Sobeck Lab

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===WELCOME TO THE SOBECK LAB===
===WELCOME TO THE SOBECK LAB===
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We are interested in deciphering signaling pathways that contribute to the maintenance of genomic stability in our cells. We are specifically investigating DNA repair pathways that are activated during the S-phase of the cell cycle when chromosomes replicate.
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We are interested in signaling pathways that contribute to the maintenance of genomic stability in our cells and prevent cancer susceptibility in humans. We are studying DNA repair pathways  
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Our current focus are the Fanconi Anemia (FA) and Breast Cancer associated (BRCA1, BRCA2) repair pathways that are suspected to act at the crossroads of DNA replication, repair, and cell cycle checkpoint activation. Our lab uses Xenopus laevis cell-free egg extracts that are naturally cell-cycle synchronized and replication competent to study roles of FA and BRCA pathway members during the DNA damage response.
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that are activated during the S-phase of the cell cycle when chromosomes replicate.
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Our research centers on the  Fanconi Anemia (FA) and Breast Cancer associated (BRCA1, BRCA2) repair pathways that are suspected have crucial functions in DNA repair and cell cycle checkpoint activation during S-phase. Humans born with mutations in FA genes have a highly elevated risk to develop certain types of cancers including acute myeloid leukemia (AML) and various types of solid tumors. Acquired mutations and silencing of FA genes have been found in different cancers in the general population and the FA genes are thus considered "caretakers" of our genome. Our goal is to understand the molecular functions of the FA/BRCA proteins (currently 15 FA/BRCA genes are known) and to elucidate how these proteins communicate with other members of the DNA damage response network to control and suppress genomic instability.
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==Lab News==
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Our lab uses a combination of human cell-based assays and extracts prepared from eggs of the African clawed frog,'' Xenopus laevis''. These extracts are naturally cell-cycle synchronized and able to replicate and repair DNA in a test tube, providing us with a cell-free system that can be manipulated in many ways and that allows us to ask specific questions about functions of individual FA/BRCA proteins during the DNA damage response.
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- Current rotation student and moose whisperer: Jordan Becker
 
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- Upcoming BMBB retreat at the Minnesota Landscape Arboretum: OCTOBER 16. Posters from our lab will be presented by Archana Sareen, PhD and Indrajit Chaudhury, PhD
 
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==<span style="color:red">!! Mark your calendars for the Fanconi Anemia Research Fund Symposium from Oct 21-24 here in downtown Minneapolis !!</span>==
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  [[image:Frog10.gif]]
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[[Image:Sobeck GROUPsmaller.jpg]]
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'''May 2013 (left to right): Maya Raghunandan, Dan Stroik, Alex Sobeck, Jung-Eun Yeo, Indrajit Chaudhury, Sarah Riman, Niki Sathish Kumar'''
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===Lab News===
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<span style="color:blue">!! Mark your calendars for the Fanconi Anemia Research Fund Symposium from October 24-27, 2013 in Houston, Texas</span>
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  [[image:Frog10.gif]]
==Useful links==
==Useful links==
*[[OpenWetWare:Welcome|Introductory tutorial]]
*[[OpenWetWare:Welcome|Introductory tutorial]]
*[[Help|OpenWetWare help pages]]
*[[Help|OpenWetWare help pages]]

Revision as of 13:44, 23 May 2013

Home/Research        Contact        Lab Members        Publications        Talks        Protocols        Internal       



WELCOME TO THE SOBECK LAB

We are interested in signaling pathways that contribute to the maintenance of genomic stability in our cells and prevent cancer susceptibility in humans. We are studying DNA repair pathways that are activated during the S-phase of the cell cycle when chromosomes replicate.

Our research centers on the Fanconi Anemia (FA) and Breast Cancer associated (BRCA1, BRCA2) repair pathways that are suspected have crucial functions in DNA repair and cell cycle checkpoint activation during S-phase. Humans born with mutations in FA genes have a highly elevated risk to develop certain types of cancers including acute myeloid leukemia (AML) and various types of solid tumors. Acquired mutations and silencing of FA genes have been found in different cancers in the general population and the FA genes are thus considered "caretakers" of our genome. Our goal is to understand the molecular functions of the FA/BRCA proteins (currently 15 FA/BRCA genes are known) and to elucidate how these proteins communicate with other members of the DNA damage response network to control and suppress genomic instability.

Our lab uses a combination of human cell-based assays and extracts prepared from eggs of the African clawed frog, Xenopus laevis. These extracts are naturally cell-cycle synchronized and able to replicate and repair DNA in a test tube, providing us with a cell-free system that can be manipulated in many ways and that allows us to ask specific questions about functions of individual FA/BRCA proteins during the DNA damage response.




Image:Sobeck GROUPsmaller.jpg



May 2013 (left to right): Maya Raghunandan, Dan Stroik, Alex Sobeck, Jung-Eun Yeo, Indrajit Chaudhury, Sarah Riman, Niki Sathish Kumar

Lab News


!! Mark your calendars for the Fanconi Anemia Research Fund Symposium from October 24-27, 2013 in Houston, Texas

 image:Frog10.gif

Useful links

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