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Research 121–150 of 1000+
- Finding Makhubu: A morphological forensic facial comparison
- <i>De novo</i> mutation in the mitochondrial tRNA<sup>Leu(UUR)</sup> gene (A3243G) with rapid segregation resulting in MELAS in the offspring
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- <i>Microsporum gypseum</i> isolated from a feline case of dermatophytosis
- 461 Identification of a Novel Pathogenic XPC:c.2420+1G>C Variant in a Patient with Xeroderma Pigmentosum
- Childhood Systemic Lupus Erythematosus: Clinical and Immunologic Patterns in Mexican Children
- <i>R</i><i>hodococcus equi</i>: Clinical Manifestations, Virulence, and Immunity
- A Transcriptome Sequencing Study on Genome-Wide Gene Expression Differences of Lung Cancer Cells Modulated by Fucoidan
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Drug Repurposing for Rare Diseases
- Genetic diversity of Armillaria spp. symbiotic with Polyporus umbellatus in China
- Adli Uygulamalarda Yeni Nesil Dizileme Teknolojilerinin Yeri ve Önemi
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- A woman with iatrogenic androgenetic alopecia responding to finasteride
- Molecular cloning, characterization, and expression of sheep FGF5 gene
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- 259 Scalp hair follicle dermal sheath fibroblasts express genes associated with promotion of skin integrity/wound healing and prevention of autoimmune responses in Recessive Dystrophic Epidermolysis Bullosa
- Towards grizzly bear population recovery in a modern landscape
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Forensic skeletal and molecular anthropology face to face: Combining expertise for identification of human remains
- Besnoitiosis in donkeys: an emerging parasitic disease of equids in Italy
- BAYONET trial: staged combination with encorafenib, binimetinib, plus cetuximab following encorafenib plus cetuximab for BRAF V600E-mutant metastatic colorectal cancer
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Mesenchymal Stem Cell‐Inspired Microneedle Platform for NIR‐responsive Immunomodulation and Accelerated Chronic Wound Healing
- Neural Stem Cells Restore Hair Growth through Activation of the Hair Follicle Niche
- Identification of a Novel MPL Loss of Function Mutation in a Patient with Cyclic Thrombocytopenia and Characterization of This Syndrome
- Postzygotic KRAS G12C mutation, associated with various malignancies, is also underling epidermal nevus syndrome
- 411 THE POTENTIAL OF CIRCULATING ENDOTHELIAL CELLS AS PROGNOSTIC BIOMARKERS IN PROSTATE CANCER
- BRCA2 in abscission