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1. Indirect study of the stellar Ar 34 (α,p) K 37 reaction rate through Ca 40 (p,t) Ca 38 reaction measurements
by Long, A.M and Adachi, T and Beard, M and Berg, G.P.A and Buthelezi, Z and Carter, J and Couder, M and Deboer, R.J and Fearick, R.W and Förtsch, S.V and Görres, J and Mira, J.P and Murray, S.H.T and Neveling, R and Papka, P and Smit, F.D and Sideras-Haddad, E and Swartz, J.A and Talwar, R and Usman, I.T and Wiescher, M and Van Zyl, J.J and Volya, A
Physical review. C, ISSN 2469-9985, 05/2017, Volume 95, Issue 5
Physical Sciences | Physics, Nuclear | Physics | Science & Technology
Journal Article
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2. Full Text Wavelet signatures of K-splitting of the Isoscalar Giant Quadrupole Resonance in deformed nuclei from high-resolution (p,p′) scattering off 146, 148, 150Nd
by Kureba, C.O and Buthelezi, Z and Carter, J and Cooper, G.R.J and Fearick, R.W and Förtsch, S.V and Jingo, M and Kleinig, W and Krugmann, A and Krumbolz, A.M and Kvasil, J and Mabiala, J and Mira, J.P and Nesterenko, V.O and von Neumann-Cosel, P and Neveling, R and Papka, P and Reinhard, P.-G and Richter, A and Sideras-Haddad, E and Smit, F.D and Steyn, G.F and Swartz, J.A and Tamii, A and Usman, I.T
Physics letters. B, ISSN 0370-2693, 04/2018, Volume 779, pp. 269 - 274
Wavelet analysis | ISGQR K-splitting | 146, 148, 150Nd([formula omitted]) | Semblance analysis | Characteristic energy scales | Nd(p,p
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3. Full Text Wavelet signatures of K-splitting of the Isoscalar Giant Quadrupole Resonance in deformed nuclei from high-resolution ( p, p ') scattering off Nd-146,Nd-148,Nd-150
by Kureba, C. O and Buthelezi, Z and Carter, J and Cooper, G. R. J and Fearick, R. W and Fortsch, S. V and Jingo, M and Kleinig, W and Krugmann, A and Krumbolz, A. M and Kvasil, J and Mabiala, J and Mira, J. P and Nesterenko, V. O and von Neumann-Cosel, P and Neveling, R and Papka, P and Reinhard, P. -G and Richter, A and Sideras-Haddad, E and Smit, F. D and Steyn, G. F and Swartz, J. A and Tamii, A and Usman, I. T
Physics letters. B, ISSN 0370-2693, 04/2018, Volume 779, pp. 269 - 274
Physical Sciences | Physics, Nuclear | Astronomy & Astrophysics | Physics, Particles & Fields | Physics | Science & Technology
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4. Full Text Wavelet signatures of K -splitting of the Isoscalar Giant Quadrupole Resonance in deformed nuclei from high-resolution (p,p ′ ) scattering off 146, 148, 150 Nd
by Von Neumann-Cosel, P and Kureba, C. O and Buthelezi, Z and Carter, J and Cooper, G. R. J and Fearick, R. W and Förtsch, S. V and Jingo, M and Kleinig, W and Krugmann, A and Krumbolz, A. M and Kvasil, J and Mabiala, J and Mira, J. P and Nesterenko, V. O and Neveling, R and Papka, P and Reinhard, P. -G and Richter, A and Sideras-Haddad, E and Smit, F. D and Steyn, G. F and Swartz, J. A and Tamii, A and Usman, I. T
Physics letters B, ISSN 0370-2693, 02/2018
Nuclear Experiment | Semblance analysis | Wavelet analysis | 146, 148, 150 Nd( p,p′ ) | Physics | ISGQR K -splitting | Characteristic energy scales
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5. Full Text Wavelet signatures of K-splitting of the Isoscalar Giant Quadrupole Resonance in deformed nuclei from high-resolution scattering off .sup.146, 148, 150Nd
by Kureba, C.O and Buthelezi, Z and Carter, J and Cooper, G.R.J and Fearick, R.W and Fortsch, S.V and Jingo, M and Kleinig, W and Krugmann, A and Krumbolz, A.M and Kvasil, J and Mabiala, J and Mira, J.P and Nesterenko, V.O and von Neumann-Cosel, P and Neveling, R and Papka, P and Reinhard, P.-G and Richter, A and Sideras-Haddad, E and Smit, F.D and Steyn, G.F and Swartz, J.A and Tamii, A and Usman, I.T
Physics letters. B, ISSN 0370-2693, 04/2018, Volume 779, p. 269
Bisphenol-A | Analysis | Nuclear physics
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6. Full Text Strange-quark contributions to parity-violating asymmetries in the forward G0 electron-proton scattering experiment
by Armstrong, D.S and Arvieux, J and Asaturyan, R and Averett, T and Bailey, S.L and Batigne, G and Beck, D.H and Beise, E.J and Benesch, J and Bimbot, L and Birchall, J and Biselli, A and Bosted, P and Boukobza, E and Breuer, H and Carlini, R and Carr, R and Chant, N and Chao, Y.-C and Chattopadhyay, S and Clark, R and Covrig, S and Cowley, A and Dale, D and Davis, C and Falk, W and Finn, J.M and Forest, T and Franklin, G and Furget, C and Gaskell, D and Grames, J and Griffioen, K.A and Grimm, K and Guillon, B and Guler, H and Hannelius, L and Hasty, R and Allen, A. Hawthorne and Horn, T and Johnston, K and Jones, M and Kammel, P and Kazimi, R and King, P.M and Kolarkar, A and Korkmaz, E and Korsch, W and Kox, S and Kuhn, J and Lachniet, J and Lee, L and Lenoble, J and Liatard, E and Liu, J and Loupias, B and Lung, A and MacLachlan, G.A and Marchand, D and Martin, J.W and McFarlane, K.W and McKee, D.W and McKeown, R.D and Merchez, F and Mkrtchyan, H and Moffit, B and Morlet, M and Nakagawa, I and Nakahara, K and Nakos, M and Neveling, R and Niccolai, S and Ong, S and Page, S and Papavassiliou, V and Pate, S.F and Phillips, S.K and Pitt, M.L and Poelker, M and Porcelli, T.A and Quéméner, G and Quinn, B and Ramsay, W.D and Rauf, A.W and Real, J.-S and Roche, J and Roos, P and Rutledge, G.A and Secrest, J and Simicevic, N and Smith, G.R and Spayde, D.T and Stepanyan, S and Stutzman, M and Sulkosky, V and Tadevosyan, V and Tieulent, R and Van De Wiele, J and Van Oers, W and G0 Collaboration
Physical review letters, ISSN 0031-9007, 08/2005, Volume 95, Issue 9, pp. 092001.1 - 092001.5
Physics, Multidisciplinary | Physical Sciences | Physics | Science & Technology | Exact sciences and technology | Nuclear Experiment | ELECTRON-PROTON INTERACTIONS | WEAK INTERACTIONS | ELECTROMAGNETIC FORM FACTORS | PHYSICS OF ELEMENTARY PARTICLES AND FIELDS | S QUARKS | PROTONS | HYDROGEN | ASYMMETRY | PARITY | SPECTROMETERS | P INVARIANCE | MOMENTUM TRANSFER | INTERFERENCE | CEBAF ACCELERATOR | LIQUIDS
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7. Full Text Complete electric dipole response and the neutron skin in Pb208
by Tamii, A and Poltoratska, I and Von Neumann-Cosel, P and Fujita, Y and Adachi, T and Bertulani, C.A and Carter, J and Dozono, M and Fujita, H and Fujita, K and Hatanaka, K and Ishikawa, D and Itoh, M and Kawabata, T and Kalmykov, Y and Krumbholz, A.M and Litvinova, E and Matsubara, H and Nakanishi, K and Neveling, R and Okamura, H and Ong, H.J and Özel-Tashenov, B and Ponomarev, V.Yu and Richter, A and Rubio, B and Sakaguchi, H and Sakemi, Y and Sasamoto, Y and Shimbara, Y and Shimizu, Y and Smit, F.D and Suzuki, T and Tameshige, Y and Wambach, J and Yamada, R and Yosoi, M and Zenihiro, J
Physical review letters, ISSN 0031-9007, 08/2011, Volume 107, Issue 6
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8. Full Text Complete Electric Dipole Response and the Neutron Skin in Pb-208
by Tamii, A and Poltoratska, I and von Neumann-Cosel, P and Fujita, Y and Adachi, T and Bertulani, C. A and Carter, J and Dozono, M and Fujita, H and Fujita, K and Hatanaka, K and Ishikawa, D and Itoh, M and Kawabata, T and Kalmykov, Y and Krumbholz, A. M and Litvinova, E and Matsubara, H and Nakanishi, K and Neveling, R and Okamura, H and Ong, H. J and Oezel-Tashenov, B and Ponomarev, V. Yu and Richter, A and Rubio, B and Sakaguchi, H and Sakemi, Y and Sasamoto, Y and Shimbara, Y and Shimizu, Y and Smit, F. D and Suzuki, T and Tameshige, Y and Wambach, J and Yamada, R and Yosoi, M and Zenihiro, J
Physical review letters, ISSN 0031-9007, 08/2011, Volume 107, Issue 6
MODES | NUCLEI | EXCITATIONS | RESONANCE | POLARIZATION TRANSFER | SCATTERING | Physics, Multidisciplinary | Physical Sciences | Physics | Science & Technology
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9. Full Text Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
by Meindl, Alfons and Wichmann, Hans E and Niederacher, Dieter and Hartmann, Linda and Schmutzler, Rita K and Kubisch, Christian and Neveling, Kornelia and Deißler, Helmut and Kiechle, Marion and Hellebrand, Heide and Hanenberg, Helmut and Lichtner, Peter and Engel, Christoph and Mathew, Christopher G and Wappenschmidt, Barbara and Erven, Verena and Honisch, Ellen and Schindler, Detlev and Freund, Marcel and Müller-Myhsok, Bertram and Wiek, Constanze and Ramser, Juliane and Kast, Karin and Schaal, Heiner
Nature genetics, ISSN 1061-4036, 05/2010, Volume 42, Issue 5, pp. 410 - 414
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Female genital diseases | Tumors | Genetic Predisposition to Disease | Humans | DNA-Binding Proteins - genetics | Case-Control Studies | Ovarian Neoplasms - genetics | Phenotype | Breast Neoplasms - genetics | Pedigree | Alleles | Germ-Line Mutation | Female | Fanconi Anemia - genetics | Models, Genetic | Mutation | Germany | Genetic susceptibility | Gene mutations | Genetic aspects | Breast cancer | Research | Health aspects | Risk factors | Ovarian cancer | Proteins | Genetics | Genes | Index Medicus
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10. Full Text Germline deletions in the tumour suppressor gene FOCAD are associated with polyposis and colorectal cancer development
by Weren, Robbert DA and Venkatachalam, Ramprasath and Cazier, Jean-Baptiste and Farin, Henner F and Kets, C Marleen and de Voer, Richarda M and Vreede, Lilian and Verwiel, Eugène Tp and van Asseldonk, Monique and Kamping, Eveline J and Kiemeney, Lambertus A and Neveling, Kornelia and Aben, Katja Kh and Carvajal-Carmona, Luis and Nagtegaal, Iris D and Schackert, Hans K and Clevers, Hans and van de Wetering, Marc and Tomlinson, Ian P and Ligtenberg, Marjolijn Jl and Hoogerbrugge, Nicoline and Geurts van Kessel, Ad and Kuiper, Roland P
The Journal of pathology, ISSN 0022-3417, 02/2015, Volume 236, Issue 2, pp. 155 - 164
cancer predisposition | polyposis and colorectal cancer | FOCAD | copy number variation | gene expression | Pathology | Oncology | Life Sciences & Biomedicine | Science & Technology | Tumor Suppressor Proteins - metabolism | Epithelial Cells - metabolism | Colorectal Neoplasms - genetics | Humans | Middle Aged | Male | DNA Copy Number Variations - genetics | Germ-Line Mutation - genetics | Open Reading Frames - genetics | Case-Control Studies | Adenomatous Polyposis Coli - metabolism | Chromosomes, Human, Pair 9 - genetics | Gene Deletion | Tumor Suppressor Proteins - genetics | Adult | Female | Heterozygote | Neoplasm Recurrence, Local - genetics | Adenomatous Polyposis Coli - genetics | Colorectal Neoplasms - metabolism | Gene Expression Regulation, Neoplastic - genetics | Genes | Genomics | Colorectal cancer | Development and progression | Genetic aspects | Tumors | Cancer | Index Medicus | Original Papers | Original Paper
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11. Full Text The Complexity of Controlling Condorcet, Fallback, and k-Veto Elections by Replacing Candidates or Voters
by Neveling, Marc and Rothe, Jörg and Zorn, Roman
06/2020, Lecture Notes in Computer Science, ISBN 303050025X
Book Chapter
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12. Full Text Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy
by Neveling, Kornelia and Martinez-Carrera, Lilian A and Hölker, Irmgard and Heister, Angelien and Verrips, Aad and Hosseini-Barkooie, Seyyed Mohsen and Gilissen, Christian and Vermeer, Sascha and Pennings, Maartje and Meijer, Rowdy and te Riele, Margot and Frijns, Catharina J.M and Suchowersky, Oksana and MacLaren, Linda and Rudnik-Schöneborn, Sabine and Sinke, Richard J and Zerres, Klaus and Lowry, R. Brian and Lemmink, Henny H and Garbes, Lutz and Veltman, Joris A and Schelhaas, Helenius J and Scheffer, Hans and Wirth, Brunhilde
American journal of human genetics, ISSN 0002-9297, 06/2013, Volume 92, Issue 6, pp. 946 - 954
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Child, Preschool | Male | Golgi Apparatus - pathology | Mutation, Missense | Muscular Atrophy, Spinal - genetics | Genes, Dominant | Base Sequence | Conserved Sequence | Adult | Female | Fibroblasts - metabolism | Genetic Linkage | Amino Acid Sequence | Muscular Atrophy, Spinal - metabolism | Genetic Association Studies | Muscular Atrophy, Spinal - congenital | Microtubule-Associated Proteins | Fibroblasts - pathology | Muscular Atrophy, Spinal - pathology | Sequence Analysis, DNA | Carrier Proteins - genetics | Carrier Proteins - metabolism | Pedigree | Golgi Apparatus - metabolism | Polymorphism, Single Nucleotide | HeLa Cells | Proteins | Neuromuscular diseases | Mutation | Insects | Neurons | Deoxyribonucleic acid--DNA | Index Medicus | Report
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13. Full Text A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular coloboma
by Ajmal, Muhammad and Khan, Muhammad Imran and Neveling, Kornelia and Khan, Yar Muhammad and Azam, Maleeha and Waheed, Nadia Khalida and Hamel, Christian P and Ben-Yosef, Tamar and De Baere, Elfride and Koenekoop, Robert K and Collin, Rob W J and Qamar, Raheel and Cremers, Frans P M
Journal of medical genetics, ISSN 0022-2593, 07/2014, Volume 51, Issue 7, pp. 444 - 448
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Coloboma - genetics | RNA Splicing Factors | Retinitis Pigmentosa - genetics | Male | Mutation, Missense | Genes, Recessive | DEAD-box RNA Helicases - genetics | DNA Mutational Analysis | Pedigree | Base Sequence | Female | Polymorphism, Single Nucleotide | Macula Lutea - abnormalities | Genetic Linkage | Causes of | Genetic aspects | Research | Gene mutations | Retinitis pigmentosa | Index Medicus
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14. Full Text Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability
by Kleefstra, Tjitske and Kramer, Jamie M and Neveling, Kornelia and Willemsen, Marjolein H and Koemans, Tom S and Vissers, Lisenka E.L.M and Wissink-Lindhout, Willemijn and Fenckova, Michaela and van den Akker, Willem M.R and Kasri, Nael Nadif and Nillesen, Willy M and Prescott, Trine and Clark, Robin D and Devriendt, Koenraad and van Reeuwijk, Jeroen and de Brouwer, Arjan P.M and Gilissen, Christian and Zhou, Huiqing and Brunner, Han G and Veltman, Joris A and Schenck, Annette and van Bokhoven, Hans
American journal of human genetics, ISSN 0002-9297, 07/2012, Volume 91, Issue 1, pp. 73 - 82
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Psychopathology. Psychiatry | Medical genetics | Intellectual deficiency | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Chromatin | Histone-Lysine N-Methyltransferase - genetics | Drosophila | Epigenesis, Genetic | Humans | Male | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Syndrome | Chromosomal Proteins, Non-Histone - genetics | Intellectual Disability - genetics | SMARCB1 Protein | Animals | Female | Mutation | Infant, Newborn | Intelligence levels | Gene mutations | Intellect | Cognition in children | Causes of | Genetic aspects | Research | Cognition disorders | Neurosciences | Genetic transcription | Methyltransferases | Genes | Proteins | Genotype & phenotype | Epigenetics | Developmental disabilities | Index Medicus
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