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Biology and Biochemistry

D-Index
47
Citations
7882
World Ranking
18718
National Ranking
7650

Overview

Stephen D. Cederbaum is affiliated with the University of California, Los Angeles in the United States. Their research primarily focuses on the fields of biochemistry, genetics, and molecular biology, with significant contributions also in medicine. Their work covers various subfields including clinical biochemistry, biochemistry, genetics, molecular biology, and physiology.

The main topics of their scientific investigation include metabolism and genetic disorders, amino acid enzymes and metabolism, neurogenetic and muscular disorders research, biochemical and molecular research, congenital heart defects research, cell adhesion molecules research, and neonatal health and biochemistry.

Frequent coauthors collaborating with Stephen D. Cederbaum include George A. Díaz, Mark Bechter, Yue Huang, Rajesh Sharma, and Pranoot Tanpaiboon.

The scientist has published articles in several scholarly venues. Prominent publication outlets include Molecular Genetics and Metabolism Reports, Journal of Inherited Metabolic Disease, Molecular Therapy - Nucleic Acids, Genetics in Medicine, and Brain Communications.

Selected recent papers authored or coauthored by Stephen D. Cederbaum are:

  • The role and control of arginine levels in arginase 1 deficiency, 2022, Journal of Inherited Metabolic Disease
  • Intermittent lipid nanoparticle mRNA administration prevents cortical dysmyelination associated with arginase deficiency, 2022, Molecular Therapy - Nucleic Acids
  • Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participants, 2024, Genetics in Medicine
  • Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemia, 2021, Molecular Genetics and Metabolism Reports
  • Characterization of spastic paraplegia in a family with a novel PSEN1 mutation, 2023, Brain Communications

Best Publications

  • Comparative properties of arginases.

    Christopher P. Jenkinson;Wayne W. Grody;Stephen D. Cederbaum

  • Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO production

    Georgette M. Buga;Rajan Singh;Shehla Pervin;Norma E. Rogers

  • Co-induction of arginase and nitric oxide synthase in murine macrophages activated by lipopolysaccharide.

    Winnie W. Wang;Christopher P. Jenkinson;Jeanette M. Griscavage;Rita M. Kern

  • Arginases I and II: do their functions overlap?

    Stephen D Cederbaum;Hong Yu;Wayne W Grody;Rita M Kern

  • Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets: Studies in patients with identical mutations

    I. D. Wexler;S. G. Hemalatha;J. McConnell;N. R M Buist

  • Cloning and characterization of the human type II arginase gene.

    Joseph G. Vockley;Christopher P. Jenkinson;Hridayabiranjan Shukla;Rita M. Kern

  • Mouse model for human arginase deficiency.

    Ramaswamy K. Iyer;Paul K. Yoo;Rita M. Kern;Nora Rozengurt

  • Arginase activity in human breast cancer cell lines: N(omega)-hydroxy-L-arginine selectively inhibits cell proliferation and induces apoptosis in MDA-MB-468 cells.

    Rajan Singh;Shehla Pervin;Ardeshir Karimi;Stephen Cederbaum

  • Cross-sectional multicenter study of patients with urea cycle disorders in the United States.

    Mendel Tuchman;Brendan Lee;Uta Lichter-Konecki;Marshall L. Summar

  • Helicobacter pylori induces macrophage apoptosis by activation of arginase II.

    Alain P. Gobert;Yulan Cheng;Jian Ying Wang;Jean Luc Boucher

  • The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study.

    B. K. Burton;B. K. Burton;D. K. Grange;A. Milanowski;G. Vockley

  • The human arginases and arginase deficiency

    R. Iyer;C. P. Jenkinson;J. G. Vockley;R. M. Kern

  • Regulation of mRNA levels for five urea cycle enzymes in rat liver by diet, cyclic AMP, and glucocorticoids.

    Sidney M. Morris;Carole L. Moncman;Katherine D. Rand;George J. Dizikes

  • A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency

    Georgianne L. Arnold;Johan Van Hove;Debra Freedenberg;Arnold Strauss

  • Hyperargininemia due to liver arginase deficiency.

    Eric A. Crombez;Stephen D. Cederbaum

  • Arginase I suppresses IL-12/IL-23p40-driven intestinal inflammation during acute schistosomiasis.

    De’Broski R. Herbert;Tatyana Orekov;Tatyana Orekov;Amanda Roloson;Amanda Roloson;Monica Ilies

  • The chondro-osseous dysplasia of adenosine deaminase deficiency with severe combined immunodeficiency†

    Stephen D. Cederbaum;Illka Kaitila;David L. Rimoin;E. Richard Stiehm

  • Newborn screening 50 years later: access issues faced by adults with PKU

    Susan A. Berry;Christine Brown;Mitzie Grant;Carol L. Greene

  • Cloning and characterization of human agmatinase.

    Ramaswamy K. Iyer;Ho K. Kim;Rosemarie W. Tsoa;Wayne W. Grody

  • Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorder.

    Brendan Lee;George A. Diaz;William Rhead;Uta Lichter-Konecki

Frequent Co-Authors

Brendan Lee
Brendan Lee Baylor College of Medicine
Jerry Vockley
Jerry Vockley University of Pittsburgh
Eric Vilain
Eric Vilain George Washington University
Ruth B. Caldwell
Ruth B. Caldwell Augusta University
Gregory M. Enns
Gregory M. Enns Stanford University
Marc Yudkoff
Marc Yudkoff Children's Hospital of Philadelphia
Rudolf Lucas
Rudolf Lucas Augusta University
Dietrich Matern
Dietrich Matern Mayo Clinic
Sidney M. Morris
Sidney M. Morris University of Pittsburgh
Anthony E. Pegg
Anthony E. Pegg Pennsylvania State University

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