Physician
Pediatrics
Dr. Owen M. Rennert, MD
Owen Rennert works in the field of Pediatrics. He studied medicine at University of Chicago Pritzker School of Medicine. University of Chicago Pritzker School of Medicine is ranked 10/19 in Research/PrimaryCare. Owen Rennert is also published. He has 100 publications published. The lastest publication: "Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BO...'
Publications
- Modulation of microRNA expression in human lung cancer cells by the G9a histone methyltransferase inhibitor BIX01294.
- Telomerase protects werner syndrome lineage-specific stem cells from premature aging.
- Identification of differentially expressed microRNAs across the developing human brain.
- Up-regulation of proliferative and migratory genes in regulatory T cells from patients with metastatic castration-resistant prostate cancer.
- The Cerebellum in Autism: Pathogenic or an Anatomical Beacon?
- Aberrant expression of long noncoding RNAs in autistic brain.
- Association of brain-derived neurotrophic factor (BDNF) haploinsufficiency with lower adaptive behaviour and reduced cognitive functioning in WAGR/11p13 deletion syndr...
- Revealing the transcriptome landscape of mouse spermatogonial cells by tiling microarray.
- Methylation profiling using methylated DNA immunoprecipitation and tiling array hybridization.
- Identification of novel long noncoding RNA transcripts in male germ cells.
- Expression of human NAA11 (ARD1B) gene is tissue-specific and is regulated by DNA methylation.
- Accessing the Genomic Effects of Naked Nanoceria in Murine Neuronal Cells.
- Generation of fertile sperm in a culture dish: clinical implications.
- Methylation patterns of Brahma during spermatogenesis and oogenesis: potential implications.
- Expression Profiling of Autism Candidate Genes during Human Brain Development Implicates Central Immune Signaling Pathways.
- Targeted disruption of Ing2 results in defective spermatogenesis and development of soft-tissue sarcomas.
- Juvenile xanthogranuloma in a child with previously unsuspected neurofibromatosis type 1 and juvenile myelomonocytic leukemia.
- Assessing the safety of nanomaterials by genomic approach could be another alternative.
- DNA methylation of cancer genome.
- Cloning, characterization, and expression analysis of the novel acetyltransferase retrogene Ard1b in the mouse.
- Two types of human malignant melanoma cell lines revealed by expression patterns of mitochondrial and survival-apoptosis genes: implications for malignant melanoma the...
- Genomic landscape of developing male germ cells.
- Brain-derived neurotrophic factor and obesity in the WAGR syndrome.
- Molecular mechanism underlying differential apoptosis between human melanoma cell lines UACC903 and UACC903(+6) revealed by mitochondria-focused cDNA microarrays.
- Reducing the impact of poverty on health and human development: scientific approaches. Preface.
- Human chorionic gonadotropin induces neuronal differentiation of PC12 cells through activation of stably expressed lutropin/choriogonadotropin receptor.
- Mitochondria as key components of the stress response.
- Third-generation human mitochondria-focused cDNA microarray and its bioinformatic tools for analysis of gene expression.
- Biological effect of a novel mutation in the third leucine-rich repeat of human luteinizing hormone receptor.
- Structural characterization and expression studies of Dby and its homologs in the mouse.
- Application of transcriptional and biological network analyses in mouse germ-cell transcriptomes.
- The complexity of antisense transcription revealed by the study of developing male germ cells.
- Expression profiling of purified male germ cells: stage-specific expression patterns related to meiosis and postmeiotic development.
- BioSilico- a functional genomics platform to identify novel candidate genes from gene expression data.
- Analysis of mouse germ-cell transcriptome at different stages of spermatogenesis by SAGE: biological significance.
- Idiopathic intracranial hypertension in cystinosis.
- A novel missense homozygous inactivating mutation in the fourth transmembrane helix of the luteinizing hormone receptor in leydig cell hypoplasia.
- Identification of differentially expressed genes in mouse spermatogenesis.
- Evidence for genetic susceptibility to thrombosis in idiopathic intracranial hypertension.
- Recurrent hepatomegaly and transient alteration of liver functions in an adolescent with diabetic acidosis.
- Metabolic alterations in diabetes mellitus.
- Acute management of diabetic ketoacidosis.
- The detection of the heterozygote and homozygote in cystic fibrosis by short term lymphocyte culture studies: a defect in RNA methylation.
- RNA methylation, a possible genetic marker in cystic fibrosis.
- How to diagnose and treat malabsorption in children.
- Diazoxide in von Gierke''s disease.
- Aminoacyl-tRNA synthetase reaction unique to early embryonic tissue of the mouse.
- Asymptomatic lead poisoning in 85 chicago children. Some diagnostic, therapeutic, prognostic and sociologic considerations.
- The embryonic tRNA methylase reaction.
- Hereditary fructosemia.
- Arsenic poisoning in childhood.
- Zinc metabolism in testicular feminization and surgical cryptorchid testes in rats.
- Acid mucopolysaccharide (AMPS) abnormality in multiple sulfatase deficiency: chemical compositions of AMPS in urine and liver.
- A case of mosaic Down syndrome with 46,XY/47,XY, + 21/46,XY, + fragment cell lines.
- Prenatal diagnosis of thalassemias and hemoglobinopathies.
- Altered glial marker expression in autistic post-mortem prefrontal cortex and cerebellum.
- Mechanisms of antibiotic-induced nephrotoxicity.
- Histochemical studies of fibroblasts from patients with Menkes kinky hair disease and Wilson''s disease.
- Silver-Russell syndrome with absence of digits and syndactylism of the fingers.
- Studies of lipids, lipoproteins, and apolipoproteins in Menkes' disease.
- A supernumerary microchromosome in amniotic cell cultures and talipes equinovarus in a live born female.
- Intestinal transport of manganese from human milk, bovine milk and infant formula in rats.
- Systematic comparison of apomorphine-induced behavioral changes in two mouse strains with inherited differences in brain dopamine receptors.
- Recombinant DNA technology: a clinical revolution in pediatrics.
- Cloning of a human acid sphingomyelinase cDNA with a new mutation that renders the enzyme inactive.
- Congenital adrenal hyperplasia: molecular genetics and alternative approaches to treatment.
- Do clocks run clockwise?
- Identification of three novel mutations in the acid sphinogomyelinase gene of Japanese patients with Niemann-Pick disease type A and B.
- Mutation screening of 17 Japanese patients with neuropathic Gaucher disease.
- Clinical and genetic studies of five fatal cases of Japanese Gaucher disease type 1.
- Kidney abnormalities in Hajdu-Cheney syndrome.
- Managed care and the Hippocratic Oath.
- Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease: identification of four novel mutations.
- Segregation of Allgrove (triple-A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers.
- Type 1 Gaucher disease: phenotypic expression and natural history in Japanese patients.
- Testicular seminoma in a patient with a constitutively activating mutation of the luteinizing hormone/chorionic gonadotropin receptor.
- Genetic heterogeneity of adrenocorticotropin (ACTH) resistance syndromes: identification of a novel mutation of the ACTH receptor gene in hereditary glucocorticoid def...
- Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BO...
- Severe skeletal complications in Japanese patients with type 1 Gaucher disease.
- Polymorphisms in the coding exons of the human luteinizing hormone receptor gene. Mutations in brief no. 124. Online.
- Case report on SHORT syndrome.
- Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutation.
- Update on the genetics and pathophysiology of type I diabetes mellitus.
- Luteinizing hormone receptor mutations in disorders of sexual development and cancer.
- Effects of enzyme replacement therapy in thirteen Japanese paediatric patients with Gaucher disease.
- Gitelman''s syndrome (familial hypokalemia-hypomagnesemia).
- Molecular aspects of sex differentiation.
- Enteroviruses and type 1 diabetes mellitus.
- A novel function of differentiation revealed by cDNA microarray profiling of p75NTR-regulated gene expression.
- Transcriptome analyses of male germ cells with serial analysis of gene expression (SAGE).
- Dysregulated mitochondrial genes and networks with drug targets in postmortem brain of patients with posttraumatic stress disorder (PTSD) revealed by human mitochondri...
- Rieger''s anomaly and other ocular abnormalities in association with osteogenesis imperfecta and a COL1A1 mutation.
- GonadSAGE: a comprehensive SAGE database for transcript discovery on male embryonic gonad development.
- Developmental staging of male murine embryonic gonad by SAGE analysis.
- Congenital generalized lipodystrophy: profile of the disease and gender differences in two siblings.
- Glycogen storage disease, type 8.
- Acrodermatitis enteropathica with immune deficiency.
- Effects of amino acid infusions on cell metabolism in hemodialyzed patients with uremia.
- Copper-histidine treatment of Menkes disease.
Schools
U Of Chgo Div Of Bio Sci Pritzker Sch Of Med
Doctors Specialties
- Clinical Biochemical Genetics
- Clinical Genetics
- Pediatrics
Accepted Insurances
Education
-
University of Chicago Pritzker School of Medicine
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