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Topic Review
ITGB2 Gene
Integrin subunit beta 2
  • 621
  • 23 Dec 2020
Topic Review
Circulating Fetal Cells for NIPD
Prenatal diagnosis plays a crucial role in clinical genetics. Non-invasive prenatal diagnosis using fetal cells circulating in maternal peripheral blood has become the goal of prenatal diagnosis, to obtain complete fetal genetic information and avoid risks to mother and fetus. The development of high-efficiency separation technologies is necessary to obtain the scarce fetal cells from the maternal circulation. 
  • 621
  • 22 Dec 2021
Topic Review
Pseudohypoaldosteronism Type 2
Pseudohypoaldosteronism type 2 (PHA2) is caused by problems that affect regulation of the amount of sodium and potassium in the body. Sodium and potassium are important in the control of blood pressure, and their regulation occurs primarily in the kidneys.
  • 620
  • 24 Dec 2020
Topic Review
Exploring Large MAF Transcription Factors
Large musculoaponeurotic fibrosarcoma (MAF) transcription factors contain acidic, basic, and leucine zipper regions. Four types of MAF have been elucidated in mice and humans, namely c-MAF, MAFA, MAFB, and NRL.
  • 620
  • 13 Oct 2023
Topic Review
ST3GAL5 Gene
ST3 beta-galactoside alpha-2,3-sialyltransferase 5
  • 619
  • 22 Dec 2020
Topic Review
PDGFRB-Associated Chronic Eosinophilic Leukemia
PDGFRB-associated chronic eosinophilic leukemia is a type of cancer of blood-forming cells.
  • 619
  • 24 Dec 2020
Topic Review
Blood Biomarkers for Breast Cancer
The expression of two oncogenic miRNAs, miR526b and miR655, in poorly metastatic breast cancer cells enhances aggressive breast cancer phenotypes. miR526b and miR655 expression in breast tumors is associated with poor patient survival.  Both miRNAs are major regulators of the tumor microenvironment and can be detected in cell-free tumor cell secretions. Precursors of both miRNAs, pri-miR526b and pri-miR655, are sensitive and robust blood biomarkers to distinguish cancer from benign plasmas. 
  • 618
  • 13 Aug 2021
Topic Review
PROKR2 Gene
prokineticin receptor 2
  • 616
  • 22 Dec 2020
Topic Review
Mucopolysaccharidosis Type VI
Mucopolysaccharidosis type VI (MPS VI), also known as Maroteaux-Lamy syndrome, is a progressive condition that causes many tissues and organs to enlarge and become inflamed or scarred. Skeletal abnormalities are also common in this condition. The rate at which symptoms worsen varies among affected individuals.
  • 616
  • 23 Dec 2020
Topic Review
TBC1D20 Gene
TBC1 domain family member 20: The TBC1D20 gene provides instructions for making a protein that helps regulate the activity of other proteins called GTPases, which control a variety of functions in cells. 
  • 616
  • 24 Dec 2020
Topic Review
IFT122 Gene
Intraflagellar transport 122
  • 615
  • 23 Dec 2020
Topic Review
Isobutyryl-CoA Dehydrogenase Deficiency
Isobutyryl-CoA dehydrogenase (IBD) deficiency is a condition that disrupts the breakdown of certain proteins.
  • 615
  • 23 Dec 2020
Topic Review
EIF2B5 Gene
Eukaryotic translation initiation factor 2B subunit epsilon
  • 615
  • 24 Dec 2020
Topic Review
Knobloch Syndrome
Knobloch syndrome is a rare condition characterized by severe vision problems and a skull defect.
  • 614
  • 23 Dec 2020
Topic Review
MYCN Gene
MYCN proto-oncogene, bHLH transcription factor
  • 613
  • 23 Dec 2020
Topic Review
IFT43 Gene
Intraflagellar transport 43
  • 613
  • 23 Dec 2020
Topic Review
RANBP2 Gene
RAN binding protein 2
  • 613
  • 23 Dec 2020
Topic Review
SCN8A Gene
sodium voltage-gated channel alpha subunit 8
  • 613
  • 24 Dec 2020
Topic Review
MIR17HG Gene
miR-17-92a-1 cluster host gene
  • 612
  • 22 Dec 2020
Topic Review
IL1A Gene
Interleukin 1 alpha
  • 612
  • 23 Dec 2020
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