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- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- Ultrahigh-Power Sonicator Lysis Enables Deep ProteomicProfiling of Hair Shafts for Fetal Growth Restriction Biomarker Discovery
- Are the Meibomian glands “hair follicles without a hair shaft” ?
- Hair keratin pattern in human hair follicles grown <i>in vitro</i>
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Localization of Cathepsins B, D, L, LAMP-1 and .MU.-Calpain in Developing Hair Follicles.
- Comparative Transcriptome Analysis of Fetal Skin Reveals Key Genes Related to Hair Follicle Morphogenesis in Cashmere Goats
- Transglutaminase 5 Expression in Human Hair Follicle
- Pili Trianguli et Canaliculi Is a Defect of Inner Root Sheath Keratinization
- Embryology, Histology, and Physiology of the Hair Follicle
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- HAIR LOSS FROM SEBUM
- Histological and dermatoscopic description of sphynx cat skin
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- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- The nude gene and the skin
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Histopathologic Criteria for Follicular Differentiation
- 성장기 모낭에서 큐티클층의 각질화 과정
- Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts
- Outer root sheath keratinization in anagen and catagen of the mammalian hair follicle. A seventh distinct type of keratinization in the hair follicle: trichilemmal keratinization.
- Keratinisation status and cytokeratins of the human Meibomian gland epithelium
- Unraveling the Comedone Switch through Single-Cell Resolution of Human Acne Lesions
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Learning from nudity: lessons from the nude phenotype
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Catagen in the hairless house mouse
- Abnormal inner root sheath of the hair follicle in the loose anagen hair syndrome: An ultrastructural study
- The Genomic Variation in Textured Hair: Implications in Developing a Holistic Hair Care Routine