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Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency

Nature immunology, 2003-03, Vol.4 (3), p.261-268

2003

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HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

Nature genetics, 2007-01, Vol.39 (1), p.86-92

2007

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Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans

Nature genetics, 2005-08, Vol.37 (8), p.820-828

2005

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Protein database searches using compositionally adjusted substitution matrices

The FEBS journal, 2005-10, Vol.272 (20), p.5101-5109

2005

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Aneuploidy, TP53 mutation, and amplification of MYC correlate with increased intratumor heterogeneity and poor prognosis of breast cancer patients

Genes chromosomes & cancer, 2018-04, Vol.57 (4), p.165-175

2018

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Improving the accuracy of PSI-BLAST protein database searches with composition-based statistics and other refinements

Nucleic acids research, 2001-07, Vol.29 (14), p.2994-3005

2001

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DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

Human molecular genetics, 2015-12, Vol.24 (25), p.7361-7372

2015

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Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

Blood, 2009-02, Vol.113 (9), p.1967-1976

2009

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High Levels of Chromosomal Copy Number Alterations and TP53 Mutations Correlate with Poor Outcome in Younger Breast Cancer Patients

The American journal of pathology, 2020-08, Vol.190 (8), p.1643-1656

2020

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Antiherpesvirus drugs: a promising spectrum of new drugs and drug targets

Nature reviews. Drug discovery, 2003-04, Vol.2 (4), p.278-288

2003

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WindowMasker: window-based masker for sequenced genomes

Bioinformatics, 2006-01, Vol.22 (2), p.134-141

2006

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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

Nucleic acids research, 1997-09, Vol.25 (17), p.3389-3402

1997

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Phylogenetic analysis of multiple FISH markers in oral tongue squamous cell carcinoma suggests that a diverse distribution of copy number changes is associated with poor prognosis

International journal of cancer, 2016-01, Vol.138 (1), p.98-109

2016

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Sucrose-to-starch metabolism in tomato fruit undergoing transient starch accumulation

Plant physiology (Bethesda), 1997-03, Vol.113 (3), p.739-746

1997

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Deconstructing common variable immunodeficiency by genetic analysis

Current opinion in genetics & development, 2007-06, Vol.17 (3), p.201-212

2007

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Developmental anomalies of the cervical spine in patients with fibrodysplasia ossificans progressiva are distinctly different from those in patients with klippel-feil syndrome : Clues from the BMP signaling pathway

Spine (Philadelphia, Pa. 1976), 2005-06, Vol.30 (12), p.1379-1385

2005

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Primary Non-Hodgkin's Lymphoma of Bone in Children

Journal of bone and joint surgery. American volume, 2006-03, Vol.88 (3), p.583

Glotzbecker, Michael P.

2006

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Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23

Science (American Association for the Advancement of Science), 1996-11, Vol.274 (5290), p.1197-1199

1996

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Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo

Blood, 2005-08, Vol.106 (4), p.1447-1453

2005

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A novel ion funnel for focusing ions at elevated pressure using electrospray ionization mass spectrometry

Rapid communications in mass spectrometry, 1997-10, Vol.11 (16), p.1813-1817

1997

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A Genetic Linkage Map of Microsatellites in the Domestic Cat (Felis catus)

Genomics (San Diego, Calif.), 1999-04, Vol.57 (1), p.9-23

1999

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A Novel Nemaline Myopathy in the Amish Caused by a Mutation in Troponin T1

American journal of human genetics, 2000-10, Vol.67 (4), p.814-821

2000

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A Novel Alkaline α-Galactosidase from Melon Fruit with a Substrate Preference for Raffinose

Plant physiology (Bethesda), 1999-03, Vol.119 (3), p.979-987

1999

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Dual Role of the Pigmentation Gene B in Affecting Carotenoid and Vitamin E Content in Squash (Cucurbita pepo) Mesocarp

Journal of agricultural and food chemistry, 2005-12, Vol.53 (25), p.9759-9763

2005

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Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency

Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans

Protein database searches using compositionally adjusted substitution matrices

Aneuploidy, TP53 mutation, and amplification of MYC correlate with increased intratumor heterogeneity and poor prognosis of breast cancer patients

Improving the accuracy of PSI-BLAST protein database searches with composition-based statistics and other refinements

DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

High Levels of Chromosomal Copy Number Alterations and TP53 Mutations Correlate with Poor Outcome in Younger Breast Cancer Patients

Antiherpesvirus drugs: a promising spectrum of new drugs and drug targets

WindowMasker: window-based masker for sequenced genomes

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

Phylogenetic analysis of multiple FISH markers in oral tongue squamous cell carcinoma suggests that a diverse distribution of copy number changes is associated with poor prognosis

Sucrose-to-starch metabolism in tomato fruit undergoing transient starch accumulation

Deconstructing common variable immunodeficiency by genetic analysis

Developmental anomalies of the cervical spine in patients with fibrodysplasia ossificans progressiva are distinctly different from those in patients with klippel-feil syndrome : Clues from the BMP signaling pathway

Primary Non-Hodgkin's Lymphoma of Bone in Children

Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23

Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo

A novel ion funnel for focusing ions at elevated pressure using electrospray ionization mass spectrometry

A Genetic Linkage Map of Microsatellites in the Domestic Cat (Felis catus)

A Novel Nemaline Myopathy in the Amish Caused by a Mutation in Troponin T1

A Novel Alkaline α-Galactosidase from Melon Fruit with a Substrate Preference for Raffinose

Dual Role of the Pigmentation Gene B in Affecting Carotenoid and Vitamin E Content in Squash (Cucurbita pepo) Mesocarp

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