Han-Xiang Deng

  • 14050 Citations
1989 …2021
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Personal profile

Research Interests

Understanding the mechanism of neurodegenerative diseases such as Amyotrophic Lateral Sclerosis.

Education/Academic qualification

MD, PhD, Hunan Medical University, China

… → 1983

Research interests

  • Amyotrophic Lateral Sclerosis
  • Cell Biology
  • Genetics
  • Neurogenetics
  • Neuromuscular Disorders

Fingerprint Dive into the research topics where Han-Xiang Deng is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 11 Similar Profiles
Amyotrophic Lateral Sclerosis Medicine & Life Sciences
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Chromosomes Medicine & Life Sciences
Human Chromosomes Medicine & Life Sciences
Transgenic Mice Medicine & Life Sciences
Microdissection Medicine & Life Sciences
Motor Neurons Medicine & Life Sciences

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Grants 2002 2021

Secretory Vesicles
Dementia
Motor Neurons
Carisoprodol
Therapeutics
Parkinson Disease
Chromosomes, Human, Pair 20
Genetic Loci
Neurodegenerative Diseases
Genes
Amyotrophic Lateral Sclerosis
Motor Neurons
Oxidation-Reduction
Clustered Regularly Interspaced Short Palindromic Repeats
Pathology
Chromosomes, Human, Pair 15
Nerve Degeneration
Motor Neuron Disease
Molecular Models
Motor Neurons

Research Output 1989 2019

HACE1, RAC1, and what else in the pathogenesis of SPPRS?

Deng, H-X., Jun 1 2019, In : Neurology: Genetics. 5, 3, e326.

Research output: Contribution to journalEditorial

Open Access

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

Deng, S., Feely, S. M. E., Shi, Y., Zhai, H., Zhan, L., Siddique, T., Deng, H-X. & Shy, M. E., Jan 1 2019, (Accepted/In press) In : Neuromolecular medicine.

Research output: Contribution to journalArticle

Mutation
Incidence
Spinal Muscular Atrophy
Vocal Cord Paralysis
Hearing Loss
6 Citations (Scopus)

Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans

Tan, Y. Q., Tu, C., Meng, L., Yuan, S., Sjaarda, C., Luo, A., Du, J., Li, W., Gong, F., Zhong, C., Deng, H-X., Lu, G., Liang, P. & Lin, G., May 1 2019, In : Genetics in Medicine. 21, 5, p. 1209-1217 9 p.

Research output: Contribution to journalArticle

Cataract
Mutation
Azoospermia
Genes
Exome
1 Citation (Scopus)
Parkinsonian Disorders
Parkinson Disease
Genes
10 Citations (Scopus)

A novel ALS-associated variant in UBQLN4 regulates motor axon morphogenesis

Edens, B. M., Yan, J., Miller, N., Deng, H-X., Siddique, T. & Ma, Y., May 2 2017, In : eLife. 6, e25453.

Research output: Contribution to journalArticle

Amyotrophic Lateral Sclerosis
Morphogenesis
Axons
beta Catenin
Wnt Signaling Pathway