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Research 691–720 of 1000+
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- Keratins: the hair shaft's backbone revealed
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Identification and characterization of Birt–Hogg–Dubé associated renal carcinoma
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- FGF5 is a crucial regulator of hair length in humans
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Pigmentary mosaicism: An update
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Genome-Wide Association Studies of Hair Whorl in Pigs