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Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy

Journal of medical genetics, 2004-03, Vol.41 (3), p.183-187

2004

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Long-term in vitro maintenance of clonal abundance and leukaemia-initiating potential in acute lymphoblastic leukaemia

Leukemia, 2016-08, Vol.30 (8), p.1691-1700

2016

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Abundant and equipotent founder cells establish and maintain acute lymphoblastic leukaemia

Leukemia, 2017-12, Vol.31 (12), p.2577-2586

2017

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Differential expression of miR-17∼92 identifies BCL2 as a therapeutic target in BCR-ABL-positive B-lineage acute lymphoblastic leukemia

Leukemia, 2014-03, Vol.28 (3), p.554-565

2014

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Evc Regulates a Symmetrical Response to Shh Signaling in Molar Development

Journal of dental research, 2013-03, Vol.92 (3), p.222-228

2013

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Differential expression of miR-17 similar to 92 identifies BCL2 as a therapeutic target in BCR-ABL-positive B-lineage acute lymphoblastic leukemia

Leukemia, 2014-03, Vol.28 (3), p.554-565

2014

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The structure of DXF34, a human X-linked sequence family with homology to a transcribed mouse Y-linked repeat

Mammalian genome, 1997-09, Vol.8 (9), p.689-691

1997

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New Insights into the Man-Mouse Comparative Map of the X Chromosome

Genomics (San Diego, Calif.), 1994-01, Vol.19 (2), p.215-220

1994

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Mouse Mutants Carrying Deletions that Remove the Genes Mutated in Coffin-Lowry Syndrome and Lactic Acidosis

Human molecular genetics, 1998-03, Vol.7 (3), p.549-555

1998

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An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome

Genomics (San Diego, Calif.), 1998-02, Vol.48 (1), p.128-131

1998

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High-Resolution Comparative Mapping of the Proximal Region of the Mouse X Chromosome

Genomics (San Diego, Calif.), 1995-07, Vol.28 (2), p.305-310

1995

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Comment on: Collaborative research: population-based data and validation are necessary

British journal of surgery, 2022-09, Vol.109 (10), p.e111-e112

2022

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High yield reproducible rat model recapitulating human Barrett’s carcinogenesis

World journal of gastroenterology : WJG, 2017-09, Vol.23 (33), p.6077-6087

2017

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t(8;21) Acute Myeloid Leukaemia Requires Active CCND-CDK4/6

Klinische Pädiatrie, 2016-05, Vol.228 (3)

2016

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Smcx lies distal to DXHX674 and DXHX679 on the mouse X chromosome

Mammalian genome, 1996-07, Vol.7 (7), p.552-552

1996

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Perspectives and Approaches

Frans H. van Eemeren, Rob Grootendorst, J. Anthony Blair, Charles A. Willard, Frans H. van Eemeren, Rob Grootendorst, J. Anthony Blair, Charles A. Willard

2011

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Across the Lines of Disciplines

Frans H. van Eemeren, Rob Grootendorst, J. Anthony Blair, Charles A. Willard, Frans H. van Eemeren, Rob Grootendorst, J. Anthony Blair, Charles A. Willard

2011

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Analysis and Practices

Frans H. van Eemeren, Rob Grootendorst, J. Anthony Blair, Charles A. Willard, Frans H. van Eemeren, Rob Grootendorst, J. Anthony Blair, Charles A. Willard

2011

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A phenotype map of the mouse X chromosome: models for human X-linked disease

Genome research, 2000-03, Vol.10 (3), p.277-292

2000

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Mapping of FMR1, the gene implicated in fragile X-linked mental retardation, on the mouse X chromosome

Genomics (San Diego, Calif.), 1992-04, Vol.12 (4), p.818-821

1992

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Mutations in Two Nonhomologous Genes in a Head-to-Head Configuration Cause Ellis-van Creveld Syndrome

American journal of human genetics, 2003-03, Vol.72 (3), p.728-732

2003

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Evaluation of human microdissection clones from the FRAXA region as tools for comparative mapping in the mouse: isolation of a conserved genomic clone close to FMR1

Mammalian genome, 1994-09, Vol.5 (9), p.584-587

1994

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Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis-van Creveld syndrome patients

Human genetics, 2007-01, Vol.120 (5), p.663-670

2007

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Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X chromosome short arm with respect to evolutionary breakpoints on the mouse X chromosome

Mammalian genome, 2000-08, Vol.11 (8), p.710-712

2000

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Encyclopedia of the mouse genome VII. Mouse chromosome X

Mammalian genome, 1998, Vol.8 Spec No, p.S361-S377

1998

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Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy

Long-term in vitro maintenance of clonal abundance and leukaemia-initiating potential in acute lymphoblastic leukaemia

Abundant and equipotent founder cells establish and maintain acute lymphoblastic leukaemia

Differential expression of miR-17∼92 identifies BCL2 as a therapeutic target in BCR-ABL-positive B-lineage acute lymphoblastic leukemia

Evc Regulates a Symmetrical Response to Shh Signaling in Molar Development

Differential expression of miR-17 similar to 92 identifies BCL2 as a therapeutic target in BCR-ABL-positive B-lineage acute lymphoblastic leukemia

The structure of DXF34, a human X-linked sequence family with homology to a transcribed mouse Y-linked repeat

New Insights into the Man-Mouse Comparative Map of the X Chromosome

Mouse Mutants Carrying Deletions that Remove the Genes Mutated in Coffin-Lowry Syndrome and Lactic Acidosis

An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome

High-Resolution Comparative Mapping of the Proximal Region of the Mouse X Chromosome

Comment on: Collaborative research: population-based data and validation are necessary

High yield reproducible rat model recapitulating human Barrett’s carcinogenesis

t(8;21) Acute Myeloid Leukaemia Requires Active CCND-CDK4/6

Smcx lies distal to DXHX674 and DXHX679 on the mouse X chromosome

Perspectives and Approaches

Across the Lines of Disciplines

Analysis and Practices

A phenotype map of the mouse X chromosome: models for human X-linked disease

Mapping of FMR1, the gene implicated in fragile X-linked mental retardation, on the mouse X chromosome

Mutations in Two Nonhomologous Genes in a Head-to-Head Configuration Cause Ellis-van Creveld Syndrome

Evaluation of human microdissection clones from the FRAXA region as tools for comparative mapping in the mouse: isolation of a conserved genomic clone close to FMR1

Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis-van Creveld syndrome patients

Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X chromosome short arm with respect to evolutionary breakpoints on the mouse X chromosome

Encyclopedia of the mouse genome VII. Mouse chromosome X

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