نتایج جستجو برای: shox2

تعداد نتایج: 132  

Journal: :Development 2016
Wenduo Ye Yingnan Song Zhen Huang Marco Osterwalder Anja Ljubojevic Jue Xu Brent Bobick Samuel Abassah-Oppong Ningsheng Ruan Ross Shamby Diankun Yu Lu Zhang Chen-Leng Cai Axel Visel Yanding Zhang John Cobb YiPing Chen

Vertebrate appendage patterning is programmed by Hox-TALE factor-bound regulatory elements. However, it remains unclear which cell lineages are commissioned by Hox-TALE factors to generate regional specific patterns and whether other Hox-TALE co-factors exist. In this study, we investigated the transcriptional mechanisms controlled by the Shox2 transcriptional regulator in limb patterning. Harn...

2010
Sandra Puskaric Stefanie Schmitteckert Alessandro D. Mori Anne Glaser Katja U. Schneider Benoit G. Bruneau Rüdiger J. Blaschke Herbert Steinbeisser Gudrun Rappold

Heart formation requires a highly balanced network of transcriptional activation of genes. The homeodomain transcription factor, Shox2, is essential for the formation of the sinoatrial valves and for the development of the pacemaking system. The elucidation of molecular mechanisms underlying the development of pacemaker tissue has gained clinical interest as defects in its patterning can be rel...

2015
XIHAI LI WENNA LIANG HONGZHI YE XIAPING WENG FAYUAN LIU PINGDONG LIN XIANXIANG LIU

The role of short stature homeobox 2 (shox2) in the development and homeostasis of the temporomandibular joint (TMJ) has been well documented. Shox2 is known to be expressed in the progenitor cells and perichondrium of the developing condyle. A previous study by our group reported that overexpression of shox2 leads to congenital dysplasia of the TMJ via downregulation of the Indian hedgehog (Ih...

2014
Miriam Aza-Carmona Veronica Barca-Tierno Alfonso Hisado-Oliva Alberta Belinchón Darya Gorbenko-del Blanco Jose Ignacio Rodriguez Sara Benito-Sanz Angel Campos-Barros Karen E. Heath

SHOX and SHOX2 transcription factors are highly homologous, with even identical homeodomains. Genetic alterations in SHOX result in two skeletal dysplasias; Léri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD), while no human genetic disease has been linked to date with SHOX2. SHOX2 is, though, involved in skeletal development, as shown by different knockout mice models. Due ...

Journal: :Cancer genomics & proteomics 2014
Peter Ilse Stefan Biesterfeld Natalia Pomjanski Christian Wrobel Martin Schramm

BACKGROUND/AIM The Epi proLung® BL Reflex Assay [short stature homeobox gene two methylation assay (SHOX2 assay)] (Epigenomics AG, Berlin, Germany) utilizes quantitative methylation-sensitive real-time polymerase chain reaction (QMSP) for the quantification of methylated short stature homeobox gene two (SHOX2) DNA. In the present study, the diagnostic utility of the SHOX2 assay was tested with ...

Journal: :Neuron 2013
Kimberly J. Dougherty Laskaro Zagoraiou Daisuke Satoh Ismini Rozani Staceyann Doobar Silvia Arber Thomas M. Jessell Ole Kiehn

Locomotion is controlled by spinal networks that generate rhythm and coordinate left-right and flexor-extensor patterning. Defined populations of spinal interneurons have been linked to patterning circuits; however, neurons comprising the rhythm-generating kernel have remained elusive. Here, we identify an ipsilaterally projecting excitatory interneuron population, marked by the expression of S...

2016
Yu-An Zhang Yunyun Zhou Xin Luo Kai Song Xiaotu Ma Adwait Sathe Luc Girard Guanghua Xiao Adi F Gazdar

BACKGROUND Diffuse gliomas, grades II and III, hereafter called lower-grade gliomas (LGG), have variable, difficult to predict clinical courses, resulting in multiple studies to identify prognostic biomarkers. The purpose of this study was to assess expression or methylation of the homeobox family gene SHOX2 as independent markers for LGG survival. METHODS We downloaded publically available g...

Journal: :Journal of cell science 2012
Brent E Bobick John Cobb

In humans, loss of SHOX gene function is responsible for the mesomelic short stature characteristic of Turner syndrome, Leri-Weill dyschondrosteosis, and Langer dysplasia. In a mouse model of SHOX deficiency, Prrx1-Cre-driven limb-specific deletion of the paralogous gene Shox2 results in severe rhizomelia. In this study, we show that Col2a1-Cre-driven deletion of Shox2 in developing chondrocyte...

Journal: :Genetics 2014
Stanley J Neufeld Fan Wang John Cobb

The growth and development of the vertebrate limb relies on homeobox genes of the Hox and Shox families, with their independent mutation often giving dose-dependent effects. Here we investigate whether Shox2 and Hox genes function together during mouse limb development by modulating their relative dosage and examining the limb for nonadditive effects on growth. Using double mRNA fluorescence in...

Journal: :Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2011
Christoph Kneip Bernd Schmidt Anke Seegebarth Sabine Weickmann Michael Fleischhacker Volker Liebenberg John K Field Dimo Dietrich

INTRODUCTION Recently, analysis of DNA methylation of the SHOX2 locus was shown to reliably identify lung cancer in bronchial aspirates of patients with disease. As a plasma-based assay would expand the possible applications of the SHOX2 biomarker, this study aimed to develop a modified SHOX2 assay for use in a blood-based test and to analyze the performance of this optimized SHOX2 methylation ...

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