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Items: 1 to 20 of 26

1.

Furriers lung

MedGen UID:
538594
Concept ID:
C0264476
Disease or Syndrome
2.

Coffee-workers lung

MedGen UID:
538589
Concept ID:
C0264468
Disease or Syndrome
3.

Malt-workers lung

MedGen UID:
510125
Concept ID:
C0155888
Disease or Syndrome
4.

Cheese-washers lung

MedGen UID:
507549
Concept ID:
C0007969
Disease or Syndrome
5.

Myofibroblastic Differentiation

A morphologic finding that indicates the presence of myofibroblastic differentiation in a cellular infiltrate of a tissue sample. [from NCI]

MedGen UID:
311021
Concept ID:
C1709101
Finding
6.

Bronchopulmonary dysplasia of newborn

A chronic lung disease developed after OXYGEN INHALATION THERAPY or mechanical ventilation (VENTILATION, MECHANICAL) usually occurring in certain premature infants (INFANT, PREMATURE) or newborn infants with respiratory distress syndrome (RESPIRATORY DISTRESS SYNDROME, NEWBORN). Histologically, it is characterized by the unusual abnormalities of the bronchioles, such as METAPLASIA, decrease in alveolar number, and formation of CYSTS. [from MeSH]

MedGen UID:
2738
Concept ID:
C0006287
Disease or Syndrome
7.

Thickened

MedGen UID:
525976
Concept ID:
C0205400
Finding
8.

Nuclear Translocation

Nuclear Translocation is a subcellular process in which activated cytoplasmic proteins are transported into the cell nucleus as part of a signal transduction pathway to modify cell function (typically gene expression) in response to a signaling event or condition. [from NCI]

MedGen UID:
273609
Concept ID:
C1518440
Molecular Function
9.

Positive

Involving advantage or good. [from NCI]

MedGen UID:
254858
Concept ID:
C1446409
Finding
10.

Mutant

An altered form of an individual, organism, population, or genetic character that differs from the corresponding wild type due to one or more alterations (mutations). [from NCI]

MedGen UID:
109303
Concept ID:
C0596988
Cell or Molecular Dysfunction
11.

Respiratory distress

A pathological increase in the effort and frequency of breathing movements. [from NCI]

MedGen UID:
96907
Concept ID:
C0476273
Sign or Symptom
12.

Dysplasia

A usually neoplastic transformation of the cell, associated with altered architectural tissue patterns. The cellular changes include nuclear and cytoplasmic abnormalities. Molecular genetic abnormalities are also often found and, in some instances, may lead to cancer. [from NCI]

MedGen UID:
87191
Concept ID:
C0334044
Pathologic Function
13.

Examined for

Having been subjected to inspection or evaluation. [from NCI]

MedGen UID:
83047
Concept ID:
C0332128
Finding
14.

Distress

A state of physiological or psychological stress that cannot be compensated for by normal adaptive measures. [from NCI]

MedGen UID:
68535
Concept ID:
C0231303
Finding
15.

Signaling Pathway

An elaboration of the known or inferred interactions involved in a signal transduction pathway. [from NCI]

MedGen UID:
39530
Concept ID:
C0086982
Molecular Function
16.

Transforming growth factor beta 1

A subtype of transforming growth factor beta that is synthesized by a wide variety of cells. It is synthesized as a precursor molecule that is cleaved to form mature TGF-beta 1 and TGF-beta1 latency-associated peptide. The association of the cleavage products results in the formation a latent protein which must be activated to bind its receptor. Defects in the gene that encodes TGF-beta1 are the cause of CAMURATI-ENGELMANN SYNDROME. [from MeSH]

MedGen UID:
316445
Concept ID:
C1704256
Amino Acid, Peptide, or Protein; Biologically Active Substance; Pharmacologic Substance
17.

Hyperoxia

An abnormal increase in the amount of oxygen in the tissues and organs. [from MeSH]

MedGen UID:
66144
Concept ID:
C0242706
Sign or Symptom
18.

Serpin

A family of serine proteinase inhibitors which are similar in amino acid sequence and mechanism of inhibition, but differ in their specificity toward proteolytic enzymes. This family includes alpha 1-antitrypsin, angiotensinogen, ovalbumin, antiplasmin, alpha 1-antichymotrypsin, thyroxine-binding protein, complement 1 inactivators, antithrombin III, heparin cofactor II, plasminogen inactivators, gene Y protein, placental plasminogen activator inhibitor, and barley Z protein. Some members of the serpin family may be substrates rather than inhibitors of SERINE ENDOPEPTIDASES, and some serpins occur in plants where their function is not known. [from MeSH]

MedGen UID:
48634
Concept ID:
C0036764
Amino Acid, Peptide, or Protein; Biologically Active Substance; Pharmacologic Substance
19.

Infant, Premature, Diseases

Diseases that occur in PREMATURE INFANTS. [from MeSH]

MedGen UID:
43873
Concept ID:
C0021295
Disease or Syndrome
20.

Respiratory symptom

Respiratory system manifestations of diseases of the respiratory tract or of other organs. [from MeSH]

MedGen UID:
20754
Concept ID:
C0037090
Sign or Symptom
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