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Research 121–150 of 1000+
- Dodatek A: Model matematyczny AL/RC/ASE. Functional Androgen Axis (FOA) - wersja operacyjna v1.2
- Skin fragility in the wild-derived, inbred mouse strain Mus pahari/EiJ
- Foxp3 Post-translational Modifications and Treg Suppressive Activity
- Improving human forensics through advances in genetics, genomics and molecular biology
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Folliculotropic mycosis fungoides of external ear: a case study
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- Deciphering the Insulin Link: Exploring Metabolic Interplay in Polycystic Ovary Syndrome
- Phenotype and metabolic profile of South Asian women with polycystic ovary syndrome (PCOS): results of a large database from a specialist Endocrine Clinic
- Biological characteristics of age-related changes in C57BL/6 mice sub-strains in the national center for geriatrics and gerontology aging farm
- Phenotypic characterization of non-dermatophyte moulds from companion animals with mycotic dermatitis
- Paraoxonase Enzyme Activity and Determination of Phenotypic Polymorphism in Patients with Acne Vulgaris
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Label Retaining Cells (LRCs) with Myoepithelial Characteristic from the Proximal Acinar Region Define Stem Cells in the Sweat Gland
- Evaluating combined therapy with myoinositol and D-chiro-inositol in infertility management across PCOS phenotypes: a comprehensive retrospective data analysis
- Causal Relationship Between Sleep Characteristics and Alopecia Areata and Other Non-Scarring Alopecia: A Two-Sample Bidirectional Mendelian Randomization Analysis
- Characteristics of non‐melanoma skin cancers of the cutaneous perioral and vermilion lip treated by Mohs micrographic surgery
- Comparing classic and newer phenotypes in Greek PCOS women: the prevalence of metabolic syndrome and their association with insulin resistance.
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Deep phenotyping of skin tissue remodeling in patients with systemic sclerosis treated with CD19-CAR T cells
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Learning from nudity: lessons from the nude phenotype
- A Simple Screening Approach for Assessing Community Prevalence and Phenotype of Polycystic Ovary Syndrome in a Semiurban Population in Sri Lanka
- Characteristic features of Japanese women's hair with aging and with progressing hair loss
- Receiver operating characteristic analysis of the performance of basal serum hormone profiles for the diagnosis of polycystic ovary syndrome in epidemiological studies
- FORENSIC MEDICAL CHARACTERISTICS OF ACUTE THALLIUM POISONING AND ITS LONG-TERM EFFECTS
- Pediatric Lichen: Epidemiological and Clinical Characteristics in Children
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice