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Research 691–720 of 1000+
- CD133-positive dermal papilla-derived Wnt ligands regulate postnatal hair growth
- Activation and regulation of the granulation tissue derived cells with stemness-related properties
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Long noncoding RNA and gene expression analysis of melatonin-exposed Liaoning cashmere goat fibroblasts indicating cashmere growth
- Activation of mitochondrial aldehyde dehydrogenase 2 promotes hair growth in human hair follicles
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Comparison of mitochondrial transplantation by using a stamp-type multineedle injector and platelet-rich plasma therapy for hair aging in naturally aging mice
- Allopregnanolone Alters the Gene Expression Profile of Human Glioblastoma Cells
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- In Vivo Evaluation of<i>Eclipta alba</i>Extract as Anticancer and Multidrug Resistance Reversal Agent
- Keratin 6A promotes skin inflammation through JAK1-STAT3 activation in keratinocytes
- Shh Gene Regulates the Proliferation and Apoptosis of Dermal Papilla Cells to Affect Its Differential Expression in Secondary Hair Follicle Growth Cycle of Cashmere Goats
- Type 1 interferon signature and cytotoxic T lymphocyte activation targeted against sweat ducts in inflammatory acquired idiopathic generalized anhidrosis
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Integrated single-cell chromatin and transcriptomic analyses of peripheral immune cells in patients with alopecia areata
- Janus kinase inhibitors for alopecia areata: a review of clinical data
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Le gène<i>hairless</i>de la souris
- Construction of regulatory network for alopecia areata progression and identification of immune monitoring genes based on multiple machine-learning algorithms
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- 277 An open label pilot clinical trial of the JAK inhibitor tofacitinib for alopecia areata
- The incidental pore: Ca<sub>V</sub>1.2 and stem cell activation in quiescent hair follicles
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis
- TRPV3 Ion Channel: From Gene to Pharmacology
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria