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Research 61–90 of 1000+
- Variation in the ovine keratin-associated protein 15-1 gene affects wool yield
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- 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
- Association of Rs231775 Genetic Variant of Cytotoxic T-lymphocyte Associated Protein 4 with Alopecia Areata Disease in Males: A Case–Control Study
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- 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 Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- 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 frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- 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
- Adenosine A2B receptor: A pathogenic factor and a therapeutic target for sensorineural hearing loss
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Characterization of Novel Cutaneous Human Papillomavirus Genotypes HPV-150 and HPV-151
- 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
- Safety Analysis of Panax Ginseng in Randomized Clinical Trials: A Systematic Review
- Sex hormone binding globulin - an important biomarker for predicting PCOS risk: A systematic review and meta-analysis
- 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
- Emerging Topics in Cardiometabolic and Psychologic Sequelae, Pathogenesis, and Treatment of Polycystic Ovarian Syndrome: A Review
- Hair follicle morphogenesis and epidermal homeostasis in we/we wal/wal mice with postnatal alopecia