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Research 361–390 of 1000+
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Role of skin enzymes in metabolism of topical drugs
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Clinical and Demographic Characteristics of Patients Diagnosed with Polycystic Ovary Syndrome: A Cross-Sectional Observational Study
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Review on Diagnostic and Managerial Consequences of PCOS Among Females
- Comparison differentiated osteoblast from adipose stem cells and normal osteoblast
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Adrenal causes of endocrine hypertension in childhood or adolescence
- The Role of Hormonal Imbalances in Amenorrhea
- Development of MALDI-TOF-MS and MALDI-MSI methods for hair analysis and evaluation of cosmetic treatments
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Keratin disorders: from gene to therapy
- Regulation of masculinization: androgen signalling for external genitalia development
- [Hormonal interaction and hair growth].
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits