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Research 361–390 of 1000+
- Melanocytes and Vitiligo (and Hair Graying)
- The Role of Histone Demethylases in Disease
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling
- Hair That Is Difficult to Manage in a Hispanic Girl
- Uncomplicated differentiation of stem cells into bipolar neurons and myelinating glia
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Uncombable hair improved by biotin
- 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증
- Trichothiodystrophy: Current Concepts
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Stem cell therapy and hair loss: Present evidence and future perspectives
- Bachmann–Bupp syndrome and treatment
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Cases Report the Cronkhite-Canada Syndrome
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Epidermal patterning and induction of different hair types during mouse embryonic development
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- New developments in the molecular treatment of ichthyosis: review of the literature
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration