{"id":59159,"date":"2020-06-22T12:57:26","date_gmt":"2020-06-22T16:57:26","guid":{"rendered":"https:\/\/rarediseases.org\/nords-jayne-holtzer-rare-disease-research-grants-program-continues-its-commitment-to-rare-disease-research-with-new-funding-opportunities\/"},"modified":"2020-06-22T12:57:26","modified_gmt":"2020-06-22T16:57:26","slug":"nords-jayne-holtzer-rare-disease-research-grants-program-continues-its-commitment-to-rare-disease-research-with-new-funding-opportunities","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/nords-jayne-holtzer-rare-disease-research-grants-program-continues-its-commitment-to-rare-disease-research-with-new-funding-opportunities\/","title":{"rendered":"NORD\u2019s Jayne Holtzer Rare Disease Research Grants Program Continues Its Commitment to Rare Disease Research with New Funding Opportunities"},"content":{"rendered":"<p><strong>Washington, DC, June 22, 2020 &#8211; <\/strong>The National Organization for Rare Disorders\u00ae (NORD), the leading independent nonprofit organization representing over 25 million Americans living with rare diseases, today announced the availability of three new funding opportunities to support the study of two rare diseases. The initial application deadline is August 25, 2020.<\/p>\n<p>NORD&#8217;s Jayne Holtzer Rare Disease Research Grants Program Rare Disease Research Grant Program is accepting proposals for scientific and\/or clinical research studies of:<\/p>\n<ul>\n<li>Appendix Cancer and Pseudomyxoma Peritonei (PMP) \u2014 Two grants of up to $50,000 (US) each<\/li>\n<li>Neuroendocrine Cell Hyperplasia of Infancy (NEHI) \u2014 One grant of up to $50,000 (US)<\/li>\n<\/ul>\n<p>NORD encourages all US and international researchers interested in studying one or more of these diseases to review the complete <a href=\"https:\/\/rarediseases.org\/for-clinicians-and-researchers\/research-opportunities\/requests-proposals\/\" data-cke-saved-href=\"https:\/\/rarediseases.org\/for-clinicians-and-researchers\/research-opportunities\/requests-proposals\/\">application guidelines<\/a> detailed in the request for proposals.<\/p>\n<p>NORD\u2019s Jayne Holtzer Rare Disease Research Grants Program provides seed funding to qualified researchers for translational or clinical studies related to the development of potential new diagnostics or treatments for rare diseases. Over the past thirty years, NORD grants have led to the development of two FDA-approved treatments and numerous peer-reviewed publications. More than 200 grants have been awarded, representing over $9 million in approved funding since the program\u2019s launch in 1989.<\/p>\n<p>\u201cAt NORD, we remain committed to accelerating the development of life-saving discoveries for the rare disease community, even in the face of the unprecedented challenges presented by COVID-19,\u201d said Vanessa Boulanger, NORD&#8217;s Director of Research Programs. \u201cWe are grateful for the continued, generous support of our donors, which makes funding opportunities to support rare disease research possible.\u201d<\/p>\n<p>Grants are made available through the generosity of allies in the rare disease community and supporters who have donated into NORD\u2019s research fund. For more information about NORD\u2019s Rare Disease Research Grant Program and rare disease research funding opportunities, visit: <a href=\"https:\/\/rarediseases.org\/research\" data-cke-saved-href=\"https:\/\/rarediseases.org\/research\">rarediseases.org\/research<\/a>.<\/p>\n<p style=\"text-align: center;\">#\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 #\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 #<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Washington, DC, June 22, 2020 &#8211; The National Organization for Rare Disorders\u00ae (NORD), the leading independent nonprofit organization representing over 25 million Americans living with rare diseases, today announced the &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/nords-jayne-holtzer-rare-disease-research-grants-program-continues-its-commitment-to-rare-disease-research-with-new-funding-opportunities\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;NORD\u2019s Jayne Holtzer Rare Disease Research Grants Program Continues Its Commitment to Rare Disease Research with New Funding Opportunities&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","_price":"","_stock":"","_tribe_ticket_header":"","_tribe_default_ticket_provider":"","_tribe_ticket_capacity":"","_ticket_start_date":"","_ticket_end_date":"","_tribe_ticket_show_description":"","_tribe_ticket_show_not_going":false,"_tribe_ticket_use_global_stock":"","_tribe_ticket_global_stock_level":"","_global_stock_mode":"","_global_stock_cap":"","_tribe_rsvp_for_event":"","_tribe_ticket_going_count":"","_tribe_ticket_not_going_count":"","_tribe_tickets_list":"[]","_tribe_ticket_has_attendee_info_fields":false,"footnotes":""},"categories":[190,504,193],"tags":[1926,2229,1932,2389,1386],"class_list":["post-59159","post","type-post","status-publish","format-standard","hentry","category-featured-news","category-press-releases","category-research","tag-appendix-cancer-and-pseudomyxoma-peritonei","tag-covid-19","tag-neuroendocrine-cell-hyperplasia-of-infancy","tag-nords-jayne-holtzer-rare-disease-research-grants-program","tag-vanessa-boulanger"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59159","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/comments?post=59159"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/59159\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=59159"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=59159"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=59159"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}