Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes.
about
Active and inactive genes localize preferentially in the periphery of chromosome territoriesConcerted evolution of the tandem array encoding primate U2 snRNA occurs in situ, without changing the cytological context of the RNU2 locusNew 5'-(CGG)n-3' repeats in the human genomeCentromere and telomere movements during early meiotic prophase of mouse and man are associated with the onset of chromosome pairingTopology of double minutes (dmins) and homogeneously staining regions (HSRs) in nuclei of human neuroblastoma cell lines.Reconstruction of genomic rearrangements in great apes and gibbons by chromosome painting.Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis typeSimultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy.The impact of the new fish technologies on the cytogenetics of haematological malignancies.Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.Emergence of the ZNF91 Krüppel-associated box-containing zinc finger gene family in the last common ancestor of anthropoideaInvolvement of chromosomes 1 and 17 in a case of neuroblastoma.The Bombyx mori karyotype and the assignment of linkage groupsCombined karyotyping, CGH and M-FISH analysis allows detailed characterization of unidentified chromosomal rearrangements in Merkel cell carcinoma.Characterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysisLibraries for each human chromosome, constructed from sorter-enriched chromosomes by using linker-adaptor PCR.Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries.Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and lossesLack of X inactivation associated with maternal X isodisomy: evidence for a counting mechanism prior to X inactivation during human embryogenesisThree-dimensional reconstruction of painted human interphase chromosomes: active and inactive X chromosome territories have similar volumes but differ in shape and surface structure.Validation of chromosome painting as a biodosimeter in human peripheral lymphocytes following acute exposure to ionizing radiation in vitro.A comparative map of the porcine and human genomes demonstrates ZOO-FISH and gene mapping-based chromosomal homologies.Comparative analysis of the cattle and human genomes: detection of ZOO-FISH and gene mapping-based chromosomal homologies.Isolation and mapping of three new polymorphic markers to chromosomes 3, 20 and 21.Fluorescene in situ hybridization establishes homology between human and silvered leaf monkey chromosomes, reveals reciprocal translocations between chromosomes homologous to human Y/5, 1/9, and 6/16, and delineates an X1X2Y1Y2/X1X1X2X2 sex-chromosoWhole library-amplification and labelling of human chromosome-specific composite probes for fluorescence in situ hybridization (FISH) using PCR.Differential involvement of chromosomes 1 and 4 in the formation of chromosomal aberrations in human lymphocytes after X-irradiation.Tumor suppression in human skin carcinoma cells by chromosome 15 transfer or thrombospondin-1 overexpression through halted tumor vascularization.Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines.Cytogenetic analysis of non Hodgkin's lymphomas by ratio-painting and comparative genomic hybridization reveals unsuspected chromosomal abnormalities.An unbalanced half-cryptic translocation involving the 6q subtelomeric region and 2p25.3 in a child with mental retardation: uses and limitations of fluorescence in situ hybridization.Emerging patterns of comparative genome organization in some mammalian species as revealed by Zoo-FISH.Chromosome aberration analysis in atomic bomb survivors and Thorotrast patients using two- and three-colour chromosome painting of chromosomal subsets.Homologous and heterologous FISH painting with PARM-PCR chromosome-specific probes in mammals.Chromosome 2 short arm translocations revealed by M-FISH analysis of neuroblastoma cell lines.Molecular cytogenetic analysis of human tumors.Subchromosomal mapping of a putative transformation suppressor gene on human chromosome 1.Use of fluorescence in situ hybridization to measure chromosome aberrations as a predictor of radiosensitivity in human tumour cells.Rapid translocation frequency analysis in humans decades after exposure to ionizing radiation.Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH.
P2860
Q22066165-5FE4B3A8-5262-48B7-9B85-22AD01791835Q24568372-F3989F99-5D21-4376-AD70-42D88B7444B1Q28287940-0C77E9EF-E2CE-41E4-82C3-BBB1CF0F2146Q28609152-FA9EEE5E-A8D2-4F62-ADFE-9308EDB7D6B7Q30956415-CE954CA2-AFB4-4390-9791-3FACBDAF2421Q31103788-A6A8146C-943E-457A-B6D2-7AED425880EEQ31106248-B0951B8B-0E5D-4540-8409-F623127B580BQ33281355-2DB20623-6E51-4B46-897C-EEEA84F5431CQ33587586-297D8BF5-9242-4FF4-B520-D51071755524Q33680969-BCE8FF65-3C05-4D9C-931C-8FDFBA616232Q33800471-013BF84F-AE74-4A9A-BFC6-751466D6E2FEQ33970264-55F04F7B-5EEA-4CD0-B81B-D5DCDA8F8F06Q34407799-C18A6990-23FB-4EDE-B7D0-CD74585D87A3Q34810928-D649CEC8-6FCC-4ED1-A4CD-9FE669D40214Q35194066-80DFDBA1-A8A5-4872-9BB6-40EF42A911DEQ35194422-2097DA22-5D4C-4D7D-A211-1E5A6BA223AAQ35194734-572FDBD3-7EC8-49C3-9BFD-15B0176F5BB8Q35834190-C97DB25F-BB76-41A3-AE3C-5E10E9A5B41EQ35882389-17AC335D-F3C3-4C99-9D45-ADD97E14875FQ36257706-186539DD-3EE0-488C-8949-6CA68E98AC28Q36741663-025F23EB-588B-4015-99EA-056F4627F53EQ36802704-260B4F6B-F2AF-4091-9C6C-0A7080952DADQ36802708-174C9667-A185-4954-9E64-4753D53F6444Q36822984-82BED027-3C48-4F46-86E2-175A8C74FD22Q36853241-8DD09352-2BC2-4CE6-8CB4-91C45018EA99Q36866657-28D9CBFC-7A37-43E4-941C-F34557B79A33Q36878788-E96E0472-F500-4381-81D6-822BBD3F4360Q37170480-E6854352-D1C5-4491-9685-3B81E869F0F4Q38492110-B7983B31-F2B5-4097-87A9-6AB896C1A0C5Q38497524-61D2CDBD-255A-4D66-BC9E-81AAF3988417Q38499915-76A0551C-F0F4-43CD-816A-5ABFE1704349Q38502527-6A464AEE-04B9-4EE8-90F5-968160657854Q38506812-160E4126-228C-4CF8-9E01-85A633A81404Q38507478-2BCE7208-0028-4434-9BAA-A9804E7FF87CQ40838808-F26E738D-8AB0-4440-8AE3-23745E5F015DQ40907983-1B84578B-9894-4101-A80D-4F6519F78510Q41347781-1D5EA60C-767A-4D38-BD7C-46CD305EBE5DQ41444932-90212462-FC0B-4C76-AD36-BE6F2E42C4ADQ46467335-45AB500E-D0D6-49DD-9FB4-95A2840144C8Q49054744-8949AC75-F7D9-4802-AEB8-9ADECF0557BE
P2860
Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes.
description
1991 nî lūn-bûn
@nan
1991 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Construction and characterizat ...... from single human chromosomes.
@ast
Construction and characterizat ...... from single human chromosomes.
@en
Construction and characterizat ...... from single human chromosomes.
@nl
type
label
Construction and characterizat ...... from single human chromosomes.
@ast
Construction and characterizat ...... from single human chromosomes.
@en
Construction and characterizat ...... from single human chromosomes.
@nl
prefLabel
Construction and characterizat ...... from single human chromosomes.
@ast
Construction and characterizat ...... from single human chromosomes.
@en
Construction and characterizat ...... from single human chromosomes.
@nl
P2093
P1433
P1476
Construction and characterizat ...... from single human chromosomes.
@en
P2093
P304
P356
10.1016/0888-7543(91)90025-A
P577
1991-12-01T00:00:00Z