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Research 541–570 of 1000+
- Nanotechnology-Based Strategies for Hair Follicle Regeneration in Androgenetic Alopecia
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Synthetic Approaches for Pharmacologically Active Decorated Six-Membered Diazines
- A New Office Based Protocol to Reverse AGA Miniaturization at Early and Advanced Stages
- Therapeutic effects of a new long-acting growth factor cocktail (Cellcurex™) injected using a microneedle on the scalp in patients with androgenetic alopecia: A split study
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Management of hypotrichosis of the eyelashes: Focus on bimatoprost
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- Histopathology of Hypotrichosis with Juvenile Macular Dystrophy
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- Homozygous Deletion in CDH3 and Hypotrichosis With Juvenile Macular Dystrophy
- A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Hair Restoration Surgery in Patients with Hypotrichosis of the Pubis
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis