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Research 871–900 of 1000+
- Cyberspace Chat
- Molecular mechanisms underlying cashmere quality differences between Jiangnan cashmere goats and Changthangi pashmina goats
- Light-Emitting Hair Follicles: Studying Skin Regeneration With In Vivo Imaging
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Keratin disorders: from gene to therapy
- Advances in Lipid Nanoparticle‐Based Disease Treatment
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Regulatory pathways implicated in male androgenetic alopecia pathogenesis
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- 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
- 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
- A review of the ethnomedicinal, antimicrobial, and phytochemical properties of Musa paradisiaca (plantain)
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- 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
- 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
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- 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