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Research 211–240 of 1000+
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- 132 Genetics of Stress Hormone Concentrations in Hair of Healthy Nursery Pigs and Their Relationship with Back Test Responses
- 268 Male-pattern baldness and its association with coronary heart disease
- Metabolic disease with autoimmune phenomena: 2 cases of SLE-like disease in young children diagnosed with lysinuric protein intolerance
- Dermatopathology and molecular genetics
- Cleave but not leave: Astrotactin proteins in development and disease
- Animal models of human skin disease
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Autoimmune skin disease pathogenesis: a chronological immune cascade and multi-hit model
- Angiogenesis and Microcirculation in Ischemic Heart Disease
- Diseases of Honeybee (Apis mellifera)
- Current issues on the genetic implications and treatment of androgenic alopecia
- The genetic basis of dermatophytosis skin infection susceptibility
- Biology and Genetics of Hair
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- Acne as a chronic systemic disease
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Finding models for skin diseases: successes and failures
- AORTOCAVAL PARAGANGLIOMA IN VON HIPPEL-LINDAU DISEASE
- DYS459, DYS391, DYS388 and DYS19 genetic loci have high allelic frequency in patients with prostate cancer
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- The role of WNT10B in physiology and disease: A 10-year update
- Identificación de la variación molecular y genética subyacente a las enfermedades de la piel
- Neonatal screening in Sweden and disease-causing variants in phenylketonuria, galactosaemia and biotinidase deficiency
- A Review on Unraveling the Complexity of Autoimmune Skin Disorders: Genetic Influences, Environmental Triggers and Innovative Management Approaches
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Joint study of the associations of HLA‐B and the transmembrane short tandem repeat polymorphism of MICA protein with alopecia areata shows independent associations of both with the disease
- So Much More Than Just Structural Support: Laminin‐332 and Its Multifaceted Functions in Skin Homeostasis and Disease