Cloning from purified high endothelial venule cells of hevin, a close relative of the antiadhesive extracellular matrix protein SPARC.
about
Sulfotransferases of two specificities function in the reconstitution of high endothelial cell ligands for L-selectinMolecular cloning and functional analysis of SUT-1, a sulfate transporter from human high endothelial venulesIdentification of sites of mannose 6-phosphorylation on lysosomal proteinsIdentification of podocalyxin-like protein as a high endothelial venule ligand for L-selectin: parallels to CD34Hevin is down-regulated in many cancers and is a negative regulator of cell growth and proliferationHeterogeneity of endothelial cells: the specialized phenotype of human high endothelial venules characterized by suppression subtractive hybridizationMolecular characterization of NF-HEV, a nuclear factor preferentially expressed in human high endothelial venulesSPARC, a matricellular glycoprotein with important biological functionsDifferential gene expression profile of human tonsil high endothelial cells: implications for lymphocyte traffickingGenetic basis for the evolution of vertebrate mineralized tissueDry eye and designer ophthalmics.Expression profile of active genes in mouse lymph node high endothelial cells.SC1/hevin. An extracellular calcium-modulated protein that binds collagen I.Tumor-suppressor function of SPARC-like protein 1/Hevin in pancreatic cancerCharacterization of Smoc-1 uncovers two transcript variants showing differential tissue and age specific expression in Bubalus bubalis.Lymphopoiesis and matrix glycoprotein SC1/ECM2.Processing of the matricellular protein hevin in mouse brain is dependent on ADAMTS4Modulation of endothelial cell adhesion by hevin, an acidic protein associated with high endothelial venules.The novel SPARC family member SMOC-2 potentiates angiogenic growth factor activity.Matricellular hevin regulates decorin production and collagen assembly.Cell proliferation and interleukin-6-type cytokine signaling are implicated by gene expression responses in early optic nerve head injury in rat glaucoma.Using In silico LD clumping and meta-analysis of genome-wide datasets as a complementary tool to investigate and validate new candidate biomarkers in Alzheimer's disease.SPARCL1, Shp2, MSH2, E-cadherin, p53, ADCY-2 and MAPK are prognosis-related in colorectal cancerMineralized tissue and vertebrate evolution: the secretory calcium-binding phosphoprotein gene cluster.Hevin plays a pivotal role in corneal wound healing.Matricellular homologs in the foreign body response: hevin suppresses inflammation, but hevin and SPARC together diminish angiogenesis.Proteolysis of the matricellular protein hevin by matrix metalloproteinase-3 produces a SPARC-like fragment (SLF) associated with neovasculature in a murine glioma model.Sialomucin CD34 is the major L-selectin ligand in human tonsil high endothelial venules.CD44 and hyaluronan-dependent rolling interactions of lymphocytes on tonsillar stroma.Sialylated, fucosylated ligands for L-selectin expressed on leukocytes mediate tethering and rolling adhesions in physiologic flow conditions.Mapping of SPARC/BM-40/osteonectin-binding sites on fibrillar collagens.Cloning and expression of murine SC1, a gene product homologous to SPARC.SPARCL1 suppresses metastasis in prostate cancer.A holistic approach to dissecting SPARC family protein complexity reveals FSTL-1 as an inhibitor of pancreatic cancer cell growth.Autotaxin, an ectoenzyme that produces lysophosphatidic acid, promotes the entry of lymphocytes into secondary lymphoid organs.The matricellular protein SPARC/osteonectin as a newly identified factor up-regulated in obesity.CD6 synergistic co-stimulation promoting proinflammatory response is modulated without interfering with the activated leucocyte cell adhesion molecule interaction.Extracellular matrix-associated protein Sc1 is not essential for mouse development.Associations of tumor suppressor SPARCL1 with cancer progression and prognosisN-acetylglucosamine-6-O-sulfotransferases 1 and 2 cooperatively control lymphocyte homing through L-selectin ligand biosynthesis in high endothelial venules.
P2860
Q22010048-F4412108-1967-485B-AF88-8EDD9AD9001BQ22010720-9B6DAE8A-339D-4D99-9C71-7AA29DB13403Q24300525-94B6FB8B-E6BB-4CFF-91A7-6AD477333C55Q24647059-A3C288C9-2E9D-44EA-9680-73D3DD559FB8Q24649170-DE55E2F0-A0D2-415C-9B22-86C7666C05FAQ24670568-8575984F-8484-444A-882A-61674D18362DQ24685626-7557460E-2720-46E3-81C3-EC9C5674FBE1Q28138199-E7CCE0F1-4A24-48A6-A38F-895D5032F087Q28242325-D4C289C9-6557-4ECB-BB5D-0FD57C08075AQ28770150-D60418A2-CFF9-49B2-BD91-C61080EA553BQ30437137-A65FE879-D6F2-442F-A664-2F586EC3610CQ30824941-7FFB1FB8-9050-4568-ABA6-49999A855D9DQ30882570-B868F449-9D25-42F0-B56C-4CBD13330ADDQ33275720-CA1F5EAB-92D6-4110-A50E-54903A9A2E2DQ33307461-BE29E3F9-8FD3-44D7-A70C-DF7B1D8E3237Q33536274-C56F75C5-83DB-477B-B91A-9E2C936CEE1DQ33648561-EF6E8913-1CAB-4E0A-9E41-EC4905B9DFB3Q34379100-8011F243-8347-456B-889C-3BF7D98499BEQ34538166-09B775BF-52D3-4FCC-BCFE-69311DC9195AQ34547905-65F70C5E-9DC3-4B0D-9E72-8CFF9A343F4CQ34646791-C4DDE68E-B9B6-44C4-BC90-F8FDCD511AC9Q34793871-00953FA7-95B5-41AF-B75B-69ADF1D326EEQ34863399-22100BEE-ABDD-442F-AB7C-C2BC39DE88B9Q34921105-36718CC0-1882-4FAD-AB47-48EA1E88EF55Q35058600-DD069DF5-20B1-45EE-88ED-0486C9CC0857Q35083699-D80EBBDE-23DB-4092-8C13-D4B6CFB22E3BQ35281840-4466BB69-AA9B-4100-8C09-549E7878A03FQ36236050-ADCDA956-2A14-4800-B16D-73E497362009Q36237249-849776D7-E5C9-4E86-B8B6-6BBADDE1D354Q36237657-F5CB7030-B6AE-4CB2-9667-FD67434FD107Q36744234-BCB00368-68AC-4380-B5BF-A7459A2FD414Q36867654-C82D1822-C355-4278-836F-6B8425FC292AQ37337322-97935B8E-E176-4521-A047-8376855220CFQ37439142-FE8D58A8-7B46-4B41-AB45-6F075C9BA7E1Q37439765-EA7C85FC-92BC-4EC7-A090-29B4594A1D4CQ38302172-AFAC1DDF-BAF8-45F2-9E22-88BFBB67B84EQ38341487-5E8334A7-F83F-406C-A22E-54C4EB48B86BQ39450526-C75931EC-B08D-4E8B-A210-C8C24BF009BDQ41613171-593D93E4-6798-4749-B797-3600CB41C6E0Q46468544-1D94F38A-54CD-4C7C-AEB8-78AF9607FD4B
P2860
Cloning from purified high endothelial venule cells of hevin, a close relative of the antiadhesive extracellular matrix protein SPARC.
description
1995 nî lūn-bûn
@nan
1995 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Cloning from purified high end ...... cellular matrix protein SPARC.
@ast
Cloning from purified high end ...... cellular matrix protein SPARC.
@en
Cloning from purified high end ...... cellular matrix protein SPARC.
@nl
type
label
Cloning from purified high end ...... cellular matrix protein SPARC.
@ast
Cloning from purified high end ...... cellular matrix protein SPARC.
@en
Cloning from purified high end ...... cellular matrix protein SPARC.
@nl
prefLabel
Cloning from purified high end ...... cellular matrix protein SPARC.
@ast
Cloning from purified high end ...... cellular matrix protein SPARC.
@en
Cloning from purified high end ...... cellular matrix protein SPARC.
@nl
P1433
P1476
Cloning from purified high end ...... cellular matrix protein SPARC.
@en
P2093
J P Girard
T A Springer
P304
P356
10.1016/1074-7613(95)90083-7
P407
P577
1995-01-01T00:00:00Z