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Research 211–240 of 1000+
- The nude gene and the skin
- The Genetics of Human Skin Disease
- The molecular pathogenesis of Trichilemmal carcinoma
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Comprehensive Genomic Profiling of Cutaneous Adnexal Carcinomas: A Genomic Landscape Study
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Intratumoral <i>De Novo</i> Steroid Synthesis Activates Androgen Receptor in Castration-Resistant Prostate Cancer and Is Upregulated by Treatment with CYP17A1 Inhibitors
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Recent advances in understanding and managing male infertility
- Epidermal Growth Factor Receptor Inhibitors: A Review of Cutaneous Adverse Events and Management
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes
- Nanomaterial-Based Therapy for Wound Healing
- What's new in the pathogeneses and triggering factors of bullous pemphigoid
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Taiwanese Dermatological Association consensus for the prevention and management of epidermal growth factor receptor tyrosine kinase inhibitor-related skin toxicities
- New developments in the molecular treatment of ichthyosis: review of the literature
- Hidradenitis Suppurativa and Wound Management
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice