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Soluble Heparin and Heparan Sulfate Glycosaminoglycans Interfere with Sonic Hedgehog Solubilization and Receptor Binding

Molecules (Basel, Switzerland), 2019-04, Vol.24 (8), p.1607

2019

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Ca2+ coordination controls sonic hedgehog structure and its Scube2-regulated release

Journal of cell science, 2017-10, Vol.130 (19), p.3261-3271

2017

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Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure

American journal of human genetics, 2006-12, Vol.79 (6), p.1030-1039

2006

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Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

The American heart journal, 2008-07, Vol.156 (1), p.161-169

2008

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C-Terminal Peptide Modifications Reveal Direct and Indirect Roles of Hedgehog Morphogen Cholesteroylation

Frontiers in cell and developmental biology, 2021-01, Vol.8, p.615698-615698

2021

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Conserved cholesterol-related activities of Dispatched 1 drive Sonic hedgehog shedding from the cell membrane

Journal of cell science, 2022-03, Vol.135 (5)

2022

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Hedgehog lipids: Promotors of alternative morphogen release and signaling?: Conflicting findings on lipidated Hedgehog transport and signaling can be explained by alternative regulated mechanisms to release the morphogen

BioEssays, 2021-11, Vol.43 (11), p.e2100133-e2100133

2021

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ERCC1 is required for FANCD2 focus formation

Molecular genetics and metabolism, 2008-09, Vol.95 (1), p.66-73

2008

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Hedgehog lipids: Promotors of alternative morphogen release and signaling?

BioEssays, 2021-11, Vol.43 (11), p.n/a

2021

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A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation

The American heart journal, 2002-12, Vol.144 (6), p.1081-1086

2002

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Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy

Journal of cardiac failure, 2002-02, Vol.8 (1), p.28-32

2002

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Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia

Blood, 2003-07, Vol.102 (1), p.7-16

2003

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Role for DNA Polymerase κ in the Processing of N2-N2-Guanine Interstrand Cross-links

The Journal of biological chemistry, 2008-06, Vol.283 (25), p.17075-17082

2008

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Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p

Nature genetics, 1995-11, Vol.11 (3), p.341-343

1995

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Scube2 enhances proteolytic Shh processing from the surface of Shh-producing cells

Journal of cell science, 2014-04, Vol.127 (Pt 8), p.1726-1737

2014

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A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

Nature genetics, 1993-06, Vol.4 (2), p.202-205

1993

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Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

Clinical and translational science, 2008-05, Vol.1 (1), p.21-26

2008

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Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2

American journal of human genetics, 2000-04, Vol.66 (4), p.1432-1436

2000

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Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome

Mammalian genome, 1999-04, Vol.10 (4), p.381-384

1999

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Ca 2+ coordination controls sonic hedgehog structure and its Scube2-regulated release

Journal of cell science, 2017-10, Vol.130 (19), p.3261

2017

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Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

Journal of cardiac failure, 2001-09, Vol.7 (3), p.249-256

2001

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Role for DNA Polymerase Kappa in the Processing of N super(2)-N super(2)-Guanine Interstrand Cross-links

The Journal of biological chemistry, 2008-06, Vol.283 (25), p.17075-17082

2008

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Role for DNA Polymerase κ in the Processing of N2-N2-Guanine Interstrand Cross-linksS

The Journal of biological chemistry, 2008-06, Vol.283 (25), p.17075-17082

2008

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Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3

American journal of human genetics, 2000-05, Vol.66 (5), p.1540-1551

2000

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Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism

Human molecular genetics, 1995-09, Vol.4 (9), p.1681-1684

1995

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Soluble Heparin and Heparan Sulfate Glycosaminoglycans Interfere with Sonic Hedgehog Solubilization and Receptor Binding

Ca2+ coordination controls sonic hedgehog structure and its Scube2-regulated release

Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

C-Terminal Peptide Modifications Reveal Direct and Indirect Roles of Hedgehog Morphogen Cholesteroylation

Conserved cholesterol-related activities of Dispatched 1 drive Sonic hedgehog shedding from the cell membrane

Hedgehog lipids: Promotors of alternative morphogen release and signaling?: Conflicting findings on lipidated Hedgehog transport and signaling can be explained by alternative regulated mechanisms to release the morphogen

ERCC1 is required for FANCD2 focus formation

Hedgehog lipids: Promotors of alternative morphogen release and signaling?

A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation

Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy

Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia

Role for DNA Polymerase κ in the Processing of N2-N2-Guanine Interstrand Cross-links

Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p

Scube2 enhances proteolytic Shh processing from the surface of Shh-producing cells

A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2

Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome

Ca 2+ coordination controls sonic hedgehog structure and its Scube2-regulated release

Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

Role for DNA Polymerase Kappa in the Processing of N super(2)-N super(2)-Guanine Interstrand Cross-links

Role for DNA Polymerase κ in the Processing of N2-N2-Guanine Interstrand Cross-linksS

Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3

Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism

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