(Q33909470)

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The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

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scholarly article

1 reference

Europe PubMed Central

29 July 2017

The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats (English)

1 reference

Europe PubMed Central

29 July 2017

Christina A Cuomo

4

1 reference

Europe PubMed Central

29 July 2017

object named as

Thoas Fioretos

12

0 references

Mattias Höglund

object named as

Mattias Höglund

6

0 references

3

object named as

Chad Nusbaum

1 reference

Europe PubMed Central

29 July 2017

James R. Lupski

11

object named as

James R Lupski

1 reference

Europe PubMed Central

29 July 2017

Pawel Stankiewicz

2

object named as

Pawel Stankiewicz

1 reference

Europe PubMed Central

29 July 2017

object named as

Felix Mitelman

10

0 references

Aikaterini Barbouti

1

object named as

Aikaterini Barbouti

1 reference

Europe PubMed Central

29 July 2017

Bertil Johansson

7

object named as

Bertil Johansson

1 reference

Europe PubMed Central

29 July 2017

Anne Hagemeijer

8

object named as

Anne Hagemeijer

1 reference

Europe PubMed Central

29 July 2017

author name string

April Cook

5

1 reference

Europe PubMed Central

29 July 2017

Sung-Sup Park

9

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Europe PubMed Central

29 July 2017

language of work or name

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publication date

8 December 2003

1 reference

Europe PubMed Central

29 July 2017

American Journal of Human Genetics

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Europe PubMed Central

29 July 2017

74

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Europe PubMed Central

29 July 2017

1-10

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Europe PubMed Central

29 July 2017

1

1 reference

Europe PubMed Central

29 July 2017

Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

An Alu Transposition Model for the Origin and Expansion of Human Segmental Duplications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Genome architecture catalyzes nonrecurrent chromosomal rearrangements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

2002 Curt Stern Award Address. Genomic disorders recombination-based disease resulting from genomic architecture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Recent segmental duplications in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Molecular-evolutionary mechanisms for genomic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

A large nucleolar U3 ribonucleoprotein required for 18S ribosomal RNA biogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Structure and evolution of the Smith-Magenis syndrome repeat gene clusters, SMS-REPs.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Cytogenetic and molecular genetic evolution of chronic myeloid leukemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Molecular mechanism of class switch recombination: linkage with somatic hypermutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Genome architecture, rearrangements and genomic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Initial sequencing and analysis of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

The Sequence of the Human Genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Long palindromic sequences induce double-strand breaks during meiosis in yeast.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Factors affecting inverted repeat stimulation of recombination and deletion in Saccharomyces cerevisiae

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Human genes encoding U3 snRNA associate with coiled bodies in interphase cells and are clustered on chromosome 17p11.2 in a complex inverted repeat structure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Palindrome resolution and recombination in the mammalian germ line

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Chromosome 17 abnormalities and inactivation of the p53 gene in chronic myeloid leukemia and their prognostic significance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

High resolution mapping using fluorescence in situ hybridization to extended DNA fibers prepared from agarose-embedded cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

Isochromosomes in neoplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

5 July 2018

The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1181896

29 October 2018

Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q)

1 reference

https://pubmed.ncbi.nlm.nih.gov/14666446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/14666446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course

1 reference

https://pubmed.ncbi.nlm.nih.gov/14666446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long AT-rich palindromes and the constitutional t(11;22) breakpoint

1 reference

https://pubmed.ncbi.nlm.nih.gov/14666446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of complex disease association and linkage studies using the University of California Santa Cruz Genome Browser

1 reference

https://pubmed.ncbi.nlm.nih.gov/14666446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cruciform structures in palindromic DNA are favored by DNA supercoiling

1 reference

https://pubmed.ncbi.nlm.nih.gov/14666446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isochromosome 17q demonstrated by interphase fluorescence in situ hybridization in primitive neuroectodermal tumors of the central nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/14666446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

1 reference

https://pubmed.ncbi.nlm.nih.gov/14666446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

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