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Research 91–120 of 1000+
- <i>De Novo</i>Transcriptome Assembly and Differential Gene Expression Profiling of Three<i>Capra hircus</i>Skin Types during Anagen of the Hair Growth Cycle
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Anatomy and Biology of Hair at Different Ages
- Untersuchungen der Fremdstoffbindung in permanenten Keratinozyten- und Melanozyten-Zelllinien sowie die Eignung von Primärkulturen aus humanen Haarfollikeln zur In-vitro-Messung der Fremdstoffaufnahme im Haar
- Radiofrequency Microporation Enhances Topical Minoxidil Delivery and Hair Regeneration in Androgenetic Alopecia
- TRICOSCOPIA – ESTRUTURAS TRICOSCÓPICAS E SUA APLICABILIDADE NAS PATOLOGIAS DO CABELO E DO COURO CABELUDO
- Did You Ever See a Creeping Hair?
- Noninvasive method for assessing the human circadian clock using hair follicle cells
- Efluvio anágeno. Hallazgos tricoscópicos
- Pathologic Diagnosis of Central Centrifugal Cicatricial Alopecia on Horizontal Sections
- Dissecting Microscope Versus Magnifying Loupes with Transilluntination in the Preparation of Follicular Unit Grafts
- Reliability of Histopathology for the Early Recognition of Fibrosis in Traction Alopecia: Correlation with Clinical Severity
- Pathologic Quiz Case: Unexplained Hair Loss—1 Boy, 2 Cats, and 1 Dog
- Sequence and Expression of Murine Type I Hair Keratins mHa2 and mHa3
- Cosmetic Approach for Healthy and Damaged Hair
- Protopanaxatirol type ginsenoside Re promotes cyclic growth of hair follicles via inhibiting transforming growth factor β signaling cascades
- New Activators and Inhibitors in the Hair Cycle Clock: Targeting Stem Cells’ State of Competence
- Hair Medulla and its variations in Doshaja Prakruti – An observational study
- Post waxing folliculitis: a clinicopathological evaluation
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Follicles Twisted During Follicular Unit Excision Could Survive in the Skin of Nude Mice
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- The nude gene and the skin
- Marine Health-Promoting Compounds: Recent Trends for Their Characterization and Human Applications
- Trichoscopic patterns of nonscarring alopecia's
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Protein extraction from human anagen head hairs 1-millimeter or less in total length
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease