Douglas Bittel: search on Z-Library

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1

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

Nagasawa, Chloe K., Kibiryeva, Nataliya, Marshall, Jennifer, O’Brien, James E., Bittel, Douglas C.

Journal:

Pediatric Cardiology

Year:

2020

Language:

english

File:

PDF, 692 KB

english, 2020

2

Quantitative Real-Time Polymerase Chain Reaction for the Verification of Genomic Imbalances Detected by Microarray-Based Comparative Genomic Hybridization

Yu, Shihui, Kielt, Matthew, Stegner, Andrew L., Kibiryeva, Nataliya, Bittel, Douglas C., Cooley, Linda D.

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2009

Language:

english

File:

PDF, 110.57 MB

english, 2009

3

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

Bittel, Douglas C., Butler, Merlin G.

Journal:

Expert Reviews in Molecular Medicine

Year:

2005

Language:

english

File:

PDF, 579 KB

english, 2005

4

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

Merlin G. Butler, William Fischer, Nataliya Kibiryeva, Douglas C. Bittel

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 194 KB

english, 2008

5

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

Riordan, Sean M., Bittel, Douglas C., Le Pichon, Jean-Baptiste, Gazzin, Silvia, Tiribelli, Claudio, Watchko, Jon F., Wennberg, Richard P., Shapiro, Steven M.

Journal:

Frontiers in Neuroscience

Year:

2016

Language:

english

File:

PDF, 1.21 MB

english, 2016

6

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

Rodemoyer, Amy, Kibiryeva, Nataliya, Bair, Alexis, Marshall, Jennifer, O’Brien, James E, Bittel, Douglas C

Journal:

Year:

2014

Language:

english

File:

PDF, 612 KB

english, 2014

7

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

Le Pichon, Jean-Baptiste, Yu, Shihui, Kibiryeva, Nataliya, Graf, William D, Bittel, Douglas C

Journal:

European Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 1.07 MB

english, 2013

8

A Comparison of Fuzzy Clustering Approaches for Quantification of Microarray Gene Expression

Yu-Ping Wang, Maheswar Gunampally, Jie Chen, Douglas Bittel, Merlin G. Butler, Wei-Wen Cai

Journal:

Journal of Signal Processing Systems

Year:

2008

Language:

english

File:

PDF, 682 KB

english, 2008

9

scaRNAs regulate splicing and vertebrate heart development

Patil, Prakash, Kibiryeva, Nataliya, Uechi, Tamayo, Marshall, Jennifer, O'Brien, James E., Artman, Michael, Kenmochi, Naoya, Bittel, Douglas C.

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Year:

2015

Language:

english

File:

PDF, 1.30 MB

english, 2015

10

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

Ahmed T. Abdelmoity, John J. Hall, Douglas C. Bittel, Shihui Yu

Journal:

European Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 584 KB

english, 2011

11

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

Butler, Merlin G, Bittel, Douglas C, Kibiryeva, Nataliya, Garg, Uttam

Journal:

Genetics in Medicine

Year:

2006

Language:

english

File:

PDF, 371 KB

english, 2006

12

Single-Amino Acid Substitutions Eliminate Lysine Inhibition of Maize Dihydrodipicolinate Synthase

Jonathan M. Shaver, Douglas C. Bittel, Janita M. Sellner, David A. Frisch, David A. Somers and Burle G. Gengenbach

Journal:

Proceedings of the National Academy of Sciences

Year:

1996

Language:

english

File:

PDF, 943 KB

english, 1996

13

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

Bittel, Douglas C., Hueros, Gregorio, Jouve, Nicolas, Gustafson, J. Perry

Journal:

Year:

1991

Language:

english

File:

PDF, 356 KB

english, 1991

14

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

Elisabeth M. Dykens, Elizabeth Roof, Douglas Bittel, Merlin G. Butler

Journal:

Journal of Child Psychology and Psychiatry

Year:

2011

Language:

english

File:

PDF, 160 KB

english, 2011

15

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

Douglas C. Bittel, Nataliya Kibiryeva, Zohreh Talebizadeh, Daniel J. Driscoll, Merlin G. Butler

Journal:

Year:

2005

Language:

english

File:

PDF, 349 KB

english, 2005

16

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

Douglas C. Bittel, Nataliya Kibiryeva, Steven G. McNulty, Daniel J. Driscoll, Merlin G. Butler, Robert A. White

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 216 KB

english, 2007

17

Gene expression in pediatric heart disease with emphasis on conotruncal defects

Douglas C. Bittel, Nataliya Kibiryeva, James E. O'Brien, Gary K. Lofland, Merlin G. Butler

Journal:

Progress in Pediatric Cardiology

Year:

2005

Language:

english

File:

PDF, 1.14 MB

english, 2005

18

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

Douglas C. Bittel, Nataliya Kibiryeva, Susan M. Sell, Theresa V. Strong, Merlin G. Butler

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 325 KB

english, 2007

19

Spontaneous Ca2+ oscillations in subcellular compartments of vascular smooth muscle cells rely on different Ca2+ pools

FEDORYAK, Olesya D, SEARLS, Yvonne, SMIRNOVA, Irina V, BURNS, Douglas M, STEHNO-BITTEL, Lisa

Journal:

Year:

2004

Language:

english

File:

PDF, 310 KB

english, 2004

20

MicroRNA-421 Dysregulation is Associated with Tetralogy of Fallot

Bittel, Douglas, Kibiryeva, Nataliya, Marshall, Jennifer, O'Brien, James

Journal:

Year:

2014

Language:

english

File:

PDF, 415 KB

english, 2014

21

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

Merlin G. Butler, Mariana F. Theodoro, Douglas C. Bittel, Paul J. Kuipers, Daniel J. Driscoll, Zohreh Talebizadeh

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 139 KB

english, 2007

22

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

Merlin G. Butler, Douglas C. Bittel, Nataliya Kibiryeva, Linda D. Cooley, Shihui Yu

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 209 KB

english, 2010

23

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

Merlin G. Butler, Mariana F. Theodoro, Douglas C. Bittel, Joseph E. Donnelly

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 218 KB

english, 2007

24

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

Jean-Baptiste LePichon, Douglas C. Bittel, William D. Graf, Shihui Yu

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 145 KB

english, 2010

25

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

Bittel, Douglas C, Kibiryeva, Nataliya, Butler, Merlin G

Journal:

Genetics in Medicine

Year:

2007

Language:

english

File:

PDF, 647 KB

english, 2007

26

Methylation-Specific Multiplex Ligation-Dependent Probe Amplification Analysis of Subjects with Chromosome 15 Abnormalities

Bittel, Douglas C., Kibiryeva, Nataliya, Butler, Merlin G.

Journal:

Genetic Testing

Year:

2007

Language:

english

File:

PDF, 346 KB

english, 2007

27

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

Stanford, John A., Shuler, Jeffrey M., Fowler, Stephen C., Stanford, Kimberly G., Ma, Delin, Bittel, Douglas C., Le Pichon, Jean-Baptiste, Shapiro, Steven M.

Journal:

Pediatric Research

Year:

2015

Language:

english

File:

PDF, 515 KB

english, 2015

28

TPH2polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes

Rebecca S. Henkhaus, Douglas C. Bittel, Merlin G. Butler

Journal:

Journal of Neurodevelopmental Disorders

Year:

2010

Language:

english

File:

PDF, 132 KB

english, 2010

29

Biology and clinical relevance of non-coding sno/scaRNAs

Cao, Thuy, Rajasingh, Sheeja, Samanta, Saheli, Dawn, Buddhadeb, Bittel, Douglas C., Rajasingh, Johnson

Journal:

Trends in Cardiovascular Medicine

Year:

2017

Language:

english

File:

PDF, 1009 KB

english, 2017

30

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

Merlin G. Butler, Douglas C. Bittel

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 177 KB

english, 2007

31

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)

Merlin G. Butler, Douglas C. Bittel, Nataliya Kibiryeva, Linda D. Cooley, Shihui Yu

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 142 KB

english, 2010

32

Gene expression in cardiac tissues from infants with idiopathic conotruncal defects

Douglas C Bittel, Merlin G Butler, Nataliya Kibiryeva, Jennifer A Marshall, Jie Chen, Gary K Lofland, James E O’Brien

Journal:

BMC Medical Genomics

Year:

2011

Language:

english

File:

PDF, 952 KB

english, 2011

33

[IEEE 2007 IEEE International Workshop on Genomic Signal Processing and Statistics - Tuusula, Finland (2007.06.10-2007.06.12)] 2007 IEEE International Workshop on Genomic Signal Processing and Statistics - Accurate Quantification of Gene Expression using Fuzzy Clustering Approaches

Wang, Yu-Ping, Gunampally, Maheswar, Chen, Jie, Bittel, Douglas, Butler, Merlin G., Cai, Wei-Wen

Year:

2007

Language:

english

File:

PDF, 1005 KB

english, 2007

34

Deletion of the insulin receptor in sensory neurons increases pancreatic insulin levels

Grote, Caleb W., Wilson, Natalie M., Katz, Natalie K., Guilford, Brianne L., Ryals, Janelle M., Novikova, Lesya, Stehno-Bittel, Lisa, Wright, Douglas E.

Journal:

Experimental Neurology

Year:

2018

Language:

english

File:

PDF, 2.29 MB

english, 2018

35

Exercise Increases Insulin Content and Basal Secretion in Pancreatic Islets in Type 1 Diabetic Mice

Huang, Han-Hung, Farmer, Kevin, Windscheffel, Jill, Yost, Katie, Power, Mary, Wright, Douglas E., Stehno-Bittel, Lisa

Journal:

Experimental Diabetes Research

Year:

2011

Language:

english

File:

PDF, 3.18 MB

english, 2011

36

Snord94 expression level alters methylation at C62 in snRNA U6

Ogren, Allison, Kibiryeva, Nataliya, Marshall, Jennifer, O’Brien, James E., Bittel, Douglas C., Preiss, Thomas

Journal:

Year:

2019

File:

PDF, 852 KB

2019

37

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

Douglas C. Bittel, Nataliya Kibiryeva, Majed Dasouki, Joan H.M. Knoll, Merlin G. Butler

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 345 KB

english, 2006

38

Testing unilateral versus bilateral normal contamination

Richard Charnigo, Qian Fan, Douglas Bittel, Hongying Dai

Journal:

Statistics & Probability Letters

Year:

2013

Language:

english

File:

PDF, 223 KB

english, 2013

39

Preparing plant chromosomes for scanning electron microscopy

Dillé, John E., Bittel, Douglas C., Ross, Kathleen, Gustafson, J. Perry

Journal:

Year:

1990

Language:

english

File:

PDF, 634 KB

english, 1990

40

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

Talebizadeh, Zohreh, Kibiryeva, Nataliya, Bittel, Douglas, Butler, Merlin

Journal:

International Journal of Molecular Medicine

Year:

2005

Language:

english

File:

PDF, 2.78 MB

english, 2005

41

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

Zohreh Talebizadeh, Douglas C. Bittel, Olivia J. Veatch, Merlin G. Butler, T. Nicole Takahashi, Judith H. Miles, Ching H. Wang

Journal:

Journal of Autism and Developmental Disorders

Year:

2004

Language:

english

File:

PDF, 59 KB

english, 2004

42

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

Nagasawa, Chloe, Ogren, Allison, Kibiryeva, Nataliya, Marshall, Jennifer, O’Brien, James, Kenmochi, Naoya, Bittel, Douglas

Journal:

Journal of Cardiovascular Development and Disease

Year:

2018

Language:

english

File:

PDF, 1.13 MB

english, 2018

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