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Research 61–90 of 1000+
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- 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
- 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
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Pentacyclic Triterpenoid Maslinic Acid Promotes Hair Growth Comparable to Minoxidil: A New Insight on the Potential Involvement of Cilia Activity
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- The role of hemp (Cannabis sativa L.) in cosmeceuticals and personal care: A systematic review
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Hair follicle morphogenesis and epidermal homeostasis in we/we wal/wal mice with postnatal alopecia
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- The Role of Micronutrients in Alopecia Areata: A Review
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Decreased Serum Ferritin is Associated With Alopecia in Women
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond