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Research 211–240 of 1000+
- Connexin mutations in human disease
- Burden of Eosinophilic Esophagitis and Gastroesophageal Reflux Disease in Metabolic Dysfunction–Associated Steatotic Liver Disease: A Comprehensive US Healthcare Analysis
- GENOME-WIDE ANALYSIS REVEALS THE MOLECULAR BASIS OF GENETIC VARIATION OF IMPORTANT ECONOMIC TRAITS IN CASHMERE GOATS ON QINGHAI-TIBET PLATEAU
- Adverse Reactions to Biologic Medications Used in Allergy and Immunology Diseases
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Adaptive 3D Self‐Assembly of Colorectal Cancer Cells With Unchanged Tumor Phenotype and Drug Sensitivity
- 010 Development of a Desmocollin-3 Active Mouse Model Recapitulating Human Atypical Pemphigus
- Unravelling the Genetics of Physical Appearance Variation in Modern Humans
- Reprogramming the wound microenvironment: identity remodeling strategies for fibroblasts, keratinocytes, and macrophages
- Author response: scRNA+TCR-seq reveals the proportion and characteristics of dual TCR Treg cells in mouse lymphoid and non-lymphoid tissues
- Unveiling the Connection between Gut Microbiome and Polycystic Ovary Syndrome (PCOS)
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Finding Long-COVID: Temporal Topic Modeling of Electronic Health Records from the N3C and RECOVER Programs
- From hair colour to diagnosis
- Síndrome de ovario poliquístico: la distancia anogenital como marcador del entorno androgénico prenatal y revisión y comparación de los criterios diagnósticos
- Dumhetens rum i bildningens mitt
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Ivarmacitinib in atopic dermatitis presenting with prurigo nodularis-like lesions and alopecia areata: a case report
- Impaired turnover of autophagolysosomes in cathepsin L deficiency
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Contact Dermatitis Associated with Alopecia and Hyperpigmentation
- Cell Polarization Defects in Early Heart Development
- Pre‐polycystic ovary syndrome and polymenorrhoea as new facets of polycystic ovary syndrome (PCOS): Evidences from a single centre data set
- Mendelian Randomization Identifies CD25+ CD4+ Tregs and Plasma Proteins in Androgenetic Alopecia Pathogenesis
- Weathering of the hairless scalp: a study using skin capacitance imaging and ultraviolet light-enhanced visualization
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Novel aspects of age-protection by spermidine supplementation are associated with preserved telomere length