نتایج جستجو برای: sall4

تعداد نتایج: 329  

2015
Jianhua Xiong Dilyana Todorova Ning-Yuan Su Jinchul Kim Pei-Jen Lee Zhouxin Shen Steven P. Briggs Yang Xu

Mouse embryonic stem cells (ESCs) are genetically more stable than somatic cells, thereby preventing the passage of genomic abnormalities to their derivatives including germ cells. The underlying mechanisms, however, remain largely unclear. In this paper, we show that the stemness factor Sall4 is required for activating the critical Ataxia Telangiectasia Mutated (ATM)-dependent cellular respons...

2012
Ulrich Elling Christian Klasen Tobias Eisenberger Katrin Anlag Mathias Treier

Sall4 is a mammalian Spalt transcription factor expressed by cells of the early embryo and germ cells, an expression pattern similar to that of both Oct4 and Sox2, which play essential roles during early murine development. We show that the activity of Sall4 is cell-autonomously required for the development of the epiblast and primitive endoderm from the inner cell mass. Furthermore, no embryon...

Malihe Bahadori Mohammad Mahdi Forghanifard Saedeh Zafar-Balannezjad

Background SALL gene family represent a group of evolutionary conserved zinc finger transcription factors which are involved in normal development. It includes four members (SALL1 to SALL4). SALL4 has significant roles in the maintenance of pluripotency and self-renewal, efficient proliferation /stabilization and cell fate decision of embryonic stem cells (ESCs). Our aim in this study was to a...

2017
Ai-Leen Chan Hue M. La Julien M.D. Legrand Juho-Antti Mäkelä Michael Eichenlaub Mia De Seram Mirana Ramialison Robin M. Hobbs

Sustained spermatogenesis in adult males and fertility recovery following germ cell depletion are dependent on undifferentiated spermatogonia. We previously demonstrated a key role for the transcription factor SALL4 in spermatogonial differentiation. However, whether SALL4 has broader roles within spermatogonia remains unclear despite its ability to co-regulate genes with PLZF, a transcription ...

2014
Su-xia Han Jun-lan Wang Xi-jing Guo Chen-chen He Xia Ying Jin-lu Ma Yuan-yuan Zhang Qian Zhao Qing Zhu

AIM Sal-like protein 4 (SALL4), is reexpressed in tissues of a subgroup of HCC associated with poor prognosis. Reports of SALL4 serological levels linked to HCC patients are meager and unclear in the prognosis of this malignancy. METHODS Immunohistochemistry and optical microscopy protocols were used to examine the presence of SALL4 in liver tissues from the following patients: 38 HCC, 11 chr...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Jianchang Yang Li Chai Taylor C Fowles Zaida Alipio Dan Xu Louis M Fink David C Ward Yupo Ma

Embryonic stem cells have potential utility in regenerative medicine because of their pluripotent characteristics. Sall4, a zinc-finger transcription factor, is expressed very early in embryonic development with Oct4 and Nanog, two well-characterized pluripotency regulators. Sall4 plays an important role in governing the fate of stem cells through transcriptional regulation of both Oct4 and Nan...

Journal: :The Journal of clinical investigation 2013
Ailing Li Youyang Yang Chong Gao Jiayun Lu Ha-Won Jeong Bee H Liu Ping Tang Xiaopan Yao Donna Neuberg Gang Huang Daniel G Tenen Li Chai

The embryonic self-renewal factor SALL4 has been implicated in the development of human acute myeloid leukemia (AML). Transgenic mice expressing the human SALL4B allele develop AML, which indicates that this molecule contributes to leukemia development and maintenance. However, the underlying mechanism of SALL4-dependent AML progression is unknown. Using SALL4B transgenic mice, we observed that...

Journal: :Molecular human reproduction 2009
Binbin Wang Lin Li Feng Ni Junjie Song Jing Wang Yuan Mu Xu Ma Yunxia Cao

Pluripotency associated transcription factor, SAL-Like 4 (SALL4), might play an important role in conferring totipotency on oocytes. In the present study, we screened SALL4 coding regions for mutations in 100 Han Chinese women with non-syndromic ovarian failure and discovered two novel non-synonymous variants in the SALL4 gene: c.541G>A (p.Val181Met) and c.2449A>G. (p.Thr817Ala). The former var...

Journal: :Blood 2008
Jianchang Yang Li Chai Chong Gao Taylor C Fowles Zaida Alipio Hien Dang Dan Xu Louis M Fink David C Ward Yupo Ma

Increasing studies suggest that SALL4 may play vital roles in leukemogenesis and stem cell phenotypes. We have mapped the global gene targets of SALL4 using chromatin immunoprecipitation followed by microarray hybridization and identified more than 2000 high-confidence, SALL4-binding genes in the human acute promyelocytic leukemic cell line, NB4. Analysis of SALL4-binding sites reveals that gen...

2013
Elizabeth J. Paik Shaun Mahony Richard M. White Emily N. Price Anthony DiBiase Bilguujin Dorjsuren Christian Mosimann Alan J. Davidson David Gifford Leonard I. Zon

Deletion of caudal/cdx genes alters hox gene expression and causes defects in posterior tissues and hematopoiesis. Yet, the defects in hox gene expression only partially explain these phenotypes. To gain deeper insight into Cdx4 function, we performed chromatin immunoprecipitation sequencing (ChIP-seq) combined with gene-expression profiling in zebrafish, and identified the transcription factor...

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