Search Results - "Otterud, Brith E."

Exome Analysis of a Family With Pleiotropic Congenital Heart Disease by Arrington, Cammon B, Bleyl, Steven B, Matsunami, Norisada, Bonnell, Gabriel D, Otterud, Brith E.M, Nielsen, Douglas C, Stevens, Jeffrey, Levy, Shawn, Leppert, Mark F, Bowles, Neil E

“…BACKGROUND—A number of single gene defects have been identified in patients with isolated or nonsyndromic congenital heart defects (CHDs). However, due to…”
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Identification of a Herpes Simplex Labialis Susceptibility Region on Human Chromosome 21 by Hobbs, Maurine R., Jones, Brandt B., Otterud, Brith E., Leppert, Mark, Kriesel, John D.

“…Background. Most of the United States population is infected with either herpes simplex virus type 1 (HSV-1), herpes simplex virus type 2, or both…”
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Leukemia-associated minor histocompatibility antigen discovery using T-cell clones isolated by in vitro stimulation of naive CD8+ T cells by Bleakley, Marie, Otterud, Brith E., Richardt, Julia L., Mollerup, Audrey D., Hudecek, Michael, Nishida, Tetsuya, Chaney, Colette N., Warren, Edus H., Leppert, Mark F., Riddell, Stanley R.

“…T-cell immunotherapy that targets minor histocompatibility (H) antigens presented selectively by recipient hematopoietic cells, including leukemia, could…”
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Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis by Spaapen, Robbert M, Lokhorst, Henk M, van den Oudenalder, Kelly, Otterud, Brith E, Dolstra, Harry, Leppert, Mark F, Minnema, Monique C, Bloem, Andries C, Mutis, Tuna

“…Some minor histocompatibility antigens (mHags) are expressed exclusively on patient hematopoietic and malignant cells, and this unique set of antigens enables…”
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Allogeneic hematopoietic cell transplantation for metastatic renal cell carcinoma after nonmyeloablative conditioning: Toxicity, clinical response, and immunological response to minor histocompatibility antigens by TYKODI, Scott S, WARREN, Edus H, THOMPSON, John A, RIDDELL, Stanley R, CHILDS, Richard W, OTTERUD, Brith E, LEPPERT, Mark F, STORB, Rainer, SANDMAIER, Brenda M

“…This phase I trial assessed the safety, efficacy, and immunologic responses to minor histocompatibility antigens following nonmyeloablative allogeneic…”
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A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22 by Butterfield, Russell J, Ramachandran, Deepa, Hasstedt, Sandra J, Otterud, Brith E, Leppert, Mark F, Swoboda, Kathryn J, Flanigan, Kevin M

“…Abstract We describe a novel form of juvenile recessive ALS (JRALS) affecting four of six offspring from a consanguineous first cousin marriage. The syndrome…”
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Molecular cloning and physical and genetic mapping of a novel human Na +/H + exchanger (NHE5/SLC9A5) to chromosome 16q22.1 by Klanke, Charles A., Su, Yan Ru, Callen, David F., Wang, Zhuo, Meneton, Pierre, Baird, Nancy, Kandasamy, Ramani A., Orlowski, John, Otterud, Brith E., Leppert, Mark, Shull, Gary E., Menon, Anil G.

“…A human genomic clone for a novel fifth member of the Na +/H + exchanger (NHE) family, NHE5 (gene symbol SLC9A5), has been isolated and partially sequenced…”
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Allogeneic Hematopoietic Cell Transplantation for Metastatic Renal Cell Carcinoma after Nonmyeloablative Conditioning by Tykodi, Scott S., Warren, Edus H., Thompson, John A., Riddell, Stanley R., Childs, Richard W., Otterud, Brith E., Leppert, Mark F., Storb, Rainer, Sandmaier, Brenda M.

“…Purpose: This phase I trial assessed the safety, efficacy, and immunologic responses to minor histocompatibility antigens following nonmyeloablative allogeneic…”
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Identification of a Herpes Simplex Labialis Susceptibility Region on Human Chromosome 21. Commentary by KOELLE, David M, BERGEMANN, Tracy L, HOBBS, Maurine R, JONES, Brandt B, OTTERUD, Brith E, LEPPERT, Mark, KRIESEL, John D

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Localization to chromosome 22 of a gene encoding a human minor histocompatibility antigen by Gubarev, MI, Jenkin, JC, Leppert, MF, Buchanan, GS, Otterud, BE, Guilbert, DA, Beatty, PG

“…In human allogeneic bone marrow transplantation, graft-vs-host disease and graft rejection can occur even if the patient and donor are genotypically matched by…”
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Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36 by Su, Y R, Klanke, C A, Houseal, T W, Linn, S C, Burk, S E, Varvil, T S, Otterud, B E, Shull, G E, Leppert, M F, Menon, A G

“…A human clone corresponding to the gene encoding anion exchanger isoform 3 (AE3) (approved gene symbol SLC2C) has been isolated and partially sequenced…”
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