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Research 961–990 of 1000+
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia
- Tissue-Specific Multi-Omics Integration Demonstrates Molecular Signatures Connecting Obesity to Immune Vulnerability
- The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- FGF5 is a crucial regulator of hair length in humans
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Transcriptomic analyses of regenerating adult feathers in chicken
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Molecular Background of Pi Deficiency-Induced Root Hair Growth in Brassica carinata – A Fasciclin-Like Arabinogalactan Protein Is Involved
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Exploring the role of CYP19A1 single nucleotide polymorphisms in the pathogenesis of female pattern hair loss
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- Rapidly progressing mycosis fungoides presenting as follicular mucinosis
- Ligand-Independent Vitamin D Receptor Actions Essential for Keratinocyte Homeostasis in the Skin
- Folliculocentric tinea versicolor: a case report
- Generalised Glucocorticoid Resistance
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish