نتایج جستجو برای: meis1

تعداد نتایج: 344  

2011
Richard C. Crist Jacquelyn J. Roth Scott A. Waldman Arthur M. Buchberg

Colorectal cancer is one of the most common cancers in developed nations and is the result of both environmental and genetic factors. Many of the genetic lesions observed in colorectal cancer alter expression of homeobox genes, which encode homeodomain transcription factors. The MEIS1 homeobox gene is known to be involved in several hematological malignancies and solid tumors and recent evidenc...

Journal: :Cell 1997
Gabrielle E Rieckhof Fernando Casares Hyung Don Ryoo Muna Abu-Shaar Richard S Mann

We show that homothorax (hth) is required for the Hox genes to pattern the body of the fruit fly, Drosophila melanogaster. hth is necessary for the nuclear localization of an essential HOX cofactor, Extradenticle (EXD), and encodes a homeodomain protein that shares extensive identity with the product of Meis1, a murine proto-oncogene. MEIS1 is able to rescue hth mutant phenotypes and can induce...

Journal: :Genome research 2014
Derek Spieler Maria Kaffe Franziska Knauf José Bessa Juan J Tena Florian Giesert Barbara Schormair Erik Tilch Heekyoung Lee Marion Horsch Darina Czamara Nazanin Karbalai Christine von Toerne Melanie Waldenberger Christian Gieger Peter Lichtner Melina Claussnitzer Ronald Naumann Bertram Müller-Myhsok Miguel Torres Lillian Garrett Jan Rozman Martin Klingenspor Valérie Gailus-Durner Helmut Fuchs Martin Hrabě de Angelis Johannes Beckers Sabine M Hölter Thomas Meitinger Stefanie M Hauck Helmut Laumen Wolfgang Wurst Fernando Casares Jose Luis Gómez-Skarmeta Juliane Winkelmann

Genome-wide association studies (GWAS) identified the MEIS1 locus for Restless Legs Syndrome (RLS), but causal single nucleotide polymorphisms (SNPs) and their functional relevance remain unknown. This locus contains a large number of highly conserved noncoding regions (HCNRs) potentially functioning as cis-regulatory modules. We analyzed these HCNRs for allele-dependent enhancer activity in ze...

Journal: :Blood 2007
Guang Jin Yukari Yamazaki Miki Takuwa Tomoko Takahara Keiko Kaneko Takeshi Kuwata Satoshi Miyata Takuro Nakamura

Cooperative activation of Meis1 and Hoxa9 perturbs myeloid differentiation and eventually leads myeloid progenitors to leukemia, yet it remains to be clarified what kinds of subsequent molecular processes are required for development of overt leukemia. To understand the molecular pathway in Hoxa9/Meis1-induced leukemogenesis, retroviral insertional mutagenesis was applied using retrovirus-media...

2015
Laurent Dupays Catherine Shang Robert Wilson Surendra Kotecha Sophie Wood Norma Towers Timothy Mohun

The homeobox transcription factors NKX2-5 and MEIS1 are essential for vertebrate heart development and normal physiology of the adult heart. We show that, during cardiac differentiation, the two transcription factors have partially overlapping expression patterns, with the result that as cardiac progenitors from the anterior heart field differentiate and migrate into the cardiac outflow tract, ...

2007
Carla Gonzalez Dejah Judelson SD Esparza J Chang DB Shankar B Zhang SF Nelson KM Sakamoto

CREB is a 43 kDa basic leucine zipper nuclear protein that is ubiquitously expressed and conserved from Drosophila to humans. Transcriptional activation by CREB is mediated through its interaction with a consensus octanucleotide sequence (TGANNTCA) termed the cyclic AMP response element or CRE, located in the promoter region of target genes. CREB constitutively binds to the CRE sequence as a he...

Journal: :American journal of human genetics 2014
Eva C Schulte Maria Kousi Perciliz L Tan Erik Tilch Franziska Knauf Peter Lichtner Claudia Trenkwalder Birgit Högl Birgit Frauscher Klaus Berger Ingo Fietze Magdolna Hornyak Wolfgang H Oertel Cornelius G Bachmann Alexander Zimprich Annette Peters Christian Gieger Thomas Meitinger Bertram Müller-Myhsok Nicholas Katsanis Juliane Winkelmann

Restless legs syndrome (RLS) is a common neurologic condition characterized by nocturnal dysesthesias and an urge to move, affecting the legs. RLS is a complex trait, for which genome-wide association studies (GWASs) have identified common susceptibility alleles of modest (OR 1.2-1.7) risk at six genomic loci. Among these, variants in MEIS1 have emerged as the largest risk factors for RLS, sugg...

Journal: :The EMBO journal 1998
E Kroon J Krosl U Thorsteinsdottir S Baban A M Buchberg G Sauvageau

Hoxa9, Meis1 and Pbx1 encode homeodomaincontaining proteins implicated in leukemic transformation in both mice and humans. Hoxa9, Meis1 and Pbx1 proteins have been shown to physically interact with each other, as Hoxa9 cooperatively binds consensus DNA sequences with Meis1 and with Pbx1, while Meis1 and Pbx1 form heterodimers in both the presence and absence of DNA. In this study, we sought to ...

2015
Hanna Grauers Wiktorin Tina Nilsson Ann Jansson Lars Palmqvist Anna Martner

BACKGROUND Acute myeloid leukemia (AML) carrying nucleophosmin 1 (NPM1) mutations (NPMc(+)) is regarded as a separate entity of myeloid neoplasms due to its distinct biological and clinical features. However, NPMc(+) alone displays low leukemogenic activity and cooperating events appear crucial for AML to develop. Dysregulation of homeobox genes, such as HOXA9 and MEIS1, is a common transcripti...

2014
Reina Ariki Satoru Morikawa Yo Mabuchi Sadafumi Suzuki Mayuka Nakatake Kentaro Yoshioka Shinya Hidano Hiromitsu Nakauchi Yumi Matsuzaki Takuro Nakamura Ryo Goitsuka

Hematopoietic stem cells in the bone marrow have the capacity to both self-renew and to generate all cells of the hematopoietic system. The balance of these two activities is controlled by hematopoietic stem cell-intrinsic regulatory mechanisms as well as extrinsic signals from the microenvironment. Here we demonstrate that Meis1, a TALE family homeodomain transcription factor involved in numer...

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