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Research 871–900 of 1000+
- 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
- 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
- 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
- TRPA1 Modulates Mechanotransduction in Cutaneous Sensory Neurons
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- SEXUAL DIMORPHISM IN MAMMALS
- Combined C3b and Factor B Autoantibodies and MPGN Type II
- Planar Cell Polarity Cadherin Celsr1 Regulates Skin Hair Patterning in the Mouse
- In vivo function of VDR in gene expression-VDR knock-out mice
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- Autotaxin-LPA signaling contributes to obesity-induced insulin resistance in muscle and impairs mitochondrial metabolism
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Differential sensitivity of epidermal cell subpopulations to β-catenin-induced ectopic hair follicle formation
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS