. PMID: 12792143

2

Genetics of amyotrophic lateral sclerosis.

Siddique T, Deng HX. Siddique T, et al. Among authors: deng hx. Hum Mol Genet. 1996;5 Spec No:1465-70. doi: 10.1093/hmg/5.supplement_1.1465. Hum Mol Genet. 1996. PMID: 8875253 Review.

3

Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis.

Deng HX, Tainer JA, Mitsumoto H, Ohnishi A, He X, Hung WY, Zhao Y, Juneja T, Hentati A, Siddique T. Deng HX, et al. Hum Mol Genet. 1995 Jun;4(6):1113-6. doi: 10.1093/hmg/4.6.1113. Hum Mol Genet. 1995. PMID: 7655471 No abstract available.

4

Midbrain dopaminergic neuronal degeneration in a transgenic mouse model of familial amyotrophic lateral sclerosis.

Kostic V, Gurney ME, Deng HX, Siddique T, Epstein CJ, Przedborski S. Kostic V, et al. Among authors: deng hx. Ann Neurol. 1997 Apr;41(4):497-504. doi: 10.1002/ana.410410413. Ann Neurol. 1997. PMID: 9124807

5

Age and founder effect of SOD1 A4V mutation causing ALS.

Saeed M, Yang Y, Deng HX, Hung WY, Siddique N, Dellefave L, Gellera C, Andersen PM, Siddique T. Saeed M, et al. Among authors: deng hx. Neurology. 2009 May 12;72(19):1634-9. doi: 10.1212/01.wnl.0000343509.76828.2a. Epub 2009 Jan 28. Neurology. 2009. PMID: 19176896 Free PMC article.

6

Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosis.

Zu JS, Deng HX, Lo TP, Mitsumoto H, Ahmed MS, Hung WY, Cai ZJ, Tainer JA, Siddique T. Zu JS, et al. Among authors: deng hx. Neurogenetics. 1997 May;1(1):65-71. doi: 10.1007/s100480050010. Neurogenetics. 1997. PMID: 10735277

7

Transgenic mouse models and human neurodegenerative disorders.

Deng HX, Siddique T. Deng HX, et al. Arch Neurol. 2000 Dec;57(12):1695-702. doi: 10.1001/archneur.57.12.1695. Arch Neurol. 2000. PMID: 11115235 Review. No abstract available.

8

Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.

Yan J, Deng HX, Siddique N, Fecto F, Chen W, Yang Y, Liu E, Donkervoort S, Zheng JG, Shi Y, Ahmeti KB, Brooks B, Engel WK, Siddique T. Yan J, et al. Among authors: deng hx. Neurology. 2010 Aug 31;75(9):807-14. doi: 10.1212/WNL.0b013e3181f07e0c. Epub 2010 Jul 28. Neurology. 2010. PMID: 20668259 Free PMC article.

9

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.

Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, Hung WY, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben-Hamida M, Pericak-Vance M, Hentati F, Siddique T. Yang Y, et al. Among authors: deng hx. Nat Genet. 2001 Oct;29(2):160-5. doi: 10.1038/ng1001-160. Nat Genet. 2001. PMID: 11586297

10

Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement.

Shibata N, Hirano A, Kobayashi M, Siddique T, Deng HX, Hung WY, Kato T, Asayama K. Shibata N, et al. Among authors: deng hx. J Neuropathol Exp Neurol. 1996 Apr;55(4):481-90. doi: 10.1097/00005072-199604000-00011. J Neuropathol Exp Neurol. 1996. PMID: 8786408

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