Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Brenda Richards"'
Autor:
Beverly A. Teicher, Johanne Kaplan, Abraham Scaria, Steve Schmid, Peter Pechan, Mindy Zhang, Brenda Richards, Min Yao, Roy Krumbholz, Stephanie Roth, Tri-Hung Nguyen, William Weber, Leslie Kurtzberg, Rebecca G. Bagley
sFLT01 is a novel fusion protein that consists of the VEGF/PlGF (placental growth factor) binding domain of human VEGFR1/Flt-1 (hVEGFR1) fused to the Fc portion of human IgG1 through a polyglycine linker. It binds to both human VEGF (hVEGF) and human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84cca7de32eec4d56b9cae5039c260c8
https://doi.org/10.1158/1535-7163.c.6535446
https://doi.org/10.1158/1535-7163.c.6535446
Autor:
Beverly A. Teicher, Johanne Kaplan, Abraham Scaria, Steve Schmid, Peter Pechan, Mindy Zhang, Brenda Richards, Min Yao, Roy Krumbholz, Stephanie Roth, Tri-Hung Nguyen, William Weber, Leslie Kurtzberg, Rebecca G. Bagley
Supplementary Table 1 from sFLT01: A Novel Fusion Protein with Antiangiogenic Activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f012f4588ebb8dfbc94d844ed9d77a3
https://doi.org/10.1158/1535-7163.22496958.v1
https://doi.org/10.1158/1535-7163.22496958.v1
Autor:
Beverly A. Teicher, Johanne Kaplan, Abraham Scaria, Steve Schmid, Peter Pechan, Mindy Zhang, Brenda Richards, Min Yao, Roy Krumbholz, Stephanie Roth, Tri-Hung Nguyen, William Weber, Leslie Kurtzberg, Rebecca G. Bagley
Supplementary Figure 1 from sFLT01: A Novel Fusion Protein with Antiangiogenic Activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3de49d4078880297abbf8fa50c243165
https://doi.org/10.1158/1535-7163.22496961.v1
https://doi.org/10.1158/1535-7163.22496961.v1
Autor:
Bing Wang, Mandy M. Smith, Stefano Zanotti, Stephen L. Madden, Hervé Husson, Vijay Modur, Laurie A. Smith, Nikolay O. Bukanov, Thomas A. Natoli, Sarah Moreno, Tyler Picariello, Katherine W. Klinger, Brenda Richards, Hyejung Park, Cheng Zhu, Oxana Ibraghimov-Beskrovnaya, Ryan J. Russo
Publikováno v:
Human Molecular Genetics
Bardet–Biedl syndrome (BBS) is a pleiotropic autosomal recessive ciliopathy affecting multiple organs. The development of potential disease-modifying therapy for BBS will require concurrent targeting of multi-systemic manifestations. Here, we show
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c7481d69b1504e2abb5077cf41fe841
https://doi.org/10.1093/hmg/ddaa138
https://doi.org/10.1093/hmg/ddaa138
Autor:
Thomas Hagerty, John F. D’Agostino, Bindhu Sebastian, Hillary Sullivan, Brenda Richards, Rosemarie Reyes
Publikováno v:
Critical care nurse. 37(3)
BACKGROUNDCatheter-associated urinary tract infections are preventable adverse outcomes that increase hospital morbidity, mortality, and costs. These infections are particularly prevalent in intensive care units.OBJECTIVESTo describe the success of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27e676f2dc87d2d6a01680a73a66635d
https://pubmed.ncbi.nlm.nih.gov/28572100
https://pubmed.ncbi.nlm.nih.gov/28572100
Autor:
Siem de Marie, A. Hasegawa, Alison McVie-Wylie, Rachel Palmer, Patrick Finn, Robert J. Pomponio, Mario Pescatori, K. So, K.M. Ciociola, Adam Palermo, Sueli Mieko Oba-Shinjo, Robert J. Mattaliano, Shruti Madhiwalla, Brenda Richards, Katherine W. Klinger, Stephen L. Madden, Mindy Zhang
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Pompe disease is a genetic disorder resulting from a deficiency of lysosomal acid alpha-glucosidase (GAA) that manifests as a clinical spectrum with regard to symptom severity and rate of progression. In this study, we used microarrays to examine gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::565df81407e9ecb8a48744db5805fe9d
https://doi.org/10.1016/j.ymgme.2012.05.004
https://doi.org/10.1016/j.ymgme.2012.05.004
Autor:
Katherine W. Klinger, Robert J. Mattaliano, Stephen L. Madden, Brenda Richards, Robert J. Pomponio, Sherry Cao, Claire A. Davies, Mark Plavsic, Adam Palermo
Publikováno v:
PDA journal of pharmaceutical science and technology. 68(6)
Next-generation sequencing has been evaluated at Genzyme as a means of identifying bioreactor contaminants due to its capability for detection of known and novel microbial species. In this approach, data obtained from next-generation sequencing is us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aae7842465d39dad85eae45b35b3266b
https://pubmed.ncbi.nlm.nih.gov/25475640
https://pubmed.ncbi.nlm.nih.gov/25475640
Autor:
Katherine W. Klinger, Viatcheslav R. Akmaev, Brian P. Cook, Dongyu Liu, Oxana Ibraghimov-Beskrovnaya, Xiaohong Cao, Clarence J. Wang, Gregory M. Landes, Douglas M. Jefferson, Brenda Richards, Hervé Husson, Bruce L. Roberts, Dana Barberio, Partha Manavalan, Ryan J. Russo, Shelley A. Grubman
Publikováno v:
Genomics. 84:497-510
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in the PKD1 or PKD2 gene, but cellular mechanisms of cystogenesis remain unclear. In an attempt to display the array of cyst-specific molecules and to elucidate the disease p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d08217a3a0d23531430c2ef9350bf17
https://doi.org/10.1016/j.ygeno.2004.03.009
https://doi.org/10.1016/j.ygeno.2004.03.009
Autor:
Brenda Richards, Leslie Kurtzberg, Peter Pechan, Johanne Kaplan, William Weber, Tri-Hung Nguyen, Beverly A. Teicher, Stephanie Roth, Roy Krumbholz, Mindy Zhang, Min Yao, Abraham Scaria, Rebecca G. Bagley, Steven Schmid
Publikováno v:
Molecular cancer therapeutics. 10(3)
sFLT01 is a novel fusion protein that consists of the VEGF/PlGF (placental growth factor) binding domain of human VEGFR1/Flt-1 (hVEGFR1) fused to the Fc portion of human IgG1 through a polyglycine linker. It binds to both human VEGF (hVEGF) and human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5052cfd62704a06661ced1b34fe84e24
https://pubmed.ncbi.nlm.nih.gov/21252283
https://pubmed.ncbi.nlm.nih.gov/21252283
Autor:
Robert C Stern, David R. Witt, Katherine W. Klinger, Brenda Richards, Henry L. Dorkin, Joel Skoletsky, Richard B. Parad, Anthony P. Shuber, Rosemary Balfour
Publikováno v:
Human Molecular Genetics. 2:159-163
Traditionally, DNA used for PCR-based diagnostic analysis has originated from white cells fractionated from whole blood. Although this method yields substantial quantities of DNA, there are some drawbacks to the procedure, including the inconvenience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6c523425a31f79ae23a7f9809a75f3b
https://doi.org/10.1093/hmg/2.2.159
https://doi.org/10.1093/hmg/2.2.159