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Research 151–180 of 1000+
- Drug repurposing—a promising approach for patients with angina but non-obstructive coronary artery disease (ANOCA)
- Role of Drug Repurposing in Sustainable Drug Discovery
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Application of big data analytics in minoxidil drug development: a data-driven model for predicting efficacy and side effect risks
- First clinical cases of leishmaniosis in meerkats (Suricata suricatta) housed in wildlife parks in Madrid, Spain
- E-Poster
- Tracking adult stem cells
- Pemphigus Vulgaris IgG and Methylprednisolone Exhibit Reciprocal Effects on Keratinocytes
- Visualising Androgen Receptor Activity in Male and Female Mice
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- Coronavirus 2019 Infectious Disease Epidemic: Where We Are, What Can Be Done and Hope For
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Integrated analysis of lncRNAs and mRNAs by RNA-Seq in secondary hair follicle development and cycling (anagen, catagen and telogen) of Jiangnan cashmere goat (Capra hircus)
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Advances in precise cell manipulation
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System
- Treatment Strategies for Cutaneous and Oral Mucosal Side Effects of Oncological Treatment in Breast Cancer: A Comprehensive Review
- Clinical, pathological, and molecular features of classical and L-type atypical-BSE in goats
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Radiomics and radiogenomics in ovarian cancer: a review with a focus on ultrasound applications
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle