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Research 931–960 of 1000+
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Expression of the β-Catenin Gene in the Skin of Embryonic Geese During Feather Bud Development
- Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia
- The genetic evolution of skin squamous cell carcinoma: tumor suppressor identity matters
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A general mathematical model for the in vitro assembly dynamics of intermediate filament proteins
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Effects of bright light exposure during daytime on peripheral clock gene expression in humans
- Polymorphic CAG Repeat Numbers in the Androgen Receptor Gene of Female Pattern Hair Loss in a Han Chinese Population
- ‘Atrichosis’, a new hairless gene with cyst formation in rats
- Identification of Potential Hub Genes in Alopecia Areata
- The Suppression Effects of Fat Mass and Obesity Associated Gene on the Hair Follicle-Derived Neural Crest Stem Cells Differentiating into Melanocyte by N6-Methyladenosine Modifying Microphthalmia-Associated Transcription Factor
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Rare Generalized Form of Fungal Dermatitis in a Horse: Case Report
- Hox in the Niche Controls Hairy-geneity
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Le gène<i>hairless</i>de la souris