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Topic Review
RFXAP Gene
regulatory factor X associated protein
  • 630
  • 24 Dec 2020
Topic Review
GUCY2D Gene
Guanylate cyclase 2D, retinal
  • 626
  • 22 Dec 2020
Topic Review
PDGFRB-Associated Chronic Eosinophilic Leukemia
PDGFRB-associated chronic eosinophilic leukemia is a type of cancer of blood-forming cells.
  • 626
  • 24 Dec 2020
Topic Review
ST3GAL5 Gene
ST3 beta-galactoside alpha-2,3-sialyltransferase 5
  • 625
  • 22 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. 
  • 625
  • 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.
  • 625
  • 13 Oct 2023
Topic Review
ITGB2 Gene
Integrin subunit beta 2
  • 624
  • 23 Dec 2020
Topic Review
KCNQ1OT1 Gene
KCNQ1 opposite strand/antisense transcript 1
  • 623
  • 23 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.
  • 623
  • 23 Dec 2020
Topic Review
IFT43 Gene
Intraflagellar transport 43
  • 622
  • 23 Dec 2020
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.
  • 622
  • 24 Dec 2020
Topic Review
PROKR2 Gene
prokineticin receptor 2
  • 621
  • 22 Dec 2020
Topic Review
MYCN Gene
MYCN proto-oncogene, bHLH transcription factor
  • 621
  • 23 Dec 2020
Topic Review
HESX1 Gene
HESX homeobox 1
  • 620
  • 22 Dec 2020
Topic Review
IFT122 Gene
Intraflagellar transport 122
  • 620
  • 23 Dec 2020
Topic Review
Isobutyryl-CoA Dehydrogenase Deficiency
Isobutyryl-CoA dehydrogenase (IBD) deficiency is a condition that disrupts the breakdown of certain proteins.
  • 619
  • 23 Dec 2020
Topic Review
SCN8A Gene
sodium voltage-gated channel alpha subunit 8
  • 618
  • 24 Dec 2020
Topic Review
EIF2B5 Gene
Eukaryotic translation initiation factor 2B subunit epsilon
  • 618
  • 24 Dec 2020
Topic Review
MIR17HG Gene
miR-17-92a-1 cluster host gene
  • 617
  • 22 Dec 2020
Topic Review
Isovaleric Acidemia
Isovaleric acidemia is a rare disorder in which the body is unable to properly break down a particular protein building block (amino acid). The condition is classified as an organic acid disorder, which is a condition that leads to an abnormal buildup of particular acids known as organic acids. Abnormal levels of organic acids in the blood (organic acidemia), urine (organic aciduria), and tissues can be toxic and can cause serious health problems.
  • 617
  • 23 Dec 2020
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