Physician
Neonat/Perinatology
Dr. Jonathan D. Gitlin, MD
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Jonathan Gitlin is an expert in the field of Neonat/Perinatology. He went to University of Pittsburgh School of Medicine. He received 1 awards: "Elected Member". Jonathan Gitlin is also published. He has 99 publications published. The lastest publication: "Genetic disorders of membrane transport. IV. Wilson's disease and Menkes disease.'
Publications
- Kinesin family member 6 (kif6) is necessary for spine development in zebrafish.
- Copper homeostasis: specialized functions of the late secretory pathway.
- Commentary: charting a course for success: excellence in clinical care and discovery in academic departments.
- Regulation of the copper chaperone CCS by XIAP-mediated ubiquitination.
- Patient safety as an academic discipline.
- Essential role for the alpha 1 chain of type VIII collagen in zebrafish notochord formation.
- Zebrafish mutants calamity and catastrophe define critical pathways of gene-nutrient interactions in developmental copper metabolism.
- Essential role for fibrillin-2 in zebrafish notochord and vascular morphogenesis.
- Coordination of development and metabolism in the pre-midblastula transition zebrafish embryo.
- The zebrafish embryo as a dynamic model of anoxia tolerance.
- In vivo correction of a Menkes disease model using antisense oligonucleotides.
- Assembling the pieces.
- Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B.
- Essential role of lysyl oxidases in notochord development.
- Conflict of interest policy for Editors of The American Journal of Clinical Nutrition.
- Copper deficiency.
- Copper and iron disorders of the brain.
- Plant science. Distributing nutrition.
- Role of the Menkes copper-transporting ATPase in NMDA receptor-mediated neuronal toxicity.
- Copper and nitric oxide meet in the plasma.
- Atp7a determines a hierarchy of copper metabolism essential for notochord development.
- Mechanisms of the copper-dependent turnover of the copper chaperone for superoxide dismutase.
- GLUT1 deficiency links nutrient availability and apoptosis during embryonic development.
- Copper homeostasis in the CNS: a novel link between the NMDA receptor and copper homeostasis in the hippocampus.
- NMDA receptor activation mediates copper homeostasis in hippocampal neurons.
- A fungal multicopper oxidase restores iron homeostasis in aceruloplasminemia.
- Role of copper in the proteosome-mediated degradation of the multicopper oxidase hephaestin.
- Wilson disease.
- The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein.
- Mechanisms of biosynthesis of mammalian copper/zinc superoxide dismutase.
- Hepatic copper metabolism: insights from genetic disease.
- Essential role for Atox1 in the copper-mediated intracellular trafficking of the Menkes ATPase.
- Mechanisms of copper incorporation into human ceruloplasmin.
- The copper-iron connection: hereditary aceruloplasminemia.
- Copper chaperones for cytochrome c oxidase and human disease.
- Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading.
- Biochemical analysis of a missense mutation in aceruloplasminemia.
- Ceruloplasmin metabolism and function.
- Mineralization of the deep gray matter with age: a retrospective review with susceptibility-weighted MR imaging.
- Identification of genes associated with stromal hyperplasia and glandular atrophy of the prostate by mRNA differential display.
- Rat hemopexin. Molecular cloning, primary structural characterization, and analysis of gene expression.
- Plasma proteins in health and disease: a scientific symposium to celebrate the career and accomplishments of Harvey R. Colten, M.D.
- Selective transfer of plasma proteins across mammary gland in lactating mouse.
- Protein binding by specific receptors on human placenta, murine placenta, and suckling murine intestine in relation to protein transport across these tissues.
- Antiproliferative B cell translocation gene 2 protein is down-regulated post-transcriptionally as an early event in prostate carcinogenesis.
- The sky blue protein.
- Clinical, molecular, and PET study of a case of aceruloplasminaemia presenting with focal cranial dyskinesia.
- Clara cell secretory protein gene expression in bronchiolar epithelium.
- Mechanisms of gene expression and cell fate determination in the developing pulmonary epithelium.
- Role of hepatocyte nuclear factor-3 alpha and hepatocyte nuclear factor-3 beta in Clara cell secretory protein gene expression in the bronchiolar epithelium.
- 5' flanking region of the Clara cell secretory protein gene specifies a unique temporal and spatial pattern of gene expression in the developing pulmonary epithelium.
- Hepatic caeruloplasmin-gene expression during development in the guinea-pig. Correlation with changes in hepatic copper metabolism.
- Diminished helper/suppressor lymphocyte ratios and natural killer activity in recipients of repeated blood transfusions.
- Intracellular localization of the Menkes and Wilson''s disease proteins and their role in intracellular copper transport.
- Characterization of a nonsense mutation in the ceruloplasmin gene resulting in diabetes and neurodegenerative disease.
- Identification of hepatocyte nuclear factor-3 binding sites in the Clara cell secretory protein gene.
- Regulation of human and murine complement: comparison of 5'' structural and functional elements regulating human and murine complement factor B gene expression.
- Induction of ceruloplasmin gene expression in rat lung during inflammation and hyperoxia.
- Aceruloplasminemia.
- Molecular cloning of a rat uterine gap junction protein and analysis of gene expression during gestation.
- Interaction of CCAAT/enhancer-binding protein alpha and beta with the rat caeruloplasmin gene promoter.
- Tissue-specific ceruloplasmin gene expression in the mammary gland.
- How to make a metalloprotein.
- Hepatic iron overload in aceruloplasminaemia.
- An international symposium on Wilson's and Menkes' diseases.
- Use of desferrioxamine in the treatment of aceruloplasminemia.
- Increased very long-chain fatty acids in erythrocyte membranes of patients with aceruloplasminemia.
- The neuronal adaptor protein X11alpha interacts with the copper chaperone for SOD1 and regulates SOD1 activity.
- CSF abnormalities in patients with aceruloplasminemia.
- Increased plasma lipid peroxidation in patients with aceruloplasminemia.
- Primary structure of hepatocyte nuclear factor/forkhead homologue 4 and characterization of gene expression in the developing respiratory and reproductive epithelium.
- Cell-specific expression of a Clara cell secretory protein-human growth hormone gene in the bronchiolar epithelium of transgenic mice.
- Transcriptional regulation of ceruloplasmin gene expression during inflammation.
- Structural and functional analysis of the 5'-flanking region of the rat ceruloplasmin gene.
- Primary structure of rat ceruloplasmin and analysis of tissue-specific gene expression during development.
- Mechanisms of caeruloplasmin biosynthesis in normal and copper-deficient rats.
- Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease.
- Hepatocyte-specific localization and copper-dependent trafficking of the Wilson's disease protein in the liver.
- Combined zebrafish-yeast chemical-genetic screens reveal gene-copper-nutrition interactions that modulate melanocyte pigmentation.
- Genetic disorders of membrane transport. IV. Wilson's disease and Menkes disease.
- Expression of the Wilson disease gene is deficient in the Long-Evans Cinnamon rat.
- Ceruloplasmin gene expression in the murine central nervous system.
- A novel pineal night-specific ATPase encoded by the Wilson disease gene.
- HAH1 is a copper-binding protein with distinct amino acid residues mediating copper homeostasis and antioxidant defense.
- Biochemical characterization of the Wilson disease protein and functional expression in the yeast Saccharomyces cerevisiae.
- Biochemical characterization and intracellular localization of the Menkes disease protein.
- The copper chaperone CCS directly interacts with copper/zinc superoxide dismutase.
- Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation.
- Functional expression of the menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases.
- Mechanisms of copper incorporation during the biosynthesis of human ceruloplasmin.
- Expression of the ceruloplasmin gene in the human retina and brain: implications for a pathogenic model in aceruloplasminemia.
- The role of copper in neurodegenerative disease.
- Intracellular pathways of copper trafficking in yeast and humans.
- Chromosomal localization of CCS, the copper chaperone for Cu/Zn superoxide dismutase.
- Structure, expression, and chromosomal localization of the mouse Atox1 gene.
- Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux.
- Genetic and molecular basis for copper toxicity.
- Identification and functional expression of HAH1, a novel human gene involved in copper homeostasis.
Schools
University of Pittsburgh Main Campus
Brigham and Women39s Hospital
Children39s Hospital
Doctors Specialties
- Pediatrics
- Neonat/Perinatology
Accepted Insurances
- Great West Healthcare-Cigna PPO
Awards
- Elected Member
Education
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Brigham and Women's Hospital -
Boston Children's Hospital -
University of Pittsburgh School of Medicine
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