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Research 751–780 of 1000+
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Agouti and Agouti-related Protein: Analogies and Contrasts
- Distinct Regulatory Programs Control the Latent Regenerative Potential of Dermal Fibroblasts during Wound Healing
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Gender differences in patients with COVID-19: a narrative review
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- A Novel In Vivo Model for Evaluating Agents that Protect Against Ultraviolet A-induced Photoaging
- Minoxidil may suppress androgen receptor-related functions
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- Evolution of Trichocyte Keratins
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Hair follicles modulate skin barrier function
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Sustained Postnatal Skin Regeneration Upon Prenatal Application of Functionalized Collagen Scaffolds
- Integrative analysis of Iso-Seq and RNA-seq data reveals transcriptome complexity and differential isoform in skin tissues of different hair length Yak
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Mechanical forces across compartments coordinate cell shape and fate transitions to generate tissue architecture
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Acne Syndromes and Mosaicism
- Current Genetics in Hair Diseases
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata