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Research 30 of 590
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Acne Syndromes and Mosaicism
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- The Genetics of Human Skin Disease
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Phylloid terminal hair nevus: A unique clinical entity
- Disruption of FGF5 in Cashmere Goats Using CRISPR/Cas9 Results in More Secondary Hair Follicles and Longer Fibers
- Lgr5+ stem cells and their progeny in mouse epidermis under regimens of exogenous skin carcinogenesis, and their absence in ensuing skin tumors
- Lgr6+ stem cells and their progeny in mouse epidermis under regimens of exogenous skin carcinogenesis, and their absence in ensuing skin tumors
- Oral Presentations
- Genetic Defects of Female Sexual Differentiation
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Modulating the stem cell niche for tissue regeneration
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- Molecular pathology of skin adnexal tumours
- Immunological aspects and gender bias during respiratory viral infections including novel Coronavirus disease‐19 (COVID‐19): A scoping review
- The clinicopathological spectrum of trichoepitheliomas: a retrospective descriptive study
- Acne
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Inherited Disorders of the Hair
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)