NOBOX homeobox mutation causes premature ovarian failure (Q24677575)

ORCID Public Data File 2021

Yingying Qin

1

object named as

Yingying Qin

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author name string

Youngsok Choi

2

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Han Zhao

3

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Joe Leigh Simpson

4

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Aleksandar Rajkovic

American Journal of Human Genetics

6

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language of work or name

English

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publication date

September 2007

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published in

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volume

81

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page(s)

576-81

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issue

3

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cites work

Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

The third helix of the homeodomain of paired class homeodomain proteins acts as a recognition helix both for DNA and protein interactions

7 April 2017

1 reference

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Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Premature luteinization and cumulus cell defects in ovarian-specific Smad4 knockout mice

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Characterization of NOBOX DNA binding specificity and its regulation of Gdf9 and Pou5f1 promoters

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Candidate genes for premature ovarian failure.

7 April 2017

1 reference

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The FMR1 premutation and reproduction

28 September 2017

1 reference

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CPEB controls oocyte growth and follicle development in the mouse

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

The genetic basis of premature ovarian failure.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

cDNA cloning and expression of the human NOBOX gene in oocytes and ovarian follicles

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Genetics of early mammalian folliculogenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Premature ovarian failure in androgen receptor-deficient mice

28 September 2017

1 reference

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Transcriptional regulation of early oogenesis: in search of masters.

28 September 2017

1 reference

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Mutational analysis of the homeobox region of the human NOBOX gene in Japanese women who exhibit premature ovarian failure

28 September 2017

1 reference

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Mutations that affect the ability of the vnd/NK-2 homeoprotein to regulate gene expression: transgenic alterations and tertiary structure

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Nobox is a homeobox-encoding gene preferentially expressed in primordial and growing oocytes.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Molecular evolution of the homeodomain family of transcription factors

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Ovarian differentiation and gonadal failure

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Association of FMR1 repeat size with ovarian dysfunction.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Characterization of Nkx3.2 DNA binding specificity and its requirement for somitic chondrogenesis

30 May 2018

1 reference

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A fork in the road to fertility.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Incidence of premature ovarian failure.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

A novel mutation in the bone morphogenetic protein 15 gene causing defective protein secretion is associated with both increased ovulation rate and sterility in Lacaune sheep.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Functional characterization of the human FSH receptor with an inactivating Ala189Val mutation

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

New natural inactivating mutations of the follicle-stimulating hormone receptor: correlations between receptor function and phenotype.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950834

Inheritance in idiopathic premature ovarian failure: analysis of 71 cases

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17701902

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Physical and functional interactions between the prostate suppressor homeoprotein NKX3.1 and serum response factor

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17701902

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/519496

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91991

91991

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1 reference

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