Molecular cloning of a translocation breakpoint hotspot in 22q11. - Wikidata - wikimedia - TriplyDB

Molecular cloning of a translocation breakpoint hotspot in 22q11.

Molecular cloning of a translocation breakpoint hotspot in 22q11.

http://www.wikidata.org/entity/Q42907947

about

Resolving the complexity of the human genome using single-molecule sequencing Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements Chromosomal translocations and palindromic AT-rich repeats Chimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiency The Immune Syntax Revisited: Opening New Windows on Language Evolution Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.Paternal origin of the de novo constitutional t(11;22)(q23;q11).Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations.Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation.DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation.Complexity of a small non-protein coding sequence in chromosomal region 22q11.2: presence of specialized DNA secondary structures and RNA exon/intron motifs.The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.Searching for non-B DNA-forming motifs using nBMST (non-B DNA motif search tool)Segmental duplication, microinversion, and gene loss associated with a complex inversion breakpoint region in Drosophila.Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13)Many or most genes in Arabidopsis transposed after the origin of the order Brassicales.Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.Chromosome aberrations resulting from double-strand DNA breaks at a naturally occurring yeast fragile site composed of inverted ty elements are independent of Mre11p and Sae2p.Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.Palindrome-mediated and replication-dependent pathogenic structural rearrangements within the NF1 gene.A family of long intergenic non-coding RNA genes in human chromosomal region 22q11.2 carry a DNA translocation breakpoint/AT-rich sequence.Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication.

P2860

Q22122132-D207773D-3A5F-49E2-B9E2-AC8FA7CCA19E Q26741394-D5CF0BEE-9CB3-45FA-87E7-874835700625 Q27024347-E26E89F5-62E5-4D05-BA6B-501259E7ADDD Q28290365-A85669E4-990D-4EDC-BAA3-C9E5032D0721 Q28602830-7CD4AC1F-231F-4F89-BEBF-5ABA27DBB6AD Q33608641-7EE81D9F-843A-4E49-9831-65E10B0A6B22 Q33904434-8AE50771-F0CE-4022-A877-018FBBE3B8C2 Q33915581-80878381-E124-4167-80CC-02F6FB2C2FB6 Q34329295-551BD9C0-C9E6-48C8-A62A-4A1660F23240 Q34332380-5E83D487-D913-4B77-9599-7D7712B4B4EA Q34631531-4364BE75-D857-41DA-865D-CB7CB524D198 Q35398079-293923A3-8A3C-4D91-BCA2-4A7771D1ECD4 Q35807265-334E37BF-DC92-48C1-BC5E-38331605F426 Q35913621-9A24AB32-196E-44A8-BD88-F4E08188B332 Q35954644-E4E2D006-8259-402F-8E8B-1488E756C3DC Q36032967-9AA75E08-A60B-4E30-87F4-33D709711FB8 Q36961261-806AF487-5DC5-4E0C-8500-984796568182 Q36995341-AAADB4B6-68EE-47AB-9A74-BD564FB0B88A Q37312490-EC6B47F0-5DC5-4711-87B9-BE145934DD08 Q37397448-74FFA432-4F50-4516-B729-399AFEEB5D32 Q42150838-20857D9F-9C3B-4355-BBA9-DDAA12AF7C1F Q44108282-43ECB7F5-CF5C-4425-9401-C0C80EB7205A Q52580542-CCECB971-A3F5-49C5-9CBC-72D7C8A1521E Q55442996-EB210E95-D0E0-4BE1-8E9D-EBECDC7958EF

P2860

Molecular cloning of a translocation breakpoint hotspot in 22q11.

http://www.wikidata.org/entity/Q42907947

description

2007 nî lūn-bûn

@nan

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

2007年论文

@zh

2007年论文

@zh-cn

name

Molecular cloning of a translocation breakpoint hotspot in 22q11.

@en

Molecular cloning of a translocation breakpoint hotspot in 22q11.

@nl

type

label

Molecular cloning of a translocation breakpoint hotspot in 22q11.

@en

Molecular cloning of a translocation breakpoint hotspot in 22q11.

@nl

prefLabel

Molecular cloning of a translocation breakpoint hotspot in 22q11.

@en

Molecular cloning of a translocation breakpoint hotspot in 22q11.

@nl

P1433

Q42907947-72FAAF70-4588-45DC-B2B4-8033F4BE2853

P1476

Q42907947-9100AF00-F755-46E4-BC21-92913A87B12E

P2093

Q42907947-0A55F473-F9CF-4008-812A-2B796BB84C68

Q42907947-7585A184-BE9B-444C-B786-F8C4B65CDEDC

Q42907947-80470073-9994-4209-AE40-E353714FC114

Q42907947-854882C8-5BE6-44B8-94FA-125A2F0C5219

Q42907947-B6F8AAAD-C356-4E5F-9EB3-BB5FECE08283

Q42907947-CB11D9DF-A289-41AF-AB0D-5C560E5C4830

Q42907947-CB430AF6-419B-4F9D-B63D-7377EFE56DBB

P2860

Q42907947-05F67FF9-0E0E-4782-B5E8-63C69D70FEC0

Q42907947-0A4B3295-E132-48AB-929F-4A229F3607AD

Q42907947-0FE2DDF3-516C-4D02-928D-E83D925A4F01

Q42907947-1F392AA8-33C0-4CC1-AE72-594D1E545B25

Q42907947-26C6925A-095C-48B0-BFFA-8513D6766094

Q42907947-31E21439-4260-40D5-AB77-32DB7583A4D3

Q42907947-3B8C3483-42FC-4406-823D-5A5B927BE9CB

Q42907947-44D42792-36BB-41AE-8449-B966376162CD

Q42907947-479E5F4C-DD72-4B63-A75F-D5C8E18B04C8

Q42907947-59DDE985-7799-4F58-A25F-C329AD9A23FE

P304

Q42907947-FBDA29C4-18CC-4E27-933C-B62F569EDC78

P31

Q42907947-8B3F66EF-5FD9-47F8-98C5-E1C6B160F809

P356

Q42907947-D4CF3874-A049-48DF-A02C-B93F50CA4EDD

P433

Q42907947-3C58E16E-E850-44A9-BFE6-3F22C5CE20FA

P478

Q42907947-C7D245DC-AD2B-40CA-AC24-611F49B57FB1

P577

Q42907947-578F459A-6E1B-4148-858C-880B52D9706D

P5875

Q42907947-85AB9507-7A46-417D-8470-EDF78069BCDB

P698

Q42907947-2DF0DAF8-44B2-4D25-B8A4-5B53B6159111

P932

Q42907947-1C6C029D-AA59-4B27-AC29-5A09B616B18C

P356

P1433

Genome Research

P1476

Molecular cloning of a translocation breakpoint hotspot in 22q11.

@en

P2093

Beverly S Emanuel

http://www.w3.org/2001/XMLSchema#string

Eriko Hosoba

http://www.w3.org/2001/XMLSchema#string

Hidehito Inagaki

http://www.w3.org/2001/XMLSchema#string

Hiroki Kurahashi

http://www.w3.org/2001/XMLSchema#string

Hiroshi Kogo

http://www.w3.org/2001/XMLSchema#string

Takema Kato

http://www.w3.org/2001/XMLSchema#string

Tamae Ohye

http://www.w3.org/2001/XMLSchema#string

P2860

Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers.

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations

A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2.

The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats.

AT-rich palindromes mediate the constitutional t(11;22) translocation.

Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).

Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families

P304

461-469

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1101/GR.5769507

http://www.w3.org/2001/XMLSchema#string

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

17

http://www.w3.org/2001/XMLSchema#string

P577

2007-01-31T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

6536483

http://www.w3.org/2001/XMLSchema#string

P698

17267815

http://www.w3.org/2001/XMLSchema#string

P932

1832093

http://www.w3.org/2001/XMLSchema#string