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Research 121–150 of 1000+
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Follikelhormone
- Androgen receptors and their biology
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Review of Fluconazole Properties and Analytical Methods for Its Determination
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Multi-omics revealed that the postbiotic of hawthorn-probiotic alleviated constipation caused by loperamide in elderly mice
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- The potential impact of melanosomal pH and metabolism on melanoma
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Bioarchitectural Design of Bioactive Biopolymers: Structure–Function Paradigm for Diabetic Wound Healing
- P78 Acrodermatitis enteropathica in children: clinical cases
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Biochemistry of Vitamin B: Metabolic Regulations, Deficiency Disorders and Emerging Therapeutic Strategies
- Autologous Platelet and Extracellular Vesicle-Rich Plasma as Therapeutic Fluid: A Review
- Polycystic ovary syndrome and its management: In view of oxidative stress
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>