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Research 31–60 of 71
- Molecular Genetics of Alopecias
- The seasonal development dynamics of the yak hair cycle transcriptome
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Inherited Disorders of the Hair
- Trichodystrophies: A hair-raising differential diagnosis
- Rhamnose-mediated modulation of hair follicle growth: insights from chemical genomics
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Genetic Hair Disorders: A Review
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Transcriptomic analyses of regenerating adult feathers in chicken
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- CD34 defines melanocyte stem cell subpopulations with distinct regenerative properties
- Transcriptome Reveals Long Non-coding RNAs and mRNAs Involved in Primary Wool Follicle Induction in Carpet Sheep Fetal Skin
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- Innate type 2 immunity controls hair follicle commensalism by Demodex mites
- Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X
- Characterization of a new, inducible transgenic mouse model with GFP expression in melanocytes and their precursors
- Transcriptome meta-analysis reveals the hair genetic rules in six animal breeds and genes associated with wool fineness
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Transcriptome Profiling of Human Follicle Dermal Papilla Cells in response to Porphyra-334 Treatment by RNA-Seq
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- The homing of exogenous hair follicle mesenchymal stem cells into hair follicle niches