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Research 61–90 of 464
- Role of the Wnt signaling pathway in keratoacanthoma
- Industry update: the latest developments in the field of therapeutic delivery, July 2018
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Inherited Epidermolysis Bullosa: A Clinical Case
- Syndromes of Severe Insulin Resistance (SSIRs)
- Androgen replacement therapy in women
- A Review on Nanoparticle Based Herbal Remedies for the Management of Alopecia
- 461 Identification of a Novel Pathogenic XPC:c.2420+1G>C Variant in a Patient with Xeroderma Pigmentosum
- Epithelial elements in superficial angiomyxomas: mimicry of adnexal development, and mesenchymal‐to‐epithelial transition
- Generalized atrophic benign epidermolysis bullosa.
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- The impact of VDR expression and regulation in vivo
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Genetic Disorders and Defects in Vitamin D Action
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- PCSK9: From Nature’s Loss to Patient’s Gain
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- WNT Signaling in Disease
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- Correlation of trichoscopic findings with clinico-epidemiological factors in male pattern&nbsp;<span style="font-size: 1rem;">hairloss: A cross-sectional study from a tertiary care center in Chengalpattu</span>
- Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1