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Research 121–150 of 131
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- The molecular anatomy of cashmere goat hair follicle during cytodifferentiation stage
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Examining the Effect of Notocactus ottonis Cold Vacuum Isolated Plant Cell Extract on Hair Growth in C57BL/6 Mice Using a Combination of Physiological and OMICS Analyses
- Hair growth promoting effect of toothpaste in C57BL/6 mice: Active components and their effects on genomic expression
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Monilethrix – Case report of a rare disease
- Molecular Genetics of Human Hair Diseases
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Circ 0020938 inhibits hair follicle stem cells proliferation via the miR-142-5p/DSG4 axis in cashmere goats
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- LB1034 Meta-analysis of scalp transcriptome defines alopecia areata subtypes and molecular response to four (4) treatments with jak inhibiting properties