RAW TOBACCO MATERIAL PROCESSING METHOD von PETRIJ A.I, RJABCHENKO A.G, PETRIJ A.A, D'JACHKIN I.I, PESTOVA L.P, NESTERENKO I.A, SAFRONOVA I.V

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BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients von Petrij-Bosch, Anne, Peelen, Tamara, van Vliet, Margreethe, Eijk, Ronald van, Olmer, Renske, Drüsedau, Marion, Hogervorst, Frans B.L, Hageman, Sandra, Arts, Petronella J.W, Ligtenberg, Marjolijn J.L, Meijers-Heijboer, Hanne, Klijn, Jan G.M, Vasen, Hans R.A, Cornelisse, Cees J, van't Veer, Laura J, Bakker, Egbert, van Ommen, Gert-Jan B, Devilee, Peter

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WATER-ABSORBING ALLOY FOR MANUFACTURING ELECTRODES von MOVLAEV EHL'SHAD ALEJ OGLY, SUNGUL CHO, MITROKHIN S.V, VASINA S.JA, PETRIJ O.A, SALAMOVA A.A, VERBETSKIJ V.N, DZHAESUK SUNG

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The association between desmopressin exposure, FVIII response and side effects von Schütte, Lisette M., Hest, Reinier M., Cnossen, Marjon H., Stoof, Sara C. M., Leebeek, Frank W. G., Mathôt, Ron A. A., Kruip, Marieke J. H. A.

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Desmopressin treatment combined with clotting factor VIII concentrates in patients with non-severe haemophilia A: protocol for a multicentre single-armed trial, the DAVID study von Schütte, Lisette M, Cnossen, Marjon H, van Hest, Reinier M, Driessens, Mariette H E, Fijnvandraat, Karin, Polinder, Suzanne, Beckers, Erik A M, Coppens, Michiel, Eikenboom, Jeroen, Laros-van Gorkom, Britta A P, Meijer, Karina, Nieuwenhuizen, Laurens, Mauser-Bunschoten, Evelien P, Leebeek, Frank W G, Mathôt, Ron A A, Kruip, Marieke J H A

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Tachyphylaxis and reproducibility of desmopressin response in perioperative persons with nonsevere hemophilia A: implications for clinical practice von Romano, L.G.R., Schütte, L.M., van Hest, R.M., Meijer, K., Laros-van Gorkom, B.A.P., Nieuwenhuizen, L., Eikenboom, J., Heubel-Moenen, F.C.J.I., Uitslager, N., Coppens, M., Fijnvandraat, K., Driessens, M.H.E., Polinder, S., Cnossen, M.H., Leebeek, F.W.G., Mathôt, R.A.A., Kruip, M.J.H.A.

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BRCA1 promoter deletions in young women with breast cancer and a strong family history: A population-based study von Smith, L.D, Tesoriero, A.A, Ramus, S.J, Dite, G, Royce, S.G, Giles, G.G, McCredie, M.R.E, Hopper, J.L, Southey, M.C

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Oligonucleotide Microarray Analysis of Genomic Imbalance in Children with Mental Retardation von Friedman, J.M., Baross, Ágnes, Delaney, Allen D., Ally, Adrian, Arbour, Laura, Asano, Jennifer, Bailey, Dione K., Barber, Sarah, Birch, Patricia, Brown-John, Mabel, Cao, Manqiu, Chan, Susanna, Charest, David L., Farnoud, Noushin, Fernandes, Nicole, Flibotte, Stephane, Go, Anne, Gibson, William T., Holt, Robert A., Jones, Steven J.M., Kennedy, Giulia C., Krzywinski, Martin, Langlois, Sylvie, Li, Haiyan I., McGillivray, Barbara C., Nayar, Tarun, Pugh, Trevor J., Rajcan-Separovic, Evica, Schein, Jacqueline E., Schnerch, Angelique, Siddiqui, Asim, Van Allen, Margot I., Wilson, Gary, Yong, Siu-Li, Zahir, Farah, Eydoux, Patrice, Marra, Marco A.

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Chromatin Acetylation, Memory, and LTP Are Impaired in CBP +/− Mice : A Model for the Cognitive Deficit in Rubinstein-Taybi Syndrome and Its Amelioration von Alarcón, Juan M, Malleret, Gaël, Touzani, Khalid, Vronskaya, Svetlana, Ishii, Shunsuke, Kandel, Eric R, Barco, Angel

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Sevoflurane suppresses ALG13 transcription in a CREBBP-dependent manner to induce hippocampal damage and cognitive impairment von Gong, Xiuping, Li, Qi, Liu, Yang

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Reversing Neurodevelopmental Disorders in Adults von Ehninger, Dan, Li, Weidong, Fox, Kevin, Stryker, Michael P., Silva, Alcino J.

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Phosphorylation of CBP Mediates Transcriptional Activation by Neural Activity and CaM Kinase IV von Impey, Soren, Fong, Amy L., Wang, Yanhong, Cardinaux, Jean-Rene, Fass, Daniel M., Obrietan, Karl, Wayman, Gary A., Storm, Daniel R., Soderling, Thomas R., Goodman, Richard H.

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Tyrosinase mutations associated with Siamese and Burmese patterns in the domestic cat (Felis catus) von Lyons, L.A, Imes, D.L, Rah, H.C, Grahn, R.A

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Localization of the transcriptional coactivator PGC-1α to GABAergic neurons during maturation of the rat brain von Cowell, Rita Marie, Blake, Kathryn Rose, Russell, James W.

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The Rubinstein–Taybi syndrome: modeling mental impairment in the mouse von Barco, A.

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Histone modifying and chromatin remodelling enzymes in cancer and dysplastic syndromes von Gibbons, Richard J

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Identification of disease genes by whole genome CGH arrays von Vissers, Lisenka E.L.M., Veltman, Joris A., van Kessel, Ad Geurts, Brunner, Han G.

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Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome von Niesler, Beate, Rao, Ercole, Breuning, Martijn H, Nordsiek, Gabriele, Ogata, Tsutomu, Binder, Gerhard, Weiss, Birgit, Fukami, Maki, Kirsch, Stefan, Heinrich, Udo, Rappold, Gudrun A, Rump, Andreas, Winkelmann, Martina, Mertz, Annelyse, Muroya, Koji, Rosenthal, André, Ranke, Michael B

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Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification von Schouten, Jan P., McElgunn, Cathal J., Waaijer, Raymond, Zwijnenburg, Danny, Diepvens, Filip, Pals, Gerard

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Bartter Syndrome: A Systematic Review of Case Reports and Case Series von Qasba, Rakhtan K, Bucharles, Anna Carolina Flumignan, Piccoli, Maria Victoria Ferreira, Sharma, Pranjal, Banga, Akshat, Kamaraj, Balakrishnan, Nawaz, Faisal A, Kumar, Harshadayani Jagadish, Happy, Mahika Afrin, Qasba, Ruman K, Kogilathota Jagirdhar, Gowthami Sai, Essar, Mohammad Yasir, Garg, Piyush, Reddy, Shiva Teja, Rama, Kaanthi, Surani, Salim, Kashyap, Rahul

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