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Research 511–540 of 1000+
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Pitfalls of PCR-Based Strategy for Genotyping <i>Cre-Loxp</i> Mice
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Keratin Gene Expression in Wool Fibre Development
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Single cell analysis of transcriptome and open chromatin reveals the dynamics of hair follicle stem cell aging
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Recombinant Goat VEGF164 Increases Hair Growth by Painting Process on the Skin of Shaved Mouse
- Cornified Epithelial Teeth of Jawless Vertebrates Contain Proteins Similar to Keratin-Associated Proteins of Mammalian Skin Appendages
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Industry updates in advanced therapy medicinal products and regenerative medicine – March 2026
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Siberian cats help in solving part of the mystery surrounding golden cats
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Competitive balance of intrabulge BMP/Wnt signaling reveals a robust gene network ruling stem cell homeostasis and cyclic activation
- The role of VEGF and thrombospondins in skin angiogenesis
- Estrogen and androgen signaling in the pathogenesis of BPH
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome