Search
for
Sort by
Research 451–480 of 1000+
- Androgen receptor gene CAG repeat polymorphism in women with polycystic ovary syndrome
- Acquired scalp alopecia. Part I: A review
- Hoxc-Dependent Mesenchymal Niche Heterogeneity Drives Regional Hair Follicle Regeneration
- Congenital hair loss disorders: Rare, but not too rare
- A Microarray-Based Analysis Reveals that a Short Photoperiod Promotes Hair Growth in the Arbas Cashmere Goat
- SLE and Serum Complement: Causative, Concomitant or Coincidental?
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Prediction of male-pattern baldness from genotypes
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- The Mesenchymal Niche of the Hair Follicle Induces Regeneration by Releasing Primed Progenitors from Inhibitory Effects of Quiescent Stem Cells
- Treatment strategies for alopecia
- Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns
- Parathyroid Hormone Hormone-Related Protein and the PTH Receptor Regulate Angiogenesis of the Skin
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- Smad1 and 5 but Not Smad8 Establish Stem Cell Quiescence Which Is Critical to Transform the Premature Hair Follicle During Morphogenesis Toward the Postnatal State
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- <i>WNT10A</i> , dermatology and dentistry
- An Ovol2‐Zeb1 transcriptional circuit regulates epithelial directional migration and proliferation
- Inhibition of glycosphingolipid synthesis reverses skin inflammation and hair loss in ApoE−/− mice fed western diet
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Hairless is a nuclear receptor corepressor essential for skin function
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- What does acne genetics teach us about disease pathogenesis?
- Enzyme Replacement Therapy Ameliorates Multiple Symptoms of Murine Homocystinuria
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?