(Q28208083)

1

0 references

Makiko Meguro

2

0 references

Hidetoshi Hoshiya

3

0 references

Masayuki Haruta

4

0 references

Yu-ki Sakamoto

5

0 references

Mitsuo Oshimura

Mechanisms of genomic imprinting

6

0 references

language of work or name

English

0 references

publication date

June 2003

0 references

published in

Genomics

0 references

volume

81

0 references

issue

6

0 references

page(s)

556-9

0 references

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Imprinting mechanisms.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Genomic imprinting: implications for human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Imprinting: focusing on the center

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Genomic imprinting and cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Asb4, Ata3, and Dcn are novel imprinted genes identified by high-throughput screening using RIKEN cDNA microarray

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Mouse A9 cells containing single human chromosomes for analysis of genomic imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Construction of 700 human/mouse A9 monochromosomal hybrids and analysis of imprinted genes on human chromosome 6.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

The molecular basis of the human serum paraoxonase activity polymorphism.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Autism: recent molecular genetic advances

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Genetic studies of autistic disorder and chromosome 7

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Cloning and characterization of two members of the vertebrate Dlx gene family

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

A highly conserved enhancer in the Dlx5/Dlx6 intergenic region is the site of cross-regulatory interactions between Dlx genes in the embryonic forebrain.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Mouse model of split hand/foot malformation type I

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Maternal uniparental disomy 7 in Silver-Russell syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Possible evidence for genomic imprinting in childhood acute myeloblastic leukaemia associated with monosomy for chromosome 7

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Comparative genomic hybridization studies in hydatidiform moles and choriocarcinoma: amplification of 7q21-q31 and loss of 8p12-p21 in choriocarcinoma.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

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://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900052-1

7 January 2021