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Research 691–720 of 1000+
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Racial variations in COVID‐19 deaths may be due to androgen receptor genetic variants associated with prostate cancer and androgenetic alopecia. Are anti‐androgens a potential treatment for COVID‐19?
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- Exploring Differentially Expressed Genes by RNA-Seq in Cashmere Goat (Capra hircus) Skin during Hair Follicle Development and Cycling
- GLP-1 Receptor Agonists: Beyond Their Pancreatic Effects
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Exosomes mediate sensory hair cell protection in the inner ear
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Genetic Basis of Alopecia Areata
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Ichthyosis with confetti: clinics, molecular genetics and management
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Inflammatory and Anti-Inflammatory Parameters in PCOS Patients Depending on Body Mass Index: A Case-Control Study
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Keratinocyte-derived follistatin regulates epidermal homeostasis and wound repair
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Integrated analysis of lncRNAs and mRNAs by RNA-Seq in secondary hair follicle development and cycling (anagen, catagen and telogen) of Jiangnan cashmere goat (Capra hircus)
- Transcriptome-based selection and validation of optimal house-keeping genes for skin research in goats (Capra hircus)
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Effect of the FA2H Gene on cashmere fineness of Jiangnan cashmere goats based on transcriptome sequencing
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells