HaMut Lam
Publications by Year
Research Areas
Hair Growth and Disorders, Skin and Cellular Biology Research, Wnt/β-catenin signaling in development and cancer, RNA Research and Splicing, melanin and skin pigmentation
Most-Cited Works
- → Alopecia Universalis Associated with a Mutation in the Human hairless Gene(1998)413 cited
- → The Molecular Pathology of Progressive Symmetric Erythrokeratoderma: A Frameshift Mutation in the Loricrin Gene and Perturbations in the Cornified Cell Envelope(1997)156 cited
- → Genomic Organization of the Human Hairless Gene (HR) and Identification of a Mutation Underlying Congenital Atrichia in an Arab Palestinian Family(1999)92 cited
- → A Locus for Autosomal Recessive Hypodontia with Associated Dental Anomalies Maps to Chromosome 16q12.1(1998)91 cited
- → A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers(1998)84 cited
- → Homozygous Variegate Porphyria: Identification of Mutations on Both Alleles of the Protoporphyrinogen Oxidase Gene in a Severely Affected Proband(1998)51 cited
- → A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis(2004)44 cited
- → Evidence for Pseudodominant Inheritance of Atrichia with Papular Lesions(2002)32 cited
- → Novel compound heterozygous nonsense mutations in the hairless gene causing atrichia with papular lesions(2005)13 cited
- Identification of a novel splice site mutation in the human hairless gene underlying atrichia with papular lesions.(2006)