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Research 811–840 of 1000+
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Familial Frontal Fibrosing Alopecia
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Microneedling plus topical dutasteride solution for androgenetic alopecia: a randomized placebo‐controlled study
- A study of the Geheimratsacken angle as predictor for early diagnosis of androgenetic alopecia in adolescent population
- The Hair Shedding Visual Scale: A Quick Tool to Assess Hair Loss in Women
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Central centrifugal cicatricial alopecia: retrospective case-control study of 54 patients from a tertiary care center
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Bioengineering the Hair Follicle
- Role of caffeine in the management of androgenetic alopecia
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Testosterone and dihydrotestosterone production in genetically furless and furred male rabbits and effects on growth.
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- 272 Structural changes in human skin after topical application of glucocorticoids assessed by in vivo imaging technologies
- 269 Down-regulatory role of cholecystokinin on psoriatic epidermal inflammation
- 270 A novel small compound HPH-15 antagonizes TGF-β/Smad signaling and ameliorates experimental skin fibrosis
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Hair growth promoting effects of adipose tissue-derived stem cells
- Premature graying of hair