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Research 931–960 of 1000+
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Construction of regulatory network for alopecia areata progression and identification of immune monitoring genes based on multiple machine-learning algorithms
- Applications of Ultrasound-Mediated Gene Delivery in Regenerative Medicine
- <i>Brassica oleracea</i> extract, glucosinlates, and sulforaphane promote hair growth in vitro and ex vivo
- Highly Conserved Keratin-Associated Protein 7-1 Gene in Yak, Taurine and Zebu Cattle
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Role of Sulfur Metabolism Gene and High-Sulfur Gene Expression in Wool Growth Regulation in the Cashmere Goat
- A computationally inferred regulatory heart aging model including post-transcriptional regulations
- Woolly Antics between the Sheaths
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- 583 Promoting hair growth and hair keratin production with a propolis extract
- 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 FRZB gene regulates hair follicle development in rabbits via the Wnt/β-catenin signaling pathway
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- 795 Bacteria induce skin regeneration
- Inherited Epidermolysis Bullosa: A Clinical Case
- Highlights
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- British Society for Dermatopathology: Summaries of Papers
- The role of mutations on gene AR, in androgenetic alopecia syndrome