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Research 451–480 of 1000+
- Association between genetically predicted rheumatoid arthritis and alopecia areata: a two-sample Mendelian randomization study
- A method for the determination of minoxidil in hair-regrowth formulations by micellar electrokinetic capillary chromatography
- Nonclassic adrenal hyperplasia
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- CCDC22 and CCDC93, two potential retriever-interacting proteins, are required for root and root hair growth in Arabidopsis
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- <i>signatureSearch</i>: environment for gene expression signature searching and functional interpretation
- Advances in single-cell transcriptomics in animal research
- Evaluation of noninvasive biospecimens for transcriptome studies
- Concurrent follicular dysplasia and interface dermatitis in Boxer dogs
- [Hormonal profile in men with premature androgenic alopecia].
- Frontal fibrosing alopecia: A review of disease pathogenesis
- Personalized Medicine in the Field of Inflammatory Skin Disorders
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- 268 Male-pattern baldness and its association with coronary heart disease
- 0040 Machine learning algorithms as tools for identifying predictive autoantibody biomarkers in pemphigus vulgaris
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women
- Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature
- Woolly Antics between the Sheaths
- Localized variant of junctional epidermolysis bullosa with R795X mutation
- THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Salt-losing tubulopathy and chronic dermatitis
- P78 Acrodermatitis enteropathica in children: clinical cases
- Фрактальный обнаружитель эхo-сигнала
- Review: Evolution and diversification of corneous beta‐proteins, the characteristic epidermal proteins of reptiles and birds
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis