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Research 601–630 of 1000+
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- Disorders linked to insufficient androgen action in male children
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Nrf2-Mediated Expansion of Pilosebaceous Cells Accelerates Cutaneous Wound Healing
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Netherton Syndrome: A Case-Based Review of Diagnosis, Management, and Emerging Treatments.
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- USING THE FROG EPIDERMIS TO UNCOVER DESMOSOME FUNCTION AND REGULATION IN THE DEVELOPING EMBRYO
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Tracing the cellular origin of cancer
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Zebrafish Model of Hereditary Pigmentary Disorders
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Netherton Syndrome
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets