Kui Ming CHAN

Prof. Kui Ming CHAN, 陳居明

  • TYB-1B-206

Accepting PhD Students

Calculated based on number of publications stored in Pure and citations from Scopus
20042025

Research activity per year

Personal profile

Author IDs

ORCID iD: 0000-0001-6430-3340
Scopus Author ID: 8631854500

Impact

Qualifications (Brief)

PhD (HKU)
Postdoc (Mayo Clinic, Rochester MN, USA)        

Biography

Dr K. M. CHAN graduated with BSc and received his PhD at HKU in 2003 and 2007 respectively. He then moved to Mayo Clinic (Rochester MN, USA) for postdoctoral training and obtained the Edward C. Kendall Research Fellowship in Biochemistry before rejoining HKU as Research Assistant Professor in June 2013. In February 2015 he joined the Department of Biomedical Sciences (BMS), City University of Hong Kong as a tenure-track Assistant Professor.

Prizes/Honours

  • Edward C. Kendall Research Fellowship in Biochemistry 2013, Mayo Clinic
  • Professional Development Award 2015, City University of Hong Kong

Position(s) Available

We are looking for Postdoctoral Fellows, Research Assistants and Postgraduate Students to join our newly established research team. Interested candidates please send your CV and a summary of past research experience to Dr Chan: (email: [email protected])

  1. Applications are invited for Research Assistant I or II. Applicants with M.Phil. degree in Biological Science, Biochemistry or a related discipline; or a Bachelor's degree with at least 1 year lab work experience are welcome to apply.
  2. PhD positions are available. BSc or MSc students with passion in basic or applied biomedical research are encouraged to apply.
  3. Postdoctoral fellow positions are available upon enquiry. Please contact Dr Chan directly for further information.

Research Interests/Areas

  • Epigenetics
  • Chromatin Biology
  • Cancer Epigenetics
  • X-Chromosome inactivation
  • DNA replication

Dr Chan is interested in understanding 1) how epigenetic information is maintained during cell division and 2) the role of epigenetics in regulating gene expression and human diseases. It is well known that genetic information is encoded by the DNA sequence. However, DNA alone does not account for the complexity of the mammalian genome. Chromatin, comprising DNA, core histone proteins, and other regulatory proteins, regulates gene expression and maintains genome stability. Recent studies using the next generation sequencing (NGS) technologies have identified for the first time mutations on histone genes in two pediatric brain cancers; diffuse intrinsic pontine gliomas (DIPG) and glioblastoma multiforme (GBM). Two recurrent somatic mutations (K27M and G34R/V) were identified in genes encoding the canonical histone H3.1 (HIST1H3B) and its variant H3.3 (H3F3A.) This revealed the important roles of histone modifications in human diseases and links epigenetic changes to tumorigenesis.

We are currently elucidating the functional significance of novel epigenetic protein factors in maintaining X Chromosome Inactivation as well as the roles of histone mutations in human diseases.

Research Interests

Expertise related to UN Sustainable Development Goals

In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):

  • SDG 3 - Good Health and Well-being
  • SDG 12 - Responsible Consumption and Production

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Collaborations from the last five years

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