A new bacteriophage P1-derived vector for the propagation of large human DNA fragments.
about
Engineering BioBrick vectors from BioBrick partsMolecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3'-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damageCharacterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development.Human ligands of the Notch receptorHuman TRH-degrading ectoenzyme cDNA cloning, functional expression, genomic structure and chromosomal assignmentMutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type IA bacterial artificial chromosome library for sequencing the complete human genomeA member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationDMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumoursHolt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familySHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb developmentLIM domains-containing protein 1 (LIMD1), a tumor suppressor encoded at chromosome 3p21.3, binds pRB and represses E2F-driven transcriptionCloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuriaIdentification of a candidate human spectrin Src homology 3 domain-binding protein suggests a general mechanism of association of tyrosine kinases with the spectrin-based membrane skeletonCloning and mapping of the human SOX1: a highly conserved gene expressed in the developing brainMolecular cloning of human GDP-mannose 4,6-dehydratase and reconstitution of GDP-fucose biosynthesis in vitroOrganization, chromosomal localization and promoter analysis of the gene encoding human acidic fibroblast growth factor intracellular binding proteinRefined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region.Molecular analysis of SALL1 mutations in Townes-Brocks syndrome.Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.Physical mapping, cloning, and identification of genes within a 500-kb region containing BRCA1An arrayed human genomic library constructed in the PAC shuttle vector pJCPAC-Mam2 for genome-wide association studies and gene therapyHigh-resolution transcript map of the region spanning D12S1629 and D12S312 at chromosome 12q13: triple A syndrome-linked regionA 7.5 Mb sequence-ready PAC contig and gene expression map of human chromosome 11p13-p14.1Physical map of human 6p21.2-6p21.3: region flanking the centromeric end of the major histocompatibility complexA 3-Mb contig from D11S987 to MLK3, a gene-rich region in 11q13A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiencyHigh-resolution analysis of DNA replication domain organization across an R/G-band boundaryThe complete nucleotide sequence of the human immunoglobulin heavy chain variable region locusPlasticity in the organization and sequences of human KIR/ILT gene familiesThe activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2Molecular genetics and structural genomics of the human protein kinase C gene moduleMinimal cross-recombination between wild-type and loxP511 sites in vivo facilitates truncating both ends of large DNA inserts in pBACe3.6 and related vectors.The human glycine receptor subunit alpha3. Glra3 gene structure, chromosomal localization, and functional characterization of alternative transcriptsStructure of the human oxytocinase/insulin-regulated aminopeptidase gene and localization to chromosome 5q21Hormonal regulation and genomic organization of the human amiloride-sensitive epithelial sodium channel alpha subunit geneMutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)Truncating mutations of hSNF5/INI1 in aggressive paediatric cancerThe proto-oncoprotein SYT interacts with SYT-interacting protein/co-activator activator (SIP/CoAA), a human nuclear receptor co-activator with similarity to EWS and TLS/FUS family of proteins
P2860
Q21202064-84168F3F-6D99-4CAA-A4C1-E3DBB7633326Q22003729-74079BE6-F2E6-43F4-A2B6-4C6F2C53695CQ22008848-85493FEF-DCB9-4F24-8C55-9FFFDAD2B9B4Q22009037-9265B4A5-B94A-4C97-8267-23D14EC96242Q22010550-9A46D2A3-2879-4749-BECE-2F014FED78FCQ22010997-D7635E7F-7D4B-4A70-9129-EE7A1C6A6434Q22065763-43502EFE-36FE-4635-AC20-27B8321B8B90Q22254646-96250AEB-F606-494E-AA0B-4DFFFEA56AE9Q24310338-2C9E13A2-7154-44EB-ACEA-0026223235FBQ24311501-482FB8C4-3FE7-47AD-98D3-62C6964BDE0AQ24314232-EC110177-682B-4F29-8ED8-D1FC7E361367Q24314650-DAB8BABA-1FF9-4116-BFC1-BD949C7F3A24Q24317481-E0F6EB67-BE3E-4166-8D80-F72296607296Q24317739-5204DA9D-2858-4D1D-9E84-A58DEB46F8B2Q24319003-71D833B5-BF97-4BAF-A138-6B8821F056A4Q24321287-C872886E-A568-4B78-AA3A-0C44BB8599EEQ24532217-13BC0B0B-EB50-49C3-A093-6E9CC3E3E6ECQ24538880-D4ACC9B8-CE72-44E1-A6F1-A2F44FFAC5CDQ24540095-330300B2-6A5D-4AA4-A8FB-DEC17DFAEB75Q24540203-C9C6ADCD-8544-42B2-BE2D-72348B7D9FA3Q24562783-765F11EB-489D-49BD-8FEB-344D78BA6B74Q24619270-A705F05D-067F-4F04-9A24-6D37B2F58F33Q24622783-38F704BE-3EF5-4C74-BF7D-17CD364C643FQ24624647-5A0EE25B-4608-46C4-B8D4-396DB5316AB2Q24627151-E185CB30-AECC-4E3E-B7D7-3518668CCCBFQ24628598-D8C81575-020E-41A1-9315-ACC60DA78043Q24629476-1FC204E0-503A-4914-8C70-13BFCD92A197Q24633221-04924AB2-5C9E-4C15-BC39-A6C6E133D596Q24644428-57C3B4F9-E4CF-470D-B833-64E01841D5A2Q24647015-A8EDE3F7-AD19-4F82-A0C1-4A225732E9ECQ24676718-D71E3ECD-83D7-4B51-9986-94DC4A17262CQ24678806-A1F00683-1B11-4A8B-9782-B184A6CF905AQ24804121-CE97C571-ECF1-4547-B61A-F897FE3C82DAQ24816022-62DB2422-1B90-479D-9F52-B99A293110EEQ28119046-40F54384-2A0E-4538-A7F8-888A99545861Q28141509-B6349D0C-3677-4893-9505-AA7509C6D584Q28142111-F8052DA5-A1DD-4443-9EA5-EB38878C4A6BQ28146138-C5DCDD0C-C486-4A7D-BBCA-52E3DB47C797Q28277002-D6F84E52-4E01-4E8E-ABA7-2875115ACAD3Q28277223-ACDF2DCF-AABB-4356-BD70-1FA2A04150A7
P2860
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments.
@ast
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments.
@en
type
label
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments.
@ast
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments.
@en
prefLabel
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments.
@ast
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments.
@en
P2093
P2860
P356
P1433
P1476
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments.
@en
P2093
Amemiya CT
Ioannou PA
Kroisel PM
de Jong PJ
P2860
P2888
P356
10.1038/NG0194-84
P407
P577
1994-01-01T00:00:00Z
P5875
P6179
1027542612