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[title] => [Alan Shuldiner, M.D. ]
[body] => [<div class="field field-type-image field-field-people-image"><div class="field-label">People Image: </div><div class="field-items"><div class="field-item"><img src="http://www.diabetescenters.org/files/Ashuldiner.jpg" alt="Ashuldiner.jpg" title="Ashuldiner.jpg" width="175" height="233" /></div></div></div><div class="field field-type-text field-field-center-name"><div class="field-label">Center Name: </div><div class="field-items"><div class="field-item">DRTC - Johns Hopkins University/University of Maryland</div></div></div><div class="field field-type-text field-field-core"><div class="field-label">Core List: </div><div class="field-items"><div class="field-item">DRTC Baltimore Clinical Investigation Core</div></div></div><div class="field field-type-text field-field-phone-number"><div class="field-label">Phone Number: </div><div class="field-items"><div class="field-item">410-706-1623</div></div></div><div class="field field-type-text field-field-people-details"><div class="field-label">People Details: </div><div class="field-items"><div class="field-item"><p><span id="lblResearchInterests"><font size="2">Dr. Shuldiner’s major research interests are in the molecular basis and genetics of type-2 diabetes, obesity and insulin resistance. He has published over 130 original articles and 50 review articles. His studies of type-2 diabetes candidate genes include studies in African Americans, Pima Indians, Mexican Americans and Caucasians. His group was the first to discover a common mutation in the beta-3-adrenergic receptor (Trp64Arg) that influences several features of the insulin resistance syndrome, including insulin resistance, obesity and visceral fat accumulation. His group was also the first to describe a common variant in the peroxisome proliferator activated receptor gamma-2 gene (Pro12Ala PPAR¿2), which associates with obesity, increased insulin sensitivity and protection from type 2 diabetes. Most recently, his group has utilized genome scan/positional cloning approaches to identify several chromosomal regions that are likely to harbor susceptibility genes for type 2 diabetes, hypertension, obesity and hyperlipidemia in the Old Order Amish. These studies in the Amish have recently been expanded to include genetic studies of cardiovascular disease, osteoporosis, osteogenesis imperfecta, autoimmune thyroid disease, longevity and pharmacogenomics. Dr. Shuldiner has broad-based financial support for his research including NIH, American Diabetes Association, Juvenile Diabetes Foundation, Ellison Foundation and biotech/pharmaceuticals.</font></span></p>
<p><a href="http://medschool.umaryland.edu/FACULTYRESEARCHPROFILE/viewprofile.aspx?id=3978"><span><font size="2">More</font></span></a></p>
</div></div></div><div class="field field-type-text field-field-center-title"><div class="field-label">center_title: </div><div class="field-items"><div class="field-item">Center Co-Director and Director, Clinical Investigation Core</div></div></div>]
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[value] => [<p><span id="lblResearchInterests"><font size="2">Dr. Shuldiner’s major research interests are in the molecular basis and genetics of type-2 diabetes, obesity and insulin resistance. He has published over 130 original articles and 50 review articles. His studies of type-2 diabetes candidate genes include studies in African Americans, Pima Indians, Mexican Americans and Caucasians. His group was the first to discover a common mutation in the beta-3-adrenergic receptor (Trp64Arg) that influences several features of the insulin resistance syndrome, including insulin resistance, obesity and visceral fat accumulation. His group was also the first to describe a common variant in the peroxisome proliferator activated receptor gamma-2 gene (Pro12Ala PPAR¿2), which associates with obesity, increased insulin sensitivity and protection from type 2 diabetes. Most recently, his group has utilized genome scan/positional cloning approaches to identify several chromosomal regions that are likely to harbor susceptibility genes for type 2 diabetes, hypertension, obesity and hyperlipidemia in the Old Order Amish. These studies in the Amish have recently been expanded to include genetic studies of cardiovascular disease, osteoporosis, osteogenesis imperfecta, autoimmune thyroid disease, longevity and pharmacogenomics. Dr. Shuldiner has broad-based financial support for his research including NIH, American Diabetes Association, Juvenile Diabetes Foundation, Ellison Foundation and biotech/pharmaceuticals.</font></span></p><p><a href="http://medschool.umaryland.edu/FACULTYRESEARCHPROFILE/viewprofile.aspx?id=3978"><span><font size="2">More</font></span></a></p>]
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<p><a href="http://medschool.umaryland.edu/FACULTYRESEARCHPROFILE/viewprofile.aspx?id=3978"><span><font size="2">More</font></span></a></p>
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<p><a href="http://medschool.umaryland.edu/FACULTYRESEARCHPROFILE/viewprofile.aspx?id=3978"><span><font size="2">More</font></span></a></p>
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[#children] => [<div class="field field-type-image field-field-people-image"><div class="field-label">People Image: </div><div class="field-items"><div class="field-item"><img src="http://www.diabetescenters.org/files/Ashuldiner.jpg" alt="Ashuldiner.jpg" title="Ashuldiner.jpg" width="175" height="233" /></div></div></div><div class="field field-type-text field-field-center-name"><div class="field-label">Center Name: </div><div class="field-items"><div class="field-item">DRTC - Johns Hopkins University/University of Maryland</div></div></div><div class="field field-type-text field-field-core"><div class="field-label">Core List: </div><div class="field-items"><div class="field-item">DRTC Baltimore Clinical Investigation Core</div></div></div><div class="field field-type-text field-field-phone-number"><div class="field-label">Phone Number: </div><div class="field-items"><div class="field-item">410-706-1623</div></div></div><div class="field field-type-text field-field-people-details"><div class="field-label">People Details: </div><div class="field-items"><div class="field-item"><p><span id="lblResearchInterests"><font size="2">Dr. Shuldiner’s major research interests are in the molecular basis and genetics of type-2 diabetes, obesity and insulin resistance. He has published over 130 original articles and 50 review articles. His studies of type-2 diabetes candidate genes include studies in African Americans, Pima Indians, Mexican Americans and Caucasians. His group was the first to discover a common mutation in the beta-3-adrenergic receptor (Trp64Arg) that influences several features of the insulin resistance syndrome, including insulin resistance, obesity and visceral fat accumulation. His group was also the first to describe a common variant in the peroxisome proliferator activated receptor gamma-2 gene (Pro12Ala PPAR¿2), which associates with obesity, increased insulin sensitivity and protection from type 2 diabetes. Most recently, his group has utilized genome scan/positional cloning approaches to identify several chromosomal regions that are likely to harbor susceptibility genes for type 2 diabetes, hypertension, obesity and hyperlipidemia in the Old Order Amish. These studies in the Amish have recently been expanded to include genetic studies of cardiovascular disease, osteoporosis, osteogenesis imperfecta, autoimmune thyroid disease, longevity and pharmacogenomics. Dr. Shuldiner has broad-based financial support for his research including NIH, American Diabetes Association, Juvenile Diabetes Foundation, Ellison Foundation and biotech/pharmaceuticals.</font></span></p>
<p><a href="http://medschool.umaryland.edu/FACULTYRESEARCHPROFILE/viewprofile.aspx?id=3978"><span><font size="2">More</font></span></a></p>
</div></div></div><div class="field field-type-text field-field-center-title"><div class="field-label">center_title: </div><div class="field-items"><div class="field-item">Center Co-Director and Director, Clinical Investigation Core</div></div></div>]
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