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Research 511–540 of 1000+
- Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- 284 Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Female Androgenetic (?) Alopecia
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Effect of Oral Minoxidil on Monilethrix
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Steatocystoma Multiplex
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Discreet monilethrix: De novo mutation on the example of polish families
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Sebaceous gland diseases: clinical picture risk factors and treatment
- Pachyonychia congenita: Sporadic onset with mutation analysis
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Full investigation of patients with polycystic ovary syndrome (PCOS) presenting to four different clinical specialties reveals significant differences and undiagnosed morbidity
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- Ichthyosis
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction