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Research 691–720 of 1000+
- Two Hydroxyproline Galactosyltransferases, GALT5 and GALT2, Function in Arabinogalactan-Protein Glycosylation, Growth and Development in Arabidopsis
- A review on computer‐aided chemogenomics and drug repositioning for rationalCOVID‐19 drug discovery
- The human gut chemical landscape predicts microbe-mediated biotransformation of foods and drugs
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Construction of the coexpression network involved in the pathogenesis of thyroid eye disease via bioinformatics analysis
- Structural Abnormalities in the Hair of a Patient with a Novel Ribosomopathy
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Mapping Human Skin: One Sequenced Cell at a Time
- Pathophysiological mechanisms implicated in postpartum depression
- Identification of drug-specific public TCR driving severe cutaneous adverse reactions
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Functional characterization of soybean strigolactone biosynthesis and signaling genes in Arabidopsis MAX mutants and GmMAX3 in soybean nodulation
- S100A4/Nonmuscle Myosin IIA/p53 Axis Contributes to Aggressive Features in Ovarian High-Grade Serous Carcinoma
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Estimation of biological heart age using cardiovascular magnetic resonance radiomics
- Organoid‐Guided Precision Medicine: From Bench to Bedside
- The fiber diameter traits of Tibetan cashmere goats are governed by the inherent differences in stress, hypoxic, and metabolic adaptations: an integrative study of proteome and transcriptome
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- In Situ Self-Assembling Liver Spheroids with Synthetic Nanoscaffolds for Preclinical Drug Screening Applications
- A genetically informed brain atlas for enhancing brain imaging genomics
- Hidradenitis Suppurativa Tunnels: Unveiling a Unique Disease Entity
- Radiomics and radiogenomics in ovarian cancer: a review with a focus on ultrasound applications
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Identification and profiling of microRNA between back and belly Skin in Rex rabbits (Oryctolagus cuniculus)
- In Silico Promoter Motif Analysis of Human Fertility-Related Genes
- The heart of the hair fiber: How the inner structure of the coat reflects adaptive variation across color, sex, age, and body region in dromedary camels (Camelus dromedarius)