Search Results - "OEFNER, P. J"

Rifaximin preserves intestinal microbiota balance in patients undergoing allogeneic stem cell transplantation by Weber, D, Oefner, P J, Dettmer, K, Hiergeist, A, Koestler, J, Gessner, A, Weber, M, Stämmler, F, Hahn, J, Wolff, D, Herr, W, Holler, E

“…Intestinal dysbiosis has been associated with acute gastrointestinal GvHD and poor outcome following allogeneic stem cell transplantation (ASCT). To assess the…”
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Nuclear magnetic resonance and mass spectrometry-based milk metabolomics in dairy cows during early and late lactation by Klein, M S, Almstetter, M F, Schlamberger, G, Nürnberger, N, Dettmer, K, Oefner, P J, Meyer, H H D, Wiedemann, S, Gronwald, W

“…Milk production in dairy cows has dramatically increased over the past few decades. The selection for higher milk yield affects the partitioning of available…”
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The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations by UNDERHILL, P. A., PASSARINO, G., LIN, A. A., SHEN, P., MIRAZÓN LAHR, M., FOLEY, R. A., OEFNER, P. J., CAVALLI-SFORZA, L. L.

“…Although molecular genetic evidence continues to accumulate that is consistent with a recent common African ancestry of modern humans, its ability to…”
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Increased incidence of chronic GvHD and CMV disease in patients with vitamin D deficiency before allogeneic stem cell transplantation by von Bahr, L, Blennow, O, Alm, J, Björklund, A, Malmberg, K-J, Mougiakakos, D, Le Blanc, A, Oefner, P J, Labopin, M, Ljungman, P, Le Blanc, K

“…Vitamin D has emerged as a central player in the immune system, with its deficiency being implicated in the pathogenesis of several autoimmune diseases,…”
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The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans: A Y Chromosome Perspective by Semino, Ornella, Passarino, Giuseppe, Oefner, Peter J., Lin, Alice A., Arbuzova, Svetlana, Beckman, Lars E., de Benedictis, Giovanna, Francalacci, Paolo, Kouvatsi, Anastasia, Limborska, Svetlana, Marcikiæ, Mladen, Mika, Anna, Mika, Barbara, Primorac, Dragan, Santachiara-Benerecetti, A. Silvana, Cavalli-Sforza, L. Luca, Underhill, Peter A.

“…A genetic perspective of human history in Europe was derived from 22 binary markers of the nonrecombining Y chromosome (NRY). Ten lineages account for >95% of…”
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High-Resolution Analysis of Human Y-Chromosome Variation Shows a Sharp Discontinuity and Limited Gene Flow between Northwestern Africa and the Iberian Peninsula by Bosch, Elena, Calafell, Francesc, Comas, David, Oefner, Peter J., Underhill, Peter A., Bertranpetit, Jaume

“…In the present study we have analyzed 44 Y-chromosome biallelic polymorphisms in population samples from northwestern (NW) Africa and the Iberian Peninsula,…”
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BITES: balanced individual treatment effect for survival data by Schrod, S, Schäfer, A, Solbrig, S, Lohmayer, R, Gronwald, W, Oefner, P J, Beißbarth, T, Spang, R, Zacharias, H U, Altenbuchinger, M

“…Abstract Motivation Estimating the effects of interventions on patient outcome is one of the key aspects of personalized medicine. Their inference is often…”
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Optimal Temperature Selection for Mutation Detection by Denaturing HPLC and Comparison to Single-Stranded Conformation Polymorphism and Heteroduplex Analysis by Jones, Alistair C, Austin, Jehannine, Hansen, Nancy, Hoogendoorn, Bastiaan, Oefner, Peter J, Cheadle, Jeremy P, O'Donovan, Michael C

“…Denaturing HPLC (DHPLC) is a semi-automated method for detecting unknown DNA sequence variants. The sensitivity of the method is dependent on the temperature…”
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Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography by Underhill, P A, Jin, L, Lin, A A, Mehdi, S Q, Jenkins, T, Vollrath, D, Davis, R W, Cavalli-Sforza, L L, Oefner, P J

“…Y chromosome haplotypes are particularly useful in deciphering human evolutionary history because they accentuate the effects of drift, migration, and range…”
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A Simple Procedure for the Analysis of Single Nucleotide Polymorphisms Facilitates Map-Based Cloning in Arabidopsis by Drenkard, Eliana, Richter, Brent G., Rozen, Steve, Lisa M. Stutius, Nathaniel A. Angell, Mindrinos, Michael, Cho, Raymond J., Oefner, Peter J., Davis, Ronald W., Ausubel, Frederick M.

“…We developed a modified allele-specific PCR procedure for assaying single nucleotide polymorphisms (SNPs) and used the procedure (called SNAP for…”
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Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection by O'Donovan, Michael C., Oefner, Peter J., Roberts, Stacy C., Austin, Jehannine, Hoogendoorn, Bastiaan, Guy, Carol, Speight, Graham, Upadhyaya, Meena, Sommer, Steve S., McGuffin, Peter

“…Denaturing high-performance liquid chromatography (DHPLC) is a novel high-capacity technique for detecting new mutations. We have evaluated the sensitivity and…”
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Genome-wide mapping with biallelic markers in Arabidopsis thaliana by Oefner, Peter J, Cho, Raymond J, Mindrinos, Michael, Richards, Daniel R, Sapolsky, Ronald J, Anderson, Mary, Drenkard, Eliana, Dewdney, Julia, Reuber, T. Lynne, Stammers, Melanie, Federspiel, Nancy, Theologis, Athanasios, Yang, Wei-Hsien, Hubbell, Earl, Au, Melinda, Chung, Edward Y, Lashkari, Deval, Lemieux, Bertrand, Dean, Caroline, Lipshutz, Robert J, Ausubel, Frederick M, Davis, Ronald W

“…Single-nucleotide polymorphisms, as well as small insertions and deletions (here referred to collectively as simple nucleotide polymorphisms, or SNPs),…”
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Reference point insensitive molecular data analysis by Altenbuchinger, M, Rehberg, T, Zacharias, H U, Stämmler, F, Dettmer, K, Weber, D, Hiergeist, A, Gessner, A, Holler, E, Oefner, P J, Spang, R

“…In biomedicine, every molecular measurement is relative to a reference point, like a fixed aliquot of RNA extracted from a tissue, a defined number of blood…”
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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 by Ophoff, R A, Terwindt, G M, Vergouwe, M N, van Eijk, R, Oefner, P J, Hoffman, S M, Lamerdin, J E, Mohrenweiser, H W, Bulman, D E, Ferrari, M, Haan, J, Lindhout, D, van Ommen, G J, Hofker, M H, Ferrari, M D, Frants, R R

“…Genes for familial hemiplegic migraine (FHM) and episodic ataxia type-2 (EA-2) have been mapped to chromosome 19p13. We characterized a brain-specific P/Q-type…”
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A Pre-Columbian Y Chromosome-Specific Transition and its Implications for Human Evolutionary History by Underhill, Peter A., Jin, Li, Zemans, Rachel, Oefner, Peter J., Cavalli-Sforza, L. Luca

“…A polymorphic C → T transition located on the human Y chromosome was found by the systematic comparative sequencing of Y-specific sequence-tagged sites by…”
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Molecular signatures that can be transferred across different omics platforms by Altenbuchinger, M, Schwarzfischer, P, Rehberg, T, Reinders, J, Kohler, Ch W, Gronwald, W, Richter, J, Szczepanowski, M, Masqué-Soler, N, Klapper, W, Oefner, P J, Spang, R

“…Molecular signatures for treatment recommendations are well researched. Still it is challenging to apply them to data generated by different protocols or…”
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Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene by Horváth, R, Scharfe, C, Hoeltzenbein, M, Do, B H, Schröder, C, Warzok, R, Vogelgesang, S, Lochmüller, H, Müller-Höcker, J, Gerbitz, K D, Oefner, P J, Jaksch, M

“…More than 100 mitochondrial (mt) DNA mutations have been described in association with different complex neurological disorders and with respiratory chain (RC)…”
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Molecular signatures that can be transferred across different omics platforms by Altenbuchinger, M, Schwarzfischer, P, Rehberg, T, Reinders, J, Kohler, Ch W, Gronwald, W, Richter, J, Szczepanowski, M, Masqué-Soler, N, Klapper, W, Oefner, P J, Spang, R

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Origins and Divergence of the Roma (Gypsies) by Gresham, David, Morar, Bharti, Underhill, Peter A., Passarino, Giuseppe, Lin, Alice A., Wise, Cheryl, Angelicheva, Dora, Calafell, Francesc, Oefner, Peter J., Shen, Peidong, Tournev, Ivailo, de Pablo, Rosario, Kuĉinskas, Vaidutis, Perez-Lezaun, Anna, Marushiakova, Elena, Popov, Vesselin, Kalaydjieva, Luba

“…The identification of a growing number of novel Mendelian disorders and private mutations in the Roma (Gypsies) points to their unique genetic heritage…”
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Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography by HOOGENDOORN, B, OWEN, M. J, OEFNER, P. J, WILLIAMS, N, AUSTIN, J, O'DONOVAN, M. C

“…We have investigated the possibility of genotyping single nucleotide polymorphisms (SNPs) by primer extension and high performance liquid chromatography…”
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