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Effects of novel inhibitors of poly(ADP-ribose) polymerase-1 and the DNA-dependent protein kinase on enzyme activities and DNA repair

Oncogene, 2004-09, Vol.23 (44), p.7322-7329

2004

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Competitive and noncompetitive inhibition of the DNA-dependent protein kinase

Cancer research (Chicago, Ill.), 1999-06, Vol.59 (11), p.2581-2586

1999

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Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway Regulating Extracellular Matrix Development and Maintenance

American journal of human genetics, 2011-06, Vol.88 (6), p.767-777

2011

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Complex responses of birds to landscape‐level fire extent, fire severity and environmental drivers

Diversity & distributions, 2014-04, Vol.20 (4), p.467-477

2014

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Mapping of Deletion and Translocation Breakpoints in 1q44 Implicates the Serine/Threonine Kinase AKT3 in Postnatal Microcephaly and Agenesis of the Corpus Callosum

American journal of human genetics, 2007-08, Vol.81 (2), p.292-303

2007

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Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth

American journal of human genetics, 2011-07, Vol.89 (1), p.148-153

2011

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Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature

Nature genetics, 2011-02, Vol.43 (2), p.127-131

2011

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Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

Nature genetics, 2011-04, Vol.43 (4), p.329-332

2011

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Complement Abnormalities in Acquired Lipodystrophy Revisited

The journal of clinical endocrinology and metabolism, 2009-01, Vol.94 (1), p.10-16

2009

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Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

Nature genetics, 2012-05, Vol.44 (5), p.491-501

2012

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How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum

European journal of human genetics : EJHG, 2012-04, Vol.20 (4), p.381-388

2012

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Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

Nature genetics, 2012-07, Vol.44 (7), p.770-776

2012

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Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy

Nature genetics, 2009-12, Vol.41 (12), p.1345-1349

2009

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Analysis of Crude Protein and Allergen Abundance in Peanuts (Arachis hypogaea cv. Walter) from Three Growing Regions in Australia

Journal of agricultural and food chemistry, 2013-04, Vol.61 (15), p.3714-3725

2013

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A randomized, double-blind, controlled study of NGX-4010, a capsaicin 8% dermal patch, for the treatment of painful HIV-associated distal sensory polyneuropathy

Journal of acquired immune deficiency syndromes (1999), 2012-02, Vol.59 (2), p.126-133

2012

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4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate

European journal of medical genetics, 2009-11, Vol.52 (6), p.454-457

2009

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Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor

European journal of human genetics : EJHG, 2009-10, Vol.17 (10), p.1309-1313

2009

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Coats' Disease of the Retina (Unilateral Retinal Telangiectasis) Caused by Somatic Mutation in the NDP Gene: A Role for Norrin in Retinal Angiogenesis

Human molecular genetics, 1999-10, Vol.8 (11), p.2031-2035

1999

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Genetic interaction between PARP and DNA-PK in V(D)J recombination and tumorigenesis

Nature genetics, 1997-12, Vol.17 (4), p.479-482

1997

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Geroderma osteodysplastica maps to a 4 Mb locus on chromosome 1q24

American journal of medical genetics. Part A, 2008-12, Vol.146A (23), p.3034-3037

2008

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Changes in homocysteine levels during normal pregnancy

American journal of obstetrics and gynecology, 1999-03, Vol.180 (3), p.660-664

1999

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An empirically derived taxonomy of common distress syndromes in the medically ill

Journal of psychosomatic research, 2003-04, Vol.54 (4), p.323-330

2003

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Nutritional and bacterial profiles of juvenile Artemia fed different enrichments and during starvation

Aquaculture, 2004-09, Vol.239 (1), p.351-373

2004

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A new X-linked mental retardation (XLMR) syndrome with late-onset primary testicular failure, short stature and microcephaly maps to Xq25–q26

European journal of medical genetics, 2007-05, Vol.50 (3), p.216-223

2007

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A comparative study of constitutive and induced alkoxyresorufin O-dealkylation and individual cytochrome P450 forms in cynomolgus monkey ( Macaca fascicularis), human, mouse, rat and hamster liver microsomes

Biochemical pharmacology, 1994-03, Vol.47 (5), p.763-773

1994

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Effects of novel inhibitors of poly(ADP-ribose) polymerase-1 and the DNA-dependent protein kinase on enzyme activities and DNA repair

Competitive and noncompetitive inhibition of the DNA-dependent protein kinase

Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway Regulating Extracellular Matrix Development and Maintenance

Complex responses of birds to landscape‐level fire extent, fire severity and environmental drivers

Mapping of Deletion and Translocation Breakpoints in 1q44 Implicates the Serine/Threonine Kinase AKT3 in Postnatal Microcephaly and Agenesis of the Corpus Callosum

Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth

Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature

Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

Complement Abnormalities in Acquired Lipodystrophy Revisited

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy

Analysis of Crude Protein and Allergen Abundance in Peanuts (Arachis hypogaea cv. Walter) from Three Growing Regions in Australia

A randomized, double-blind, controlled study of NGX-4010, a capsaicin 8% dermal patch, for the treatment of painful HIV-associated distal sensory polyneuropathy

4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate

Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor

Coats' Disease of the Retina (Unilateral Retinal Telangiectasis) Caused by Somatic Mutation in the NDP Gene: A Role for Norrin in Retinal Angiogenesis

Genetic interaction between PARP and DNA-PK in V(D)J recombination and tumorigenesis

Geroderma osteodysplastica maps to a 4 Mb locus on chromosome 1q24

Changes in homocysteine levels during normal pregnancy

An empirically derived taxonomy of common distress syndromes in the medically ill

Nutritional and bacterial profiles of juvenile Artemia fed different enrichments and during starvation

A new X-linked mental retardation (XLMR) syndrome with late-onset primary testicular failure, short stature and microcephaly maps to Xq25–q26

A comparative study of constitutive and induced alkoxyresorufin O-dealkylation and individual cytochrome P450 forms in cynomolgus monkey ( Macaca fascicularis), human, mouse, rat and hamster liver microsomes

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