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Research 391–420 of 1000+
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Intrauterine botulinum toxin A administration promotes endometrial regeneration mediated by IGFBP3-dependent OPN proteolytic cleavage in thin endometrium
- Variation in the ovine trichohyalin gene and its association with wool curvature
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- The Role of Vitamin D3 Deficiency and Colonization of the Oral Mucosa by Candida Yeast-like Fungi in the Pathomechanism of Psoriasis
- De novo assembly and annotation of Asiatic lion (<i>Panthera leo persica</i>) genome
- Is Dutasteride a Therapeutic Alternative for Amyotrophic Lateral Sclerosis?
- Male polycystic ovarian syndrome phenotype: a meta-analysis of endocrine-metabolic dysregulation in fathers and brothers of PCOS-affected women
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Genetics of infertility and “assisted fertilization” in the Bible: The case of Abraham and his family
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Free Testosterone Levels in Patients with Covid-19 and its Association with Disease Severity
- Human acellular amniotic membrane incorporating exosomes from adipose-derived mesenchymal stem cells promotes diabetic wound healing
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- Safety concerns of paternal drug exposure on fertility, pregnancy and offspring: An analysis based on the FDA adverse event reporting system
- Human Hair Keratin‐Associated Proteins (KAPs)
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- The Genetic Architecture of Alopecia Areata
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Multiomics global landscape of stemness-related gene clusters in adipose-derived mesenchymal stem cells
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Conjoint analysis of methylation, transcriptomic, and proteomic profiles in pemphigus vulgaris
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- A phase 2a randomized, placebo-controlled study to evaluate the efficacy and safety of the oral Janus kinase inhibitors ritlecitinib and brepocitinib in alopecia areata: 24-week results