IU Health PhysiciansIU Methodist Trauma Center 1701 Senate Blvd STE B238, Indianapolis, IN 46202 3179625339 (phone), 3179622082 (fax)
Education:
Medical School Indiana University School of Medicine Graduated: 2008
Conditions:
Cholelethiasis or Cholecystitis
Languages:
English
Description:
Dr. Browne graduated from the Indiana University School of Medicine in 2008. He works in Indianapolis, IN and specializes in Traumatic Surgery and General Surgery. Dr. Browne is affiliated with Indiana University Health Methodist Hospital.
Dr. Browne graduated from the University of Connecticut School of Medicine in 2002. He works in Raleigh, NC and 1 other location and specializes in Diagnostic Radiology. Dr. Browne is affiliated with Rex Hospital.
Joan C. Egrie - Newbury Park CA, US Steven G. Elliott - Newbury Park CA, US Jeffrey K. Browne - Camarillo CA, US Karen C. Sitney - Studio City CA, US
Assignee:
Amgen Inc. - Thousand Oaks CA
International Classification:
C07K 14/505 C07K 16/46 C07H 21/00
US Classification:
536 2351, 530397, 5303873
Abstract:
Methods for increasing and maintaining hematocrit in a mammal comprising administering a hyperglycosylated analog of erythropoietin are disclosed. An analog may be administered less frequently than an equivalent molar amount of recombinant human erythropoietin to obtain a comparable target hematocrit and treat anemia. Alternatively, a lower molar amount of a hyperglycosylated analog may be administered to obtain a comparable target hematocrit and treat anemia. Also disclosed are new hyperglycosylated erythopoietin analogs, methods of production of the analogs, and compositions comprising the analogs.
Methods And Compositions For The Prevention And Treatment Of Anemia
Joan C. Egrie - Newbury Park CA, US Steven G. Elliott - Newbury Park CA, US Jeffrey K. Browne - Camarillo CA, US Karen C. Sitney - Studio City CA, US
Assignee:
Amgen Inc. - Thousand Oaks CA
International Classification:
A61K 38/18 C07K 14/505
US Classification:
514 77, 514 11, 530350, 530395
Abstract:
Methods for increasing and maintaining hematocrit in a mammal comprising administering a hyperglycosylated analog of erythropoietin are disclosed. An analog may be administered less frequently than an equivalent molar amount of recombinant human erythropoietin to obtain a comparable target hematocrit and treat anemia. Alternatively, a lower molar amount of a hyperglycosylated analog may be administered to obtain a comparable target hematocrit and treat anemia. Also disclosed are new hyperglycosylated erythropoietin analogs, methods of production of the analogs, and compositions comprising the analogs.
Methods And Compositions For The Prevention And Treatment Of Anemia
Joan C. Egrie - Newbury Park CA, US Steven G. Elliott - Newbury Park CA, US Jeffrey K. Browne - Camarillo CA, US Karen C. Sitney - Studio City CA, US
Assignee:
Amgen Inc. - Thousand Oaks CA
International Classification:
C07K 14/505 A61K 38/16
US Classification:
514 8, 530397
Abstract:
Methods for increasing and maintaining hematocrit in a mammal comprising administering a hyperglycosylated analog of erythropoietin are disclosed. An analog may be administered less frequently than an equivalent molar amount of recombinant human erythropoietin to obtain a comparable target hematocrit and treat anemia. Alternatively, a lower molar amount of a hyperglycosylated analog may be administered to obtain a comparable target hematocrit and treat anemia. Also disclosed are new hyperglycosylated erythopoietin analogs, methods of production of the analogs, and compositions comprising the analogs.
Methods And Compositions For The Prevention And Treatment Of Anemia
Joan C. Egrie - Newbury Park CA, US Steven G. Elliott - Newbury Park CA, US Jeffrey K. Browne - Camarillo CA, US Karen C. Sitney - Studio City CA, US
Assignee:
Amgen Inc. - Thousand Oaks CA
International Classification:
C12N 15/00 C12N 5/00 C12N 1/00 C07K 14/505
US Classification:
435 691, 435325, 4353201, 530397
Abstract:
Methods for increasing and maintaining hematocrit in a mammal comprising administering a hyperglycosylated analog of erythropoietin are disclosed. An analog may be administered less frequently than an equivalent molar amount of recombinant human erythropoietin to obtain a comparable target hematocrit and treat anemia. Alternatively, a lower molar amount of a hyperglycosylated analog may be administered to obtain a comparable target hematocrit and treat anemia. Also disclosed are new hyperglycosylated erythopoietin analogs, methods of production of the analogs, and compositions comprising the analogs.
Methods And Compositions For The Prevention And Treatment Of Anemia
Methods for increasing and maintaining hematocrit in a mammal comprising administering a hyperglycosylated analog of erythropoietin are disclosed. An analog may be administered less frequently than an equivalent molar amount of recombinant human erythropoietin to obtain a comparable target hematocrit and treat anemia. Alternatively, a lower molar amount of a hyperglycosylated analog may be administered to obtain a comparable target hematocrit and treat anemia. Also disclosed are new hyperglycosylated erythropoietin analogs, methods of production of the analogs, and compositions comprising the analogs.
Methods And Compositions For The Prevention And Treatment Of Anemia
Joan C. EGRIE - Newbury Park CA, US Steven G. Elliot - Newbury Park CA, US Jeffrey K. Browne - Camarillo CA, US Karen C. Sitney - Studio City CA, US
International Classification:
A61K 38/18 C07K 14/505
US Classification:
514 77, 530380
Abstract:
Methods for increasing and maintaining hematocrit in a mammal comprising administering a hyperglycosylated analog of erythropoietin are disclosed. An analog may be administered less frequently than an equivalent molar amount of recombinant human erythropoietin to obtain a comparable target hematocrit and treat anemia. Alternatively, a lower molar amount of a hyperglycosylated analog may be administered to obtain a comparable target hematocrit and treat anemia. Also disclosed are new hyperglycosylated erythopoietin analogs, methods of production of the analogs, and compositions comprising the analogs.
Method For Producing Secretable Glycosyltransferases And Other Golgi Processing Enzymes
James C. Paulson - Sherman Oaks CA Karen J. Colley - Los Angeles CA Beverly Adler - Newbury Park CA Jeffrey K. Browne - Camarillo CA
Assignee:
The Regents of the Univ. of California - Oakland CA
International Classification:
C12N 1500 C12N 1554 C12N 1563 C12N 1579
US Classification:
435193
Abstract:
A method for genetically engineering cells to produce soluble and secretable Golgi processing enzymes instead of naturally occurring membrane-bound enzymes. Cells are genetically engineered to express glycosyltransferases which lack both a membrane anchor and a r This invention was made with government support under Grant Contract Nos. GM-27904 and GM-11557 awarded by the National Institute of Health. The government has certain rights in this invention. The publications and other reference materials referred to herein to describe the background of the invention and to provide additional detail regarding its practice are hereby incorporated by reference. For convenience, the reference materials are numerically referenced and grouped in the appended bibliography.
Method For Producing Secretable Glycosyltransferases And Other Golgi Processing Enzymes
James C. Paulson - Del Mar CA Karen J. Colley - Chicago IL Beverly Adler - Newbury Park CA Jeffrey K. Browne - Camarillo CA Jasminder Weinstein - Westlake Village CA
Assignee:
The Regents of the University of California - Oakland CA Amgen - Thousand Oaks CA
International Classification:
C12P 1918 C12P 2106 C12P 100 C12N 1552
US Classification:
435 41
Abstract:
A method for genetically engineering cells to produce soluble and secretable Golgi processing enzymes instead of naturally occurring membrane-bound enzymes. Cells are genetically engineered to express glycosyltransferases which lack both a membrane anchor and a retention signal. The resulting altered enzyme becomes soluble and secretable by the cell without losing its catalytic activity. Secretion of the soluble glycosyltransferase by the cell provides for increased production and simplified recovery of glycosyltransferase.
Christopher Gibson Elementary School Dorchester MA 1960-1962, Henry L. Higginson Elementary School Roxbury MA 1962-1963, James P. Timilty Middle School Roxbury MA 1963-1966
Community:
Michael Lodico, Napoleon Santos, Adalgisa Melenciano, James Cunniff, Robert Rocha, Joanne Shaw, John Haidul, Joel Gibbons, Richard Julian, Patty Cameron, Ralph Macleod, Linda Grieco