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Research 31–60 of 1000+
- Hyaluronic Acid Filler Injection as an Alternative to Surgery for the Correction of Canine Entropion
- Centella asiatica L. Urb. Extracellular Vesicle and Growth Factor Essence for Hair and Scalp Health: A 56-Day Exploratory Randomized Trial
- Differentiation of cultured hair follicle neural crest stem cells into functional melanocytes
- Prevalence, Phenotypes, and Comorbidities of Polycystic Ovary Syndrome Among Indian Women
- Sesquiterpene-Enriched Extract of <i>Curcuma aeruginosa</i> Roxb. Retards Axillary Hair Growth: A Randomised, Placebo-Controlled, Double-Blind Study
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Overexpression of hypoxia-inducible factor-1α in hidradenitis suppurativa: the link between deviated immunity and metabolism
- Blimp1+ cells generate functional mouse sebaceous gland organoids in vitro
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Endoscopic Browplasty
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- New Progesterone Esters as 5.ALPHA.-Reductase Inhibitors.
- Ozenoxacin suppresses sebum production by inhibiting mTORC1 activation in differentiated hamster sebocytes
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Subcellular localization of the five members of the human steroid 5α-reductase family
- MECHANISM OF PROTEINURIA
- Molecular interactions of progesterone derivatives with 5α-reductase types 1 and 2 and androgen receptors
- Chitosan/LiCl composite scaffolds promote skin regeneration in full-thickness loss
- Combination of autologous FCS and MPG versus each technique alone in the treatment of stable vitiligo
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Carbon, nitrogen, and sulfur elemental and isotopic variations in mouse hair and bone collagen during short-term graded calorie restriction
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Design, proof-of-concept of single robotic hair transplant mechanisms for both harvest and implant of hair grafts
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- Co-presentation of Tapia's syndrome and pressure alopecia—A rare event after septorhinoplasty: A case report and literature review
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Recent Progress in Health Benefits of Hederagenin and Its Glycosides