The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome (Q24677893)

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English	The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome	scientific article

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scholarly article

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The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome (English)

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Սիլվեր-Ռասսելի համախտանիշ

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based on heuristic

inferred from title

object named as

P Stanier

10

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author name string

L Bentley

1

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K Nakabayashi

2

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D Monk

3

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C Beechey

4

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J Peters

5

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Z Birjandi

6

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F E Khayat

7

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M Patel

8

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M A Preece

9

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S W Scherer

11

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G E Moore

12

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language of work or name

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publication date

April 2003

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Journal of Medical Genetics

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40

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4

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249-56

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Identification and characterization of three members of the human metallocarboxypeptidase gene family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

Carboxypeptidase A3 (CPA3): a novel gene highly induced by histone deacetylase inhibitors during differentiation of prostate epithelial cancer cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

Human PEG1/MEST, an imprinted gene on chromosome 7

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

An imprinted PEG1/MEST antisense expressed predominantly in human testis and in mature spermatozoa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

The novel gene, gamma2-COP (COPG2), in the 7q32 imprinted domain escapes genomic imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

Evidence against a major role of PEG1/MEST in Silver-Russell syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

Assignment of growth factor receptor-bound protein 10 (GRB10) to human chromosome 7p11.2-p12

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

7 April 2017

A syndrome of intra-uterine dwarfism recognizable at birth with cranio-facial dysostosis, disproportionately short arms, and other anomalies (5 examples).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

Carboxypeptidases from A to z: implications in embryonic development and Wnt binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

Maternal uniparental disomy 7--review and further delineation of the phenotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

The search for the gene for Silver-Russell syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

Mechanisms of genomic imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

Developmental differences in methylation of human Alu repeats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

Carboxypeptidase A Isoforms Produced by Distinct Genes or Alternative Splicing in Brain and Other Extrapancreatic Tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 September 2017

Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

30 May 2018

Allele-specific replication timing of imprinted gene regions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

30 May 2018

Mosaic and polymorphic imprinting of the WT1 gene in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

30 May 2018

The gene TSGA14, adjacent to the imprinted gene MEST, escapes genomic imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 November 2018

Divergent evolution in M6P/IGF2R imprinting from the Jurassic to the Quaternary

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 November 2018

Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 November 2018

Peg1/Mest locates distal to the currently defined imprinting region on mouse proximal chromosome 6 and identifies a new imprinting region affecting growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 November 2018

Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 November 2018

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 November 2018

Polymorphic and tissue-specific imprinting of the human Wilms tumor gene, WT1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735416

28 November 2018

Functional Polymorphism in the Parental Imprinting of the Human IGF2R Gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/12676894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphic functional imprinting of the human IGF2 gene among individuals, in blood cells, is associated with H19 expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/12676894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paternal expression of WT1 in human fibroblasts and lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12676894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1136/JMG.40.4.249

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