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Insulin Resistance in Dairy Cows

The Veterinary clinics of North America. Food animal practice, 2013-07, Vol.29 (2), p.299-322

2013

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Antibodies to MOG are transient in childhood acute disseminated encephalomyelitis

Neurology, 2011-08, Vol.77 (6), p.580-588

2011

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Merely presenting one’s own name along with target items is insufficient to produce a memory advantage for the items: A critical role of relational processing

Psychonomic bulletin & review, 2019-02, Vol.26 (1), p.360-366

2019

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Numerical simulation of fluid flow through random packs of ellipses

Physics of fluids (1994), 2015-02, Vol.27 (2)

2015

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Antibodies to MOG are transient in childhood acute disseminated encephalomyelitis

Neurology, 2011-08, Vol.77 (6), p.580

2011

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Self-reference and cognitive effort: source memory for affectively neutral information is impaired following negative compared to positive self-referential processing

Journal of cognitive psychology (Hove, England), 2022-10, Vol.34 (7), p.833-845

2022

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High Frequency of Mosaicism among Patients with Neurofibromatosis Type 1 (NF1) with Microdeletions Caused by Somatic Recombination of the JJAZ1 Gene

American journal of human genetics, 2004-09, Vol.75 (3), p.410-423

2004

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Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

Nature genetics, 1998, Vol.18 (1), p.38-43

1998

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Autoprocessing of neutrophil elastase near its active site reduces the efficiency of natural and synthetic elastase inhibitors

Nature communications, 2015-04, Vol.6 (1), p.6722-6722, Article 6722

2015

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Regulation of Cysteine-Protease Activity Prevents Graft Dysfunction during Ischemia-Lung Reperfusion

The Journal of heart and lung transplantation, 2020-04, Vol.39 (4), p.S356-S357

2020

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Cleavage of La protein by granzyme H induces cytoplasmic translocation and interferes with La-mediated HCV-IRES translational activity

Cell death and differentiation, 2009-02, Vol.16 (2), p.340-348

2009

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Quantitative analysis of protease recognition by inhibitors in plasma using microscale thermophoresis

Scientific reports, 2016-10, Vol.6 (1), p.35413-35413, Article 35413

2016

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Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin

Nature genetics, 2000-02, Vol.24 (2), p.163-166

2000

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Induction of MHC Class I Genes in Neurons

Science (American Association for the Advancement of Science), 1995-07, Vol.269 (5223), p.549-552

1995

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Migratory Activity and Functional Changes of Green Fluorescent Effector Cells before and during Experimental Autoimmune Encephalomyelitis

Immunity (Cambridge, Mass.), 2001-05, Vol.14 (5), p.547-560

2001

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Molecular Structure and Functional Characterization of a Human Complement Cytolysis Inhibitor Found in Blood and Seminal Plasma: Identity to Sulfated Glycoprotein 2, a Constituent of Rat Testis Fluid

Proceedings of the National Academy of Sciences - PNAS, 1989-09, Vol.86 (18), p.7123-7127

1989

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Mitotic recombination mediated by the JJAZF1 (KIAA0160) gene causing somatic mosaicism and a new type of constitutional NF1 microdeletion in two children of a mosaic female with only few manifestations

Journal of medical genetics, 2003-07, Vol.40 (7), p.520-525

2003

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Major histocompatibility complex (MHC) class I gene expression in single neurons of the central nervous system: differential regulation by interferon (IFN)-gamma and tumor necrosis factor (TNF)-alpha

The Journal of experimental medicine, 1997-01, Vol.185 (2), p.305-316

1997

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Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region

Journal of medical genetics, 2003-10, Vol.40 (10), p.e116-116

2003

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Production and applications of recombinant proteinase 3, Wegener's autoantigen: problems and perspectives

Clinical nephrology, 2006-09, Vol.66 (3), p.153

2006

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γ-secretase directly sheds the survival receptor BCMA from plasma cells

Nature communications, 2015-06, Vol.6 (1), p.7333-7333, Article 7333

2015

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Molecular Characterization and Gene Content of Breakpoint Boundaries in Patients with Neurofibromatosis Type 1 with 17q11.2 Microdeletions

American journal of human genetics, 2001-09, Vol.69 (3), p.516-527

2001

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Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene

European journal of human genetics : EJHG, 2000-06, Vol.8 (6), p.455-459

2000

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Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy 7 is caused by a DES mutation

European journal of human genetics : EJHG, 2012-09, Vol.20 (9), p.984-985

2012

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Clusterin (complement lysis inhibitor) forms a high density lipoprotein complex with apolipoprotein A-I in human plasma

The Journal of biological chemistry, 1991-06, Vol.266 (17), p.11030-11036

1991

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Insulin Resistance in Dairy Cows

Antibodies to MOG are transient in childhood acute disseminated encephalomyelitis

Merely presenting one’s own name along with target items is insufficient to produce a memory advantage for the items: A critical role of relational processing

Numerical simulation of fluid flow through random packs of ellipses

Antibodies to MOG are transient in childhood acute disseminated encephalomyelitis

Self-reference and cognitive effort: source memory for affectively neutral information is impaired following negative compared to positive self-referential processing

High Frequency of Mosaicism among Patients with Neurofibromatosis Type 1 (NF1) with Microdeletions Caused by Somatic Recombination of the JJAZ1 Gene

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

Autoprocessing of neutrophil elastase near its active site reduces the efficiency of natural and synthetic elastase inhibitors

Regulation of Cysteine-Protease Activity Prevents Graft Dysfunction during Ischemia-Lung Reperfusion

Cleavage of La protein by granzyme H induces cytoplasmic translocation and interferes with La-mediated HCV-IRES translational activity

Quantitative analysis of protease recognition by inhibitors in plasma using microscale thermophoresis

Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin

Induction of MHC Class I Genes in Neurons

Migratory Activity and Functional Changes of Green Fluorescent Effector Cells before and during Experimental Autoimmune Encephalomyelitis

Molecular Structure and Functional Characterization of a Human Complement Cytolysis Inhibitor Found in Blood and Seminal Plasma: Identity to Sulfated Glycoprotein 2, a Constituent of Rat Testis Fluid

Mitotic recombination mediated by the JJAZF1 (KIAA0160) gene causing somatic mosaicism and a new type of constitutional NF1 microdeletion in two children of a mosaic female with only few manifestations

Major histocompatibility complex (MHC) class I gene expression in single neurons of the central nervous system: differential regulation by interferon (IFN)-gamma and tumor necrosis factor (TNF)-alpha

Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region

Production and applications of recombinant proteinase 3, Wegener's autoantigen: problems and perspectives

γ-secretase directly sheds the survival receptor BCMA from plasma cells

Molecular Characterization and Gene Content of Breakpoint Boundaries in Patients with Neurofibromatosis Type 1 with 17q11.2 Microdeletions

Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene

Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy 7 is caused by a DES mutation

Clusterin (complement lysis inhibitor) forms a high density lipoprotein complex with apolipoprotein A-I in human plasma

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