Yan Li

发表

Generation and Characterization of Mice with Myh9 Deficiency

A. Lalwani, A. Mhatre, Graham Atkin, 2007, NeuroMolecular Medicine.

Expression of Myh9 in the mammalian cochlea: Localization within the stereocilia

A. Lalwani, A. Mhatre, A. Maghnouj, 2006, Journal of neuroscience research.

MYH9-siRNA and MYH9 mutant alleles: expression in cultured cell lines and their effects upon cell structure and function.

A. Lalwani, D. Friedmann, A. Mhatre, 2008, Cell motility and the cytoskeleton.

Alternative splice variants of MYH9.

A. Lalwani, A. Mhatre, Yan Li, 2008, DNA and cell biology.

Clinical and molecular genetic analysis of a family with macrothrombocytopenia and early onset sensorineural hearing loss.

A. Lalwani, S. Janssens, A. Mhatre, 2009, European journal of medical genetics.

Localization in stereocilia, plasma membrane, and mitochondria suggests diverse roles for NMHC-IIa within cochlear hair cells

D. Hillman, A. Lalwani, A. Mhatre, 2008, Brain Research.

Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study

H. Christen, M. Reith, S. Heales, 2010, The Lancet Neurology.

Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.

Paul Gissen, Shu-Yuan Cheng, M. Reith, 2009, The Journal of clinical investigation.

Mutation associated with Crouzon syndrome causes ligand‐independent dimerization and activation of FGF receptor‐2

C. Basilico, A. Mansukhani, Yan Li, 1997, Journal of cellular physiology.

Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood

E. Puffenberger, K. Strauss, M. Reith, 2014, Brain : a journal of neurology.

Interrelation of dopamine transporter oligomerization and surface presence as studied with mutant transporter proteins and amphetamine

M. Reith, Shu-Yuan Cheng, N. Chen, 2010, Journal of neurochemistry.

LncRNA MEG3 downregulation mediated by DNMT3b contributes to nickel malignant transformation of human bronchial epithelial cells via modulating PHLPP1 transcription and HIF-1α translation

Jingxia Li, Dongyun Zhang, Q. Xie, 2017, Oncogene.