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Research 781–810 of 1000+
- 14-3-3σ Is Required for Club Hair Retention
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- 519 Phase I/IIa clinical trial for recessive dystrophic epidermolysis bullosa using genetically corrected autologous keratinocytes
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Canonical prolactin signaling and global mRNA expression in the skin of Holstein heifers carrying the SLICK1 allele of the prolactin receptor gene
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia.
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Effect of calcium supplementation on bone deformity and histopathological findings of skin papules in a pediatric patient with vitamin D–dependent rickets type 2A: a case report
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- LB1007 Systemic treatment with a KLK5 inhibitor shows efficacy in a murine model of Netherton syndrome
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Emerging interactions between skin stem cells and their niches
- A small multigene hydroxyproline-O-galactosyltransferase family functions in arabinogalactan-protein glycosylation, growth and development in Arabidopsis
- Two Hydroxyproline Galactosyltransferases, GALT5 and GALT2, Function in Arabinogalactan-Protein Glycosylation, Growth and Development in Arabidopsis
- Recombinant human hair keratin proteins for halting bleeding
- Activation of TRPV4 Induces Exocytosis and Ferroptosis in Human Melanoma Cells
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Normalization of hair growth in sparse fur-abnormal skin and hair (SPF-ASH) mice by introduction of the rat ornithine transcarbamylase (OTC) gene
- Medication-induced hair loss: An update
- Efficacy of autogenic, allogenic and heterogenic platelet rich plasma (PRP) on Avulsion skin wounds in rabbit model
- Investigation of Paraoxanase Enzyme Polymorphism in Patients with Alopecia Areata
- SEXUAL DIMORPHISM IN MAMMALS