University of Pittsburgh

University of Washington

The University of North Carolina at Chapel Hill

The Cleveland Clinic Foundation

Other

David C Whitcomb

Katherine Lea Pogue-Geile

Teresa A Brentnall

Ru Chen

Mary Patricia Bronner

Carol A Otey

Garth David Ehrlich

Michael Gorry

The present application discloses methods for predicting the risk of developing, or the presence of, recurrent acute pancreatitis and/or chronic pancreatitis, in a subject, by identifying the presence of an rs12688220 T allele, an rs7057398 T allele, and/or an rs10273639 C allele in a sample from the subject. The present application also discloses methods for treating or preventing pancreatitis in a human subject in need thereof.

Method for diagnosing and assessing risk of pancreatitis using genetic variants

The present invention provides methods and compositions involving detecting the presence of and/or assessing the risk of cancer in a subject. These methods include methods of detecting and diagnosing cancer in an individual; methods of identifying individuals at risk of developing a cancer; and methods of staging a cancer. The methods generally involve detecting a palladin gene nucleotide sequence alteration that has been found to be associated with cancer and/or detecting a level of a palladin mRNA and/or protein in a biological sample. The present invention further provides nucleic acid probes, nucleic acid primers, and antibodies, as well as kits comprising one or more of the same, for use in a subject method.

Compositions and methods for detecting cancer

A method for determining whether a human patient is susceptible to hereditary pancreatitis. The method comprises the steps of obtaining nucleic acid from the human patient. Then there is the step of checking the nucleic acid for a mutation that indicates hereditary pancreatitis. A primer which reacts with a human trypsinogen gene to identify hereditary pancreatitis. A method for detecting in a human a mutation in a trypsinogen gene indicative of hereditary pancreatitis. The invention comprises the steps of obtaining a sample having DNA of the patient. Then there is the step of processing the sample so the DNA will be recognized by a desired restriction enzyme. Next there is the step of introducing the desired restriction enzyme to the DNA wherein the recognizing of the desired restriction enzyme to the DNA indicates the presence of the mutation.

Method for determining whether a human patient is susceptible to hereditary pancreatitis, and primers therefore

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Allison Park, PA, United States of America

David C Whitcomb