Search
for
Sort by
Research 211–240 of 251
- Reawakening GDNF's regenerative past in mice and humans
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Repurposing DPP4-Inhibition to Improve Hair Follicle Activation and Regeneration
- 5α-reductase Inhibitors: Finasteride and Dutasteride in Feminising Therapy
- Platelet-Rich Plasma in the Treatment of Androgenetic Alopecia: An Equation with Many Unknowns
- Cyberbabes: (Self-) representation of women and the virtual male gaze
- Androgenic Effects on Ventricular Repolarization
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Scalp Dysesthesia
- Extraction and Detection of mRNA from Horsehair
- DRUG‐ASSOCIATED ALOPECIA
- HAIR DISEASES
- Contraceptive implant use among inner city teens
- Hair transparency decoding in Asia: From stylists’ perception to in vitro measurement
- Oral isotretinoin for acne
- COVID-19 and hypopituitarism
- Pathogenicity and enzyme screening of some selected non-dermatophytic moulds
- The significance of the apelinergic system in doxorubicin-induced cardiotoxicity
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- NLKFill: high-resolution image inpainting with a novel large kernel attention
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Reporting in clinical studies on platelet-rich plasma therapy among all medical specialties: A systematic review of Level I and II studies
- Boundary Conditions Cause Different Generic Bifurcation Structures in Turing Systems
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin