Search
for
Sort by
Research 241–270 of 1000+
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Hair Follicle Immune Privilege Revisited: The Key to Alopecia Areata Management
- The Okuda Papers: an extraordinary - but unfortunately unrecognized - piece of work that could have changed the history of hair transplantation
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Learning from nudity: lessons from the nude phenotype
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Proliferation, but Not Apoptosis, Is Associated with Distinct β-Catenin Expression Patterns in Non-Small-Cell Lung Carcinomas
- The character “hairless” in the mouse
- A Clinical Approach to Severe Insulin Resistance
- Skin manifestations among<i>GATA2</i>-deficient patients
- The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis
- Tsukushi is involved in the wound healing by regulating the expression of cytokines and growth factors
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- Alopecia: Association with Resistance to Thyroid Hormones
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Cyclosporine-Induced Alopecia in Childhood Nephrotic Syndrome – A Case Report
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy