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7 INGENIERÍA Y TECNOLOGÍA
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Article
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gene
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Angiotensin II
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Subject:
gene
Subject:
EGFR gene
Subject:
Article
Year:
2018
Document Type:
Artículo
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Title:
Partial IGF-1 deficiency is sufficient to reduce heart contractibility, angiotensin II sensibility, and alter gene expression of structural and functional cardiac proteins
Language:
Inglés
Repository:
34
Subject:
angiotensin II
/
calcium
/
connective tissue growth factor
/
contractile protein
/
protein Grem1
/
scleroprotein
/
somatomedin B
/
somatomedin B receptor
/
somatomedin binding protein 1
/
somatomedin binding protein 2
/
somatomedin binding protein 3
/
somatomedin binding protein 4
/
somatomedin binding protein 5
/
somatomedin binding protein 6
/
somatomedin C
/
somatomedin C receptor
/
unclassified drug
/
bradykinin
/
animal experiment
/
animal model
/
animal tissue
/
Article
/
calcium homeostasis
/
controlled study
/
coronary artery blood flow
/
Ctgf gene
/
extracellular matrix
/
gene
/
gene expression
/
Grem1 gene
/
heart muscle contractility
/
heart muscle fibrosis
/
heart weight
/
histology
/
Igf1 gene
/
Igf1r gene
/
Igf2 gene
/
Igf2r gene
/
Igfbp1 gene
/
Igfbp2 gene
/
Igfbp3 gene
/
Igfbp4 gene
/
Igfbp5 gene
/
Igfbp6 gene
/
male
/
mouse
/
nonhuman
/
protein blood level
/
real time polymerase chain reaction
/
regulatory mechanism
/
reperfusion injury
/
animal
/
body weight
/
cardiac muscle
/
deficiency
/
drug effects
/
gene expression regulation
/
genetics
/
heart contraction
/
hemodynamics
/
metabolism
/
organ size
/
pathology
/
perfusion
/
transgenic mouse
/
vasoconstriction
/
vasodilatation
/
Angiotensin II
/
Animals
/
Body Weight
/
Bradykinin
/
Extracellular Matrix
/
Gene Expression Regulation
/
Hemodynamics
/
Insulin-Like Growth Factor I
/
Mice, Transgenic
/
Myocardial Contraction
/
Myocardium
/
Organ Size
/
Perfusion
/
Real-Time Polymerase Chain Reaction
/
Vasoconstriction
/
Vasodilation
/
7 INGENIERÍA Y TECNOLOGÍA
Acceder
Title:
Multiple hereditary osteochondromatosis in a family [Osteocondromatosis múltiple hereditaria en una familia]
Language:
Español
Repository:
34
Subject:
Article
/
autosomal dominant inheritance
/
case report
/
exostosin gene
/
gene
/
hand movement
/
hereditary multiple exostosis
/
human
/
leg movement
/
multigene family
/
radiology
/
shoulder disease
/
wrist movement
/
7 INGENIERÍA Y TECNOLOGÍA
Acceder
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