Items where Division is "Medicine > Lehrstuhl für Humangenetik" and Year is 2009

A

Allikmets, Rando and Bergen, Arthur A. and Dean, Michael and Guymer, Robyn H. and Hageman, Gregory S. and Klaver, Caroline C. and Stefansson, Kari and Weber, Bernhard H. (2009) Geographic Atrophy in Age-Related Macular Degeneration and TLR3. NEW ENGLAND JOURNAL OF MEDICINE, 360 (21). pp. 2252-2254. ISSN 0028-4793, 1533-4406

Allikmets, Rando and Dean, Michael and Hageman, Gregory S. and Baird, Paul N. and Klaver, Caroline C. and Bergen, Arthur A. and Weber, Bernhard H. (2009) The SERPING1 gene and age-related macular degeneration. LANCET, 374 (9693). pp. 875-876. ISSN 0140-6736, 1474-547X

Antoniou, Antonis C. and Sinilnikova, Olga M. and McGuffog, Lesley and Healey, Sue and Nevanlinna, Heli and Heikkinen, Tuomas and Simard, Jacques and Spurdle, Amanda B. and Beesley, Jonathan and Chen, Xiaoqing and Neuhausen, Susan L. and Ding, Yuan C. and Couch, Fergus J. and Wang, Xianshu and Fredericksen, Zachary and Peterlongo, Paolo and Peissel, Bernard and Bonanni, Bernardo and Viel, Alessandra and Bernard, Loris and Radice, Paolo and Szabo, Csilla I. and Foretova, Lenka and Zikan, Michal and Claes, Kathleen and Greene, Mark H. and Mai, Phuong L. and Rennert, Gad and Lejbkowicz, Flavio and Andrulis, Irene L. and Ozcelik, Hilmi and Glendon, Gord and Gerdes, Anne-Marie and Thomassen, Mads and Sunde, Lone and Caligo, Maria A. and Laitman, Yael and Kontorovich, Tair and Cohen, Shimrit and Kaufman, Bella and Dagan, Efrat and Baruch, Ruth Gershoni and Friedman, Eitan and Harbst, Katja and Barbany-Bustinza, Gisela and Rantala, Johanna and Ehrencrona, Hans and Karlsson, Per and Domchek, Susan M. and Nathanson, Katherine L. and Osorio, Ana and Blanco, Ignacio and Lasa, Adriana and Benitez, Javier and Hamann, Ute and Hogervorst, Frans B. L. and Rookus, Matti A. and Collee, J. Margriet and Devilee, Peter and Ligtenberg, Marjolijn J. and van der Luijt, Rob B. and Aalfs, Cora M. and Waisfisz, Quinten and Wijnen, Juul and van Roozendaal, Cornelis E. P. and Peock, Susan and Cook, Margaret and Frost, Debra and Oliver, Clare and Platte, Radka and Evans, D. Gareth and Lalloo, Fiona and Eeles, Rosalind and Izatt, Louise and Davidson, Rosemarie and Chu, Carol and Eccles, Diana and Cole, Trevor and Hodgson, Shirley and Godwin, Andrew K. and Stoppa-Lyonnet, Dominique and Buecher, Bruno and Leone, Melanie and Bressac-de Paillerets, Brigitte and Remenieras, Audrey and Caron, Olivier and Lenoir, Gilbert M. and Sevenet, Nicolas and Longy, Michel and Ferrer, Sandra Fert and Prieur, Fabienne and Goldgar, David and Miron, Alexander and John, Esther M. and Buys, Saundra S. and Daly, Mary B. and Hopper, John L. and Terry, Mary Beth and Yassin, Yosuf and Singer, Christian and Gschwantler-Kaulich, Daphne and Staudigl, Christine and Hansen, Thomas V. O. and Barkardottir, Rosa Bjork and Kirchhoff, Tomas and Pal, Prodipto and Kosarin, Kristi and Offit, Kenneth and Piedmonte, Marion and Rodriguez, Gustavo C. and Wakeley, Katie and Boggess, John F. and Basil, Jack and Schwartz, Peter E. and Blank, Stephanie V. and Toland, Amanda E. and Montagna, Marco and Casella, Cinzia and Imyanitov, Evgeny N. and Allavena, Anna and Schmutzler, Rita K. and Versmold, Beatrix and Engel, Christoph and Meindl, Alfons and Ditsch, Nina and Arnold, Norbert and Niederacher, Dieter and Deissler, Helmut and Fiebig, Britta and Suttner, Christian and Schoenbuchner, Ines and Gadzicki, Dorothea and Caldes, Trinidad and de la Hoya, Miguel and Pooley, Karen A. and Easton, Douglas F. and Chenevix-Trench, Georgia (2009) Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. HUMAN MOLECULAR GENETICS, 18 (22). pp. 4442-4456. ISSN 0964-6906, 1460-2083

B

Bals-Pratsch, M. and Hehr, A. and Seifert, B. and Hehr, U. (2009) Birth Following Vitrification of Oocytes and Polar Body Diagnosis for Cystic Fibrosis. GEBURTSHILFE UND FRAUENHEILKUNDE, 69 (6). pp. 541-544. ISSN 0016-5751, 1438-8804

Bauer, Peter and Winner, Beate and Schuele, Rebecca and Bauer, Claudia and Haefele, Veronika and Hehr, Ute and Bonin, Michael and Walter, Michael and Karle, Kathrin and Ringer, Thomas M. and Riess, Olaf and Winkler, Juergen and Schoels, Ludger (2009) Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization. NEUROGENETICS, 10 (1). pp. 43-48. ISSN 1364-6745, 1364-6753

Bohring, Axel and Stamm, Thomas and Spaich, Christiane and Haase, Claudia and Spree, Kerstin and Hehr, Ute and Hoffmann, Mandy and Ledig, Susanne and Sel, Saadettin and Wieacker, Peter and Roepke, Albrecht (2009) WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes. AMERICAN JOURNAL OF HUMAN GENETICS, 85 (1). pp. 97-105. ISSN 0002-9297

C

Cullen, Paul and Funke, Harald and Klein, Hanns-Georg and Langmann, Thomas and Miethke, Thomas and Neumaier, Michael and Sauter, Guido (2009) Multiparametric diagnostic methods in pathology. LABORATORIUMSMEDIZIN-JOURNAL OF LABORATORY MEDICINE, 33 (3). pp. 149-154. ISSN 0342-3026

E

Ebenrett, I. and Koerber, F. and Gabriel, H. and Hehr, U. and Heller, R. and Hoopmann, Markus (2009) Targeted Genetic Diagnosis After First Trimester Ultrasound for Lethal Fetal Skeletal Dysplasia. GEBURTSHILFE UND FRAUENHEILKUNDE, 69 (3). pp. 244-247. ISSN 0016-5751, 1438-8804

Ebert, Stefanie and Weigelt, Karin and Drobnik, Wolfgang and Mauerer, Richard and Hume, David A. and Weber, Bernhard H. F. and Langmann, Thomas (2009) Docosahexaenoic acid (22:6n-3) protects from early retinal degeneration and attenuates microglial activation. CHEMISTRY AND PHYSICS OF LIPIDS, 160 (Suppl). S25-S26. ISSN 0009-3084

Ebert, Stefanie and Weigelt, Karin and Walczak, Yana and Drobnik, Wolfgang and Mauerer, Richard and Hume, David A. and Weber, Bernhard H. F. and Langmann, Thomas (2009) Docosahexaenoic acid attenuates microglial activation and delays early retinal degeneration. JOURNAL OF NEUROCHEMISTRY, 110 (6). pp. 1863-1875. ISSN 0022-3042, 1471-4159

Ernst, Wolfgang and Saugspier, Michael and Felthaus, Oliver and Driemel, Oliver and Morsczeck, Christian (2009) Comparison of murine dental follicle precursor and retinal progenitor cells after neural differentiation in vitro. CELL BIOLOGY INTERNATIONAL, 33 (7). pp. 758-764. ISSN 1065-6995, 1095-8355

F

Farwick, A. and Dasch, B. and Weber, B. H. F. and Pauleikhoff, D. and Stoll, M. and Hense, H. -W. (2009) Variations in five genes and the severity of age-related macular degeneration: results from the Muenster aging and retina study. EYE, 23 (12). pp. 2238-2244. ISSN 0950-222X, 1476-5454

Ferreira de Lima, Renata. L. L. and Hoper, Sarah A. and Ghassibe, Michella and Cooper, Margaret E. and Rorick, Nicholas K. and Kondo, Shinji and Katz, Lori and Marazita, Mary L. and Compton, John and Bale, Sherri and Hehr, Ute and Dixon, Michael J. and Daack-Hirsch, Sandra and Boute, Odile and Bayet, Benedicte and Revencu, Nicole and Verellen-Dumoulin, Christine and Vikkula, Miikka and Richieri-Costa, Antonio and Moretti-Ferreira, Danilo and Murray, Jeffrey C. and Schutte, Brain C. (2009) Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. GENETICS IN MEDICINE, 11 (4). pp. 241-247. ISSN 1098-3600, 1530-0366

Foerster, Johanna R. and Lochnit, Guenter and Stoehr, Heidi (2009) Proteomic analysis of the membrane palmitoylated protein-4 (MPP4)-associated protein complex in the retina. EXPERIMENTAL EYE RESEARCH, 88 (1). pp. 39-46. ISSN 0014-4835, 1096-0007

Fritsche, Lars G. and Freita-Wolf, Sandra and Bettecken, Thomas and Meitinger, Thomas and Keilhauer, Claudia N. and Krawczak, Michael and Weber, Bernhard H. F. (2009) Age-Related Macular Degeneration and Functional Promoter and Coding Variants of the Apolipoprotein E Gene. HUMAN MUTATION, 30 (7). pp. 1048-1053. ISSN 1059-7794, 1098-1004

G

Gnewuch, Carsten and Liebisch, Gerhard and Langmann, Thomas and Dieplinger, Benjamin and Mueller, Thomas and Haltmayer, Meinhard and Dieplinger, Hans and Zahn, Alexandra and Stremmel, Wolfgang and Rogler, Gerhard and Schmitz, Gerd (2009) Serum bile acid profiling reflects enterohepatic detoxification state and intestinal barrier function in inflammatory bowel disease. WORLD JOURNAL OF GASTROENTEROLOGY, 15 (25). pp. 3134-3141. ISSN 1007-9327, 2219-2840

H

Hartmaier, Ryan J. and Tchatchou, Sandrine and Richter, Alexandra S. and Wang, Jay and McGuire, Sean E. and Skaar, Todd C. and Rae, Jimmy M. and Hemminki, Kari and Sutter, Christian and Ditsch, Nina and Bugert, Peter and Weber, Bernhard H. F. and Niederacher, Dieter and Arnold, Norbert and Varon-Mateeva, Raymonda and Wappenschmidt, Barbara and Schmutzler, Rita K. and Meindl, Alfons and Bartram, Claus R. and Burwinkel, Barbara and Oesterreich, Steffi (2009) Nuclear receptor coregulator SNP discovery and impact on breast cancer risk. BMC CANCER, 9: 438. ISSN 1471-2407

Hendig, Doris and Langmann, Thomas and Zarbock, Ralf and Schmitz, Gerd and Kleesiek, Knut and Goetting, Christian (2009) Characterization of the ATP-binding cassette transporter gene expression profile in Y79: a retinoblastoma cell line. MOLECULAR AND CELLULAR BIOCHEMISTRY, 328 (1-2). pp. 85-92. ISSN 0300-8177, 1573-4919

J

Judas, M. and Sedmak, G. and Rados, M. and Sarnavka, V. and Fumic, K. and Willer, T. and Gross, C. and Hehr, U. and Strahl, S. and Cuk, M. and Baric, I. (2009) POMT1-Associated Walker-Warburg Syndrome: A Disorder of Dendritic Development of Neocortical Neurons. NEUROPEDIATRICS, 40 (1). pp. 6-14. ISSN 0174-304X, 1439-1899

K

Kellner, Simone and Kellner, Ulrich and Weber, Bernhard H. F. and Fiebig, Britta and Weinitz, Silke and Ruether, Klaus (2009) Lipofuscin- and Melanin-related Fundus Autofluorescence in Patients with ABCA4-associated Retinal Dystrophies. AMERICAN JOURNAL OF OPHTHALMOLOGY, 147 (5). pp. 895-902. ISSN 0002-9394, 1879-1891

Kellner, U. and Kellner, S. and Renner, A. B. and Fiebig, B. S. and Weinitz, S. and Weber, B. H. F. (2009) Evidence-Based Diagnostic Approach to Inherited Retinal Dystrophies 2009. KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 226 (12). pp. 999-1011. ISSN 0023-2165

Kellner, U. and Kellner, S. and Weber, B. H. F. and Fiebig, B. and Weinitz, S. and Ruether, K. (2009) Lipofuscin- and melanin-related fundus autofluorescence visualize different retinal pigment epithelial alterations in patients with retinitis pigmentosa. EYE, 23 (6). pp. 1349-1359. ISSN 0950-222X

Krumbiegel, Mandy and Pasutto, Francesca and Mardin, Christian Y. and Weisschuh, Nicole and Paoli, Daniela and Gramer, Eugen and Zenkel, Matthias and Weber, Bernhard H. F. and Kruse, Friedrich E. and Schloetzer-Schrehardt, Ursula and Reis, Andre (2009) Exploring Functional Candidate Genes for Genetic Association in German Patients with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 50 (6). pp. 2796-2801. ISSN 0146-0404, 1552-5783

L

Lacbawan, F. and Solomon, B. D. and Roessler, E. and El-Jaick, K. and Domene, S. and Velez, J. I. and Zhou, N. and Hadley, D. and Balog, J. Z. and Long, R. and Fryer, A. and Smith, W. and Omar, S. and McLean, S. D. and Clarkson, K. and Lichty, A. and Clegg, N. J. and Delgado, M. R. and Levey, E. and Stashinko, E. and Potocki, L. and VanAllen, M. I. and Clayton-Smith, J. and Donnai, D. and Bianchi, D. W. and Juliusson, P. B. and Njolstad, P. R. and Brunner, H. G. and Carey, J. C. and Hehr, U. and Muesebeck, J. and Wieacker, P. F. and Postra, A. and Hennekam, R. C. M. and van den Boogaard, M-J H. and van Haeringen, A. and Paulussen, A. and Herbergs, J. and Schrander-Stumpel, C. T. R. M. and Janecke, A. R. and Chitayat, D. and Hahn, J. and McDonald-McGinn, D. M. and Zackai, E. H. and Dobyns, W. B. and Muenke, M. (2009) Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. JOURNAL OF MEDICAL GENETICS, 46 (6). pp. 389-398. ISSN 0022-2593, 1468-6244

Langmann, Thomas and Ebert, Stefanie and Walczak, Yana and Weigelt, Karin and Ehrengruber, Markus U. and Stiewe, Thorsten and Weber, Bernhard H. F. (2009) Induction of Early Growth Response-1 Mediates Microglia Activation In Vitro But is Dispensable In Vivo. NEUROMOLECULAR MEDICINE, 11 (2). pp. 87-96. ISSN 1535-1084, 1559-1174

M

Mauerer, Richard and Ebert, Stefanie and Langmann, Thomas (2009) High glucose, unsaturated and saturated fatty acids differentially regulate expression of ATP-binding cassette transporters ABCA1 and ABCG1 in human macrophages. EXPERIMENTAL AND MOLECULAR MEDICINE, 41 (2). pp. 126-132. ISSN 1226-3613, 2092-6413

Morsczeck, Christian and Petersen, Jorgen and Voellner, Florian and Driemel, Oliver and Reichert, Torsten and Beck, Hans Christian (2009) Proteomic analysis of osteogenic differentiation of dental follicle precursor cells. ELECTROPHORESIS, 30 (7). pp. 1175-1184. ISSN 0173-0835, 1522-2683

Morsczeck, Christian and Schmalz, Gottfried and Reichert, Torsten Eugen and Voellner, Florian and Saugspier, Michael and Viale-Bouroncle, Sandra and Driemel, Oliver (2009) Gene expression profiles of dental follicle cells before and after osteogenic differentiation in vitro. CLINICAL ORAL INVESTIGATIONS, 13 (4). pp. 383-391. ISSN 1432-6981, 1436-3771

Moser, Christian and Lang, Sven and Hackl, Christina and Weber, Bernard and Zhang, Hong and Schlitt, Hans and Geissler, Edward and Stoeltzing, Oliver (2009) Inhibition of heat shock protein 90 (Hsp90) modulates macrophage stimulating-1 receptor (MSR1) expression and signaling, and reduces pancreatic tumor growth. CANCER RESEARCH, 69 (9suppl): 2835. ISSN 0008-5472, 1538-7445

O

Osorio, A. and Milne, R. L. and Pita, G. and Peterlongo, P. and Heikkinen, T. and Simard, J. and Chenevix-Trench, G. and Spurdle, A. B. and Beesley, J. and Chen, X. and Healey, S. and Neuhausen, S. L. and Ding, Y. C. and Couch, F. J. and Wang, X. and Lindor, N. and Manoukian, S. and Barile, M. and Viel, A. and Tizzoni, L. and Szabo, C. I. and Foretova, L. and Zikan, M. and Claes, K. and Greene, M. H. and Mai, P. and Rennert, G. and Lejbkowicz, F. and Barnett-Griness, O. and Andrulis, I. L. and Ozcelik, H. and Weerasooriya, N. and Gerdes, A-M and Thomassen, M. and Cruger, D. G. and Caligo, M. A. and Friedman, E. and Kaufman, B. and Laitman, Y. and Cohen, S. and Kontorovich, T. and Gershoni-Baruch, R. and Dagan, E. and Jernstrom, H. and Askmalm, M. S. and Arver, B. and Malmer, B. and Domchek, S. M. and Nathanson, K. L. and Brunet, J. and Ramon y Cajal, T. and Yannoukakos, D. and Hamann, U. and Hogervorst, F. B. L. and Verhoef, S. and Gomez Garcia, E. B. and Wijnen, J. T. and van den Ouweland, A. and Easton, D. F. and Peock, S. and Cook, M. and Oliver, C. T. and Frost, D. and Luccarini, C. and Evans, D. G. and Lalloo, F. and Eeles, R. and Pichert, G. and Cook, J. and Hodgson, S. and Morrison, P. J. and Douglas, F. and Godwin, A. K. and Sinilnikova, O. M. and Barjhoux, L. and Stoppa-Lyonnet, D. and Moncoutier, V. and Giraud, S. and Cassini, C. and Olivier-Faivre, L. and Revillion, F. and Peyrat, J-P and Muller, D. and Fricker, J-P and Lynch, H. T. and John, E. M. and Buys, S. and Daly, M. and Hopper, J. L. and Terry, M. B. and Miron, A. and Yassin, Y. and Goldgar, D. and Singer, C. F. and Gschwantler-Kaulich, D. and Pfeiler, G. and Spiess, A-C and Hansen, Thomas v. O. and Johannsson, O. T. and Kirchhoff, T. and Offit, K. and Kosarin, K. and Piedmonte, M. and Rodriguez, G. C. and Wakeley, K. and Boggess, J. F. and Basil, J. and Schwartz, P. E. and Blank, S. V. and Toland, A. E. and Montagna, M. and Casella, C. and Imyanitov, E. N. and Allavena, A. and Schmutzler, R. K. and Versmold, B. and Engel, C. and Meindl, A. and Ditsch, N. and Arnold, N. and Niederacher, D. and Deissler, H. and Fiebig, B. and Varon-Mateeva, R. and Schaefer, D. and Froster, U. G. and Caldes, T. and de la Hoya, M. and McGuffog, L. and Antoniou, A. C. and Nevanlinna, H. and Radice, P. and Benitez, J. (2009) Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA). BRITISH JOURNAL OF CANCER, 101 (12). pp. 2048-2054. ISSN 0007-0920

P

Pasutto, Francesca and Matsumoto, Tomoya and Mardin, Christian Y. and Sticht, Heinrich and Brandstaetter, Johann H. and Michels-Rautenstrauss, Karin and Weisschuh, Nicole and Gramer, Eugen and Ramdas, Wishal D. and van Koolwijk, Leonieke M. E. and Klaver, Caroline C. W. and Vingerling, Johannes R. and Weber, Bernhard H. F. and Kruse, Friedrich E. and Rautenstrauss, Bernd and Barde, Yves-Alain and Reis, Andre (2009) Heterozygous NTF4 Mutations Impairing Neurotrophin-4 Signaling in Patients with Primary Open-Angle Glaucoma. AMERICAN JOURNAL OF HUMAN GENETICS, 85 (4). pp. 447-456. ISSN 0002-9297, 1537-6605

Q

Qi, Jian Hua and Dai, Ganying and Luthert, Philip and Chaurasia, Shyam and Hollyfield, Joe and Weber, Bernhard H. F. and Stoehr, Heidi and Anand-Apte, Bela (2009) S156C Mutation in Tissue Inhibitor of Metalloproteinases-3 Induces Increased Angiogenesis. JOURNAL OF BIOLOGICAL CHEMISTRY, 284 (30). pp. 19927-19936. ISSN 0021-9258, 1083-351X

R

Renner, Agnes B. and Fiebig, Britta S. and Cropp, Elke and Weber, Bernhard H. F. and Kellner, Ulrich (2009) Progression of Retinal Pigment Epithelial Alterations During Long-term Follow-up in Female Carriers of Choroideremia and Report of a Novel CHM Mutation. ARCHIVES OF OPHTHALMOLOGY, 127 (7). pp. 907-912. ISSN 0003-9950, 1538-3601

Renner, Agnes B. and Fiebig, Britta S. and Weber, Bernhard H. F. and Wissinger, Bernd and Andreasson, Sten and Gal, Andreas and Cropp, Elke and Kohl, Susanne and Kellner, Ulrich (2009) Phenotypic Variability and Long-term Follow-up of Patients With Known and Novel PRPH2/RDS Gene Mutations. AMERICAN JOURNAL OF OPHTHALMOLOGY, 147 (3). pp. 518-530. ISSN 0002-9394

Roessler, Erich and El-Jaick, Kenia B. and Dubourg, Christele and Velez, Jorge I. and Solomon, Benjamin D. and Pineda-Alvarez, Daniel E. and Lacbawan, Felicitas and Zhou, Nan and Ouspenskaia, Maia and Paulussen, Aimee and Smeets, Hubert J. and Hehr, Ute and Bendavid, Claude and Bale, Sherri and Odent, Sylvie and David, Veronique and Muenke, Maximilian (2009) The Mutational Spectrum of Holoprosencephaly-Associated Changes within the SHH Gene in Humans Predicts Loss-of-Function Through Either Key Structural Alterations of the Ligand or Its Altered Synthesis. HUMAN MUTATION, 30 (10). E921-E935. ISSN 1059-7794, 1098-1004

Rudnik-Schoeneborn, S. and Hehr, U. and von Kalle, T. and Bornemann, A. and Winkler, J. and Zerres, K. (2009) Andermann Syndrome can be a Phenocopy of Hereditary Motor and Sensory Neuropathy - Report of a Discordant Sibship with a Compound Heterozygous Mutation of the KCC3 Gene. NEUROPEDIATRICS, 40 (3). pp. 129-133. ISSN 0174-304X

S

Schell-Apacik, Chayirn Can and Ertl-Wagner, Birgit and Panzel, Axel and Klausener, Kerstin and Rausch, Gisbert and Muenke, Maximilian and von Voss, Hubertus and Hehr, Ute (2009) Maternally Inherited Heterozygous Sequence Change in the Sonic Hedgehog Gene in a Male Patient with Bilateral Closed-Lip Schizencephaly and Partial Absence of the Corpus Callosum. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 149A (7). pp. 1592-1594. ISSN 1552-4825

Schuele, R. and Schlipf, N. and Synofzik, M. and Klebe, S. and Klimpe, S. and Hehr, U. and Winner, B. and Lindig, T. and Dotzer, A. and Riess, O. and Winkler, J. and Schoels, Ludger and Bauer, P. (2009) Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 80 (12). pp. 1402-1404. ISSN 0022-3050, 1468-330X

Siebzehnrubl, Florian A. and Jeske, Ina and Mueller, Dorit and Buslei, Rolf and Coras, Roland and Hahnen, Eric and Huttner, Hagen B. and Corbeil, Denis and Kaesbauer, Johanna and Appl, Thomas and von Hoersten, Stephan and Bluemcke, Ingmar (2009) Spontaneous In Vitro Transformation of Adult Neural Precursors into Stem-Like Cancer Cells. BRAIN PATHOLOGY, 19 (3). pp. 399-408. ISSN 1015-6305, 1750-3639

Stoecker, Katharina and Weigelt, Karin and Ebert, Stefanie and Karlstetter, Marcus and Walczak, Yana and Langmann, Thomas (2009) Induction of STAP-1 promotes neurotoxic activation of microglia. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 379 (1). pp. 121-126. ISSN 0006-291X, 1090-2104

Stoehr, Heidi and Heisig, Julia B. and Benz, Peter M. and Schoeberl, Simon and Milenkovic, Vladimir M. and Strauss, Olaf and Aartsen, Wendy M. and Wijnholds, Jan and Weber, Bernhard H. F. and Schulz, Heidi L. (2009) TMEM16B, A Novel Protein with Calcium-Dependent Chloride Channel Activity, Associates with a Presynaptic Protein Complex in Photoreceptor Terminals. JOURNAL OF NEUROSCIENCE, 29 (21). pp. 6809-6818. ISSN 0270-6474

T

Tchatchou, Sandrine and Jung, Anke and Hemminki, Kari and Sutter, Christian and Wappenschmidt, Barbara and Bugert, Peter and Weber, Bernhard H. F. and Niederacher, Dieter and Arnold, Norbert and Varon-Mateeva, Raymonda and Ditsch, Nina and Meindl, Alfons and Schmutzler, Rita K. and Bartram, Claus R. and Burwinkel, Barbara (2009) A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women. CARCINOGENESIS, 30 (1). pp. 59-64. ISSN 0143-3334, 1460-2180

U

Uyanik, G. and Hehr, U. (2009) Congenital brain malformations and mental retardation. MEDIZINISCHE GENETIK, 21 (2). pp. 217-223. ISSN 1863-5490

V

Voellner, Florian and Ernst, Wolfgang and Driemel, Oliver and Morsczeck, Christian (2009) A two-step strategy for neuronal differentiation in vitro of human dental follicle cells. DIFFERENTIATION, 77 (5). pp. 433-441. ISSN 0301-4681, 1432-0436

W

Weigelt, Karin and Lichtinger, Monika and Rehli, Michael and Langmann, Thomas (2009) Transcriptomic profiling identifies a PU.1 regulatory network in macrophages. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 380 (2). pp. 308-312. ISSN 0006-291X, 1090-2104

Wieczorek, Dagmar and Gener, Blanca and Martinez Gonzalez, Ma Jesus and Seland, Saskia and Fischer, Sven and Hehr, Ute and Kuechler, Alma and Hoefsloot, Lies H. and de Leeuw, Nicole and Gillessen-Kaesbach, Gabriele and Lohmann, Dietmar R. (2009) Microcephaly, Microtia, Preauricular Tags, Choanal Atresia and Developmental Delay in Three Unrelated Patients: A Mandibulofacial Dysostosis Distinct From Treacher Collins Syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 149A (5). pp. 837-843. ISSN 1552-4825

Y

Yang, Rongxi and Chen, Bowang and Hemminki, Kari and Wappenschmidt, Barbara and Engel, Christoph and Sutter, Christian and Ditsch, Nina and Weber, Bernhard H. F. and Niederacher, Dieter and Arnold, Norbert and Meindl, Alfons and Bartram, Claus R. and Schmutzler, Rita K. and Burwinkel, Barbara (2009) Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk. BREAST CANCER RESEARCH AND TREATMENT, 118 (2). pp. 407-413. ISSN 0167-6806

Yis, Uluc and Uyanik, Goekhan and Kurul, Semra Hiz and Cakmakci, Handan and Ozer, Erdener and Dirik, Eray and Hehr, Ute and Morris-Rosendahl, Deborah J. (2009) Evaluation of cases with congenital muscular dystrophy. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, 44 (1). pp. 23-28. ISSN 1306-0015