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Research 391–420 of 1000+
- Abnormal essential fatty acid composition of tissue lipids in genetically diabetic mice is partially corrected by dietary linoleic and γ-linolenic acids
- Androgens trigger different growth responses in genetically identical human hair follicles in organ culture that reflect their epigenetic diversity in life
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Biochemical features of primary cells from a pediatric patient with a gain-of-function <i>ODC1</i> genetic mutation
- MiR‐200c‐3p as a novel genetic marker and therapeutic tool for alopecia areata
- Thrombotic risk minimization for Diane‐35 and generics
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Clinical benefits and adverse effects of genetically-elevated free testosterone levels: a Mendelian randomization analysis
- Early onset female pattern hair loss: a case–control study for analyzing clinical features and genetic variants
- RETRACTED: Thyroid Dysfunction and Alopecia Areata: A Genetic Prediction Causality Analysis Study
- Diverse northern Asian and Jomon-related genetic structure discovered among socially complex Three Kingdoms period Gaya region Koreans
- Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
- Craniometric Ancestry Proportions among Groups Considered Hispanic: Genetic Biological Variation, Sex-Biased Asymmetry, and Forensic Applications
- Woodhouse-Sakati Syndrome: The New Genetic Variant of DCAF17 In 2 Adult Sisters
- Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases
- A Study on the Pattern of Genetic Inheritance of Polycystic Ovarian Syndrome
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Table 1_Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review.xlsx
- Tru9I Variant as a Novel Genetic Marker for Vitamin D Deficiency in Alopecia Areata
- Identificación de la variación molecular y genética subyacente a las enfermedades de la piel
- A genome‐wide association study identified a genetic variant associated with hair thinning in Japanese women
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- 918 Tissue engineered human hair follicles from genetically, environmentally and extrinsically reprogrammed dermal papilla cells
- Assessment of The Influence of Non-Genetic Risk Factors on The Disease Onset and Progression of Androgenetic Alopecia in Egyptian Males
- Androgenetic alopecia risk IDed with genetic test
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- Clinical Management of Prostate Cancer in High-Risk Genetic Mutation Carriers
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Epidemiology, Genetics & Risk factors in Alopecia Androgenetics