Search
for
Sort by
Research 571–600 of 1000+
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Roles of steroid sulfatase in brain and other tissues
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- INTERFERONS IN DERMATOLOGY
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Congenital adrenal hyperplasia
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men
- Male androgenetic alopecia (Part II)
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Investigating the Safety and Efficacy of Platelet-Rich Plasma (PRP) Treatment for Female Androgenetic Alopecia: Review of the Literature
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- Function of KLF4 in Stem Cell Biology
- Ectodysplasin-A2 induces dickkopf 1 expression in human balding dermal papilla cells overexpressing the ectodysplasin A2 receptor
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Design and development of cosmeceutical cream for hyperpigmentation and anti-aging
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn