Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates.
about
New approaches to the analysis of palindromic sequences from the human genome: evolution and polymorphism of an intronic site at the NF1 locusPalindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal RearrangementsChromosomal translocations and palindromic AT-rich repeatsSnaps and mends: DNA breaks and chromosomal translocationsPalindrome-mediated chromosomal translocations in humans.GAP-Seq: a method for identification of DNA palindromes.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.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.AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12.Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.Reliable handling of highly A/T-rich genomic DNA for efficient generation of knockin strains of Dictyostelium discoideum.Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.Self-catalyzed site-specific depurination of G residues mediated by cruciform extrusion in closed circular DNA plasmids.Decoding NF1 Intragenic Copy-Number Variations.Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.Molecular cloning of a translocation breakpoint hotspot in 22q11.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.
P2860
Q24810641-C852B3EE-0AC0-4693-B101-03A3C76726A4Q26741394-B8BFCB66-DEB1-4E77-952E-85DEFF47AA57Q27024347-700E78AD-7825-4580-A963-A975B002368BQ28082525-33D8231D-86FF-414C-88E9-B563A920EC21Q33668703-8668487C-D26E-4CC4-A990-44BF68DACF43Q33755253-75875761-1B07-421D-B0FD-792A01F71BA4Q33904434-B9BAC184-5607-4425-8115-C120B7A4B1CBQ33915581-4818C2B2-A283-4F65-97FC-6AC4859AE616Q34332380-7FCE2A7C-F0E3-4118-A5D2-BA8595987168Q34631531-1CCBC5FC-0C2D-4937-8137-491416347E8AQ35398079-F412D5BD-CE94-4685-8F85-9BF124D183A6Q35698928-9B53229A-9DFD-431D-839F-9CEB33CE5FBBQ35749729-953CA58E-4104-414D-866F-BD8F5A41517EQ35913621-83EF28E8-F4C7-4DF1-92F2-A897CE583EA3Q35989107-62F35C8E-2CD3-4A56-85D9-E0CF71FC8379Q37312490-2A9488B4-92C4-4DE9-8DE8-25F88ABD1C85Q38743430-E503D615-9BAC-4CE3-A989-12A91F2DD01CQ41908846-2B36ADEF-5D31-4E93-B24A-619AC0645D5CQ42150838-D3CF68E7-0D6F-40FD-B946-9F3111D31058Q42907947-3B8C3483-42FC-4406-823D-5A5B927BE9CBQ44108282-096F6DC2-8662-4C21-AE3C-ACCE97BE6A61Q52580542-B2D79F52-80F7-4516-B2DB-AFC8CD4D890E
P2860
Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Palindromic AT-rich repeat in ...... onarily conserved in primates.
@en
type
label
Palindromic AT-rich repeat in ...... onarily conserved in primates.
@en
prefLabel
Palindromic AT-rich repeat in ...... onarily conserved in primates.
@en
P2093
P2860
P356
P1433
P1476
Palindromic AT-rich repeat in ...... ionarily conserved in primates
@en
P2093
Beverly S Emanuel
Hidehito Inagaki
Hiroe Kowa
Hiroki Kurahashi
Kouji Yamada
Tamae Ohye
Tamim H Shaikh
P2860
P304
P356
10.1002/HUMU.20228
P50
P577
2005-10-01T00:00:00Z