DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function (Englisch)
- Neue Suche nach: Jin, Bilian
- Neue Suche nach: Tao, Qian
- Neue Suche nach: Peng, Jinrong
- Neue Suche nach: Soo, Hui Meng
- Neue Suche nach: Wu, Wei
- Neue Suche nach: Ying, Jianming
- Neue Suche nach: Fields, C. Robert
- Neue Suche nach: Delmas, Amber L.
- Neue Suche nach: Liu, Xuefeng
- Neue Suche nach: Qiu, Jingxin
- Neue Suche nach: Robertson, Keith D.
- Neue Suche nach: Jin, Bilian
- Neue Suche nach: Tao, Qian
- Neue Suche nach: Peng, Jinrong
- Neue Suche nach: Soo, Hui Meng
- Neue Suche nach: Wu, Wei
- Neue Suche nach: Ying, Jianming
- Neue Suche nach: Fields, C. Robert
- Neue Suche nach: Delmas, Amber L.
- Neue Suche nach: Liu, Xuefeng
- Neue Suche nach: Qiu, Jingxin
- Neue Suche nach: Robertson, Keith D.
In:
Human molecular genetics
;
17
, 5
;
690-
;
2008
- Aufsatz (Zeitschrift) / Elektronische Ressource
-
Titel:DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function
-
Beteiligte:Jin, Bilian ( Autor:in ) / Tao, Qian ( Autor:in ) / Peng, Jinrong ( Autor:in ) / Soo, Hui Meng ( Autor:in ) / Wu, Wei ( Autor:in ) / Ying, Jianming ( Autor:in ) / Fields, C. Robert ( Autor:in ) / Delmas, Amber L. ( Autor:in ) / Liu, Xuefeng ( Autor:in ) / Qiu, Jingxin ( Autor:in )
-
Erschienen in:Human molecular genetics ; 17, 5 ; 690-
-
Verlag:
- Neue Suche nach: Oxford University Press
-
Erscheinungsdatum:01.03.2008
-
ISSN:
-
DOI:
-
Medientyp:Aufsatz (Zeitschrift)
-
Format:Elektronische Ressource
-
Sprache:Englisch
-
Datenquelle:
Inhaltsverzeichnis – Band 17, Ausgabe 5
Zeige alle Jahrgänge und Ausgaben
Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
- 631
-
Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndromeFarrington-Rock, Claire / Kirilova, Veneta / Dillard-Telm, Lisa / Borowsky, Alexander D. / Chalk, Sara / Rock, Matthew J. / Cohn, Daniel H. / Krakow, Deborah et al. | 2008
- 642
-
Long, abundantly expressed non-coding transcripts are altered in cancerPerez, Damon S. / Hoage, Tiffany R. / Pritchett, Jay R. / Ducharme-Smith, Allison L. / Halling, Meredith L. / Ganapathiraju, Sree C. / Streng, Paul S. / Smith, David I. et al. | 2008
- 656
-
SLC4A11 mutations in Fuchs endothelial corneal dystrophyVithana, Eranga N. / Morgan, Patricio E. / Ramprasad, Vedam / Tan, Donald T.H. / Yong, Victor H.K / Venkataraman, Divya / Venkatraman, Anandalakshmi / Yam, Gary H.F. / Nagasamy, Soumittra / Law, Ricky W.K. et al. | 2008
- 667
-
Regulation of glycogen synthesis by the laforin-malin complex is modulated by the AMP-activated protein kinase pathwaySolaz-Fuster, Maria Carmen / Gimeno-Alcañiz, José Vicente / Ros, Susana / Fernandez-Sanchez, Maria Elena / Garcia-Fojeda, Belen / Garcia, Olga Criado / Vilchez, David / Dominguez, Jorge / Garcia-Rocha, Mar / Sanchez-Piris, Maribel et al. | 2008
- 679
-
Loss of CHK1 function impedes DNA damage-induced FANCD2 monoubiquitination but normalizes the abnormal G2 arrest in Fanconi anemiaGuervilly, Jean-Hugues / Macé-Aimé, Gaëtane / Rosselli, Filippo et al. | 2008
- 690
-
DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune functionJin, Bilian / Tao, Qian / Peng, Jinrong / Soo, Hui Meng / Wu, Wei / Ying, Jianming / Fields, C. Robert / Delmas, Amber L. / Liu, Xuefeng / Qiu, Jingxin et al. | 2008
- 710
-
Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic peopleHewitt, Alex W. / Sharma, Shiwani / Burdon, Kathryn P. / Wang, Jie Jin / Baird, Paul N. / Dimasi, David P. / Mackey, David A. / Mitchell, Paul / Craig, Jamie E. et al. | 2008
- 717
-
A novel, putative gain-of-function haplotype at SLC6A4 associates with obsessive-compulsive disorderWendland, Jens R. / Moya, Pablo R. / Kruse, Matthew R. / Ren-Patterson, Renee F. / Jensen, Catherine L. / Timpano, Kiara R. / Murphy, Dennis L. et al. | 2008
- 724
-
The neuronal nicotinic receptor subunit genes (CHRNA6 and CHRNB3) are associated with subjective responses to tobaccoZeiger, Joanna S. / Haberstick, Brett C. / Schlaepfer, Isabel / Collins, Allan C. / Corley, Robin P. / Crowley, Thomas J. / Hewitt, John K. / Hopfer, Christian J. / Lessem, Jeffrey / McQueen, Matthew B. et al. | 2008
- 735
-
The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissuesAl-Mahdawi, Sahar / Pinto, Ricardo Mouro / Ismail, Ozama / Varshney, Dhaval / Lymperi, Stefania / Sandi, Chiranjeevi / Trabzuni, Daniah / Pook, Mark et al. | 2008
- 747
-
A network of dopaminergic gene variations implicated as risk factors for schizophreniaTalkowski, Michael E. / Kirov, George / Bamne, Mikhil / Georgieva, Lyudmila / Torres, Gonzalo / Mansour, Hader / Chowdari, Kodavali V. / Milanova, Vihra / Wood, Joel / McClain, Lora et al. | 2008
- 759
-
Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's diseaseLi, Yonghong / Grupe, Andrew / Rowland, Charles / Holmans, Peter / Segurado, Ricardo / Abraham, Richard / Jones, Lesley / Catanese, Joseph / Ross, David / Mayo, Kevin et al. | 2008
- 768
-
A genome-wide association study of sporadic ALS in a homogenous Irish populationCronin, Simon / Berger, Stephen / Ding, Jinhui / Schymick, Jennifer C / Washecka, Nicole / Hernandez, Dena G. / Greenway, Matthew J. / Bradley, Daniel G. / Traynor, Bryan J. / Hardiman, Orla et al. | 2008