D. Bittel

发表

Comparison of X-chromosome inactivation patterns in multiple tissues from human females

Z. Talebizadeh, M. Theodoro, M. Butler, 2007, Journal of Medical Genetics.

Viability, yield and expansion capability of feline MSCs obtained from subcutaneous and reproductive organ adipose depots

L. Stehno-Bittel, M. Filla, F. Karanu, 2021, BMC Veterinary Research.

TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome.

M. Butler, D. Bittel, E. Dykens, 2011, Journal of child psychology and psychiatry, and allied disciplines.

Snord94 expression level alters methylation at C62 in snRNA U6

Jennifer A. Marshall, D. Bittel, N. Kibiryeva, 2019, PloS one.

Energy expenditure and physical activity in Prader–Willi syndrome: Comparison with obese subjects

J. Donnelly, M. Theodoro, M. Butler, 2007, American journal of medical genetics. Part A.

Plasma obestatin and ghrelin levels in subjects with Prader–Willi syndrome

M. Butler, D. Bittel, M. Butler, 2007, American journal of medical genetics. Part A.

Noonan syndrome patient-specific induced cardiomyocyte model carrying SOS1 gene variant c.1654A>G.

A. Czirók, N. Gurusamy, Sheeja Rajasingh, 2021, Experimental cell research.

Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region

Z. Talebizadeh, M. Butler, D. Bittel, 2002, Journal of medical genetics.

Circulating adiponectin levels, body composition and obesity-related variables in Prader–Willi syndrome: comparison with obese subjects

M. Butler, R. Torto, S. Kalra, 2006, International Journal of Obesity.

Biology and clinical relevance of non-coding sno/scaRNAs

Saheli Samanta, Sheeja Rajasingh, B. Dawn, 2018 .

Viability, yield and expansion capability of feline MSCs obtained from subcutaneous and reproductive organ adipose depots

L. Stehno-Bittel, M. Filla, F. Karanu, 2020, BMC Veterinary Research.

Shear stress associated with cardiopulmonary bypass induces expression of inflammatory cytokines and necroptosis in monocytes

A. Aliseda, R. Savan, M. Scatena, 2020, JCI insight.

1.39 Mb inherited interstitial deletion in 12p13.33 associated with developmental delay.

D. Bittel, A. Abdelmoity, John J. Hall, 2011, European journal of medical genetics.

Plasma Peptide YY and Ghrelin Levels in Infants and Children with Prader-Willi Syndrome

Z. Talebizadeh, M. Butler, D. Bittel, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

Expression and Regulation of Nampt in Human Islets

S. Ye, L. Stehno-Bittel, Dara J Watkins, 2013, PloS one.

Competition between iron(III)-selective chelators and zinc-finger domains for zinc(II).

G. Andrews, R. Hider, D. Bittel, 1999, Biochemical pharmacology.

The Role of scaRNAs in Adjusting Alternative mRNA Splicing in Heart Development

N. Kenmochi, Jennifer A. Marshall, D. Bittel, 2018, Journal of cardiovascular development and disease.

Prader–Willi Syndrome

M. Butler, D. Bittel, 2009 .

Coenzyme Q10 levels in Prader‐Willi syndrome: Comparison with obese and non‐obese subjects

S. Dimauro, M. Butler, M. Dasouki, 2003, American journal of medical genetics. Part A.

scaRNAs regulate splicing and vertebrate heart development.

P. Patil, N. Kenmochi, T. Uechi, 2015, Biochimica et biophysica acta.

TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes

M. Butler, R. Henkhaus, D. Bittel, 2010, Journal of Neurodevelopmental Disorders.

Preparing plant chromosomes for scanning electron microscopy

K. Ross, D. Bittel, J. P. Gustafson, 1990 .

Whole genome microarray analysis of gene expression in Prader–Willi syndrome

D. Bittel, N. Kibiryeva, S. Sell, 2007, American journal of medical genetics. Part A.

Hyperactivity in the Gunn rat model of neonatal jaundice: age-related attenuation and emergence of gait deficits

S. Shapiro, J. Stanford, S. Fowler, 2014, Pediatric Research.

Mammalian metal response element-binding transcription factor-1 functions as a zinc sensor in yeast, but not as a sensor of cadmium or oxidative stress.

D. Winge, G. Andrews, D. Bittel, 2002, Nucleic acids research.

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

Z. Talebizadeh, M. Theodoro, M. Butler, 2005, Journal of Medical Genetics.

Ultra High-Resolution Gene Centric Genomic Structural Analysis of a Non-Syndromic Congenital Heart Defect, Tetralogy of Fallot

D. Bittel, N. Kibiryeva, J. O’Brien, 2014, PloS one.

Gene expression in pediatric heart disease with emphasis on conotruncal defects.

M. Butler, G. Lofland, D. Bittel, 2005, Progress in pediatric cardiology.

A 9‐year‐old male with a duplication of chromosome 3p25.3p26.2: Clinical report and gene expression analysis

J. Knoll, M. Dasouki, D. Bittel, 2006, American journal of medical genetics. Part A.

A tissue-specific gene expression template portrays heart development and pathology

D. Bittel, N. Kibiryeva, J. O'Brien, 2014, Human Genomics.

Array comparative genomic hybridization (aCGH) analysis in Prader–Willi syndrome

M. Butler, D. Bittel, N. Kibiryeva, 2008, American journal of medical genetics. Part A.

Prader–Willi syndrome: clinical genetics, cytogenetics and molecular biology

M. Butler, D. Bittel, 2005, Expert Reviews in Molecular Medicine.

Prader-Willi syndrome and a deletion / duplication within the 15 q 11-q 13 region

Z. Talebizadeh, M. Butler, D. Bittel, 2002 .

Participation of upstream stimulator factor (USF) in cadmium-induction of the mouse metallothionein-I gene.

G. Andrews, D. Bittel, Q. Li, 1998, Nucleic acids research.

Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH

M. Butler, D. Bittel, N. Kibiryeva, 2009, Cytogenetic and Genome Research.

Biology and clinical relevance of noncoding sno/scaRNAs.

Saheli Samanta, Sheeja Rajasingh, B. Dawn, 2018, Trends in cardiovascular medicine.

A Hypothesis for Using Pathway Genetic Load Analysis for Understanding Complex Outcomes in Bilirubin Encephalopathy

Sean M. Riordan, R. Wennberg, J. Watchko, 2016, Front. Neurosci..

Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis.

D. Bittel, N. Kibiryeva, L. Cooley, 2009, American journal of clinical pathology.

Noncoding RNA Expression in Myocardium From Infants With Tetralogy of Fallot

G. Lofland, M. Artman, Jennifer A. Marshall, 2012, Circulation. Cardiovascular genetics.

Zinc and Cadmium Can Promote Rapid Nuclear Translocation of Metal Response Element-binding Transcription Factor-1*

G. Andrews, Huimin Jiang, D. Bittel, 2000, The Journal of Biological Chemistry.

Activation of metallothionein gene expression by hypoxia involves metal response elements and metal transcription factor-1.

A. Giaccia, K. Webster, D. J. Discher, 1999, Cancer research.

Oxidative Stress Activates Metal-responsive Transcription Factor-1 Binding Activity

Luchuan Liang, Qing X. Li, G. Andrews, 1996, The Journal of Biological Chemistry.

Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization.

D. Bittel, N. Kibiryeva, L. Cooley, 2009, Genetic testing and molecular biomarkers.

Letter to the Editor: Do Known Mutations in Neuroligin Genes (NLGN3 and NLGN4) Cause Autism?

Z. Talebizadeh, Ching H. Wang, M. Butler, 2004, Journal of autism and developmental disorders.

No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)

Z. Talebizadeh, M. Butler, J. Miles, 2002, Journal of medical genetics.

An interstitial 15q11‐q14 deletion: Expanded Prader‐Willi syndrome phenotype

M. Butler, D. Bittel, N. Kibiryeva, 2010, American journal of medical genetics. Part A.

Genetic Subtype Differences in Neural Circuitry of Food Motivation in Prader-Willi Syndrome

C. Savage, W. Brooks, L. Holsen, 2008, International Journal of Obesity.

Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities.

M. Butler, D. Bittel, N. Kibiryeva, 2007, Genetic testing.

Expression of 4 Genes Between Chromosome 15 Breakpoints 1 and 2 and Behavioral Outcomes in Prader-Willi Syndrome

M. Butler, D. Bittel, N. Kibiryeva, 2006, Pediatrics.

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.

Z. Talebizadeh, M. Butler, D. Bittel, 2004, Pediatrics.

Reversible activation of mouse metal response element-binding transcription factor 1 DNA binding involves zinc interaction with the zinc finger domain

G. Andrews, T. Dalton, D. Bittel, 1997, Molecular and cellular biology.

The Role of Alternative mRNA Splicing in Heart Development

P. Patil, N. Kenmochi, T. Uechi, 2020, Molecular Mechanism of Congenital Heart Disease and Pulmonary Hypertension.

Methylation at nucleotide C62 in spliceosomal RNA U6 alters mRNA splicing which is important for embryonic development

Jennifer A. Marshall, D. Bittel, N. Kibiryeva, 2019, bioRxiv.

X‐chromosome inactivation patterns in females with Prader–Willi syndrome

D. J. Driscoll, Z. Talebizadeh, M. Theodoro, 2007, American journal of medical genetics. Part A.

Brief Report: Non-Random X Chromosome Inactivation in Females with Autism

Z. Talebizadeh, M. Butler, D. Bittel, 2005, Journal of autism and developmental disorders.

scaRNA1 Levels Alter Pseudouridylation in Spliceosomal RNA U2 Affecting Alternative mRNA Splicing and Embryonic Development

Jennifer A. Marshall, D. Bittel, N. Kibiryeva, 2020, Pediatric Cardiology.

Genome-wide gene expression in a patient with 15q13.3 homozygous microdeletion syndrome

Denise Daley, Moira Chan-Yeung, Reza Alizadehfar, 2013, European Journal of Human Genetics.

Dosage response of rye genes in a wheat background

D. Bittel, J. P. Gustafson, 1992, Theoretical and Applied Genetics.

Single-amino acid substitutions eliminate lysine inhibition of maize dihydrodipicolinate synthase.

D. Somers, D. Frisch, D. Bittel, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader–Willi syndrome

D. J. Driscoll, D. Bittel, N. Kibiryeva, 2007, American journal of medical genetics. Part A.

Gene expression in cardiac tissues from infants with idiopathic conotruncal defects

Jie Chen, M. Butler, G. Lofland, 2011, BMC Medical Genomics.

Analysis of the Prader‐Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array

D. Bittel, H. Newkirk, M. Butler, 2008, American journal of medical genetics. Part A.

A 15q13.3 homozygous microdeletion associated with a severe neurodevelopmental disorder suggests putative functions of the TRPM1, CHRNA7, and other homozygously deleted genes

D. Bittel, W. Graf, Shihui Yu, 2010, American journal of medical genetics. Part A.

MicroRNA-421 Dysregulation is Associated with Tetralogy of Fallot

Douglas C. Bittel, Nataliya Kibiryeva, Jennifer A. Marshall, 2014, Cells.

Cadmium-mediated Activation of the Metal Response Element in Human Neuroblastoma Cells Lacking Functional Metal Response Element-binding Transcription Factor-1*

Jeffrey A. Johnson, G. Andrews, D. Bittel, 1999, The Journal of Biological Chemistry.

New insights into the mechanisms of cadmium regulation of mouse metallothionein-I gene expression

Jeffrey A. Johnson, Qingwen Li, G. Andrews, 1999 .

Factor-1 Involves Metal Response Elements and Metal Transcription Activation of Metallothionein Gene Expression by Hypoxia

K. Webster, D. J. Discher, K. Laderoute, 1999 .

Erratum to: An Interstitial 15q11–q14 Deletion: Expanded Prader–Willi Syndrome Phenotype (DOI 10.1002/ajmg.a.33197; Am J Med Genet Part A 152A:404–408)

M. Butler, D. Bittel, N. Kibiryeva, 2010 .

Transcriptome profiling reveals activation of inflammation and apoptosis in the neonatal striatum after deep hypothermic circulatory arrest.

P. Pastuszko, A. Pastuszko, A. Timms, 2019, The Journal of thoracic and cardiovascular surgery.

Functional Heterogeneity in the Zinc Fingers of Metalloregulatory Protein Metal Response Element-binding Transcription Factor-1*

G. Andrews, D. Bittel, Douglas C. Bittel, 2000, The Journal of Biological Chemistry.

Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

A J Agopian, Cristina E. Trevino, D. Cutler, 2020, Scientific Reports.

Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD

Z. Talebizadeh, M. Butler, D. Bittel, 2003, Journal of medical genetics.

microRNA Expression Levels Change in Neonatal Patients During and After Exposure to Cardiopulmonary Bypass

A. Paquette, K. Vickers, P. Pastuszko, 2021, bioRxiv.

Ghrelin, peptide YY and their receptors: gene expression in brain from subjects with and without Prader-Willi syndrome.

Z. Talebizadeh, M. Butler, D. Bittel, 2005, International journal of molecular medicine.

Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD.

D. J. Driscoll, Z. Talebizadeh, M. Butler, 2005, Genomics.

Dosage Response of Rye Genes in a Wheat Background. I. Selection of Lines with Multiple Copies of 1RS

N. Jouve, D. Bittel, J. P. Gustafson, 1992 .

Changes in expression of seed storage protein genes effected by chromosome 1D of wheat

N. Jouve, G. Hueros, D. Bittel, 1991 .

C-reactive protein levels in subjects with Prader-Willi syndrome and obesity

M. Butler, U. Garg, D. Bittel, 2006, Genetics in Medicine.

Activation of mouse metallothionein I promoter by cadmium in human neuroblastoma cells

Jeffrey A. Johnson, G. Andrews, D. Bittel, 1999 .

PRACTICE PARAMETER: EVALUATION OF THE CHILD WITH MICROCEPHALY (AN EVIDENCE-BASED REVIEW): REPORT OF THE QUALITY STANDARDS SUBCOMMITTEE OF THE AMERICAN ACADEMY OF NEUROLOGY AND THE PRACTICE COMMITTEE OF THE CHILD NEUROLOGY SOCIETY

D. Bittel, A. Abdelmoity, J. Le Pichon, 2010, Neurology.

Whole genome microarray analysis of gene expression in subjects with fragile X syndrome

M. Butler, D. Bittel, N. Kibiryeva, 2007, Genetics in Medicine.

or Type II Deletion and Maternal Disomy Behavioral Differences Among Subjects With Prader-Willi Syndrome and Type I

Z. Talebizadeh, M. Butler, D. Bittel, 2007 .

ATM mutations in Finnish breast cancer patients

A. Børresen-Dale, R. Winqvist, Z. Talebizadeh, 2002, Journal of medical genetics.

X‐chromosome inactivation patterns in females with Prader–Willi syndrome

D. J. Driscoll, Z. Talebizadeh, M. Theodoro, 2007, American journal of medical genetics. Part A.

A tissue-specific gene expression template portrays heart development and pathology

Jennifer A. Marshall, D. Bittel, N. Kibiryeva, 2014, Human Genomics.

Sustained radiation reduction following initial quality improvement intervention in a paediatric cardiac catheterisation laboratory

Jennifer A. Marshall, D. Bittel, S. Kaine, 2022, Cardiology in the Young.

patterns in multiple tissues from human females Comparison of X-chromosome inactivation

Z. Talebizadeh, M. Theodoro, M. Butler, 2008 .

Energy expenditure and physical activity in Prader–Willi syndrome: Comparison with obese subjects

J. Donnelly, M. Theodoro, M. Butler, 2007, American journal of medical genetics. Part A.

Testing unilateral versus bilateral normal contamination

Richard Charnigo, Hongying Dai, R. Charnigo, 2013 .

Lysine accumulation in maize cell cultures transformed with a lysine-insensitive form of maize dihydrodipicolinate synthase

D. Bittel, B. G. Gengenbach, J. Shaver, 2004, Theoretical and Applied Genetics.