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----
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<p><b>Lab News</b>
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'''Lab News'''
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;For news, follow the [http://twitter.com/HoatlinLab Hoatlin lab Twitter]
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<dl><dt>For news, follow the <a href="http://twitter.com/HoatlinLab" class="external text" title="http://twitter.com/HoatlinLab" rel="nofollow">Hoatlin lab Twitter</a>
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<br>
Our laboratory is interested in understanding the molecular function of the Fanconi anemia (FA) protein network in context with other proteins that regulate or influence genomic stability. Fanconi anemia is a rare genetic disease that is typically associated with developmental abnormalities, bone marrow failure and increased risk of cancer. Because the majority of the FA proteins are unique with no significant homologies, we expect the results of our studies to shed new light on fundamental mechanisms that control the integrity of the human genome and influence cancer susceptibility.  The FA pathway is part of a network of proteins that contains BRCA2 and two other recently identified FA genes (FANCN and FANCJ) that influence breast cancer susceptibility.  Ultimately, insights into the mechanism of the FA/BRCA network of proteins will lead to an understanding of the underlying molecular defect in FA and may lead to more effective avenues of treatment for this devastating pediatric disease and cancer.  
Our laboratory is interested in understanding the molecular function of the Fanconi anemia (FA) protein network in context with other proteins that regulate or influence genomic stability. Fanconi anemia is a rare genetic disease that is typically associated with developmental abnormalities, bone marrow failure and increased risk of cancer. Because the majority of the FA proteins are unique with no significant homologies, we expect the results of our studies to shed new light on fundamental mechanisms that control the integrity of the human genome and influence cancer susceptibility.  The FA pathway is part of a network of proteins that contains BRCA2 and two other recently identified FA genes (FANCN and FANCJ) that influence breast cancer susceptibility.  Ultimately, insights into the mechanism of the FA/BRCA network of proteins will lead to an understanding of the underlying molecular defect in FA and may lead to more effective avenues of treatment for this devastating pediatric disease and cancer.  
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</p><p>We work in <a href="/wiki/Hoatlin:Portland_Oregon" title="Hoatlin:Portland Oregon"> Portland, Oregon</a> at <a href="http://www.ohsu.edu/" class="external text" title="http://www.ohsu.edu/" rel="nofollow">OHSU</a>, in the <a href="http://www.ohsu.edu/biochem/" class="external text" title="http://www.ohsu.edu/biochem/" rel="nofollow">Department of Biochemistry &amp; Molecular Biology</a> and the <a href="http://www.ohsucancer.com/" class="external text" title="http://www.ohsucancer.com/" rel="nofollow">OHSU Knight Cancer Institute</a>.  
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We work in [[Hoatlin:Portland Oregon| Portland, Oregon]] at [http://www.ohsu.edu/ OHSU], in the [http://www.ohsu.edu/biochem/ Department of Biochemistry & Molecular Biology] and the [http://www.ohsucancer.com/ OHSU Knight Cancer Institute].  
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<a name="Quick_Teaching_Links"></a><h2><span class="editsection">[<a href="/index.php?title=Hoatlin_Lab&amp;action=edit&amp;section=1" title="Edit section: Quick Teaching Links">edit</a>]</span> <span class="mw-headline">Quick Teaching Links</span></h2>
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<ul><li>Our lab's Fanconi Anemia antibodies are available from <a href="http://www.novusbio.com" class="external text" title="http://www.novusbio.com" rel="nofollow">Novus Biologicals</a>
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==Quick Teaching Links==
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*Our lab's Fanconi Anemia antibodies are available from [http://www.novusbio.com Novus Biologicals]
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<p><a href="/wiki/Hoatlin:OHSU_Genetic_Mechanisms_Class" title="Hoatlin:OHSU Genetic Mechanisms Class"> Genetic Mechanisms Class (CON662)</a>
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[[Hoatlin:OHSU_Genetic_Mechanisms_Class| Genetic Mechanisms Class (CON662)]]
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</p><p><a href="/wiki/Hoatlin:OHSU_Replication%2C_Recombination_and_Repair_%28R3%29_Club" class="mw-redirect" title="Hoatlin:OHSU Replication, Recombination and Repair (R3) Club"> OHSU DNA Replication, Recombination and Repair (R3) Club</a>.
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</p><p><a href="/wiki/Hoatlin:BMB_Seminar_Series_%2709-%2710" title="Hoatlin:BMB Seminar Series '09-'10"> BMB Seminar Series for 2009-2010</a>
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[[Hoatlin:OHSU Replication, Recombination and Repair (R3) Club| OHSU DNA Replication, Recombination and Repair (R3) Club]].
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</p><p><a href="/wiki/BMCB625" title="BMCB625">Advanced Topics in Molecular Biology(BMB625)</a>
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</p><p><a href="/wiki/Hoatlin:_CSF" title="Hoatlin: CSF">Med Students Cell Structure Function 2011 (CSF)</a>
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[[Hoatlin:BMB_Seminar_Series_%2709-%2710| BMB Seminar Series for 2009-2010]]
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Revision as of 14:16, 18 March 2011

Equipped with his five senses, man explores the universe around him and calls the adventure Science.  ~Edwin Powell Hubble, The Nature of Science, 1954

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Our laboratory is interested in understanding the molecular function of the Fanconi anemia (FA) protein network in context with other proteins that regulate or influence genomic stability. Fanconi anemia is a rare genetic disease that is typically associated with developmental abnormalities, bone marrow failure and increased risk of cancer. Because the majority of the FA proteins are unique with no significant homologies, we expect the results of our studies to shed new light on fundamental mechanisms that control the integrity of the human genome and influence cancer susceptibility. The FA pathway is part of a network of proteins that contains BRCA2 and two other recently identified FA genes (FANCN and FANCJ) that influence breast cancer susceptibility. Ultimately, insights into the mechanism of the FA/BRCA network of proteins will lead to an understanding of the underlying molecular defect in FA and may lead to more effective avenues of treatment for this devastating pediatric disease and cancer.

We work in Portland, Oregon at OHSU, in the Department of Biochemistry & Molecular Biology and the OHSU Knight Cancer Institute.

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Genetic Mechanisms Class (CON662)

OHSU DNA Replication, Recombination and Repair (R3) Club.

BMB Seminar Series for 2009-2010

Advanced Topics in Molecular Biology(BMB625)

Med Students Cell Structure Function 2011 (CSF)

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