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Results: 1 to 20 of 21

1.

Oxygen

An element with atomic symbol O, atomic number 8, and atomic weight [15.99903; 15.99977]. It is the most abundant element on earth and essential for respiration. [from MeSH]

MedGen UID:
45267
Concept ID:
C0030054
Pharmacologic Substance
2.

Strand breaks

MedGen UID:
549441
Concept ID:
C0301647
Molecular Function
3.

Thyroid hormone plasma membrane transport defect

MedGen UID:
396060
Concept ID:
C1861101
Disease or Syndrome
4.

Acyl-CoA thioester hydrolase, long-chain, 1

MedGen UID:
351308
Concept ID:
C1865144
5.

Xeroderma pigmentosum, group F

Xeroderma pigmentosum (XP) is characterized by: Sun sensitivity (severe sunburn with blistering, persistent erythema on minimal sun exposure in ~60% of affected individuals, and marked freckle-like pigmentation of the face before age 2 years in most affected individuals); Ocular involvement (photophobia, keratitis, atrophy of the skin of the lids); and Greatly increased risk of cutaneous neoplasms (basal cell carcinoma, squamous cell carcinoma, melanoma). Approximately 25% of affected individuals have neurologic manifestations (acquired microcephaly, diminished or absent deep tendon stretch reflexes, progressive sensorineural hearing loss, and progressive cognitive impairment). The most common causes of death are skin cancer, neurologic degeneration, and internal cancer. The median age at death in persons with XP with neurodegeneration (29 years) was found to be younger than that in persons with XP without neurodegeneration (37 years). [from GeneReviews]

MedGen UID:
120612
Concept ID:
C0268140
Disease or Syndrome
6.

Severe

A term used to describe cells that look abnormal under a microscope. These cells are more likely to grow and spread quickly than cells in low-grade cancer or in growths that may become cancer. [from NCI]

MedGen UID:
104640
Concept ID:
C0205082
7.

Lesion

An area of abnormal tissue. A lesion may be benign (not cancer) or malignant (cancer). [from NCI]

MedGen UID:
65128
Concept ID:
C0221198
Finding
8.

MedGen UID:
195886
Concept ID:
C0699404
9.

MedGen UID:
181798
Concept ID:
C0949336
10.

MedGen UID:
148496
Concept ID:
C0699403
11.

Hydrogen Peroxide

A strong oxidizing agent used in aqueous solution as a ripening agent, bleach, and topical anti-infective. It is relatively unstable and solutions deteriorate over time unless stabilized by the addition of acetanilide or similar organic materials. [from MeSH]

MedGen UID:
9340
Concept ID:
C0020281
Pharmacologic Substance
12.

Deoxyribonucleases

Enzymes which catalyze the hydrolases of ester bonds within DNA. EC 3.1.-. [from MeSH]

MedGen UID:
8321
Concept ID:
C0011522
Pharmacologic Substance
13.

Electrolyte

substance that while in solution or its pure state will conduct an electric current by means of the movement of ions; in physiology, usually refers to compounds such as sodium, potassium, magnesium and calcium which dissociate fluids into ions that conduct electric currents and that constitute the major force in controlling fluid balance within the body. [from CRISP]

MedGen UID:
3997
Concept ID:
C0013832
Pharmacologic Substance
14.

DNA damage

Injuries to DNA that introduce deviations from its normal, intact structure and which may, if left unrepaired, result in a MUTATION or a block of DNA REPLICATION. These deviations may be caused by physical or chemical agents and occur by natural or unnatural, introduced circumstances. They include the introduction of illegitimate bases during replication or by deamination or other modification of bases; the loss of a base from the DNA backbone leaving an abasic site; single-strand breaks; double strand breaks; and intrastrand (PYRIMIDINE DIMERS) or interstrand crosslinking. Damage can often be repaired (DNA REPAIR). If the damage is extensive, it can induce APOPTOSIS. [from MeSH]

MedGen UID:
3880
Concept ID:
C0012860
Cell or Molecular Dysfunction
15.

Acetates

a chemical substance [from CHV]

MedGen UID:
1699
Concept ID:
C0000979
Pharmacologic Substance
16.

Enzyme deficiency agent

MedGen UID:
732777
Concept ID:
C1445728
Pharmacologic Substance
17.

Deficiency of carbon-oxygen lyase

MedGen UID:
713890
Concept ID:
C1291594
Disease or Syndrome
18.

Deficiency of endoribonuclease

MedGen UID:
713847
Concept ID:
C1291549
Disease or Syndrome
19.

Deficiency of ribonuclease

MedGen UID:
713845
Concept ID:
C1291547
Disease or Syndrome
20.

Deficiency of aminoacyltransferase

MedGen UID:
713736
Concept ID:
C1291432
Disease or Syndrome

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