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Research 30 of 462
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Potential Involvement of miR-144 in the Regulation of Hair Follicle Development and Cycle Through Interaction with Lhx2
- The citrullinating enzyme PADI4 governs progenitor cell proliferation and translation in developing hair follicles
- IL-36γ drives skin toxicity induced by EGFR/MEK inhibition and commensal Cutibacterium acnes
- A Signature of Genes Featuring FGF11 Revealed Aberrant Fibroblast Activation and Immune Infiltration Properties in Keloid Tissue
- The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Transgenic mice overexpressing CD109 in the epidermis display decreased inflammation and granulation tissue and improved collagen architecture during wound healing
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Association of follicle-stimulating hormone receptor gene ser680 asn (rs6166) polymorphism with polycystic ovarian syndrome
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Mechanistic synergy of hair growth promotion by the Avicennia marina extract and its active constituent (avicequinone C) in dermal papilla cells isolated from androgenic alopecia patients
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Role of Annexin A2 isoform 2 on the aggregative growth of dermal papillae cells
- Identification and expression of the target gene SLC24A2 of oar-miR-377 and its novel SNPs effects on wool traits in sheep
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway
- Oxidative Activity of the Type 2 Isozyme of 17β-Hydroxysteroid Dehydrogenase (17β-HSD) Predominates in Human Sebaceous Glands
- Increased Vibrissa Growth in Transgenic Mice Expressing Insulin-like Growth Factor 1
- Meis1 Regulates Epidermal Stem Cells and Is Required for Skin Tumorigenesis
- The mRNA for Protease Nexin-1 is Expressed in Human Dermal Papilla Cells and its Level is Affected by Androgen
- Identification and characterization of an antisense RNA transcript (gfg) from the human basic fibroblast growth factor gene.