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A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient

Clinical genetics, 2014-12, Vol.86 (6), p.539-544

2014

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Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome

Clinical genetics, 2015-09, Vol.88 (3), p.261-266

2015

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A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors

Journal of biochemistry (Tokyo), 2000-11, Vol.128 (5), p.847-853

2000

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The Mouse Murr1 Gene Is Imprinted in the Adult Brain, Presumably Due to Transcriptional Interference by the Antisense-Oriented U2af1-rs1 Gene

Molecular and Cellular Biology, 2004-01, Vol.24 (1), p.270-279

2004

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An NsiI RFLP in the human long QT intronic transcript 1 (LIT1)

Journal of human genetics, 2000-03, Vol.45 (2), p.96-97

2000

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Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5 : long-stretches of unusually well conserved intronic sequences of Kvlqt1 between mouse and human

DNA research, 2000-06, Vol.7 (3), p.195-206

2000

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Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region

Genome research, 2002-12, Vol.12 (12), p.1860-1870

2002

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Osteoclast-Derived Zinc Finger (OCZF) Protein With POZ Domain, a Possible Transcriptional Repressor, Is Involved in Osteoclastogenesis

Blood, 1999-09, Vol.94 (6), p.1987-1997

1999

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Osteoclast-derived zinc finger (OCZF) protein with POZ domain, a possible transcriptional repressor, is involved in osteoclastogenesis

Blood, 1999-09, Vol.94 (6), p.1987-1997

1999

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Loss of CpG Methylation Is Strongly Correlated with Loss of Histone H3 Lysine 9 Methylation at DMR-LIT1 in Patients with Beckwith-Wiedemann Syndrome

American journal of human genetics, 2003-10, Vol.73 (4), p.948-956

2003

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Expression and Sequence of the Only Detectable Aldolase in Chlamydomonas reinhardtii

Archives of biochemistry and biophysics, 1994-08, Vol.313 (1), p.173-178

1994

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High frequency of fusion transcripts of exon 11 and exon 4/5 in AF-4 gene is observed in cord blood, as well as leukemic cells from infant leukemia patients with t(4;11)(q21;q23)

Leukemia, 1998-09, Vol.12 (9), p.1398-1403

1998

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MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene products

Genes & Genetic Systems, 2008, Vol.83(2), pp.199-208

2008

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A Novel Human Homolog of a Dead-Box RNA Helicase Family

Biochemical and biophysical research communications, 1994-03, Vol.199 (2), p.748-754

1994

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Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in mice

Gene, 2006-01, Vol.366 (1), p.77-86

2006

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Tissue-specific expression of rat aldolase A mRNAs. Three molecular species differing only in the 5'-terminal sequences

The Journal of biological chemistry, 1986-03, Vol.261 (7), p.3347-3354

1986

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Characterization and Imprinting Status of OBPH1/Obph1 Gene: Implications for an Extended Imprinting Domain in Human and Mouse

Genomics (San Diego, Calif.), 2002-12, Vol.80 (6), p.575-584

2002

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A developmental biological study of aldolase gene expression in Xenopus laevis

Cell research, 2002-06, Vol.12 (2), p.85-96

2002

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Nucleotide sequence of rat liver aldolase B messenger RNA

The Journal of biological chemistry, 1984-12, Vol.259 (23), p.14572-14575

1984

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C11orf21, a novel gene within the Beckwith–Wiedemann syndrome region in human chromosome 11p15.5

Gene, 2000-10, Vol.256 (1), p.311-317

2000

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Expression of rat aldolase A gene and analysis of AH promoter region of the gene

Progress in clinical and biological research, 1990, Vol.344, p.53

1990

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Caenorhabditis elegans has two isozymic forms, CE-1 and CE-2, of fructose-1,6-bisphosphate aldolase which are encoded by different genes

Archives of biochemistry and biophysics, 1997-03, Vol.339 (1), p.226-234

1997

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Structure and expression of human and rat aldolase isozyme genes: multiple mRNA species of aldolase A produced from a single gene

Isozymes, 1987, Vol.14, p.153

1987

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The structure of the brain-specific rat aldolase C gene and its regional expression

Biochemical and biophysical research communications, 1991-01, Vol.174 (2), p.1035-1042

1991

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Molecular Evolution of Amphioxus Fructose-1,6- bisphosphate Aldolase

Archives of biochemistry and biophysics, 1997-12, Vol.348 (2), p.329-336

1997

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A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient

Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome

A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors

The Mouse Murr1 Gene Is Imprinted in the Adult Brain, Presumably Due to Transcriptional Interference by the Antisense-Oriented U2af1-rs1 Gene

An NsiI RFLP in the human long QT intronic transcript 1 (LIT1)

Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5 : long-stretches of unusually well conserved intronic sequences of Kvlqt1 between mouse and human

Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region

Osteoclast-Derived Zinc Finger (OCZF) Protein With POZ Domain, a Possible Transcriptional Repressor, Is Involved in Osteoclastogenesis

Osteoclast-derived zinc finger (OCZF) protein with POZ domain, a possible transcriptional repressor, is involved in osteoclastogenesis

Loss of CpG Methylation Is Strongly Correlated with Loss of Histone H3 Lysine 9 Methylation at DMR-LIT1 in Patients with Beckwith-Wiedemann Syndrome

Expression and Sequence of the Only Detectable Aldolase in Chlamydomonas reinhardtii

High frequency of fusion transcripts of exon 11 and exon 4/5 in AF-4 gene is observed in cord blood, as well as leukemic cells from infant leukemia patients with t(4;11)(q21;q23)

MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene products

A Novel Human Homolog of a Dead-Box RNA Helicase Family

Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in mice

Tissue-specific expression of rat aldolase A mRNAs. Three molecular species differing only in the 5'-terminal sequences

Characterization and Imprinting Status of OBPH1/Obph1 Gene: Implications for an Extended Imprinting Domain in Human and Mouse

A developmental biological study of aldolase gene expression in Xenopus laevis

Nucleotide sequence of rat liver aldolase B messenger RNA

C11orf21, a novel gene within the Beckwith–Wiedemann syndrome region in human chromosome 11p15.5

Expression of rat aldolase A gene and analysis of AH promoter region of the gene

Caenorhabditis elegans has two isozymic forms, CE-1 and CE-2, of fructose-1,6-bisphosphate aldolase which are encoded by different genes

Structure and expression of human and rat aldolase isozyme genes: multiple mRNA species of aldolase A produced from a single gene

The structure of the brain-specific rat aldolase C gene and its regional expression

Molecular Evolution of Amphioxus Fructose-1,6- bisphosphate Aldolase

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