A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids (Q28208083)

1

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Makiko Meguro

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Hidetoshi Hoshiya

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Masayuki Haruta

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Yu-ki Sakamoto

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Mitsuo Oshimura

Mechanisms of genomic imprinting

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language of work or name

English

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publication date

June 2003

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published in

Genomics

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volume

81

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issue

6

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page(s)

556-9

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cites work

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Imprinting mechanisms.

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Genomic imprinting: implications for human disease

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Imprinting: focusing on the center

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Genomic imprinting and cancer

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

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

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

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

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

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

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

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

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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

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The molecular basis of the human serum paraoxonase activity polymorphism.

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Autism: recent molecular genetic advances

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Genetic studies of autistic disorder and chromosome 7

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

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

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

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Mouse model of split hand/foot malformation type I

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Maternal uniparental disomy 7 in Silver-Russell syndrome

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

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

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

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7 January 2021

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

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

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