Blood-Stage Plasmodium Berghei ANKA Infection Promotes Hepatic Fibrosis by Enhancing Hedgehog Signaling in Mice
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Blood-Stage Plasmodium Berghei ANKA Infection Promotes Hepatic Fibrosis by Enhancing Hedgehog Signaling in Mice ; volume:50 ; number:4 ; year:2018 ; pages:1414-1428
Cellular physiology and biochemistry ; 50, Heft 4 (2018), 1414-1428
- Creator
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Kim, Jieun
Wang, Sihyung
Lee, Chanbin
Sung, Sumi
Shin, Yongbo
Song, Kyoung Seob
Cha, Hee-Jae
Ock, Meesun
Jung, Youngmi
- DOI
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10.1159/000494604
- URN
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urn:nbn:de:101:1-2018111423264875685652
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:01 AM CEST
Data provider
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Associated
- Kim, Jieun
- Wang, Sihyung
- Lee, Chanbin
- Sung, Sumi
- Shin, Yongbo
- Song, Kyoung Seob
- Cha, Hee-Jae
- Ock, Meesun
- Jung, Youngmi
Other Objects (12)
Upper gastrointestinal pathophysiology due to mouse malaria Plasmodium berghei ANKA infection
Germinal center architecture disturbance during Plasmodium berghei ANKA infection in CBA mice
Antimalarial efficacy of Pongamia pinnata (L) Pierre against Plasmodium falciparum (3D7 strain) and Plasmodium berghei (ANKA)
Elevated IL-17 levels in semi-immune anaemic mice infected with Plasmodium berghei ANKA
Retraction Note: Antimalarial efficacy of Pongamia pinnata (L) Pierre against Plasmodium falciparum (3D7 strain) and Plasmodium berghei (ANKA)
Bone marrow chimeric mice reveal a dual role for CD36 in Plasmodium berghei ANKA infection
In vitro culture of Plasmodium berghei-ANKA maintains infectivity of mouse erythrocytes inducing cerebral malaria
Tim-3 signaling blockade with α-lactose induces compensatory TIGIT expression in Plasmodium berghei ANKA-infected mice
The cytokine IL-22 modulates the immune response during Plasmodium berghei ANKA infection in mice (mus musculus)
Lambda-carrageenan treatment exacerbates the severity of cerebral malaria caused by Plasmodium berghei ANKA in BALB/c mice
Exogenous nitric oxide decreases brain vascular inflammation, leakage and venular resistance during Plasmodium berghei ANKA infection in mice
Immune regulation in Plasmodium berghei ANKA infected mice either lacking type I interferon signalling or mimicking malaria tolerance
Upper gastrointestinal pathophysiology due to mouse malaria Plasmodium berghei ANKA infection
Germinal center architecture disturbance during Plasmodium berghei ANKA infection in CBA mice
Antimalarial efficacy of Pongamia pinnata (L) Pierre against Plasmodium falciparum (3D7 strain) and Plasmodium berghei (ANKA)
Elevated IL-17 levels in semi-immune anaemic mice infected with Plasmodium berghei ANKA
Retraction Note: Antimalarial efficacy of Pongamia pinnata (L) Pierre against Plasmodium falciparum (3D7 strain) and Plasmodium berghei (ANKA)
Bone marrow chimeric mice reveal a dual role for CD36 in Plasmodium berghei ANKA infection
In vitro culture of Plasmodium berghei-ANKA maintains infectivity of mouse erythrocytes inducing cerebral malaria
Tim-3 signaling blockade with α-lactose induces compensatory TIGIT expression in Plasmodium berghei ANKA-infected mice
The cytokine IL-22 modulates the immune response during Plasmodium berghei ANKA infection in mice (mus musculus)
Lambda-carrageenan treatment exacerbates the severity of cerebral malaria caused by Plasmodium berghei ANKA in BALB/c mice
Exogenous nitric oxide decreases brain vascular inflammation, leakage and venular resistance during Plasmodium berghei ANKA infection in mice
Immune regulation in Plasmodium berghei ANKA infected mice either lacking type I interferon signalling or mimicking malaria tolerance
Upper gastrointestinal pathophysiology due to mouse malaria Plasmodium berghei ANKA infection
Germinal center architecture disturbance during Plasmodium berghei ANKA infection in CBA mice
Antimalarial efficacy of Pongamia pinnata (L) Pierre against Plasmodium falciparum (3D7 strain) and Plasmodium berghei (ANKA)
Elevated IL-17 levels in semi-immune anaemic mice infected with Plasmodium berghei ANKA
Retraction Note: Antimalarial efficacy of Pongamia pinnata (L) Pierre against Plasmodium falciparum (3D7 strain) and Plasmodium berghei (ANKA)
Bone marrow chimeric mice reveal a dual role for CD36 in Plasmodium berghei ANKA infection
In vitro culture of Plasmodium berghei-ANKA maintains infectivity of mouse erythrocytes inducing cerebral malaria
Tim-3 signaling blockade with α-lactose induces compensatory TIGIT expression in Plasmodium berghei ANKA-infected mice
The cytokine IL-22 modulates the immune response during Plasmodium berghei ANKA infection in mice (mus musculus)
Lambda-carrageenan treatment exacerbates the severity of cerebral malaria caused by Plasmodium berghei ANKA in BALB/c mice
Exogenous nitric oxide decreases brain vascular inflammation, leakage and venular resistance during Plasmodium berghei ANKA infection in mice