檢索結果 - Meindl, Alfons

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

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

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Hereditary Breast and Ovarian Cancer: New Genes, New Treatments, New Concepts 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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... 由 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 由 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 由 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... 由 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 由 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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