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Research 901–930 of 1000+
- <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development
- Dermal white adipose tissue development and metabolism: The role of transcription factor Foxn1
- The effects of extended photoperiod and warmth on hair growth in ponies and horses at different times of year
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Hair Growth Cycle Is Arrested in SCD1 Deficiency by Impaired Wnt3a-Palmitoleoylation and Retrieved by the Artificial Lipid Barrier
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Evaluation of Scalp Hydration and pH Values in Hijab-Wearing and Non-Hijab-Wearing Women
- Differences between ultrastructure and protein composition in straight hair fibres
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Sequences and differential expression of three novel human type-II hair keratins
- Hair Keratins and Hair Follicle–Specific Epithelial Keratins
- Structural changes in trichocyte keratin intermediate filaments during keratinization
- The epidermis: rising to the surface
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- Ceramide: A New Approach to Hair Protection and Conditioning.
- Quality of Life in Patients Living with Andro-gentic Alopecia: A Cross Sectional Observational Study
- Highlights from Recent Cancer Literature
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Das Phototrichogramm als Verfahren zur Beurteilung haarwachstumsfördernder Präparate am Beispiel einer Kombination von Hirsefruchtextrakt, L-Cystin und Calciumpantothenat : Ergebnisse einer in vivo Untersuchung bei Frauen mit androgenetischem Haarausfall
- A meadowfoam seed oil derivative and its activity on human hair : From a natural, biodegradable source comes a silicone derivative that can penetrate and repair human hair