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Research 481–510 of 1000+
- Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- RNA-seq analysis identifies key genes enhancing hoof strength to withstand barefoot racing in Standardbred trotters
- A missense mutation in Lama3 causes androgen alopecia
- Androgenetic alopecia: An update
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Developmental origin of polycystic ovary syndrome - a hypothesis
- An Update of Congenital Adrenal Hyperplasia
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- Androgenetic alopecia: An update
- Review: Evolution and diversification of corneous beta‐proteins, the characteristic epidermal proteins of reptiles and birds
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- Zebrafish Model of Hereditary Pigmentary Disorders
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- Psoriasis del cuero cabelludo etiología, diagnóstico y tratamiento
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Clinical case of alopecia totalis in pediatric practice
- The Case | Bilateral kidney tumors and lung cysts
- Hair Diseases (Alopecia Areata and Androgenetic Alopecia)
- Low-level laser treatment accelerated hair regrowth in a rat model of chemotherapy-induced alopecia (CIA)