Search
for
Sort by
Research 481–510 of 1000+
- Analysis of pediatric dermatology inpatient consultations in a pediatric teaching hospital
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Substrate specific sulfatase activity from hair follicles in recessive X-linked ichthyosis
- Androgenetic Alopecia in Gender Minority Patients
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Association of Single Nucleotide Polymorphisms in the CYP19A1 Gene with Female Pattern Hair Loss in a Chinese Population
- Hair Loss Diagnosis Using Artificial Neural Networks
- Lipin 1 Gene Polymorphisms in Polycystic Ovary Syndrome
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Retinoids Putting the “A” in Alopecia
- Pharmacological Inhibition of DGAT1 Induces Sebaceous Gland Atrophy in Mouse and Dog Skin While Overt Alopecia Is Restricted to the Mouse
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Responses of prolactin and hair growth to selection for age at puberty in Angus cattle
- Pediatric dermatoses pattern at a Brazilian reference center
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Integrative analysis of Iso-Seq and RNA-seq data reveals transcriptome complexity and differential isoform in skin tissues of different hair length Yak
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- PLCD1 and Pilar Cysts
- Variation and Heritability in Hair Diameter and Curvature in an Australian Twin Sample
- Prevalence and treatment of Alopecia areata in Taif area, KSA
- Novel compound heterozygous mutations in the<i>desmoplakin</i>gene cause hair shaft abnormalities and culminate in lethal cardiomyopathy
- Three-dimensional reconstructions of mechanosensory end organs suggest a unifying mechanism underlying dynamic, light touch
- Atopic dermatitis and risk of autoimmune diseases: a systematic review and meta-analysis
- Evaluation of serum level of omentin‐1 in females with hirsutism