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Research 481–510 of 1000+
- Adsorption of Diclofenac and PFBS on a Hair Keratin Dimer
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Congenital triangular alopecia: Is it always confined to fronto-temporal region?
- 549 Temporary cell cycle arrest in human scalp hair follicles and their epithelial stem cells by ALRN-6924: A novel strategy to selectively protect p53-wildtype cells against paclitaxel-induced alopecia
- Discreet monilethrix: De novo mutation on the example of polish families
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- MULTIPLE HEMANGIOMAS OF THE TONGUE AND ORAL CAVITY IN A MYOTONIC DYSTROPHY TYPE 1 PATIENT: A CASE REPORT
- Hair Anomalies in a 6-Year-Old Girl
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Platelet-Rich Plasma Therapy for Male and Female Pattern Hair Loss
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Delayed Cutaneous Wound Healing and Aberrant Expression of Hair Follicle Stem Cell Markers in Mice Selectively Lacking Ctip2 in Epidermis
- Mineral Malnutrition Following Bariatric Surgery
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Natural killer cells in atopic and autoimmune diseases of the skin
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- The developmental basis of fingerprint pattern formation and variation
- Profile of tofacitinib citrate and its potential in the treatment of moderate-to-severe chronic plaque psoriasis
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Concise Review: Translating Regenerative Biology into Clinically Relevant Therapies: Are We on the Right Path?
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament