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Full and Booster Doses of SARS-CoV-2 mRNA-1273 Vaccine Increase Waning Antibody Levels After Completed Vaccination Among Dialysis Patients at a Large Dialysis Organization

International journal of nephrology and renovascular disease, 2022-01, Vol.15, p.319-321

2022

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POS-534 TRAJECTORIES OF CLINICAL AND LABORATORY CHARACTERISTICS ASSOCIATED WITH COVID-19 IN HEMODIALYSIS PATIENTS BY SURVIVAL

Kidney international reports, 2021-04, Vol.6 (4), p.S232-S233

2021

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Fungal gene expression in early symbiotic interactions between Laccaria bicolor and red pine

Plant and soil, 2002-07, Vol.244 (1/2), p.117-128

2002

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Human serum biotinidase: cDNA cloning, sequence, and characterization

The Journal of biological chemistry, 1994-03, Vol.269 (9), p.6566-6570

1994

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Front-end specifications and construction claims

Proceedings of the Institution of Civil Engineers. Management, procurement and law, 2011-08, Vol.164 (3), p.139-146

Hymes, Sidney J.

2011

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The use of biotinylated compounds or reagents is much more complicated than originally thought

Journal of neuroscience methods, 2000-06, Vol.98 (2), p.171-173

2000

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SUN-183 DIURNAL RHYTHMS OF SERUM PHOSPHATE IN HEMODIALYSIS PATIENTS

Kidney international reports, 2020-03, Vol.5 (3), p.S275-S275

2020

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Isolation and analysis of a symbiosis-regulated and Ras-interacting vesicular assembly protein gene from the ectomycorrhizal fungus Laccaria bicolor

The New phytologist, 2004-02, Vol.161 (2), p.529-538

2004

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Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. Online

Human mutation, 1998, Vol.11 (5), p.410-410

1998

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A New Infrared Spectral Library of Controlled and Noncontrolled Drug Standards Using Internal Reflection Spectroscopy

Journal of forensic sciences, 2000-07, Vol.45 (4), p.876-881

2000

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Brassinosteroid-independent function of BRI1/CLV1 chimeric receptors

Functional plant biology : FPB, 2006-01, Vol.33 (8), p.723

2006

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Growth and Materials Characterization of Native Germanium Oxynitride Thin Films on Germanium

Journal of the Electrochemical Society, 1988-04, Vol.135 (4), p.961-965

1988

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Angiotensin in progressive renal diseases: theory and practice

Journal of the American Society of Nephrology, 1996-10, Vol.7 (10), p.2025-2043

1996

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Amino Acid Homologies between Human Biotinidase and Bacterial Aliphatic Amidases: Putative Identification of the Active Site of Biotinidase

Molecular genetics and metabolism, 2000-02, Vol.69 (2), p.111-115

2000

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Human biotinidase isn't just for recycling biotin

The Journal of nutrition, 1999-02, Vol.129 (2), p.485-489

1999

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Plasma and photon interactions with organosilicon polymers for directed self-assembly patterning applications

Journal of vacuum science and technology. B, Nanotechnology & microelectronics, 2016-11, Vol.34 (6)

2016

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Biotinidase and its roles in biotin metabolism

Clinica Chimica Acta, 1996-11, Vol.255 (1), p.1-11

1996

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Mutations in BTD causing biotinidase deficiency

Human mutation, 2001-11, Vol.18 (5), p.375-381

2001

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Identification of alternatively spliced human biotinidase mRNAs and putative localization of endogenous biotinidase

Molecular genetics and metabolism, 2004-04, Vol.81 (4), p.300-312

2004

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Higher 25-Hydroxyvitamin D Associates With Gastrointestinal Bleeding Events

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2022, Vol.33 (11), p.287

2022

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Prediction of Gastrointestinal Bleeding Hospitalization in Hemodialysis

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2022, Vol.33 (11), p.712

2022

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Prediction of Severe Gastrointestinal Bleeding Events in Hemodialysis: Collaborative Development of Machine Learning Model Within INSPIRE

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2021, Vol.32 (10), p.309

2021

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Mutations causing profound biotinidase deficiency in children ascertained by newborn screening in the United States occur at different frequencies than in symptomatic children

Pediatric research, 1999-07, Vol.46 (1), p.20-27

1999

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Prenatal diagnosis of heterozygosity for biotinidase deficiency by enzymatic and molecular analyses

Prenatal diagnosis, 1998-02, Vol.18 (2), p.117-122

1998

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Biotinylation of Histones by Human Serum Biotinidase: Assessment of Biotinyl-Transferase Activity in Sera from Normal Individuals and Children with Biotinidase Deficiency

Biochemical and molecular medicine, 1995-10, Vol.56 (1), p.76-83

1995

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Full and Booster Doses of SARS-CoV-2 mRNA-1273 Vaccine Increase Waning Antibody Levels After Completed Vaccination Among Dialysis Patients at a Large Dialysis Organization

POS-534 TRAJECTORIES OF CLINICAL AND LABORATORY CHARACTERISTICS ASSOCIATED WITH COVID-19 IN HEMODIALYSIS PATIENTS BY SURVIVAL

Fungal gene expression in early symbiotic interactions between Laccaria bicolor and red pine

Human serum biotinidase: cDNA cloning, sequence, and characterization

Front-end specifications and construction claims

The use of biotinylated compounds or reagents is much more complicated than originally thought

SUN-183 DIURNAL RHYTHMS OF SERUM PHOSPHATE IN HEMODIALYSIS PATIENTS

Isolation and analysis of a symbiosis-regulated and Ras-interacting vesicular assembly protein gene from the ectomycorrhizal fungus Laccaria bicolor

Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. Online

A New Infrared Spectral Library of Controlled and Noncontrolled Drug Standards Using Internal Reflection Spectroscopy

Brassinosteroid-independent function of BRI1/CLV1 chimeric receptors

Growth and Materials Characterization of Native Germanium Oxynitride Thin Films on Germanium

Angiotensin in progressive renal diseases: theory and practice

Amino Acid Homologies between Human Biotinidase and Bacterial Aliphatic Amidases: Putative Identification of the Active Site of Biotinidase

Human biotinidase isn't just for recycling biotin

Plasma and photon interactions with organosilicon polymers for directed self-assembly patterning applications

Biotinidase and its roles in biotin metabolism

Mutations in BTD causing biotinidase deficiency

Identification of alternatively spliced human biotinidase mRNAs and putative localization of endogenous biotinidase

Higher 25-Hydroxyvitamin D Associates With Gastrointestinal Bleeding Events

Prediction of Gastrointestinal Bleeding Hospitalization in Hemodialysis

Prediction of Severe Gastrointestinal Bleeding Events in Hemodialysis: Collaborative Development of Machine Learning Model Within INSPIRE

Mutations causing profound biotinidase deficiency in children ascertained by newborn screening in the United States occur at different frequencies than in symptomatic children

Prenatal diagnosis of heterozygosity for biotinidase deficiency by enzymatic and molecular analyses

Biotinylation of Histones by Human Serum Biotinidase: Assessment of Biotinyl-Transferase Activity in Sera from Normal Individuals and Children with Biotinidase Deficiency

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