(Q22253268)

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STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion

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STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion (English)

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Stromal antigen 3

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GOA release 2020-03-11

synaptonemal complex assembly

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GOA release 2020-03-11

Stromal antigen 3

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GOA release 2020-03-11

Williams-Beuren syndrome

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inferred from title

object named as

LEONOR KREMER

3

author given names

L

author last names

Kremer

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PubMed publication ID

7 February 2023

author name string

N Pezzi

1

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I Prieto

2

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L A Pérez Jurado

4

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C Valero

5

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J Del Mazo

6

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C Martínez-A

7

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J L Barbero

8

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NIEVES PEZZI

1

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IGNACIO PRIETO

2

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LUIS A. PÉREZ JURADO

4

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CARMEN VALERO

5

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JESÚS DEL MAZO

6

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CARLOS MARTÍNEZ-A

7

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JOSÉ L. BARBERO

8

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language of work or name

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publication date

March 2000

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14

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3

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581-92

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581-592

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A coiled-coil related protein specific for synapsed regions of meiotic prophase chromosomes

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Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin

1 reference

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based on heuristic

inferred from DOI database lookup

Two discrete regions of deletion at 7q in uterine leiomyomas

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based on heuristic

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A new essential gene located on Saccharomyces cerevisiae chromosome IX.

1 reference

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based on heuristic

inferred from DOI database lookup

Analysis of the 5' region of PMS2 reveals heterogeneous transcripts and a novel overlapping gene

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

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based on heuristic

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Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

7 January 2021

based on heuristic

inferred from DOI database lookup

PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7.

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

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based on heuristic

inferred from DOI database lookup

Dynamics of meiotic prophase I during spermatogenesis: from pairing to division

1 reference

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Meiotic arrest at first spermatocyte level: a new inherited infertility disorder

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Natural history of Williams syndrome: physical characteristics

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis

1 reference

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based on heuristic

inferred from DOI database lookup

Meiotic pachytene arrest in MLH1-deficient mice

1 reference

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based on heuristic

inferred from DOI database lookup

The meiosis-specific Hop2 protein of S. cerevisiae ensures synapsis between homologous chromosomes

1 reference

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based on heuristic

inferred from DOI database lookup

Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis

1 reference

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based on heuristic

inferred from DOI database lookup

SA-1, a nuclear protein encoded by one member of a novel gene family: molecular cloning and detection in hemopoietic organs

1 reference

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based on heuristic

inferred from DOI database lookup

2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

7 January 2021

based on heuristic

inferred from DOI database lookup

Mammalian MutS homologue 5 is required for chromosome pairing in meiosis

1 reference

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based on heuristic

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

1 reference

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Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of morc (microrchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouse

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular cloning and expression of stromalin protein from Drosophila melanogaster: homologous to mammalian stromalin family of nuclear proteins

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Distribution of the Rad51 recombinase in human and mouse spermatocytes

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

7 January 2021

based on heuristic

inferred from DOI database lookup

Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

7 January 2021

based on heuristic

inferred from DOI database lookup

The human autosomal gene DAZLA: testis specificity and a candidate for male infertility

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

7 January 2021

based on heuristic

inferred from DOI database lookup

A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

7 January 2021

based on heuristic

inferred from DOI database lookup

High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions.

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

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based on heuristic

inferred from DOI database lookup

A comprehensive set of sequence analysis programs for the VAX

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

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based on heuristic

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Preparation of spermatogonia, spermatocytes, and round spermatids for analysis of gene expression using fluorescence-activated cell sorting

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

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based on heuristic

inferred from DOI database lookup

Identification of Xenopus SMC protein complexes required for sister chromatid cohesion

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

7 January 2021

based on heuristic

inferred from DOI database lookup

Maintenance of sister-chromatid cohesion at the centromere by the Drosophila MEI-S332 protein

1 reference

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based on heuristic

inferred from DOI database lookup

Yeast cohesin complex requires a conserved protein, Eco1p(Ctf7), to establish cohesion between sister chromatids during DNA replication

1 reference

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based on heuristic

inferred from DOI database lookup

A high-resolution microsatellite map of the mouse genome

1 reference

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Heterogeneity in the phosphorylation of microtubule-associated protein MAP1B during rat brain development

1 reference

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The gene encoding a major component of the lateral elements of synaptonemal complexes of the rat is related to X-linked lymphocyte-regulated genes

1 reference

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Case-control study of whether subfertility in men is familial

1 reference

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based on heuristic

inferred from DOI database lookup

Williams syndrome

1 reference

https://api.crossref.org/works/10.1096%2FFASEBJ.14.3.581

7 January 2021

based on heuristic

inferred from DOI database lookup

Centromere pattern in different mouse seminiferous tubule cells

1 reference

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based on heuristic

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Microtubule-associated proteins during mouse spermatogenesis: localization of a protein immunologically related to brain MAP1B protein in the synaptonemal complex.

1 reference

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A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease

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Identifiers

10.1096/FASEBJ.14.3.581

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OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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