Faster access than browser!Similarities between Cerebral cortex and Rett syndrome
Cerebral cortex and Rett syndrome have 11 things in common (in Unionpedia): Brain-derived neurotrophic factor, Cerebral cortex, Dendrite, Fragile X syndrome, Hippocampus, MECP2, Mutation, Pons, Protein, Science (journal), Substantia nigra.
Brain-derived neurotrophic factor
Brain-derived neurotrophic factor, also known as BDNF, is a protein that, in humans, is encoded by the BDNF gene.
Brain-derived neurotrophic factor and Cerebral cortex · Brain-derived neurotrophic factor and Rett syndrome ·
Cerebral cortex
The cerebral cortex is the largest region of the cerebrum in the mammalian brain and plays a key role in memory, attention, perception, cognition, awareness, thought, language, and consciousness.
Cerebral cortex and Cerebral cortex · Cerebral cortex and Rett syndrome ·
Dendrite
Dendrites (from Greek δένδρον déndron, "tree"), also dendrons, are branched protoplasmic extensions of a nerve cell that propagate the electrochemical stimulation received from other neural cells to the cell body, or soma, of the neuron from which the dendrites project.
Cerebral cortex and Dendrite · Dendrite and Rett syndrome ·
Fragile X syndrome
Fragile X syndrome (FXS) is a genetic disorder.
Cerebral cortex and Fragile X syndrome · Fragile X syndrome and Rett syndrome ·
Hippocampus
The hippocampus (named after its resemblance to the seahorse, from the Greek ἱππόκαμπος, "seahorse" from ἵππος hippos, "horse" and κάμπος kampos, "sea monster") is a major component of the brains of humans and other vertebrates.
Cerebral cortex and Hippocampus · Hippocampus and Rett syndrome ·
MECP2
MECP2 (methyl CpG binding protein 2 (Rett syndrome)) is a gene that encodes the protein MECP2.
Cerebral cortex and MECP2 · MECP2 and Rett syndrome ·
Mutation
In biology, a mutation is the permanent alteration of the nucleotide sequence of the genome of an organism, virus, or extrachromosomal DNA or other genetic elements.
Cerebral cortex and Mutation · Mutation and Rett syndrome ·
Pons
The pons (Latin for "bridge") is part of the brainstem, and in humans and other bipeds lies inferior to the midbrain, superior to the medulla oblongata and anterior to the cerebellum.
Cerebral cortex and Pons · Pons and Rett syndrome ·
Protein
Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.
Cerebral cortex and Protein · Protein and Rett syndrome ·
Science (journal)
Science, also widely referred to as Science Magazine, is the peer-reviewed academic journal of the American Association for the Advancement of Science (AAAS) and one of the world's top academic journals.
Cerebral cortex and Science (journal) · Rett syndrome and Science (journal) ·
Substantia nigra
The substantia nigra (SN) is a basal ganglia structure located in the midbrain that plays an important role in reward and movement.
Cerebral cortex and Substantia nigra · Rett syndrome and Substantia nigra ·
The list above answers the following questions
- What Cerebral cortex and Rett syndrome have in common
- What are the similarities between Cerebral cortex and Rett syndrome
Cerebral cortex and Rett syndrome Comparison
Cerebral cortex has 216 relations, while Rett syndrome has 86. As they have in common 11, the Jaccard index is 3.64% = 11 / (216 + 86).
References
This article shows the relationship between Cerebral cortex and Rett syndrome. To access each article from which the information was extracted, please visit:
