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Research 751–780 of 1000+
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Superior Root Hair Formation Confers Root Efficiency in Some, But Not All, Rice Genotypes upon P Deficiency
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings
- Susan Lee Lindquist (1949–2016)—pioneer in the study of cellular protein folding and disease
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Expression and Analysis of TBX3 Gene in the Skin from Three Locations on Dun Mongolian Bider Horse
- An ethnomedicinal survey of several regions of Pabna district, Bangladesh
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Peripheral Skin Temperature and Circadian Biological Clock in Shift Nurses after a Day off
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Molecular landscape of lung cancer: insights into therapeutic targets and clinical outcomes
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- RNA-seq analysis identifies key genes enhancing hoof strength to withstand barefoot racing in Standardbred trotters