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781
Using machine intelligence to uncover Alzheimer’s disease progression heterogeneity
Published 2020-12-01“…Conclusions: Using a limited transcriptomic public database, six different classes that drive AD were uncovered, supporting the premise that AD is a heterogeneously complex disorder. The perspective classes highlighted genetic pathways associated with vasculogenesis, cellular signaling and differentiation, metabolic function, mitochondrial function, nitric oxide, and metal ion metabolism. …”
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782
Relationship of Bacteria Isolated from Antral Gastric Biopsy with the Incidence of Dyspepsia in Patients Referred to Mehrad and Labbafinejad Hospitals, Tehran, Iran, in 2018
Published 2022-03-01“…Discussion & Conclusion: Bacterial species living in this area can be highly diverse, and therefore, in addition to other epigenetic involved factors, the studying of other factors, such as environment, nutrition, lifestyle, and the host's genetic, will increase our understanding of the pathogenesis of this complex disorder…”
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783
Characterization of a novel mutation V136L in bone morphogenetic protein 15 identified in a woman affected by POI
Published 2021-06-01“…We identified and characterized a novel BMP15 mutation, providing an additional elucidation of molecular basis of this complex disorder.…”
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784
The susceptibility of FSHB -211G > T and FSHR G-29A, 919A > G, 2039A > G polymorphisms to men infertility: an association study and meta-analysis
Published 2017-08-01“…Abstract Background Male infertility is a complex disorder caused by genetic, developmental, endocrine, or environmental factors as well as unknown etiology. …”
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785
Long-term effects of GH therapy in adult patients with Prader-Willi syndrome: a longitudinal study
Published 2023-05-01“…IntroductionPrader-Willi syndrome (PWS) is a complex disorder resulting from the failure of expression of paternal alleles in the PWS region of chromosome 15. …”
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786
Reference Genes across Nine Brain Areas of Wild Type and Prader-Willi Syndrome Mice: Assessing Differences in <i>Igfbp7</i>, <i>Pcsk1</i>, <i>Nhlh2</i> and <i>Nlgn3</i> Expression
Published 2022-08-01“…We provide a valuable tool for expression analysis of specific genes across different areas of the mouse brain and for comparative investigation of <i>PWScr</i> mouse models to discover and verify different regulatory pathways affecting this complex disorder.…”
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787
The Vastus Lateralis Muscle Interstitium Proteome Changes after an Acute Nociception in Patients with Fibromyalgia Compared to Healthy Subjects—A Microdialysis Study
Published 2023-01-01“…Fibromyalgia (FM) is a complex disorder and a clinical challenge to diagnose and treat. …”
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788
Comparative Study of Ultrasonographic and Anthropometric Measurements of Regional Adiposity in Metabolic Syndrome
Published 2017-08-01“…Introduction: Metabolic syndrome is complex disorder unifying dyslipidemia, insulin resistance and hyper insulinemia. …”
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789
Peripheral Blood-Based Gene Expression Studies in Schizophrenia: A Systematic Review
Published 2021-10-01“…We conclude that well-designed cohort studies across diverse populations, use of high-throughput sequencing technology, and use of artificial intelligence (AI) based computational analysis will significantly improve our understanding and diagnostic capabilities for this complex disorder.…”
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790
Effect of a nutrition education programme on the metabolic syndrome in type 2 diabetes mellitus patients at a level 5 Hospital in Kenya: “a randomized controlled trial”
Published 2020-08-01“…It worsens in the presence of the metabolic syndrome (MetS), a complex disorder characterized by co-occurrence of at least three of such factors as hypertension, obesity, dyslipidemia and insulin resistance. …”
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791
Fenotipos clínicos en el síndrome de apnea obstructiva del sueño
Published 2021-09-01“…Summary: Obstructive sleep apnea and hypopnea syndrome is characterized by repetitive episodes of upper airway obstruction and is increasingly recognized as a heterogeneous and complex disorder, proposing multiple phenotypes based on its pathogenic mechanism, polysomnographic alterations, and clinical presentation. …”
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792
Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5.
Published 2013-01-01“…Hypercalciuria is a major cause of nephrolithiasis, and is a common and complex disorder involving genetic and environmental factors. …”
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793
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
Published 2010-06-01“…Osteoporosis is a complex disorder and commonly leads to fractures in elderly persons. …”
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794
Atypical gaze patterns in autistic adults are heterogeneous across but reliable within individuals
Published 2022-09-01“…Conclusions These findings pave the way for the investigation of autism subtypes, and for elucidating the specific visual features that best discriminate gaze patterns—directions that will also combine with and inform neuroimaging and genetic studies of this complex disorder.…”
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795
Genome-wide association Scan of dental caries in the permanent dentition
Published 2012-12-01“…Dental caries is a complex disorder affected by both individual susceptibility and environmental factors. …”
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796
Role of glycated hemoglobin in microvascular complications in type 2 diabetes mellitus: cross sectional study
Published 2022-10-01“…Diabetes mellitus (DM) is a complex disorder which defects mainly vascular complications. …”
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797
Síndrome metabólica, resistência à ação da insulina e doença cardiovascular no diabete melito tipo 1 Síndrome metabólico, resistencia a la acción de la insulina y enfermedad cardio...
Published 2010-01-01“…<br>Metabolic syndrome (MS) is a complex disorder represented by a cluster of cardiovascular risk factors related to central fat distribution and insulin resistance (IR), and is associated with early mortality in non-diabetic individuals and in patients with type-2 diabetes mellitus (DM). …”
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798
Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome
Published 2022-07-01“…Abstract Background Prader-Willi syndrome (PWS) is a complex disorder caused by impaired paternally expressed genes on chromosome 15q11-q13. …”
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799
Time-course analysis of frontal gene expression profiles in the rat model of posttraumatic stress disorder and a comparison with the conditioned fear model
Published 2023-11-01“…Posttraumatic stress disorder (PTSD) is a complex disorder that involves physiological, emotional, and cognitive dysregulation that may occur after exposure to a life-threatening event. …”
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800
Aryl Hydrocarbon Receptor Activation Ameliorates Acute Respiratory Distress Syndrome through Regulation of Th17 and Th22 Cells in the Lungs
Published 2023-04-01“…Collectively, the current study suggests that AhR activation can attenuate ARDS and may serve as a therapeutic modality by which to treat this complex disorder. IMPORTANCE Acute respiratory distress syndrome (ARDS) is a type of respiratory failure that is triggered by a variety of bacterial and viral infections, including the coronavirus SARS-CoV2. …”
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