Resultados da pesquisa - Meindl, Alfons

Identification of Novel Susceptibility Genes for Breast Cancer – Genome-Wide Association Studies or Evaluation of Candidate Genes? Por Meindl, Alfons

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Breast cancer susceptibility: current knowledge and implications for genetic counselling Por Ripperger, Tim, Gadzicki, Dorothea, Meindl, Alfons, Schlegelberger, Brigitte

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Hereditary Breast and Ovarian Cancer: New Genes, New Treatments, New Concepts Por Meindl, Alfons, Ditsch, Nina, Kast, Karin, Rhiem, Kerstin, Schmutzler, Rita K.

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Vitamin D receptor, Retinoid X receptor and peroxisome proliferator-activated receptor γ are overexpressed in BRCA1 mutated breast cancer and predict prognosis Por Heublein, Sabine, Mayr, Doris, Meindl, Alfons, Kircher, Alexandra, Jeschke, Udo, Ditsch, Nina

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Thyroid Hormone Receptors Predict Prognosis in BRCA1 Associated Breast Cancer in Opposing Ways Por Heublein, Sabine, Mayr, Doris, Meindl, Alfons, Angele, Martin, Gallwas, Julia, Jeschke, Udo, Ditsch, Nina

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Non-collagenous extracellular matrix protein dermatopontin may play a role as another component of transforming growth factor-β signaling pathway in colon carcinogenesis Por Sadr-Nabavi, Ariane, Bouromand-Noughabi, Samaneh, Tayebi-Meybodi, Naser, Dadkhah, Kimia, Amini, Nafiseh, Meindl, Alfons, Abbaszadegan, Mohammad Reza

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Strong Association of a Common Dihydropyrimidine Dehydrogenase Gene Polymorphism with Fluoropyrimidine-Related Toxicity in Cancer Patients Por Gross, Eva, Busse, Birgit, Riemenschneider, Matthias, Neubauer, Steffi, Seck, Katharina, Klein, Hanns-Georg, Kiechle, Marion, Lordick, Florian, Meindl, Alfons

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Transcription factor 7-like 2 (TCF7L2) variant is associated with familial breast cancer risk: a case-control study Por Burwinkel, Barbara, Shanmugam, Kalai S, Hemminki, Kari, Meindl, Alfons, Schmutzler, Rita K, Sutter, Christian, Wappenschmidt, Barbara, Kiechle, Marion, Bartram, Claus R, Frank, Bernd

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BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study Por Frank, Bernd, Hemminki, Kari, Meindl, Alfons, Wappenschmidt, Barbara, Sutter, Christian, Kiechle, Marion, Bugert, Peter, Schmutzler, Rita K, Bartram, Claus R, Burwinkel, Barbara

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Downregulation of Serine Protease HTRA1 Is Associated with Poor Survival in Breast Cancer Por Lehner, Anna, Magdolen, Viktor, Schuster, Tibor, Kotzsch, Matthias, Kiechle, Marion, Meindl, Alfons, Sweep, Fred C. G. J., Span, Paul N., Gross, Eva

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Novel Truncating Mutations in the Polyglutamine Tract Binding Protein 1 Gene (PQBP1) Cause Renpenning Syndrome and X-Linked Mental Retardation in Another Family with Microcephaly Por Lenski, Claus, Abidi, Fatima, Meindl, Alfons, Gibson, Alice, Platzer, Matthias, Frank Kooy, R., Lubs, Herbert A., Stevenson, Roger E., Ramser, Juliane, Schwartz, Charles E.

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TP53 germline mutations in the context of families with hereditary breast and ovarian cancer: a clinical challenge Por Grill, Sabine, Ramser, Juliane, Hellebrand, Heide, Pfarr, Nicole, Boxberg, Melanie, Brambs, Christine, Ditsch, Nina, Meindl, Alfons, Groß, Eva, Meitinger, Thomas, Kiechle, Marion, Quante, Anne S.

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The Reduced Expression of the HADH2 Protein Causes X-Linked Mental Retardation, Choreoathetosis, and Abnormal Behavior Por Lenski, Claus , Frank Kooy, R. , Reyniers, Edwin , Loessner, Daniela , Wanders, Ronald J. A. , Winnepenninckx, Birgitta , Hellebrand, Heide , Engert, Stefanie , Schwartz, Charles E. , Meindl, Alfons , Ramser, Juliane 

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Girls homozygous for an IL-2–inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation Por Huck, Kirsten, Feyen, Oliver, Niehues, Tim, Rüschendorf, Franz, Hübner, Norbert, Laws, Hans-Jürgen, Telieps, Tanja, Knapp, Stefan, Wacker, Hans-Heinrich, Meindl, Alfons, Jumaa, Hassan, Borkhardt, Arndt

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Analysis of 30 Putative BRCA1 Splicing Mutations in Hereditary Breast and Ovarian Cancer Families Identifies Exonic Splice Site Mutations That Escape In Silico Prediction Por Wappenschmidt, Barbara, Becker, Alexandra A., Hauke, Jan, Weber, Ute, Engert, Stefanie, Köhler, Juliane, Kast, Karin, Arnold, Norbert, Rhiem, Kerstin, Hahnen, Eric, Meindl, Alfons, Schmutzler, Rita K.

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Criteria of the German Consortium for Hereditary Breast and Ovarian Cancer for the Classification of Germline Sequence Variants in Risk Genes for Hereditary Breast and Ovarian Canc... Por Wappenschmidt, Barbara, Hauke, Jan, Faust, Ulrike, Niederacher, Dieter, Wiesmüller, Lisa, Schmidt, Gunnar, Groß, Evi, Gehrig, Andrea, Sutter, Christian, Ramser, Juliane, Rump, Andreas, Arnold, Norbert, Meindl, Alfons

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RAD51C deletion screening identifies a recurrent gross deletion in breast cancer and ovarian cancer families Por Schnurbein, Gioia, Hauke, Jan, Wappenschmidt, Barbara, Weber-Lassalle, Nana, Engert, Stefanie, Hellebrand, Heide, Garbes, Lutz, Becker, Alexandra, Neidhardt, Guido, Rhiem, Kerstin, Meindl, Alfons, Schmutzler, Rita K, Hahnen, Eric

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Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy Por Ramser, Juliane, Ahearn, Mary Ellen, Lenski, Claus, Yariz, Kemal O., Hellebrand, Heide, von Rhein, Michael, Clark, Robin D., Schmutzler, Rita K., Lichtner, Peter, Hoffman, Eric P., Meindl, Alfons, Baumbach-Reardon, Lisa

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Identification of BRCA1-like triple-negative breast cancers by quantitative multiplex-ligation-dependent probe amplification (MLPA) analysis of BRCA1-associated chromosomal regions... Por Gross, Eva, van Tinteren, Harm, Li, Zhou, Raab, Sandra, Meul, Christina, Avril, Stefanie, Laddach, Nadja, Aubele, Michaela, Propping, Corinna, Gkazepis, Apostolos, Schmitt, Manfred, Meindl, Alfons, Nederlof, Petra M., Kiechle, Marion, Lips, Esther H.

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Full-Length L1CAM and Not Its Δ2Δ27 Splice Variant Promotes Metastasis through Induction of Gelatinase Expression Por Hauser, Stephanie, Bickel, Laura, Weinspach, Dirk, Gerg, Michael, Schäfer, Michael K., Pfeifer, Marco, Hazin, John, Schelter, Florian, Weidle, Ulrich H., Ramser, Juliane, Volkmann, Juliane, Meindl, Alfons, Schmitt, Manfred, Schrötzlmair, Florian, Altevogt, Peter, Krüger, Achim

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