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Research 181–210 of 1000+
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Identification of Potential miRNA–mRNA Regulatory Network Associated with Growth and Development of Hair Follicles in Forest Musk Deer
- 137 Loss of myeloid Mcpip1 suppresses hair growth and development of epidermal papilloma of the skin
- 1345 A single-cell RNA map of perinatal developing mouse skin
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Di-Genic Inheritance in Genodermatoses: Insights from Two Consanguineous Cases in a Reference Lebanese Center within the Middle East and North Africa (MENA) Region
- ASH2L mediates epidermal differentiation and hair follicle morphogenesis via H3K4me3 modification
- [Monilethrix is a hereditary hair shaft disorder].
- Analysis of LncRNA and mRNA Expression Profiles in Skin Tissues of Super Merino Sheep and Small-Tailed Han Sheep
- Profibrotic Subsets of SPP1+ Macrophages and POSTN+ Fibroblasts Contribute to Fibrotic Scarring in Acne Keloidalis
- Transcriptome-based selection and validation of optimal house-keeping genes for skin research in goats (Capra hircus)
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Gene Expression in Rat Dermal Papilla Cells: Analysis of 2529 ESTs
- Keratin Gene Expression in Wool Fibre Development
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- Disease causing homozygous variants in the human hairless gene
- Single-Cell Sequencing Technology in Ruminant Livestock: Challenges and Opportunities
- Differences in cell subsets between sun-exposed and unexposed skin: preliminary single-cell sequencing and biological analysis from a single case
- 5α Reductase Deficiency—a Rare Cause of Ambiguous Genitalia and Gender Dysphoria
- Association between DNA Methylation in the Core Promoter Region of the CUT-like Homeobox 1 (CUX1) Gene and Lambskin Pattern in Hu Sheep
- Integrative Phenotypic and Transcriptomic Dynamics of Hair Follicle Development and Fur Quality in Rex Rabbits
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Heterozygous <i>COL5A1</i> deletion in a cat with classical Ehlers–Danlos syndrome
- 1410 Single-cell RNA sequencing reveals POUF51 and HES3 as regulators of the stem cell population in psoriasis
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- scINSIGHT for interpreting single-cell gene expression from biologically heterogeneous data