Your search matched a total of 18 documents. Results 1 - 10.
Mus musculus
Gene: ... High impact information on Kcnq1ot1 The KvDMR, which maps within intron 10 of Kcnq1, contains the promoter for a paternally expressed, noncoding, antisense transcript, Kcnq1ot1. We show that the lack of a full- length Kcnq1ot1 transcript on the paternal chromosome leads to the expression of genes...
Homo sapiens
Gene: ... G and histone H3 lysine 9 methylation at DMR- LIT1 in esophageal cancer. Biological context of KCNQ1OT1 All four...Disease relevance of KCNQ1OT1 Biallelic expression of the KCNQ1OT1 transcript is the primary... with imprinting defects at KCNQ1OT1 was a Wilms' tumor. Loss of imprinting of long QT intronic transcript 1...
MeSH term: ... with UPD for 11p15 or H19 hypermethylation, none of the embryonal tumors with imprinting defects at KCNQ1OT1 was a Wilms' tumor. We show that miR- 562, a microRNA within the candidate region, is expressed... from the United Kingdom Childrens Cancer Study Group. All nephroblastomas induced by transplacental...
MeSH term: ... an imprinting defect at KCNQ1OT1 on 11p15, whereas the unaffected twin did not. In humans, insulin- stimulated... fusion gene in identical twins with leukemia. All genotype examinations were consistent... or corticosteroids were not major determinants of this abnormality. All 6 pairs of identical twins with CPAF, of whom...
MeSH term: ... imprinting defects of KCNQ1OT1. Molecular characterization of Beckwith- Wiedemann syndrome( BWS) patients...
Homo sapiens
Gene: ... SRS patients for epimutations in ICR1 and KCNQ1OT1 by methylation sensitive Southern blot analyses....
Homo sapiens
Gene: ... correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial... sites cause this disease. The promoter region of H19 is hypomethylated at all stages of placental... regions. H19 imprinting was maintained in all 18 informative fresh- frozen and paraffin- embedded formalin...
Mus musculus
Gene: ... , antisense transcript, Kcnq1ot1. Targeted disruption of the Kvlqt1 gene causes deafness and gastric... reporter genes was observed, suggesting that NF- Y- mediated Kcnq1ot1 transcription is critical... whether the Kcnq1ot1 RNA plays a role in the bidirectional silencing activity of the Kcnq1 ICR, we have...
Homo sapiens
Gene: ... that is thought to contain the promoter for the KCNQ1OT1 transcript, and another is in the CDKN1C gene. Mutation... on chromosome 11p15. The 11p15 LOH and absence of CDKN1C peptide staining are demonstrated in all Fo... with the loss of methylation at DMR- LIT1 in all but three. To clarify this, we investigated the CpG methylation...
MeSH term: ... - associated protein, p41, were present in all cases of AIDS and pre- AIDS but were absent in nearly 10 per...
Links to contributing authors:
Steven Johnsen and Donald R. Forsdyke and Kehinde Ross and Andrew Perry and Jonathan Eisen and A. Shimabukuro-Vornhagen and Giuseppe Rotondo and Gordon Laurie and Berkley Lynch and Kung-Hao Liang and Matthias Gstaiger and Thomas Pfeiffer and Marta Ramirez and Grant MacGregor and Jingyu Li and Fedik Rahimov and M El Gizouli and Marta Ramirez Gaite and Oswaldo Ribeiro-filho and Ralf Weigel and Bjoern Hamberger and Alexander Kanitz and Andreas Zankl and Chunming Ding and Maruf Yunus and Jonathan S. Berg and Michael Cariaso and Zakir Thomas and Monique Timberlake-Brady and LC Dore and Nan Shen and R. Eric Collins and Kuang-Mao Chiang and Brendan McMahon and John Chew and Wen-Ming Yang and Robert Hoffmann and J.B. Stewart and Manuela Cucerea and Ignacio García and William James and Thomas Kelder and Gregory Melahn and YINGDE ZHU and Andres Muro and Gabriel Santpere and Jeff Freilich and Junbin Qian and Steffen Poulsen and Eric Villard and Rafael Sidi and Grant Cramer and Chris Sander and Alexandre Chigaev and Florian Uhle and Carl Fulp and Andrew Brown and Xiaozhu Zhou and Corina Dutu and Hilary Spencer and david germano and Abbas Dehghan and Eung-ju PARK and Chris Sander and Albert Vilella and Miao Tian and Anjali Bheda and Michael Nevels and Jun Liu and D Delano and Chitose Taya and Soomi Cheong and David Kavanagh and Maha Karnoub and Hilmar Lapp and Christian Pallasch and Daniel Mietchen and Biju Balakrishnan and Keith Ashman and Juan Carlos Sobrino and Anshu Bhardwaj and Grzegorz Wickiel and Matthew Day and Anthony Sebastian and Vedran Katavic and Liang Long and Barry Wanner and Sarah Snelling and Fernando Montanes and Omobosede Fashedemi and Gustavo Cervantes and Manoj Kumar and Edward D Great and Paul Paukstelis and Roy Soetikno and Ana I Caño-Delgado and Minsoo Choi and Lei Wang and Brenda Riley and A Michelle Moon and Jon Moulton and Mahmoud Elshahawy and Meagan Gillespie and Banundari Rachmawati and Qian Han and Eric Danner and Xavier Fouillet and Madhusudhan Acharya and Brian Young and Chandra Sekhar Mukhopadhyay and shrawan bhattacharjee and Marieke van der Linden and cj hoban and Sandi Pniauskas and jackie gao and Metin Bilgin and Gillian L. Dalgliesh and Karl Wotton and Iveta Herichova and Yuji Morita and Marta Hernandez and Gregor Krings and Marco Briones and Tim D. Smith and Yiumo Michael Chan and Zhenyu Guo and Barry Barclay and Hong Wang and tarali chowdhury and Tilman Brummer and Nuno Faria and Tamir Ben David and Myles Axton and Yannick Fonseca and Francis Castets and Modesto Redrejo-Rodríguez and Bruce Herron and Toshio Fujita and Elena Puccetti and Zhang Zhang and John Osborne and Illes J Farkas and Fernando Andres and Phyllis Pugh and Jonathan Court and Tim Vickers and Nir Friedman and Holger Dick and Ya-Chen Liang and Jonathan Froehlich and Haitham Sobhy and David Abraham and Stephane Krief and Yaroslav Nikolaev and Qiping Feng and d gupta and R Thapar and Susan Wee and Michael Rehman and SOUMITRA GHOSH and Mohamed Eweida and Cedric Uytingco and Nie hongchuan and David Steenblock and Mark A. Kukucka and Zoli Fekete and Sergei Kozlov and Javier Jara and Osama Naguib and Felix Benninger and jean-marc lo-guidice and VASUDEVA BHAT and Anne O. Summers and Bjoern Titz and Anna Levine and Klas Udekwu and Robert Hoffmann
