Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region.

A Mouse Model for Imprinting of the Human Retinoblastoma Gene.

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif.

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region.

Linkage, but not gene order, of homologous loci, including alpha-L-iduronidase (Idua), is conserved in the Huntington disease region of the mouse and human genomes.

Parental imprinting of the mouse H19 gene.

The human homolog of the mouse brown gene maps to the short arm of chromosome 9 and extends the known region of homology with mouse chromosome 4.

Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q.

Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkage.

Parental imprinting of the human H19 gene.

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4.

Human in vitro oocyte maturation is not associated with increased imprinting error rates at LIT1, SNRPN, PEG3 and GTL2.

Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene.

The mouse dopamine D2A receptor gene: sequence homology with the rat and human genes and expression of alternative transcripts.

Gametic imprinting and the manifestation of the fused gene in the house mouse.

Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt).

Maternal bias and escape from X chromosome imprinting in the midgestation mouse placenta.

Linkage of a gene for neural cell adhesion molecule, L1 (CamL1) to the Rsvp region of the mouse X chromosome.

Gene order in linkage group XVI of the house mouse.

Genomic imprinting of DIO3, a candidate gene for the syndrome associated with human uniparental disomy of chromosome 14.

Imprinting analysis of the mouse chromosome 7C region in DNMT1-null embryos.

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.

Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase beta-subunit gene in mouse and human: tight linkage to the Huntington disease region (4p16.3).

Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome.

Sequence of the human factor VIII-associated gene is conserved in mouse.

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A Mouse Model for Imprinting of the Human Retinoblastoma Gene.

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif.

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region.

Linkage, but not gene order, of homologous loci, including alpha-L-iduronidase (Idua), is conserved in the Huntington disease region of the mouse and human genomes.

Parental imprinting of the mouse H19 gene.

The human homolog of the mouse brown gene maps to the short arm of chromosome 9 and extends the known region of homology with mouse chromosome 4.

Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q.

Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkage.

Parental imprinting of the human H19 gene.

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4.

Human in vitro oocyte maturation is not associated with increased imprinting error rates at LIT1, SNRPN, PEG3 and GTL2.

Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene.

The mouse dopamine D2A receptor gene: sequence homology with the rat and human genes and expression of alternative transcripts.

Gametic imprinting and the manifestation of the fused gene in the house mouse.

Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt).

Maternal bias and escape from X chromosome imprinting in the midgestation mouse placenta.

Linkage of a gene for neural cell adhesion molecule, L1 (CamL1) to the Rsvp region of the mouse X chromosome.

Gene order in linkage group XVI of the house mouse.

Genomic imprinting of DIO3, a candidate gene for the syndrome associated with human uniparental disomy of chromosome 14.

Imprinting analysis of the mouse chromosome 7C region in DNMT1-null embryos.

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.

Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase beta-subunit gene in mouse and human: tight linkage to the Huntington disease region (4p16.3).

Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome.

Sequence of the human factor VIII-associated gene is conserved in mouse.

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region.

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