Search
for
Sort by
Research 541–570 of 1000+
- Testosterone and dihydrotestosterone production in genetically furless and furred male rabbits and effects on growth.
- Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- 575 An extract of Leontopodium alpinum prolongs anagen phase in human hair follicles ex vivo
- A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE
- 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
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Update on Frontal Fibrosing Alopecia
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Hair growth promoting effects of adipose tissue-derived stem cells
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Nonclassic Congenital Adrenal Hyperplasia
- Premature graying of hair
- Clinical effects of non-ablative and ablative fractional lasers on various hair disorders: a case series of 17 patients
- 5-Alpha reductase deficiency
- <i>WNT10A</i> , dermatology and dentistry
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Further Clinical Evidence for the Effect of IGF-1 on Hair Growth and Alopecia
- Congenital adrenal hyperplasia
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Curcumin derivatives inhibit testicular 17β-hydroxysteroid dehydrogenase 3