A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice (Q33806355)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23677977%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

title

A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice (English)

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1 March 2020

1

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1 March 2020

author name string

John R McCarrey

series ordinal

2

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1 March 2020

P Jeremy Wang

series ordinal

3

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language of work or name

English

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inferred from

Biology of Reproduction

publication date

27 June 2013

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1 March 2020

published in

Biology of Reproduction

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1 March 2020

volume

88

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issue

6

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1 March 2020

page(s)

159

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Aneuploidy causes proteotoxic stress in yeast

1 March 2020

cites work

1 reference

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Non-muscle myosin IIB is essential for cytokinesis during male meiotic cell divisions

4 July 2018

1 reference

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Transcriptional consequences of aneuploidy

4 July 2018

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Interplay between synaptonemal complex, homologous recombination, and centromeres during mammalian meiosis

4 July 2018

1 reference

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Synaptonemal complex components persist at centromeres and are required for homologous centromere pairing in mouse spermatocytes.

4 July 2018

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Fragile X and X-linked intellectual disability: four decades of discovery

4 July 2018

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Aneuploidy drives genomic instability in yeast

4 July 2018

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Nxf3 is expressed in Sertoli cells, but is dispensable for spermatogenesis

4 July 2018

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Deficiency in the multicopy Sycp3-like X-linked genes Slx and Slxl1 causes major defects in spermatid differentiation

4 July 2018

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2q37 Microdeletion Syndrome

4 July 2018

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A review of current large-scale mouse knockout efforts

4 July 2018

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Genetics of mammalian meiosis: regulation, dynamics and impact on fertility

4 July 2018

1 reference

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The multicopy gene Sly represses the sex chromosomes in the male mouse germline after meiosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Regulation of male fertility by X-linked genes

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Isolation and short-term culture of mouse spermatocytes for analysis of meiosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Inactivation of Nxf2 causes defects in male meiosis and age-dependent depletion of spermatogonia

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Many X-linked microRNAs escape meiotic sex chromosome inactivation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion.

4 July 2018

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Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

The mouse X chromosome is enriched for multicopy testis genes showing postmeiotic expression

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Meiotic failure in male mice lacking an X-linked factor

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Generation of a germ cell-specific mouse transgenic Cre line, Vasa-Cre

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Meiotic sex chromosome inactivation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Abnormal sperm in mice lacking the Taf7l gene

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

High expression of the mammalian X chromosome in brain

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Mouse SYCP2 is required for synaptonemal complex assembly and chromosomal synapsis during male meiosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Del 1p36 syndrome: a newly emerging clinical entity

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Mouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

An assessment of the sequence gaps: unfinished business in a finished human genome

4 July 2018

1 reference

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

4 July 2018

1 reference

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Recent segmental duplications in the human genome

4 July 2018

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An abundance of X-linked genes expressed in spermatogonia

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

4 July 2018

The pachytene checkpoint

1 reference

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Localization of SCP2 and SCP3 protein molecules within synaptonemal complexes of the rat

4 July 2018

1 reference

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Acquisition of competence to condense metaphase I chromosomes during spermatogenesis.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

The annual incidence of DiGeorge/velocardiofacial syndrome

4 July 2018

1 reference

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SCP2: a major protein component of the axial elements of synaptonemal complexes of the rat

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

A drying-down technique for the spreading of mammalian meiocytes from the male and female germline

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Kinetochore structure, duplication, and distribution in mammalian cells: analysis by human autoantibodies from scleroderma patients

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

The 13q-deletion syndrome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Fertile male mice with three sex chromosomes: Evidence that infertility in XYY male mice is an effect of two Y chromosomes

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Sexually antagonistic genes: experimental evidence

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Inactivation of Dicer1 has a severe cumulative impact on the formation of mature germ cells in mouse testes.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Hsp90β1 knockout targeted to male germline: a mouse model for globozoospermia

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Impaired striatum-dependent behavior in GASP-1-knock-out mice

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Familial 1.1 Mb deletion in chromosome Xq22.1 associated with mental retardation and behavioural disorders in female patients

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Attenuated behavioural responses to acute and chronic cocaine in GASP-1-deficient mice

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Pachytene asynapsis drives meiotic sex chromosome inactivation and leads to substantial postmeiotic repression in spermatids.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Mutant meiotic chromosome core components in mice can cause apparent sexual dimorphic endpoints at prophase or X-Y defective male-specific sterility

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

The mouse X chromosome is enriched for sex-biased genes not subject to selection by meiotic sex chromosome inactivation

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Analysis of Fgf8 gene function in vertebrate development

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Synaptonemal complex proteins: occurrence, epitope mapping and chromosome disjunction

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4070866

Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions

30 October 2018

1 reference

12 December 2020

Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome

1 reference

12 December 2020

Nonhomologous synapsis of the XY during early pachynema in In(X)1H male mice

1 reference

12 December 2020

Purification, culture, and fractionation of spermatogenic cells

1 reference

12 December 2020

Immunocytology of chiasmata and chromosomal disjunction at mouse meiosis

1 reference

12 December 2020

Postmeiotic sex chromatin in the male germline of mice

1 reference

12 December 2020

Distal 3p deletion syndrome: detailed molecular cytogenetic and clinical characterization of three small distal deletions and review

1 reference

12 December 2020

10.1095/BIOLREPROD.112.106963

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23677977%20AND%20SRC:MED&resulttype=core&format=json

release_asutlj3cybdtxhc3k56gakhrui

1 March 2020

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/asutlj3cybdtxhc3k56gakhrui

24 November 2022

mapped directly with Wikidata item

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23677977%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

PubMed publication ID

23677977

1 reference