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Research 541–570 of 1000+
- Gene expression profile of human follicle dermal papilla cells in response to <i>Camellia japonica</i> phytoplacenta extract
- Expression of Plectin-1 and Trichohyalin in Human Tongue Cancer Cells
- SOX18 Promotes the Proliferation of Dermal Papilla Cells via the Wnt/β-Catenin Signaling Pathway
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Seasonal Variability in Transcript Expression of Type I and Type II Keratins in Wool Follicles of Lustrous Fleece-Producing Magra Sheep
- A comparative study of skin transcriptomes and histological observations for black and white hair colors of giant panda
- Understanding the Secular Decline in Testosterone: Mechanisms, Consequences, and Clinical Perspectives
- Predicting Physical Appearance from Low Template: State of the Art and Future Perspectives
- Gastric cancer; actualities and perspectives of early diagnosis and targeted therapy
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- Human Hair Keratin‐Associated Proteins (KAPs)
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Congenital atrichia with papular lesions
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Presence of Uterine Leiomyomas Has No Significant Impact on Gene Expression Profile in the Scalp of Patients with Central Centrifugal Cicatricial Alopecia
- Culturing of Melanocytes from the Equine Hair Follicle Outer Root Sheath
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- FORENSIC DNA PHENOTYPING FOR CRIMINAL IDENTIFICATION
- Abstracts from the 4th Annual Student Medical Summit
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- BJD Editor's Choice
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Comparison of allogeneic stem cell transplant conditioning regimens in AML, MDS and CLL
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up