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Research 181–210 of 1000+
- Lymphoid Enhancer-binding Factor-1 (LEF1) Interacts with the DNA-binding Domain of the Vitamin D Receptor
- The secondary role of UV light in swimmers melanoma genesis
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Dermatopathology and molecular genetics
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Diagnostic approach to low‐renin hypertension
- Syndromes of Severe Insulin Resistance (SSIRs)
- Morphological Approach to Hair Disorders
- Androgen receptors and their biology
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Current Genetics in Hair Diseases
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- FGF5 is a crucial regulator of hair length in humans
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- A kindred with mutant IKAROS and autoimmunity
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Recently Identified Forms of Epidermolysis Bullosa
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Multiple cyclic nucleotide‐gated channels coordinate calcium oscillations and polar growth of root hairs
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse