PvuII RFLPs in the DMD gene detected by a subclone (cDMD1a) of the cDNADENG HAN-XIANG; NIIKAWA, N.Nucleic acids research. 1990, Vol 18, Num 10, issn 0305-1048, p. 3107Article

Molecular cloning and chromosomal assignment of the gene for human Zn-α₂-glycoproteinUEYAMA, H; DENG HAN-XIANG; OHKUBO, I et al.Biochemistry (Easton). 1993, Vol 32, Num 48, pp 12968-12976, issn 0006-2960Article

Transgenic mouse models and human neurodegenerative disordersDENG, Han-Xiang; SIDDIQUE, Teepu.Archives of neurology (Chicago). 2000, Vol 57, Num 12, pp 1695-1702, issn 0003-9942Article

Chromosomal mapping of the human smooth muscle actin gene (enteric type, ACTA3) to 2p13.1 and molecular nature of the HindIII polymorphismUEYAMA, H; INAZAWA, J; NISHINO, H et al.Genomics (San Diego, Calif.). 1995, Vol 25, Num 3, pp 720-723, issn 0888-7543Article

Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouseLIJUN WANG; DENG, Han-Xiang; GRISOTTI, Gabriella et al.Human molecular genetics (Print). 2009, Vol 18, Num 9, pp 1642-1651, issn 0964-6906, 10 p.Article

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisYI YANG; HENTATI, Afif; COLE, Natalie et al.Nature genetics. 2001, Vol 29, Num 2, pp 160-165, issn 1061-4036Article

Differential Involvement of Optineurin in Amyotrophic Lateral Sclerosis With or Without SOD1 MutationsDENG, Han-Xiang; BIGIO, Eileen H; SUFIT, Robert et al.Archives of neurology (Chicago). 2011, Vol 68, Num 8, pp 1057-1061, issn 0003-9942, 5 p.Article

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementiaDENG, Han-Xiang; CHEN, Wenjie; HUJUN JIANG et al.Nature (London). 2011, Vol 477, Num 7363, pp 211-215, issn 0028-0836, 5 p.Article

SQSTM1 Mutations in Familial and Sporadic Amyotrophic Lateral SclerosisFECTO, Faisal; JIANHUA YAN; DONKERVOORT, Sandra et al.Archives of neurology (Chicago). 2011, Vol 68, Num 11, pp 1440-1446, issn 0003-9942, 7 p.Article

FUS-Immunoreactive Inclusions Are a Common Feature in Sporadic and Non-SOD1 Familial Amyotrophic Lateral SclerosisDENG, Han-Xiang; HONG ZHAI; SIDDIQUE, Nailah et al.Annals of neurology. 2010, Vol 67, Num 6, pp 739-748, issn 0364-5134, 10 p.Article

Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approachDENG, Han-Xiang; JIANG HUJUN; FU RONGGEN et al.Human molecular genetics (Print). 2008, Vol 17, Num 15, pp 2310-2319, issn 0964-6906, 10 p.Article

Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4DENG, Han-Xiang; KLEIN, Christopher J; HEDLEY-WHYTE, E. Tessa et al.Nature genetics. 2010, Vol 42, Num 2, pp 165-169, issn 1061-4036, 5 p.Article

Distal axonopathy in an alsin-deficient mouse modelDENG, Han-Xiang; HONG ZHAI; RONGGEN FU et al.Human molecular genetics (Print). 2007, Vol 16, Num 23, pp 2911-2920, issn 0964-6906, 10 p.Article