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Research 871–900 of 1000+
- Investigation of Paraoxanase Enzyme Polymorphism in Patients with Alopecia Areata
- TRPA1 Modulates Mechanotransduction in Cutaneous Sensory Neurons
- 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
- Generalized atrophic benign epidermolysis bullosa.
- 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
- A kindred with mutant IKAROS and autoimmunity
- 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
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- RNA sequencing reveals lncRNA-mediated non-mendelian inheritance of feather growth change in chickens
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- Participation of CD34-enriched mouse adipose cells in hair morphogenesis
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Skin morphology of the mutant hairless USP mouse
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Establishment of Tsc2-deficient rat embryonic stem cells
- Congenital atrichia with papular lesions
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Homozygous whole body <i>Cbs</i> knockout in adult mice features minimal pathology during ageing despite severe homocysteinemia
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- Pitfalls of PCR-Based Strategy for Genotyping <i>Cre-Loxp</i> Mice
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Exploring the efficacy of testosterone undecanoate in male children with 5α‐reductase deficiency
- Ashwagandha root in the treatment of non-classical adrenal hyperplasia