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A 109-amino-acid C-terminal fragment of Alzheimer's-disease amyloid precursor protein contains a sequence, -RHDS-, that promotes cell adhesion

Biochemical journal, 1992-12, Vol.288 (3), p.1053-1059

1992

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Intact Alzheimer amyloid precursor protein (APP) is present in platelet membranes and is encoded by platelet mRNA

Biochemical and biophysical research communications, 1990-12, Vol.173 (3), p.1292-1298

1990

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Characterization of Alzheimer amyloid precursor protein transcripts in platelets and megakarocytes

Neuroscience letters, 1992-04, Vol.138 (2), p.229-232

1992

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Characterization of a novel processing pathway for Alzheimer's amyloid β precursor protein

Neuroscience letters, 1994-04, Vol.171 (1), p.213-216

1994

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Beta protein precursor expression in human platelets and a megakaryocyte cell line. Possible implications for the origin of cerebral amyloidosis in Alzheimer's disease

Laboratory investigation, 1992-09, Vol.67 (3), p.303

1992

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High-level expression and in vitro mutagenesis of a fibrillogenic 109-amino-acid C-terminal fragment of Alzheimer's-disease amyloid precursor protein

Biochemical journal, 1993-09, Vol.294 (3), p.667-674

1993

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Eugenic sterilization in America and North Carolina

North Carolina medical journal (Durham, N.C.), 1995-02, Vol.56 (2), p.106

Gardella, J E

1995

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Medicine in Nazi Germany: 1933-1945

North Carolina medical journal (Durham, N.C.), 1994-05, Vol.55 (5), p.188

Gardella, J E

1994

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Hermansky-Pudlak syndrome: Pulmonary manifestations of a ceroid storage disorder

The American journal of medicine, 1979-01, Vol.66 (5), p.737-747

1979

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Salzburg Consensus Criteria for Non-Convulsive Status Epilepticus – approach to clinical application

Epilepsy & behavior, 2015-08, Vol.49, p.158-163

2015

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Total synthesis and structure-activity relationship studies of a series of selective G protein inhibitors

Nature chemistry, 2016-11, Vol.8 (11), p.1035-1041

2016

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GEBR‐7b, a novel PDE4D selective inhibitor that improves memory in rodents at non‐emetic doses

British journal of pharmacology, 2011-12, Vol.164 (8), p.2054-2063

2011

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Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

Nature genetics, 2006-04, Vol.38 (4), p.452-457

2006

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Mutations in KCNT1 cause a spectrum of focal epilepsies

Epilepsia (Copenhagen), 2015-09, Vol.56 (9), p.e114-e120

2015

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Beyond Ecosystem Modeling: A Roadmap to Community Cyberinfrastructure for Ecological Data-Model Integration

Global change biology, 2021-01, Vol.27 (1), p.13-26

2021

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Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of function

Brain (London, England : 1878), 2020-04, Vol.143 (4), p.1114-1126

2020

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EP01.47: Accurate AI measurements of ventricular area in second trimester fetal ultrasound video clips

Ultrasound in obstetrics & gynecology, 2024-09, Vol.64 (S1), p.120-121

2024

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Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Brain (London, England : 1878), 2017-05, Vol.140 (5), p.1316-1336

2017

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OP02.05: AI‐enhanced detection of congenital heart disease suspicion in second trimester ultrasounds by OBGYN and MFM

Ultrasound in obstetrics & gynecology, 2024-09, Vol.64 (S1), p.63-63

2024

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Transmission electron microscopy for the evaluation and optimization of crystal growth

Acta crystallographica. Section D, Structural biology, 2016-05, Vol.72 (5), p.603-615

2016

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Structural mapping of GABRB3 variants reveals genotype–phenotype correlations

Genetics in medicine, 2022-03, Vol.24 (3), p.681-693

2022

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New evidence of risk factors for community-acquired pneumonia: a population-based study

The European respiratory journal, 2008-06, Vol.31 (6), p.1274-1284

2008

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Abstracts of the 34th World Congress on Ultrasound in Obstetrics and Gynecology, 15-18 September 2024, Budapest, Hungary

Ultrasound in obstetrics & gynecology, 2024-09, Vol.64 Suppl 1, p.120

2024

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The spectrum of intermediate SCN8A‐related epilepsy

Epilepsia (Copenhagen), 2019-05, Vol.60 (5), p.830-844

2019

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A 109-amino-acid C-terminal fragment of Alzheimer's-disease amyloid precursor protein contains a sequence, -RHDS-, that promotes cell adhesion

Intact Alzheimer amyloid precursor protein (APP) is present in platelet membranes and is encoded by platelet mRNA

Characterization of Alzheimer amyloid precursor protein transcripts in platelets and megakarocytes

Characterization of a novel processing pathway for Alzheimer's amyloid β precursor protein

Beta protein precursor expression in human platelets and a megakaryocyte cell line. Possible implications for the origin of cerebral amyloidosis in Alzheimer's disease

High-level expression and in vitro mutagenesis of a fibrillogenic 109-amino-acid C-terminal fragment of Alzheimer's-disease amyloid precursor protein

Eugenic sterilization in America and North Carolina

Medicine in Nazi Germany: 1933-1945

Hermansky-Pudlak syndrome: Pulmonary manifestations of a ceroid storage disorder

Salzburg Consensus Criteria for Non-Convulsive Status Epilepticus – approach to clinical application

Total synthesis and structure-activity relationship studies of a series of selective G protein inhibitors

GEBR‐7b, a novel PDE4D selective inhibitor that improves memory in rodents at non‐emetic doses

Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

Mutations in KCNT1 cause a spectrum of focal epilepsies

Beyond Ecosystem Modeling: A Roadmap to Community Cyberinfrastructure for Ecological Data-Model Integration

Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of function

EP01.47: Accurate AI measurements of ventricular area in second trimester fetal ultrasound video clips

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

OP02.05: AI‐enhanced detection of congenital heart disease suspicion in second trimester ultrasounds by OBGYN and MFM

Transmission electron microscopy for the evaluation and optimization of crystal growth

Structural mapping of GABRB3 variants reveals genotype–phenotype correlations

New evidence of risk factors for community-acquired pneumonia: a population-based study

Prognostic and biological implications of genetic abnormalities in multiple myeloma undergoing autologous stem cell transplantation : t(4;14) is the most relevant adverse prognostic factor, whereas RB deletion as a unique abnormality is not associated with adverse prognosis

Abstracts of the 34th World Congress on Ultrasound in Obstetrics and Gynecology, 15-18 September 2024, Budapest, Hungary

The spectrum of intermediate SCN8A‐related epilepsy

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