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Research 721–750 of 1000+
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- Cessation of Hairline Recession following Open Forehead Rejuvenation
- Ablative 2940-nm Er: YAG fractional laser for the treatment of male androgenetic alopecia with predominantly frontal hairline recession
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Trichoscopic evaluation of frontal hairline recession in Egyptian female patients
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study
- Faculty Opinions recommendation of Association of topical minoxidil with autosomal recessive woolly hair/hypotrichosis caused by LIPH pathogenic variants.
- A Randomized Cohort Study: Is It Worth the Time to Receive Antiandrogenic Pretreatment Before Ovulation Induction for Women With Polycystic Ovary Syndrome?
- 441 Anti-melanoma gene signature in dermal sheath fibroblasts from scalp hair follicles in Recessive Dystrophic Epidermolysis Bullosa (RDEB)
- Mechanical forces in skin disorders
- Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
- First symposium on natural gene therapy of the skin
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- 688 Precise and efficient editing of the COL7A1 gene in RDEB derived iPSCs with CRISPR/Cas9 and prime editing
- TERMIS ‐ AMERICAS Toronto, Ontario, Canada July 10–13, 2022
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Disorders of Keratinization
- Research Snippets
- Tissue engineering strategies for human hair follicle regeneration: How far from a hairy goal?
- Follicle-innervating Aδ-low threshold mechanoreceptors organize through a population-dependent mechanism
- Prevalence of Male and Female Pattern Hair Loss in Maryborough
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Enanthem in Patients With COVID-19 and Skin Rash
- Genetics of Inherited Ichthyoses and Related Diseases