(Q37448159)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

review article

1 reference

title

Recent advance in our understanding of the molecular nature of chromosomal abnormalities (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

1

Hiroki Kurahashi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

6

Hidehito Inagaki

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

5

Makiko Tsutsumi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

7

Tamae Ohye

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

3

Takema Kato

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

author name string

Hasbaira Bolor

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

publication date

17 April 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

26 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

volume

54

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

page(s)

253-260

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19373258%20AND%20SRC:MED&resulttype=core&format=json

Chromosomal translocations mediated by palindromic DNA.

26 January 2020

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DNA double-strand breaks: signaling, repair and the cancer connection

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7 January 2021

Chromosomal stability and the DNA double-stranded break connection

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7 January 2021

Frequent chromosomal translocations induced by DNA double-strand breaks

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7 January 2021

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

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7 January 2021

Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit

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7 January 2021

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

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7 January 2021

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

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7 January 2021

The DNA sequence of human chromosome 22

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7 January 2021

A common molecular basis for rearrangement disorders on chromosome 22q11

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7 January 2021

Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints

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7 January 2021

Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).

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7 January 2021

A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients

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7 January 2021

NF1 microdeletion breakpoints are clustered at flanking repetitive sequences

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7 January 2021

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

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7 January 2021

Identification of a 3.0-kb major recombination hotspot in patients with Sotos syndrome who carry a common 1.9-Mb microdeletion

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7 January 2021

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

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7 January 2021

Segmental duplications: an 'expanding' role in genomic instability and disease

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7 January 2021

Primate segmental duplications: crucibles of evolution, diversity and disease

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7 January 2021

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion

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7 January 2021

Unequal exchange at the Charcot-Marie-Tooth disease type 1A recombination hot-spot is not elevated above the genome average rate

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7 January 2021

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

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7 January 2021

The first BCR gene intron contains breakpoints in Philadelphia chromosome positive leukemia

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7 January 2021

Human chromosomal translocations at CpG sites and a theoretical basis for their lineage and stage specificity

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7 January 2021

Dual-color fish analysis of breakpoints on Robertsonian translocations

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7 January 2021

Robertsonian translocations: mechanisms of formation, aneuploidy, and uniparental disomy and diagnostic considerations

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7 January 2021

Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22).

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Molecular cloning of a translocation breakpoint hotspot in 22q11.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Two different forms of palindrome resolution in the human genome: deletion or translocation.

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates.

1 reference

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7 January 2021

New approaches to the analysis of palindromic sequences from the human genome: evolution and polymorphism of an intronic site at the NF1 locus

1 reference

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7 January 2021

A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22)

1 reference

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7 January 2021

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

1 reference

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7 January 2021

A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies

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7 January 2021

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

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7 January 2021

Genetic variation affects de novo translocation frequency.

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7 January 2021

Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats

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7 January 2021

Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.

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7 January 2021

A non-B-DNA structure at the Bcl-2 major breakpoint region is cleaved by the RAG complex

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7 January 2021

Chromosome territories, nuclear architecture and gene regulation in mammalian cells

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7 January 2021

Spatial proximity of translocation-prone gene loci in human lymphomas

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7 January 2021

Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22)

1 reference

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7 January 2021

Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males

1 reference

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7 January 2021

Palindrome-mediated chromosomal translocations in humans

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7 January 2021

Long DNA palindromes, cruciform structures, genetic instability and secondary structure repair

1 reference

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7 January 2021

Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm

1 reference

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7 January 2021

Trinucleotide expansion in haploid germ cells by gap repair

1 reference

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7 January 2021

Effect of paternal age on the frequency of cytogenetic abnormalities in human spermatozoa

1 reference

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7 January 2021

Sorting out chromosome errors.

1 reference

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7 January 2021

Nonhomologous Robertsonian translocations form predominantly during female meiosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

The origins, patterns and implications of human spontaneous mutation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

To err (meiotically) is human: the genesis of human aneuploidy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

Mouse genetic models for aneuploidy induction in germ cells

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

Playing for half the deck: the molecular biology of meiosis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

Clarifying the mechanics of DNA strand exchange in meiotic recombination

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

The origin of human aneuploidy: where we have been, where we are going

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

Chromosomal abnormalities and embryo development in recurrent miscarriage couples

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

Trisomy recurrence: a reconsideration based on North American data

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

Mutations of the SYCP3 gene in women with recurrent pregnancy loss

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https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

Dissecting the mammalian synaptonemal complex using targeted mutations.

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7 January 2021

Female germ cell aneuploidy and embryo death in mice lacking the meiosis-specific protein SCP3

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7 January 2021

Chromosomal influence on meiotic spindle assembly: abnormal meiosis I in female Mlh1 mutant mice

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

RAD51C deficiency in mice results in early prophase I arrest in males and sister chromatid separation at metaphase II in females

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https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021

Azoospermia in patients heterozygous for a mutation in SYCP3

1 reference

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7 January 2021

The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility

1 reference

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7 January 2021

Sex matters in meiosis

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7 January 2021

Male infertility in reciprocal translocation carriers: the sex body affair.

1 reference

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7 January 2021

Chiasma frequency and maternal age in mammals.

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7 January 2021

Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome

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7 January 2021

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination

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7 January 2021

Association between maternal age and meiotic recombination for trisomy 21.

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7 January 2021

SMC1beta-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.35

7 January 2021