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Research 931–960 of 1000+
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Cellular heterogeneity and microenvironmental control of skin cancer
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Past, Present and Future Perspectives of Forensic Genetics
- Developmental Genetics of Color Pattern Establishment in Cats
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Structural heterogeneity of cellular K5/K14 filaments as revealed by cryo-electron microscopy
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Red Blood Cells Folate Level in Patients with Alopecia Areata
- Contraception hormonale et cancer du sein : Une question de contexte
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- An Update of Congenital Adrenal Hyperplasia
- In vivo function of VDR in gene expression-VDR knock-out mice
- Therapeutics for COVID-19 and post COVID-19 complications: An update
- Recently Identified Forms of Epidermolysis Bullosa
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Phytochemical study of <i>Bituminaria basaltica</i> aerial parts, an Italian endemism
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Nonclassical Congenital Adrenal Hyperplasia and Pregnancy
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Characterization of Rickets Type II Model Rats to Reveal Functions of Vitamin D and Vitamin D Receptor
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Author response: Interplay of opposing fate choices stalls oncogenic growth in murine skin epithelium