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Research 391–420 of 511
- Quantitation of human mitochondrial DNA and whole mtGenomes sequencing of fingernail/hair shaft samples
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Proteomic Analysis of Crimped and Straight Wool in Chinese Tan Sheep
- Intra-host SARS-CoV-2 single-nucleotide variants emerged during the early stage of COVID-19 pandemic forecast population fixing mutations
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Capsaicin: an in-depth review of its chemical properties, health benefits, and challenges in food applications
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- The Role of Vitamin D3 Deficiency and Colonization of the Oral Mucosa by Candida Yeast-like Fungi in the Pathomechanism of Psoriasis
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- Study of the Thyroid Profile of Patients with Alopecia
- Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation
- Frontal fibrosing alopecia: A review of disease pathogenesis
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Author response: Effects of lifelong testosterone exposure on health and disease using Mendelian randomization
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Prolonged Drug-Induced Hypersensitivity Syndrome/DRESS With Alopecia Areata and Autoimmune Thyroiditis
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Risk of autoimmune thyroid diseases in individuals with alopecia areata: A nationwide case‐control study
- Whole-genome resequencing to investigate the genetic diversity and the molecular basis underlying key economic traits in indigenous sheep breeds adapted to hypoxic environments
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Food Administration and Not Genetic Variants Causes Pharmacokinetic Variability of Tadalafil and Finasteride
- Genotyping of the rs1800440 Polymorphism in CYP1B1 Gene and the rs9258883 Polymorphism in HLA-B Gene in a Spanish Cohort of 223 Patients with Frontal Fibrosing Alopecia