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Sumoylation at chromatin governs coordinated repression of a transcriptional program essential for cell growth and proliferation

Genome research, 2013-10, Vol.23 (10), p.1563-1579

2013

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Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly

American journal of human genetics, 2008-07, Vol.83 (1), p.18-29

2008

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Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans

Human genetics, 2009-05, Vol.125 (4), p.393-400

2009

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Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly

Molecular genetics and metabolism, 2009-10, Vol.98 (1), p.225-234

2009

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An early requirement for maternal FoxH1 during zebrafish gastrulation

Developmental biology, 2007-10, Vol.310 (1), p.10-22

2007

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Measurement of Residual Leukemia during Remission in Childhood Acute Lymphoblastic Leukemia

The New England journal of medicine, 1997-01, Vol.336 (5), p.317-323

1997

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Residual leukaemia after bone marrow transplant in children with acute lymphoblastic leukaemia after first haematological relapse or with poor initial presenting features

British journal of haematology, 2003-02, Vol.120 (4), p.711-715

2003

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full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism

Human mutation, 2009-04, Vol.30 (4), p.E541-E554

2009

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mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis

Human mutation, 2009-10, Vol.30 (10), p.E921-E935

2009

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Risk classification at the time of diagnosis differentially affects the level of residual disease in children with B-precursor acute lymphoblastic leukemia after completion of therapy

Leukemia research, 2003-08, Vol.27 (8), p.743-750

2003

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Functional analysis of mutations in TGIF associated with holoprosencephaly

Molecular genetics and metabolism, 2007-01, Vol.90 (1), p.97-111

2007

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FISH diagnosis of the common 57-kb deletion in CTNS causing cystinosis

Human genetics, 2004-11, Vol.115 (6), p.510-514

2004

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Accurate quantitation of residual B-precursor acute lymphoblastic leukemia by limiting dilution and a PCR-based detection system : a description of the method and the principles involved

Leukemia, 1995-02, Vol.9 (2), p.321-328

1995

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Cloning of the chicken α3(IX) collagen chain completes the primary structure of type IX collagen

European journal of biochemistry, 1992-04, Vol.205 (2), p.443-449

1992

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Persistence of self-renewing leukemia cell progenitors during remission in children with B-precursor acute lymphoblastic leukemia

Leukemia, 1994, Vol.8 (1), p.46-52

1994

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Minimal residual leukaemia

The Lancet (British edition), 1994-04, Vol.343 (8901), p.858-859

1994

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Cloning of the chicken alpha 3(IX) collagen chain completes the primary structure of type IX collagen

European journal of biochemistry, 1992-04, Vol.205 (2), p.443-449

1992

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Sumoylation at chromatin governs coordinated repression of a transcriptional program essential for cell growth and proliferation

Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly

Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly

An early requirement for maternal FoxH1 during zebrafish gastrulation

Measurement of Residual Leukemia during Remission in Childhood Acute Lymphoblastic Leukemia

Residual leukaemia after bone marrow transplant in children with acute lymphoblastic leukaemia after first haematological relapse or with poor initial presenting features

full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism

mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis

Risk classification at the time of diagnosis differentially affects the level of residual disease in children with B-precursor acute lymphoblastic leukemia after completion of therapy

Functional analysis of mutations in TGIF associated with holoprosencephaly

FISH diagnosis of the common 57-kb deletion in CTNS causing cystinosis

Accurate quantitation of residual B-precursor acute lymphoblastic leukemia by limiting dilution and a PCR-based detection system : a description of the method and the principles involved

Cloning of the chicken α3(IX) collagen chain completes the primary structure of type IX collagen

Persistence of self-renewing leukemia cell progenitors during remission in children with B-precursor acute lymphoblastic leukemia

Minimal residual leukaemia

Cloning of the chicken alpha 3(IX) collagen chain completes the primary structure of type IX collagen

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