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Results: 11

1.

Death

Irreversible cessation of all bodily functions, manifested by absence of spontaneous breathing and total loss of cardiovascular and cerebral functions. [from MeSH]

MedGen UID:
3696
Concept ID:
C0011065
2.

Neurodegeneration

MedGen UID:
506929
Concept ID:
CN178344
Disease or Syndrome
3.

Neurodegeneration

Progressive loss of neural cells and tissue. [from HPO]

MedGen UID:
505144
Concept ID:
CN001976
Finding
4.

Chronic

A disease or condition that persists or progresses over a long period of time. [from NCI]

MedGen UID:
104657
Concept ID:
C0205191
5.

Finding

The result of an examination or inquiry. [from NCI]

MedGen UID:
66215
Concept ID:
C0243095
Finding
6.

Acute

Symptoms or signs that begin and worsen quickly; not chronic. [from NCI]

MedGen UID:
61381
Concept ID:
C0205178
7.

Clinical finding

clinical manifestations that can be either objective when observed by a physician, or subjective when perceived by the patient. [from CRISP]

MedGen UID:
19974
Concept ID:
C0037088
Sign or Symptom
8.

Transforming Growth Factor beta1

Transforming Growth Factor Beta 1, encoded by the TGFB1 gene, is a member of the TGF-beta family. This secreted multifunctional peptide controls proliferation, differentiation, and other functions in many cell types. Many cells synthesize TGF-Beta 1 and essentially all of them have specific receptors for this peptide. TGF-Beta 1 regulates the actions of many other peptide growth factors and determines a positive or negative direction of their effects. (from Swiss-Prot) [from NCI]

MedGen UID:
316445
Concept ID:
C1704256
Pharmacologic Substance
9.

Astrocytosis

MedGen UID:
199599
Concept ID:
C0751171
Pathologic Function
10.

Gliosis

The production of a dense fibrous network of neuroglia; includes astrocytosis, which is a proliferation of astrocytes in the area of a degenerative lesion. [from MeSH]

MedGen UID:
4899
Concept ID:
C0017639
Pathologic Function
11.

Chronic Encephalopathy, Post-Concussive

MedGen UID:
315935
Concept ID:
C1527318
Disease or Syndrome

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