about
In vitro activation of CPP32 and Mch3 by Mch4, a novel human apoptotic cysteine protease containing two FADD-like domainsIntegrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kbIsolation of human and mouse genes based on homology to REC2, a recombinational repair gene from the fungus Ustilago maydisThe gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor geneHigh-resolution physical and transcript map of human chromosome 2p21 containing the sitosterolaemia locus.ODS2: a multiplatform software application for creating integrated physical and genetic maps.An integrated physical map for the short arm of human chromosome 5.Fine mapping suggests that the goat Polled Intersex Syndrome and the human Blepharophimosis Ptosis Epicanthus Syndrome map to a 100-kb homologous region.Construction of a BAC contig map of chromosome 16q by two-dimensional overgo hybridization.Characterization of three maize bacterial artificial chromosome libraries toward anchoring of the physical map to the genetic map using high-density bacterial artificial chromosome filter hybridization.Parallel radiation hybrid mapping: a powerful tool for high-resolution genomic comparison.Screening for overlapping bacterial artificial chromosome clones by PCR analysis with an arbitrary primerHigh-resolution restriction maps of bacterial artificial chromosomes constructed by optical mappingHuGeMap: a distributed and integrated Human Genome Map database.Comparative genomics and host resistance against infectious diseasesRieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193A 4 Mb cryptic deletion associated with inv(8)(q13.1q24.11) in a patient with trichorhinophalangeal syndrome type I.Partial trisomy 1(q42-->qter): a new case with a mild phenotypeCharacterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISH.The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes.NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes.Anchoring 9,371 maize expressed sequence tagged unigenes to the bacterial artificial chromosome contig map by two-dimensional overgo hybridization.Assignment of the tibial muscular dystrophy locus to chromosome 2q31.Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene.Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.Production and characterization of maize chromosome 9 radiation hybrids derived from an oat-maize addition line.Contig maps and genomic sequencing identify candidate genes in the usher 1C locus.Mapping ESTs by fiber-FISHHigh-resolution physical and genetic mapping of the critical region for Meckel syndrome and Mulibrey Nanism on chromosome 17q22-q23.High-resolution landmark framework for the sequence-ready mapping of Xq23-q26.1.Irruption of genomics in the search for disease related genes.Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes.Two translocations of chromosome 15q associated with dyslexia.Absence of somatic alterations of the EB1 gene adenomatous polyposis coli-associated protein in human sporadic colorectal cancersConstruction and validation of yeast artificial chromosome contig maps by RecA-assisted restriction endonuclease cleavage.Direct isolation of human transcribed sequences from yeast artificial chromosomes through the application of RNA fingerprintingAnalysis of the 10q23 chromosomal region and the PTEN gene in human sporadic breast carcinoma.Multiple-complete-digest restriction fragment mapping: generating sequence-ready maps for large-scale DNA sequencing
P2860
Q24315787-DB8809DF-AF2E-49D9-AC5A-5F74A3E63D7CQ24628031-B7EFE070-B73E-4FA2-9D29-6E6531BD58BAQ24655556-65DEE08A-4686-47A0-9D7A-C0914DFE3551Q24677660-6E905C34-BBF5-462D-812E-32D49B0E7628Q28365983-D06D9F7A-806E-4653-82EC-6C0F22C667E6Q30657331-7FE424F4-D3CA-47BE-95CC-4F286FB8D583Q30829664-F6E266C6-B76B-4EB4-8483-6A1758724C97Q30847309-2B8B4EC2-C384-44D9-8795-E7268155B13CQ30870515-25261633-531F-4847-A0C5-44CAC1B04DD1Q31121405-3983565A-55B0-4A16-A32C-F8C22E447BFBQ32048269-AF115E07-BD7D-4308-9B1C-6EB5563C543AQ32064784-39CC0237-336A-40B5-AC05-7A7DE3CD00C2Q32081389-59D6B389-25A4-4CB0-B7C6-1656D735284EQ32177943-57748335-7F5B-41F3-896A-E294BEB7F9C7Q33542428-5BF1FD58-8F22-4A0E-9643-F4998D28307EQ33678523-47846686-E42A-498F-91D9-2770B860F524Q33678721-606BC050-26AB-488A-840F-2FFEF4DEA18EQ33680104-FEC452FD-A7A6-4CB7-9552-5096B7D5D5A2Q33680213-7BADD8F2-E11B-4158-8572-26456A965758Q33948853-EE7E5D0A-B3E1-4CDD-B045-4FA335949C50Q34146044-CCA32611-549C-43E4-9F1F-2B1220D72D77Q34305879-6732D86D-F94D-47B2-A76F-7935442E5B84Q34384680-B0FE1254-811A-4919-AFB0-8AD0DEDC82DBQ34387473-F014B549-B8FB-4205-9504-51024F94B0F4Q34387487-825C441F-ACD9-42EF-A86C-92C65CA3F9FDQ34389112-D82CB2FA-CA21-470A-8F6F-9F345D753691Q34610419-9105C205-550A-4C73-93AD-66952BEE5CA8Q35020837-18B0B07E-74D4-4C68-9EC2-C0733D996F79Q35021078-124AEF2F-C875-4B7A-92BD-C117758BCDA8Q35021975-B331058D-EE56-4DEB-9631-8097A28AA26CQ35024299-6D691D6D-9B1D-470B-8306-B726F9AA70C0Q35090212-EC261FDA-DA27-446F-A198-A3CC219D54CAQ35238579-C6C66DC4-43BE-4D2B-998D-178B773F97EAQ35432122-A2312B81-35AD-4BA9-9896-91699DEE99D2Q35559715-C880F615-9565-42ED-B0BA-82FA0F80A944Q36115708-10A2337D-3647-4D33-A77D-594DA0B64037Q36309949-73014460-D935-4A05-915A-534256A06F53Q36586708-FD6EAD07-E5C7-4EA8-94FE-400313940458Q36618853-7ECC10E3-9C53-49CC-9DB5-DF95743AE62CQ36769605-94EC7C3D-7DBC-4094-A669-8C02005952A3
P2860
description
1995 nî lūn-bûn
@nan
1995 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի սեպտեմբերին 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
A YAC contig map of the human genome.
@ast
A YAC contig map of the human genome.
@en
A YAC contig map of the human genome.
@nl
type
label
A YAC contig map of the human genome.
@ast
A YAC contig map of the human genome.
@en
A YAC contig map of the human genome.
@nl
prefLabel
A YAC contig map of the human genome.
@ast
A YAC contig map of the human genome.
@en
A YAC contig map of the human genome.
@nl
P2093
P356
P1433
P1476
A YAC contig map of the human genome.
@en
P2093
Bellanné-Chantelot C
Billault A
Chumakov IM
Guasconi G
Poullier E
Soularue P
P2888
P304
P356
10.1038/377175A0
P407
P433
6547 Suppl
P577
1995-09-01T00:00:00Z