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Human ubiquitin-protein ligase Nedd4: expression, subcellular localization and selective interaction with ubiquitin-conjugating enzymesA human homolog of Drosophila lethal(3)malignant brain tumor (l(3)mbt) protein associates with condensed mitotic chromosomesCloning, expression, and genetic mapping of Sema W, a member of the semaphorin familyA novel NE-dlg/SAP102-associated protein, p51-nedasin, related to the amidohydrolase superfamily, interferes with the association between NE-dlg/SAP102 and N-methyl-D-aspartate receptorA novel human nucleoside diphosphate (NDP) kinase, Nm23-H6, localizes in mitochondria and affects cytokinesisSPACRCAN, a novel human interphotoreceptor matrix hyaluronan-binding proteoglycan synthesized by photoreceptors and pinealocytesAtp11p and Atp12p are assembly factors for the F(1)-ATPase in human mitochondriaCloning of the cDNA and chromosome localization of the gene for human thymidine kinase 2Identification of a novel human homolog of the Drosophila dlg, P-dlg, specifically expressed in the gland tissues and interacting with p55Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuriaSerine phosphorylation, chromosomal localization, and transforming growth factor-beta signal transduction by human bsp-1High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridizationExpression, purification and characterization of a human serine-dependent phospholipase A2 with high specificity for oxidized phospholipids and platelet activating factorThe gene for severe combined immunodeficiency disease in Athabascan-speaking Native Americans is located on chromosome 10p.Localization of the fourth locus (GLC1E) for adult-onset primary open-angle glaucoma to the 10p15-p14 region.Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.Genotype/phenotype correlation in autosomal recessive lamellar ichthyosisLocalization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22.Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations.Identification of transcribed sequences in Arabidopsis thaliana by using high-resolution genome tiling arraysCoiled bodies preferentially associate with U4, U11, and U12 small nuclear RNA genes in interphase HeLa cells but not with U6 and U7 genesIdentification of human epidermal differentiation complex (EDC)-encoded genes by subtractive hybridization of entire YACs to a gridded keratinocyte cDNA libraryStructure, tissue distribution, and chromosomal localization of the prepronociceptin geneThe Genexpress IMAGE knowledge base of the human brain transcriptome: a prototype integrated resource for functional and computational genomicsIntegrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kbThe human genome browser at UCSCMolecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growthThe gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor geneHMGI(Y) activation by chromosome 6p21 rearrangements in multilineage mesenchymal cells from pulmonary hamartomaThe locus for combined factor V-factor VIII deficiency (F5F8D) maps to 18q21, between D18S849 and D18S1103Current status of human chromosome 14A variant of Freeman-Sheldon syndrome maps to 11p15.5-pterThe necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouseThe forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25Genes for the neuronal immunoglobulin domain cell adhesion molecules neurofascin and Nr-CAM map to mouse chromosomes 1 and 12 and homologous human chromosomesReceptor protein tyrosine kinase DDR is up-regulated by p53 protein2006 expressed-sequence tags derived from human chromosome 7-enriched cDNA libraries09/15: Comparative genomics of a conserved chromosomal region associated with a complex human phenotypeHigh-resolution physical and transcript map of human chromosome 2p21 containing the sitosterolaemia locus.Molecular characterization of a human scavenger receptor, human MARCO
P2860
Q22001440-0814090C-E624-4056-96C0-1462C2469639Q22003771-7ADDED0C-5022-4A4F-B60B-ADE12A24939FQ22008846-B5F86830-5D43-4E7E-A780-5727F8B2C062Q22010730-B5323894-AB05-4473-AED9-C6BB89AFAE4CQ22011007-A710EB8D-62AF-4B24-B9EB-05DF6CB41F69Q22253277-7A6BC584-1B39-4ABA-A179-5A46593DBB62Q24291338-74FD647A-41DC-4AF8-AD66-274031DF9AC1Q24310289-CA5A29FC-2438-4B05-9DC7-A50E64573569Q24314178-E58799A9-D518-449E-9058-DE552895AE28Q24317481-A5EEA2C0-8294-4005-BEC1-B11BD5C51659Q24322007-46940F3F-6F39-4E2C-9444-53EFB6C48A4EQ24530660-EAC84286-F25F-4BF2-9E42-7184F97DA5EBQ24530703-EED91A70-273E-4161-A93C-C0EB7367761BQ24538682-44440996-00C2-497B-8C98-80234BAA70BBQ24538831-E988A230-1800-4CF4-8290-221D2C962842Q24538838-4B8DE1C5-99F0-4AA5-9FD7-40B58D9A63EFQ24538901-761632F2-C782-44A4-83BD-44B6A6F38396Q24539075-1BE1C2D1-30BA-469F-84DD-BCB9321988F5Q24540255-F4EAF3F8-2F9C-4A9F-9B72-9D73B6C3FD8AQ24555755-013362B9-DAE1-4BB5-B773-D61F8CE023B6Q24609646-8C5F7E0E-F006-432F-A5E3-ED130B7B68FAQ24621533-A45C3C3E-1239-4619-ABAE-3632E4732AA0Q24626729-C06D8400-9872-4D81-B67B-4F11920E06C1Q24627734-BA4AF3DA-3FC5-4E84-A4ED-ED2073A0230EQ24628031-2CFB4B34-C27B-42F6-9BE1-013CBE0D81C1Q24672361-A90CF3F1-3742-451D-8834-43B6455DAE63Q24675777-60B6599A-C695-47FE-8551-9CFBED8A6667Q24677660-C015B8BC-93E9-4E11-8353-18EA03BA8C41Q24678728-5A1AB5D1-02CD-416E-B3B2-985CBACD0F83Q24678839-86028928-69FC-4DF5-9038-E00B6DAF4470Q24679620-368FB680-21E4-4383-BE61-B91040C08E2CQ24681011-E2E8EF96-2EBB-4868-87FB-98C88CFC5DFFQ28249408-1755750E-1F24-4719-A95D-3B49A9421980Q28273225-23FC2623-BAAC-4E84-96F2-EFFFC73B53A6Q28282723-7060BCFF-26BA-4A41-93F2-EAB395EF599CQ28300103-E29C5828-B017-4D8C-B257-CCF276AF927AQ28306343-978E156B-D7F6-430D-AF20-C88BDB787B6DQ28363526-10DE6F42-F6DF-4F0A-ACDF-C15BA1739CC4Q28365983-FBC36773-C63E-486A-9641-77510023FABAQ28647588-058801C9-BCFF-42B1-A59B-B6FB0B8F9D20
P2860
description
1995 nî lūn-bûn
@nan
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
1995年论文
@zh
1995年论文
@zh-cn
name
An STS-based map of the human genome.
@en
type
label
An STS-based map of the human genome.
@en
prefLabel
An STS-based map of the human genome.
@en
P2093
P1433
P1476
An STS-based map of the human genome.
@en
P2093
Anderson MO
Baptista R
Colbert AM
Collymore AJ
Courtney DF
DeAngelis MM
P304
P356
10.1126/SCIENCE.270.5244.1945
P407
P577
1995-12-01T00:00:00Z