The novel imprinted carboxypeptidase A4 gene ( CPA4) in the 7q32 imprinting domain (Q34173196)

31 July 2017

The novel imprinted carboxypeptidase A4 gene ( CPA4) in the 7q32 imprinting domain (English)

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31 July 2017

12

Norio Niikawa

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31 July 2017

7

Koh-ichiro Yoshiura

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31 July 2017

5

Nobutomo Miwa

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31 July 2017

1

Tomohiko Kayashima

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31 July 2017

6

Tohru Ohta

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31 July 2017

9

Yoshibumi Nakane

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31 July 2017

13

Tatsuya Kishino

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31 July 2017

2

Kentaro Yamasaki

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31 July 2017

Takahiro Yamada

3

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31 July 2017

Hideki Sakai

4

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31 July 2017

Naomichi Matsumoto

8

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31 July 2017

Hiroshi Kanetake

10

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31 July 2017

Fumitoshi Ishino

11

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31 July 2017

28 January 2003

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31 July 2017

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31 July 2017

112

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31 July 2017

3

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31 July 2017

220-226

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https://scigraph.springernature.com/pub.10.1007/s00439-002-0891-3

31 July 2017

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cites work

Promoter-specific imprinting of the human insulin-like growth factor-II gene

1 reference

12 December 2020

Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting status

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12 December 2020

Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy.

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12 December 2020

Identification of two new polymorphisms (c2447-125A>G; c2532G>A) in the ?2-COP (COPG2) gene by screening of Silver-Russell syndrome patients

1 reference

12 December 2020

Metallocarboxypeptidases and their protein inhibitors. Structure, function and biomedical properties

1 reference

12 December 2020

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

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12 December 2020

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

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12 December 2020

Genomic imprinting and carcinogenesis.

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12 December 2020

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

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12 December 2020

Genomewide scan for prostate cancer-aggressiveness loci.

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12 December 2020

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

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12 December 2020

Advances in metallo-procarboxypeptidases. Emerging details on the inhibition mechanism and on the activation process

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Frequent loss of imprinting of PEG1/MEST in invasive breast cancer

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12 December 2020

Genomic imprinting and Beckwith-Wiedemann syndrome

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12 December 2020

DNA methylation in genomic imprinting, development, and disease

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12 December 2020

Loss of heterozygosity in human primary prostate carcinomas: a possible tumor suppressor gene at 7q31.1

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12 December 2020

DNA methylation, imprinting and cancer

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12 December 2020

PipMaker--a web server for aligning two genomic DNA sequences

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12 December 2020

Epigenetics: regulation through repression

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12 December 2020

Molecular genetic profiling of Gleason grade 4/5 prostate cancers compared to benign prostatic hyperplasia

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12 December 2020

The role of histone acetylation in the allelic expression of the imprinted human insulin-like growth factor II gene

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12 December 2020

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

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12 December 2020

gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome

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12 December 2020

Allele-specific histone acetylation accompanies genomic imprinting of the insulin-like growth factor II receptor gene

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma

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12 December 2020

10.1007/S00439-002-0891-3

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