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Research 601–630 of 1000+
- Integrative skin phenotypic and transcriptomic analyses reveal candidate genes for coat color and fiber length in four Chinese goat breeds (<i>Capra hircus</i>)
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Cornified Epithelial Teeth of Jawless Vertebrates Contain Proteins Similar to Keratin-Associated Proteins of Mammalian Skin Appendages
- Persistent hyperparathyroidism in vitamin D-dependent rickets type 2A does not prevent normalization of hypophosphatemia or healing of the rickets
- The Effects of Single Testosterone Administration and Stress Induction on Steroid Hormone Levels in Hair
- 8507 Misdiagnosis of Graves’ and RAI Treatment in Patient with THRB Gene Mutation
- Pilomatricoma in the infraorbital region
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Reshaped DNA methylation cooperating with homoeolog‐divergent expression promotes improved root traits in synthesized tetraploid wheat
- 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
- A missense mutation in Lama3 causes androgen alopecia
- mTOR signaling in hair follicle and hair diseases: recent progress
- Uncombable hair improved by biotin
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- 921 Generation of a new rodent model of scleroderma
- P78 Acrodermatitis enteropathica in children: clinical cases
- 821 Pigmentation and autophagy in alopecia areata pathogenesis
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus
- Generalised Glucocorticoid Resistance
- Does Vitamin D play a role on Msx1 homeoprotein expression involving an endogenous antisense mRNA?*1
- [Androgenetic alopecia].
- Metabolic Regulation of Hematopoietic Stem Cells in the Hypoxic Niche
- The Functional Organization of Cutaneous Low-Threshold Mechanosensory Neurons
- <i>OsPHR2</i> Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
- The JAK/STAT signaling pathway: from bench to clinic