نتایج جستجو برای: shox2

تعداد نتایج: 132  

2016
YUANYUAN FENG PAN YANG SHOUMING LUO ZHIHUI ZHANG HUAKANG LI PING ZHU ZHIYUAN SONG

Sinoatrial node (SAN) dysfunction is a common cardiovascular problem, and the development of a cell sourced biological pacemaker has been the focus of cardiac electrophysiology research. The aim of biological pacemaker therapy is to produce SAN-like cells, which exhibit spontaneous activity characteristic of the SAN. Short stature homeobox 2 (Shox2) is an early cardiac transcription factor and ...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2011
Alexandra Scott Hiroshi Hasegawa Katsuyasu Sakurai Avraham Yaron John Cobb Fan Wang

Dorsal root ganglia (DRG) contain somatosensory neurons of diverse sensory modalities. Among these different types of sensory neurons, the molecular mechanisms that regulate the development and specification of touch neurons are the least well understood. We took a candidate approach and searched for transcription factors that are expressed in subsets of DRG neurons, and found that the transcri...

2014
Xihai Li Wenna Liang Hongzhi Ye Xiaping Weng Fayuan Liu Xianxiang Liu

Our previous study reported that inactivation of Shox2 led to dysplasia and ankylosis of the temporomandibular joint (TMJ), and that replacing Shox2 with human Shox partially rescued the phenotype with a prematurely worn out articular disc. However, the mechanisms of Shox2 activity in TMJ development remain to be elucidated. In this study, we investigated the molecular and cellular basis for th...

2017
Chenzi Zhang Wenjun Yu Lin Wang Mingna Zhao Qiaomei Guo Shaogang Lv Xiaomeng Hu Jiatao Lou

Introduction: Currently the majority of lung cancer patients are diagnosed as advanced diseases for no sensitive and specific biomarkers exist, noninvasive biomarkers with high sensitivity and specificity are urgently needed in lung cancer diagnosis. Bronchoscopy is a standard procedure of the diagnostic work-up of patients with suspected lung cancer despite of the limited diagnostic accuracy. ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2006
John Cobb Andrée Dierich Yolande Huss-Garcia Denis Duboule

Deficiencies or mutations in the human pseudoautosomal SHOX gene are associated with a series of short-stature conditions, including Turner syndrome, Leri-Weill dyschondrosteosis, and Langer mesomelic dysplasia. Although this gene is absent from the mouse genome, the closely related paralogous gene Shox2 displays a similar expression pattern in developing limbs. Here, we report that the conditi...

Journal: :Circulation 2007
Rüdiger J Blaschke Nathan D Hahurij Sanne Kuijper Steffen Just Lambertus J Wisse Kirsten Deissler Tina Maxelon Konstantinos Anastassiadis Jessica Spitzer Stefan E Hardt Hans Schöler Harma Feitsma Wolfgang Rottbauer Martin Blum Frits Meijlink Gudrun Rappold Adriana C Gittenberger-de Groot

BACKGROUND Identifying molecular pathways regulating the development of pacemaking and coordinated heartbeat is crucial for a comprehensive mechanistic understanding of arrhythmia-related diseases. Elucidation of these pathways has been complicated mainly by an insufficient definition of the developmental structures involved in these processes and the unavailability of animal models specificall...

2015
Wenduo Ye Yingnan Song Diankun Yu Cheng Sun Chao Liu Fading Chen Yanding Zhang Fen Wang Richard P. Harvey Laura Schrader James F. Martin YiPing Chen

In humans, atrial fibrillation is often triggered by ectopic pacemaking activity in the myocardium sleeves of the pulmonary vein (PV) and systemic venous return. The genetic programs that abnormally reinforce pacemaker properties at these sites and how this relates to normal sinoatrial node (SAN) development remain uncharacterized. It was noted previously that Nkx2-5, which is expressed in the ...

Journal: :Archives of general psychiatry 2003
Marjan Kromkamp Harry B M Uylings Marten P Smidt Anita J C G M Hellemons J Peter H Burbach René S Kahn

CONTEXT A shared vulnerability to develop psychosis can be related to abnormalities in thalamic circuits in schizophrenia and bipolar disorder and could be a genetic link between these disorders. Homeobox genes involved in development and differentiation of the brain could play an important role in these disorders. OBJECTIVE To determine whether patients with schizophrenia and bipolar disorde...

Journal: :International journal of oncology 2012
Dimo Dietrich Christoph Kneip Olaide Raji Triantafillos Liloglou Anke Seegebarth Thomas Schlegel Nadja Flemming Sebastian Rausch Jürgen Distler Michael Fleischhacker Bernd Schmidt Thomas Giles Martin Walshaw Chris Warburton Volker Liebenberg John K Field

In the identification of subjects with lung cancer, increased DNA methylation of the SHOX2 gene locus in bronchial aspirates has previously been proven to be a clinically valuable biomarker. This is particularly true in cases where the cytological and histological results following bronchoscopy are undetermined. This previous case control study wa...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2013
K Darwiche P Zarogoulidis K Baehner S Welter R Tetzner J Wohlschlaeger D Theegarten T Nakajima L Freitag

BACKGROUND Endobronchial ultrasound with transbronchial needle aspiration (EBUS-TBNA) is a well-established method to assess mediastinal lymph nodes for lung cancer. However, a proportion of patients require further investigation, due to the low negative predictive value (NPV). The objective of this study was to determine whether the assessment of short stature homeobox 2 (SHOX2) DNA methylatio...

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