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Research 301–330 of 1000+
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Insulin resistance as risk factor for the development of type 2 diabetes mellitus: a systematic approach
- Gene Variant in Amish a Clue to Better Aging
- Acne Vulgaris
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- Reconsidering the Polycystic Ovary Syndrome (PCOS)
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Dermoscopy of Chronic Radiation-Induced Dermatitis in Patients with Head and Neck Cancers Treated with Radiotherapy
- Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Australasian Society for Dermatology Research Meeting, May 2006
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- Pathways to inflammation: acne pathophysiology
- Inherited Disorders of the Hair
- Alopecia and its medical management
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- Female pattern hair loss
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Diagnostic approach to low‐renin hypertension
- The human gut chemical landscape predicts microbe-mediated biotransformation of foods and drugs
- LPA3, a unique G protein-coupled receptor for lysophosphatidic acid
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome