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Research 151–180 of 256
- Fluorescence Microscopy—An Outline of Hardware, Biological Handling, and Fluorophore Considerations
- A systematic summary of survival and death signalling during the life of hair follicle stem cells
- PolyQ length co-evolution in neural proteins
- Novel Technologies for Exploring the Skin–Brain Axis
- Extracellular Vesicles in Alzheimer’s Disease: Dual Roles in Pathogenesis, Promising Avenues for Diagnosis and Therapy
- Part II. Common questions and misconceptions about creatine supplementation: what does the scientific evidence really show?
- The Role of Nutrition on Thyroid Function
- Iron Deficiency in Menstruating Adult Women: Much More than Anemia
- The Role of 11-Oxygenated Androgens and Endocrine Disruptors in Androgen Excess Disorders in Women
- Inhibition of prolactin promotes secondary skin follicle activation in cashmere goats
- Analysis of Adverse Drug Reactions in Pediatric Patients with Epilepsy: An Intensive Pharmacovigilance Study
- Aligning Stem Cell Models and Postmortem Studies to Query Striatal Neurodevelopment in Schizophrenia
- Glycol Ethers and Neurodevelopment: Investigating the Impact of Prenatal Exposures
- Gain‐of‐function variants in the <i>ODC1</i> gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities
- EFFECT OF ANTIANDROGENS ON VALPROIC ACID-INDUCED NEURODEVELOPMENTAL CHANGES IN RATS
- The role of AUTS2 in neurodevelopment and human evolution
- Great Expectations: Induced pluripotent stem cell technologies in neurodevelopmental impairments
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Zinc in the Soil and Its Importance for the Plants and Human Health. An integrated review
- Abnormal neuronal differentiation and mitochondrial dysfunction in hair follicle-derived induced pluripotent stem cells of schizophrenia patients
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Two parietal cephaloceles in a female neonate
- A Rare Case of Biotinidase Deficiancy
- Pemilihan Obat Anti-Epilepsi (OAE) untuk Penyandang Epilepsi Wanita Usia Subur
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Cleave but not leave: Astrotactin proteins in development and disease
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