{"id":5,"date":"2024-12-09T14:12:35","date_gmt":"2024-12-09T19:12:35","guid":{"rendered":"https:\/\/web.uri.edu\/howlett-draft\/home\/"},"modified":"2025-06-03T09:55:30","modified_gmt":"2025-06-03T13:55:30","slug":"home","status":"publish","type":"page","link":"https:\/\/web.uri.edu\/howlett-lab\/","title":{"rendered":"Home"},"content":{"rendered":"<section class=\"cl-wrapper cl-hero-wrapper\"><div class=\"cl-hero super   cl-has-accessibility-controls\"><div class=\"cl-hero-proper\"><div class=\"overlay\"><div class=\"block\"><h1>Howlett Lab<\/h1><\/div><\/div><div class=\"still\" style=\"background-image:url(https:\/\/web.uri.edu\/howlett-lab-draft\/wp-content\/uploads\/sites\/2252\/Team-FARF-II.jpg);background-position:53% 39%;\"><\/div><div class=\"cl-accessibility-controls-container\"><div class=\"cl-accessibility-controls\"><div class=\"cl-accessibility-icon\" title=\"Accessibility controls\">Accessibility controls<\/div><div class=\"cl-accessibility-control cl-accessibility-motion-control cl-accessibility-control-hidden\"><div class=\"cl-accessibility-control-default\"><div class=\"cl-accessibility-control-button\" title=\"Pause motion\">Pause motion<\/div><div class=\"cl-accessibility-control-label\">Motion: <span class=\"cl-accessibility-syntax\">On<\/span><\/div><\/div><div class=\"cl-accessibility-control-alternate\"><div class=\"cl-accessibility-control-button\" title=\"Play motion\">Play motion<\/div><div class=\"cl-accessibility-control-label\">Motion: <span class=\"cl-accessibility-syntax\">Off<\/span><\/div><\/div><\/div><div class=\"cl-accessibility-control cl-accessibility-contrast-control\"><div class=\"cl-accessibility-control-default\"><div class=\"cl-accessibility-control-button\" title=\"Increase text contrast\">Increase text contrast<\/div><div class=\"cl-accessibility-control-label\">Contrast: <span class=\"cl-accessibility-syntax\">Standard<\/span><\/div><\/div><div class=\"cl-accessibility-control-alternate\"><div class=\"cl-accessibility-control-button\" title=\"Reset text contrast\">Reset text contrast<\/div><div class=\"cl-accessibility-control-label\">Contrast: <span class=\"cl-accessibility-syntax\">High<\/span><\/div><\/div><\/div><div class=\"cl-accessibility-system-setting\"><div class=\"cl-accessibility-toggle\" title=\"Apply my preferences site-wide\"><\/div><div class=\"cl-accessibility-toggle-label\">Apply site-wide<\/div><\/div><\/div><\/div><\/div><div class=\"cl-hero-caption-wrapper\"><div class=\"cl-hero-caption\">Team FARF pictured after the 2016 Pell Bridge Run, a 4 mile run\/walk across the Claiborne Pell Bridge from Jamestown to Newport, R.I. Team FARF 2016 included the Fiaschetti, Eminger, and Mackowicz families and friends as well as members of the Howlett lab.<\/div><\/div><\/div><\/section>\n\n\n<p class=\"has-text-align-left\">The Howlett Lab is located in the\u00a0<a href=\"https:\/\/web.uri.edu\/cmb\/\" target=\"_blank\" rel=\"noreferrer noopener\">Department of Cell and Molecular Biology<\/a>\u00a0at the\u00a0<a href=\"https:\/\/www.uri.edu\/\" target=\"_blank\" rel=\"noreferrer noopener\">University of Rhode Island<\/a>. We study the eukaryotic cellular DNA damage response and the maintenance of genome stability. We study these topics primarily through the lens of a rare genetic disease,\u00a0<a href=\"https:\/\/omim.org\/entry\/227650\" target=\"_blank\" rel=\"noreferrer noopener\">Fanconi anemia<\/a>.<\/p>\n\n\n\n<p>Fanconi anemia (FA) is clinically characterized by congenital malformations, increased risk for bone marrow failure and cancer, and premature mortality. Several recent clinical reports have described pleiotropic neurological symptoms in FA patients, including abnormal brain MRIs, seizures, brain lesions, and early-onset cognitive decline. This constellation of neurological symptoms is collectively referred to as Fanconi Anemia Neurological Syndrome (FANS). The molecular etiology of FANS is unknown.<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"195\" src=\"https:\/\/web.uri.edu\/howlett-lab-draft\/wp-content\/uploads\/sites\/2252\/D2-PCNA-Foci-copy-1024x195.jpg\" alt=\"\" class=\"wp-image-15\" srcset=\"https:\/\/web.uri.edu\/howlett-lab\/wp-content\/uploads\/sites\/2252\/D2-PCNA-Foci-copy-1024x195.jpg 1024w, https:\/\/web.uri.edu\/howlett-lab\/wp-content\/uploads\/sites\/2252\/D2-PCNA-Foci-copy-300x57.jpg 300w, https:\/\/web.uri.edu\/howlett-lab\/wp-content\/uploads\/sites\/2252\/D2-PCNA-Foci-copy-768x146.jpg 768w, https:\/\/web.uri.edu\/howlett-lab\/wp-content\/uploads\/sites\/2252\/D2-PCNA-Foci-copy-364x69.jpg 364w, https:\/\/web.uri.edu\/howlett-lab\/wp-content\/uploads\/sites\/2252\/D2-PCNA-Foci-copy-500x95.jpg 500w, https:\/\/web.uri.edu\/howlett-lab\/wp-content\/uploads\/sites\/2252\/D2-PCNA-Foci-copy-1000x191.jpg 1000w, https:\/\/web.uri.edu\/howlett-lab\/wp-content\/uploads\/sites\/2252\/D2-PCNA-Foci-copy.jpg 1122w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n<\/div>\n\n\n<p>FA is both autosomal and X-linked (<em>FA complementation group B is caused by mutation in the X-linked FANCB gene<\/em>). The incidence of FA in the U.S. is approximately 1 in 120,000 live births. FA is caused by mutation of any one of 23 genes:&nbsp;<em>FANCA, FANCB, FANCC, BRCA2\/FANCD1, FANCD2, FANCE, FANCF, FANCG, FANCI, BRIP1\/FANCJ, FANCL, FANCM, PALB2\/FANCN, RAD51C\/FANCO, SLX4\/FANCP, ERCC4\/FANCQ, RAD51\/FANCR, BRCA1\/FANCS, UBE2T\/FANCT, XRCC2\/FANCU, MAD2L2\/FANCV, RFWD3\/FANCW<\/em>, and<em>&nbsp;REV7\/FANCY<\/em>.<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"alignright\"><img decoding=\"async\" src=\"https:\/\/web.uri.edu\/howlett\/wp-content\/uploads\/sites\/2252\/100_0466-scaled-e1670510424555-300x187.jpg\" alt=\"\" class=\"wp-image-320\"\/><\/figure>\n<\/div>\n\n\n<p><em>In vitro<\/em>&nbsp;studies have established that the FA proteins function together to orchestrate the repair of DNA interstrand crosslinks (ICLs), induced by DNA crosslinking agents such as mitomycin C and cisplatin. However, the endogenous source of genome instability for FA patients remains to be elucidated. Recent studies have strongly suggested that reactive aldehydes generated through normal metabolic processes, e.g., acetaldehyde and formaldehyde, may be particularly genotoxic to FA patient cells.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The Howlett Lab is located in the\u00a0Department of Cell and Molecular Biology\u00a0at the\u00a0University of Rhode Island. We study the eukaryotic cellular DNA damage response and the maintenance of genome stability. We study these topics primarily through the lens of a rare genetic disease,\u00a0Fanconi anemia. Fanconi anemia (FA) is clinically characterized by congenital malformations, increased risk [&hellip;]<\/p>\n","protected":false},"author":5144,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":"","_links_to":"","_links_to_target":""},"class_list":["post-5","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/web.uri.edu\/howlett-lab\/wp-json\/wp\/v2\/pages\/5","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/web.uri.edu\/howlett-lab\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/web.uri.edu\/howlett-lab\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/web.uri.edu\/howlett-lab\/wp-json\/wp\/v2\/users\/5144"}],"replies":[{"embeddable":true,"href":"https:\/\/web.uri.edu\/howlett-lab\/wp-json\/wp\/v2\/comments?post=5"}],"version-history":[{"count":4,"href":"https:\/\/web.uri.edu\/howlett-lab\/wp-json\/wp\/v2\/pages\/5\/revisions"}],"predecessor-version":[{"id":122,"href":"https:\/\/web.uri.edu\/howlett-lab\/wp-json\/wp\/v2\/pages\/5\/revisions\/122"}],"wp:attachment":[{"href":"https:\/\/web.uri.edu\/howlett-lab\/wp-json\/wp\/v2\/media?parent=5"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}