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Disruption of Fnip1 Reveals a Metabolic Checkpoint Controlling B Lymphocyte Development

Immunity (Cambridge, Mass.), 2012-05, Vol.36 (5), p.769-781

2012

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The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

Nature genetics, 2001-01, Vol.27 (1), p.20-21

2001

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Evolutionary history of Tibetans inferred from whole-genome sequencing

PLoS genetics, 2017-04, Vol.13 (4), p.e1006675-e1006675

2017

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Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein

American journal of human genetics, 2001-03, Vol.68 (3), p.577-589

2001

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Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse

Nature genetics, 2001-01, Vol.27 (1), p.68-73

2001

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X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

Nature genetics, 2001-01, Vol.27 (1), p.18-20

2001

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Osteocyte control of bone formation via sclerostin, a novel BMP antagonist

The EMBO journal, 2003-12, Vol.22 (23), p.6267-6276

2003

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Rare variants in neuronal excitability genes influence risk for bipolar disorder

Proceedings of the National Academy of Sciences - PNAS, 2015-03, Vol.112 (11), p.3576-3581

2015

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Sclerostin: how human mutations have helped reveal a new target for the treatment of osteoporosis

Drug discovery today, 2013-07, Vol.18 (13-14), p.637-643

2013

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The Amount of Scurfin Protein Determines Peripheral T Cell Number and Responsiveness

The Journal of immunology (1950), 2001-12, Vol.167 (11), p.6312-6320

2001

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A point mutation in the murine Hem1 gene reveals an essential role for Hematopoietic protein 1 in lymphopoiesis and innate immunity

The Journal of experimental medicine, 2008-11, Vol.205 (12), p.2899-2913

2008

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Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

Genes & development, 1993-09, Vol.7 (9), p.1663-1673

1993

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Identification of copy number variants in whole-genome data using Reference Coverage Profiles

Frontiers in genetics, 2015-02, Vol.6, p.45-45

2015

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Cellular and Molecular Characterization of the scurfy Mouse Mutant

The Journal of immunology (1950), 1999-03, Vol.162 (5), p.2546-2554

1999

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A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA-->AAUGAA) leads to the IPEX syndrome

Immunogenetics (New York), 2001-08, Vol.53 (6), p.435-439

2001

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Whole-genome sequencing suggests a chemokine gene cluster that modifies age at onset in familial Alzheimer's disease

Molecular psychiatry, 2015-11, Vol.20 (11), p.1294-1300

2015

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Polymorphisms in the Sclerosteosis/van Buchem Disease Gene ( SOST) Region Are Associated with Bone-Mineral Density in Elderly Whites

American journal of human genetics, 2004-12, Vol.75 (6), p.1032-1045

2004

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Spin- and angle-resolved photoemission studies of the electronic structure of Si(110)“ 16 × 2 ” surfaces

Physical review. B, 2019-08, Vol.100 (7), p.1, Article 075302

2019

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Domain formation mechanism of the Si(110) “ 16 × 2 ” reconstruction

Physical review. B, 2017-05, Vol.95 (20), p.205306, Article 205306

2017

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Measurement of Organ-Specific and Acute-Phase Blood Protein Levels in Early Lyme Disease

Journal of proteome research, 2020-01, Vol.19 (1), p.346-359

2020

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Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's disease

Alzheimer's & dementia, 2014-10, Vol.10 (5), p.S277-S283.e10

2014

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Ectopic expression of the H19 gene in mice causes prenatal lethality

Genes & development, 1991-06, Vol.5 (6), p.1092-1101

1991

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Metal accumulation in eggs of the red-eared slider ( Trachemys scripta elegans) in the Lower Illinois River

Chemosphere (Oxford), 2006-03, Vol.63 (1), p.39-48

2006

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A Novel Mutation in CD83 Results in the Development of a Unique Population of CD4+ T Cells

The Journal of immunology (1950), 2004-09, Vol.173 (5), p.2995-3001

2004

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Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

PloS one, 2015-05, Vol.10 (5), p.e0127045-e0127045

2015

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Disruption of Fnip1 Reveals a Metabolic Checkpoint Controlling B Lymphocyte Development

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

Evolutionary history of Tibetans inferred from whole-genome sequencing

Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein

Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

Osteocyte control of bone formation via sclerostin, a novel BMP antagonist

Rare variants in neuronal excitability genes influence risk for bipolar disorder

Sclerostin: how human mutations have helped reveal a new target for the treatment of osteoporosis

The Amount of Scurfin Protein Determines Peripheral T Cell Number and Responsiveness

A point mutation in the murine Hem1 gene reveals an essential role for Hematopoietic protein 1 in lymphopoiesis and innate immunity

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

Identification of copy number variants in whole-genome data using Reference Coverage Profiles

Cellular and Molecular Characterization of the scurfy Mouse Mutant

A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA-->AAUGAA) leads to the IPEX syndrome

Whole-genome sequencing suggests a chemokine gene cluster that modifies age at onset in familial Alzheimer's disease

Polymorphisms in the Sclerosteosis/van Buchem Disease Gene ( SOST) Region Are Associated with Bone-Mineral Density in Elderly Whites

Spin- and angle-resolved photoemission studies of the electronic structure of Si(110)“ 16 × 2 ” surfaces

Domain formation mechanism of the Si(110) “ 16 × 2 ” reconstruction

Measurement of Organ-Specific and Acute-Phase Blood Protein Levels in Early Lyme Disease

Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's disease

Ectopic expression of the H19 gene in mice causes prenatal lethality

Metal accumulation in eggs of the red-eared slider ( Trachemys scripta elegans) in the Lower Illinois River

A Novel Mutation in CD83 Results in the Development of a Unique Population of CD4+ T Cells

Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

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