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Published in 2025 at "Advanced Science"
DOI: 10.1002/advs.202401760
Abstract: Liquid biopsy is a promising approach for early detection of gynecological malignancies. In the PERCEIVE‐I study, gynecological Cancer cases (n = 249) and age‐matched non‐cancer controls (n = 249) are randomly divided into training and…
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Keywords:
early detection;
gynecological malignancies;
multi omics;
detection gynecological ... See more keywords
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Published in 2025 at "Advanced Science"
DOI: 10.1002/advs.202501095
Abstract: Chimeric antigen receptor T (CAR‐T) cell therapies, a cornerstone of immunotherapy, have demonstrated remarkable efficacy in treating hematological malignancies and have more recently expanded into applications for solid tumors and autoimmune diseases. Emerging multidimensional profiling…
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Keywords:
visualization;
multi omics;
therapy;
car cell ... See more keywords
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Published in 2020 at "Biotechnology journal"
DOI: 10.1002/biot.201900565
Abstract: Chinese hamster ovary (CHO) cells are currently the primary host cell lines used in biotherapeutic manufacturing of monoclonal antibodies (mAbs) and other biopharmaceuticals. Cellular energy metabolism and endoplasmic reticulum (ER) stress are known to greatly…
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Keywords:
multi omics;
metabolism;
productivity;
cell ... See more keywords
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Published in 2021 at "Biotechnology and Bioengineering"
DOI: 10.1002/bit.27899
Abstract: A robust monoclonal antibody (mAb) bioprocess requires physiological parameters such as temperature, pH, or dissolved oxygen to be well‐controlled as even small variations in them could potentially impact the final product quality. For instance, pH…
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Keywords:
culture;
cell;
product quality;
multi omics ... See more keywords
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Published in 2025 at "Brain and Behavior"
DOI: 10.1002/brb3.70792
Abstract: Stroke has a high mortality and disability rate, yet its underlying mechanisms remain not fully understood. The occurrence of stroke is influenced by a combination of environmental factors, genetic factors, and their interaction, making its…
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Keywords:
decoding stroke;
stroke etiology;
multi omics;
etiology ... See more keywords
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Published in 2022 at "Cancer medicine"
DOI: 10.1002/cam4.4594
Abstract: BACKGROUND Many studies showed that the prognosis of hepatocellular carcinoma (HCC) was significantly associated with the expressions of TP53 and LRP1B. However, the potential influence of the two genes on the malignant progression of HCC…
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Keywords:
analysis;
multi omics;
hcc;
gene ... See more keywords
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Published in 2022 at "Cancer medicine"
DOI: 10.1002/cam4.5320
Abstract: The copper metabolism MURR1 domain (COMMD) protein family is involved in tumorigenicity of malignant tumors. However, as the member of COMMD, the role of COMMD2 in human tumors remains unknown.
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Keywords:
commd2 human;
copper metabolism;
multi omics;
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Published in 2018 at "ELECTROPHORESIS"
DOI: 10.1002/elps.201700476
Abstract: Over the last few years, the application of high‐throughput meta‐omics methods has provided great progress in improving the knowledge of the gut ecosystem and linking its biodiversity to host health conditions, offering complementary support to…
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Keywords:
multi omics;
elucidate gut;
approach elucidate;
omics approach ... See more keywords
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Published in 2024 at "Genetic Epidemiology"
DOI: 10.1002/gepi.22601
Abstract: Transcriptome‐wide association studies (TWAS) have been widely used to identify thousands of likely causal genes for diseases and complex traits using predicted expression models. However, most existing TWAS methods rely on gene expression alone and…
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Keywords:
causal gene;
multi omics;
identification;
gene ... See more keywords
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Published in 2022 at "Hepatology"
DOI: 10.1002/hep.32713
Abstract: BACKGROUND & AIMS Hepatoblastoma (HB) is the most common primary liver malignancy in childhood, and lacks targeted therapeutic options. We previously engineered the first Yes Associated Protein 1 (YAP1S127A )-inducible mouse model of HB, demonstrating…
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Keywords:
novel yap1;
multi omics;
mouse;
yap1 ... See more keywords
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Published in 2022 at "Human Mutation"
DOI: 10.1002/humu.24440
Abstract: Prader–Willi syndrome (PWS; MIM# 176270) is a neurodevelopmental disorder caused by the loss of expression of paternally imprinted genes within the PWS region located on 15q11.2. It is usually caused by either maternal uniparental disomy…
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Keywords:
translocation;
multi omics;
prader willi;
omics analysis ... See more keywords