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Research 721–750 of 1000+
- Pseudallescheria boydii infection associated with IgG4-related disease
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Large Language Model versus Clinician Written Summaries of Research Papers
- 455 Beyond Immunity: TEC and JAK3 Kinase Activation in Melanocytes Drives Inflammation in Vitiligo
- Investigation of ROP GTPase Activity and Cytoskeleton Dynamics During Tip Growth in Root Hairs and Pollen Tubes
- Post SARS-CoV-2 vaccination effluvium
- Arecaceae
- Book reviews
- A child with generalized hypertrichosis due to secondary topical minoxidil exposure
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Hair follicle-specific keratins and their diseases
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Update on detection, morphology and fragility in pili annulati in three kindreds
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Formononetin: A Pathway to Protect Neurons
- Calcitriol-resistant rickets with alopecia
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Myrtus communis L.
- Neem (Azadirachta indica): A Panacea of all Diseases
- Focal Dermal Hypoplasia Associated With Lymphedema: A Case Report From Saudi Arabia
- Arabidopsis Oil Body-Expressed Oleosin-rhFGF5 Inhibits Hair Growth in Mouse
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Divergent genetic mechanism leads to spiny hair in rodents
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Формирование межнациональной толерантности у детей старшего дошкольного возраста в условиях социального партнерства семьи и детского сада
- Alex de la Iglesia: "Todos somos perversos"