Regulation of lymph node vascular growth by dendritic cells. - Wikidata - wikimedia - TriplyDB

Regulation of lymph node vascular growth by dendritic cells.

Regulation of lymph node vascular growth by dendritic cells.

http://www.wikidata.org/entity/Q36228770

about

Stromal cells control soluble material and cellular transport in lymph nodes The Role of Lymphatic Niches in T Cell Differentiation Lymphoid Tissue Mesenchymal Stromal Cells in Development and Tissue Remodeling Control of CD8 T-Cell Infiltration into Tumors by Vasculature and Microenvironment Understanding high endothelial venules: Lessons for cancer immunology Organ-wide 3D-imaging and topological analysis of the continuous microvascular network in a murine lymph node Using magnetic resonance imaging to evaluate dendritic cell-based vaccination On-lattice simulation of T cell motility, chemotaxis, and trafficking in the lymph node paracortex Mouse mesenchymal stem cells inhibit high endothelial cell activation and lymphocyte homing to lymph nodes by releasing TIMP-1.In vivo imaging of therapy-induced anti-cancer immune responses in humans.Tertiary Lymphoid Structures in Cancers: Prognostic Value, Regulation, and Manipulation for Therapeutic Intervention The CLEC-2-podoplanin axis controls the contractility of fibroblastic reticular cells and lymph node microarchitecture.Laminins affect T cell trafficking and allograft fate.Power Doppler ultrasonographic assessment of the joint-draining lymph node complex in rheumatoid arthritis: a prospective, proof-of-concept study on treatment with tumor necrosis factor inhibitors.A Unique Cellular and Molecular Microenvironment Is Present in Tertiary Lymphoid Organs of Patients with Spontaneous Prostate Cancer Regression.Dendritic cells produce CXCL13 and participate in the development of murine small intestine lymphoid tissues.Implications of Lymphatic Transport to Lymph Nodes in Immunity and Immunotherapy Random migration and signal integration promote rapid and robust T cell recruitment TGF-beta1 induces mouse dendritic cells to express VEGF and its receptor (Flt-1) under hypoxic conditions.Normalization of the lymph node T cell stromal microenvironment in lpr/lpr mice is associated with SU5416-induced reduction in autoantibodies.Stromal and hematopoietic cells in secondary lymphoid organs: partners in immunity.Multiple CD11c+ cells collaboratively express IL-1β to modulate stromal vascular endothelial growth factor and lymph node vascular-stromal growth Using an agent-based model to analyze the dynamic communication network of the immune response.Nitric oxide and TNFα are critical regulators of reversible lymph node vascular remodeling and adaptive immune response.Stromal cell contributions to the homeostasis and functionality of the immune system.CD4+ T cells support cytotoxic T lymphocyte priming by controlling lymph node input.LIGHT regulates inflamed draining lymph node hypertrophy.A critical role for dendritic cells in the formation of lymphatic vessels within tertiary lymphoid structures Tertiary Lymphoid Structure-Associated B Cells are Key Players in Anti-Tumor Immunity.Coordinated regulation of lymph node vascular-stromal growth first by CD11c+ cells and then by T and B cells.Lymph node hypertrophy following Leishmania major infection is dependent on TLR9.Systems biology approaches for understanding cellular mechanisms of immunity in lymph nodes during infection The Lymphatic Endothelial mCLCA1 Antibody Induces Proliferation and Growth of Lymph Node Lymphatic Sinuses.Depletion of Regulatory T Cells Induces High Numbers of Dendritic Cells and Unmasks a Subset of Anti-Tumour CD8+CD11c+ PD-1lo Effector T Cells.Lymph node biophysical remodeling is associated with melanoma lymphatic drainage.Zinc finger transcription factor zDC is a negative regulator required to prevent activation of classical dendritic cells in the steady state.Optical projection tomography reveals dynamics of HEV growth after immunization with protein plus CFA and features shared with HEVs in acute autoinflammatory lymphadenopathy.Thermal facilitation of lymphocyte trafficking involves temporal induction of intravascular ICAM-1.Role of dendritic cells in the regulation of antitumor immunity Form follows function: lymphoid tissue microarchitecture in antimicrobial immune defence.

P2860

Q21131218-8E350BD5-D1CC-4BDA-AE85-CEF55F1F91E4 Q26745851-76DA472E-8EA8-4105-90AD-FC7D3F7B988B Q26748792-55406EA3-C869-45E8-B266-3592C9420AF7 Q26799117-7AF682D9-D21E-4728-89F0-81CC5D54AA30 Q27005794-A0793B09-DDC9-46C6-8693-2D3329EB5CA4 Q27306661-86EF9716-D678-4446-BD26-B36F3E3FEED8 Q27316977-5A636BF1-CA87-4EF0-AD53-D3B161E15B0C Q27318400-3D1B1BF0-1B4A-4B93-88DD-6D928C41571A Q27320221-C4162956-36D5-47DC-A752-0C105C74A3CC Q27693338-A1B08763-7BC3-42B0-AAF5-38CFF41A687B Q28073895-E957D5FD-06AE-4C05-80F8-579D2FB0CBD4 Q30090178-4ACB9C34-35FE-4BC4-A9CF-64732310927C Q30577194-85CF2802-3AB8-465B-9D20-C2549C5E293C Q30825520-CB9359BC-036E-4356-B899-06255CA65E1D Q33694988-4250F990-BEBF-4336-B069-95FC27A51B55 Q33816393-69C28539-382D-4926-B6EA-EFB642E3AF33 Q33920298-1B6E9C43-6611-43A5-AFFE-C069E9D72237 Q34015142-3FAFEB63-7E3A-4BA2-82E1-4F14E32B4425 Q34161224-0F265177-4DA2-4B79-8F69-CB3687EA8A25 Q34193426-48408ABA-A3E3-461B-A807-366D560D7206 Q34320316-F9D292D7-4857-4F79-B575-62BE0507A874 Q34393236-FC35D563-2B1B-4635-AAAA-08D417AA73B1 Q34547306-5AA67D84-C53D-4CEE-9F57-B6D9F1341C6D Q34662099-D5D9A1AF-F2AD-45D9-9DFB-B7660B1E20C1 Q34994909-6829BB79-BBD5-490F-A8D2-B0F341871FBB Q35008302-96DB54E6-D9D2-433D-BF86-12905925DD63 Q35032485-231254EF-4C3D-48E8-93DA-D459CE909345 Q35108664-C3F8BD77-6AE6-4FCB-ADBE-77CB2EFA5E60 Q35110486-45E43C1C-43F7-4283-BDD8-BD9370C18BEF Q35566574-59D6F43F-2173-4915-96D9-03AA99601AFC Q35685422-EEC4CAAD-F8E6-4C4A-B4D7-BA9516BED766 Q35858319-F3BD4C71-A840-48F4-8C98-4726AC8C5A2C Q36029195-2A878BED-B6BA-4061-A61A-9E4EA54662FA Q36061021-FD10C2EF-111E-4A2A-AEC2-F45BB9725240 Q36171323-9A6FF3BC-BA21-4F2A-97B4-EE73CEB8BBC0 Q36193523-E330422F-C793-4C83-AB7C-94C6DE013341 Q36213800-95EA80CD-2E21-448C-A629-F4F1E14DD4BF Q36507703-458E23FF-3084-4047-BDB1-E73228F3E219 Q36845842-4B402B2D-B59C-4406-8202-9CFF58EB8411 Q37282246-B5E30230-EF8D-4F08-B6F0-3A819AC62875

P2860

Regulation of lymph node vascular growth by dendritic cells.

http://www.wikidata.org/entity/Q36228770

description

2006 nî lūn-bûn

@nan

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

2006年论文

@zh

2006年论文

@zh-cn

name

Regulation of lymph node vascular growth by dendritic cells.

@ast

Regulation of lymph node vascular growth by dendritic cells.

@en

type

label

Regulation of lymph node vascular growth by dendritic cells.

@ast

Regulation of lymph node vascular growth by dendritic cells.

@en

prefLabel

Regulation of lymph node vascular growth by dendritic cells.

@ast

Regulation of lymph node vascular growth by dendritic cells.

@en

P1433

Q36228770-B6BD2D36-4AB3-4596-8A74-21FD1F9BEE19

P1476

Q36228770-CC91F441-816A-4292-8590-CD9B87533DA4

P2093

Q36228770-5ED21CE0-0373-4C7D-81BE-A7E95D5839BD

Q36228770-69CA254D-6DE4-4471-8D14-4F3B3BD7481A

Q36228770-77951211-0FC6-47CB-B576-C6503681C932

Q36228770-F685E80D-DBEF-4250-955E-8FE69EC521F1

P2860

Q36228770-04612523-CE7B-4291-B416-2E237EBC5747

Q36228770-1569B441-B6D5-437D-9A4E-E7235B110FED

Q36228770-1647A295-9D81-4D2E-8B95-2306321B85BB

Q36228770-1A15391D-E781-4337-8714-B16811448134

Q36228770-1CBFC977-C5C6-488F-ABAA-63969C043BC4

Q36228770-1E0158C2-CBD3-4F33-BBEE-591928347103

Q36228770-1F18E7FF-D16B-4957-B960-1D41FCB019EB

Q36228770-23056060-783C-4B1E-A78F-3732F17970B4

Q36228770-2ADD849E-8469-4F9B-B451-5946A1E2B3CE

Q36228770-338467F2-AD40-4905-AD2C-B1F3772C6CB8

P304

Q36228770-FB9E1D5D-C2C3-4303-BF2F-EF4FECD50729

P31

Q36228770-8773220F-2EBF-49C9-9C99-AB25AE9A7B24

P356

Q36228770-FA9D5E78-AAA5-438F-8D3F-051AF1BAFF70

P407

Q36228770-3DFAB1EE-4A82-49D6-A395-876D22FD88C3

P433

Q36228770-D4D9C045-2898-44D4-8B11-284997793FA9

P478

Q36228770-2A282958-FC8C-4F58-8605-C79DF81975BA

P50

Q36228770-18556FA0-2F99-4CD9-8247-13D33A87C51C

Q36228770-89E53688-3101-4BFE-993B-3932515EEF00

P577

Q36228770-B16C5D6D-8F2D-4E52-B949-AFF480C380F7

P5875

Q36228770-4D4FBF8C-116C-474E-B4F1-A20B6B00A76D

P698

Q36228770-FE9CDDB1-C03C-4AB1-A5AC-30B1FFCB4EBF

P921

Q36228770-EC02E6B3-760D-45C8-8866-942B5166AAF7

P932

Q36228770-7AB5D5B4-F3C6-42D9-B39F-098B28C510B8

P356

P1433

Journal of Experimental Medicine

P1476

Regulation of lymph node vascular growth by dendritic cells

@en

P2093

Eric H Ekland

http://www.w3.org/2001/XMLSchema#string

Lucila M Agle

http://www.w3.org/2001/XMLSchema#string

Regina Ruggieri

http://www.w3.org/2001/XMLSchema#string

Susan Chyou

http://www.w3.org/2001/XMLSchema#string

P2860

LYVE-1, a new homologue of the CD44 glycoprotein, is a lymph-specific receptor for hyaluronan

PECAM-1 (CD31) cloning and relation to adhesion molecules of the immunoglobulin gene superfamily

A novel endothelial-specific membrane protein is a marker of cell-cell contacts

Openings between defective endothelial cells explain tumor vessel leakiness

Dendritic cells and the control of immunity

T-cell priming by dendritic cells in lymph nodes occurs in three distinct phases

Isolation of putative progenitor endothelial cells for angiogenesis

Expression of VCAM-1 and E-selectin in an in vivo model of endothelial activation

Angiogenesis-inflammation cross-talk: vascular endothelial growth factor is secreted by activated T cells and induces Th1 polarization

RAG-1-deficient mice have no mature B and T lymphocytes

P304

1903-1913

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1084/JEM.20052272

http://www.w3.org/2001/XMLSchema#string

P407

P433

8

http://www.w3.org/2001/XMLSchema#string

P478

203

http://www.w3.org/2001/XMLSchema#string

P50

P577

2006-07-10T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

6953555

http://www.w3.org/2001/XMLSchema#string

P698

16831898

http://www.w3.org/2001/XMLSchema#string

P921

P932

2118366

http://www.w3.org/2001/XMLSchema#string