Publications | Lund University Publications

1031 – 1040 of 1941

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2014
Mark Clear cell sarcoma of the kidney demonstrates an embryonic signature indicative of a primitive nephrogenic origin.
Karlsson, Jenny ^LU ; Holmquist Mengelbier, Linda ^LU ; Ciornei, Cristina ^LU ; Naranjo, Arlene ; O'Sullivan, Maureen J and Gisselsson Nord, David ^LU (2014) In Genes, Chromosomes and Cancer 53(5). p.381-391
- Contribution to journal › Article
Mark DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
Osorio, Ana ; Milne, Roger L ; Kuchenbaecker, Karoline ; Vaclová, Tereza ; Pita, Guillermo ; Alonso, Rosario ; Peterlongo, Paolo ; Blanco, Ignacio ; de la Hoya, Miguel and Duran, Mercedes , et al. (2014) In PLoS Genetics 10(4).
- Contribution to journal › Article
Mark Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
Lange, Leslie A ; Hu, Youna ; Zhang, He ; Xue, Chenyi ; Schmidt, Ellen M ; Tang, Zheng-Zheng ; Bizon, Chris ; Lange, Ethan M ; Smith, Joshua D and Turner, Emily H , et al. (2014) In American Journal of Human Genetics 94(2). p.233-245
- Contribution to journal › Article
Mark TERT promoter mutations in cancer development.
Heidenreich, Barbara ; Rachakonda, P Sivaramakrishna ; Hemminki, Kari ^LU and Kumar, Rajiv (2014) In Current Opinion in Genetics & Development 24(Dec 20). p.30-37
- Contribution to journal › Article
Mark Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations
Yoneyama, Sachiko ; Guo, Yiran ; Lanktree, Matthew B. ; Barnes, Michael R. ; Elbers, Clara C. ; Karczewski, Konrad J. ; Padmanabhan, Sandosh ; Bauer, Florianne ; Baumert, Jens and Beitelshees, Amber , et al. (2014) In Human Molecular Genetics 23(9). p.2498-2510
- Contribution to journal › Article
Mark Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes.
Sharoyko, Vladimir ^LU ; Abels, Mia ^LU ; Sun, Jiangming ^LU ; Nicholas, Lisa ^LU ; Mollet, Ines ^LU ; Stamenkovic, Jelena ^LU ; Göhring, Isabel ^LU ; Malmgren, Siri ^LU ; Storm, Petter ^LU and Fadista, Joao ^LU , et al. (2014) In Human Molecular Genetics 23(21). p.5733-5749
- Contribution to journal › Article
Mark Performance of Protein Disorder Prediction Programs on Amino Acid Substitutions
Ali, Heidi ; Urolagin, Siddhaling ; Gurarslan, Omer and Vihinen, Mauno ^LU (2014) In Human Mutation 35(7). p.794-804
- Contribution to journal › Scientific review
Mark FTO genetic variants, dietary intake and body mass index: insights from 177 330 individuals.
Qi, Qibin ; Kilpeläinen, Tuomas O ; Downer, Mary K ; Tanaka, Toshiko ; Smith, Caren E ; Sluijs, Ivonne ; Sonestedt, Emily ^LU ; Chu, Audrey Y ; Renström, Frida ^LU and Lin, Xiaochen , et al. (2014) In Human Molecular Genetics 23(25). p.6961-6972
- Contribution to journal › Article
Mark Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma.
Płaszczyca, Anna ; Nilsson, Jenny ^LU ; Magnusson, Linda ^LU ; Brosjö, Otte ; Larsson, Olle ; Vult von Steyern, Fredrik ^LU ; Domanski, Henryk ^LU ; Lilljebjörn, Henrik ^LU ; Fioretos, Thoas ^LU and Tayebwa, Johnbosco ^LU , et al. (2014) In International Journal of Biochemistry & Cell Biology 53(Apr 8). p.475-481
- Contribution to journal › Article
Mark Reply to Heng: Inborn aneuploidy and chromosomal instability
Valind, Anders ^LU and Gisselsson Nord, David ^LU (2014) In Proceedings of the National Academy of Sciences 111(11). p.973-973
- Contribution to journal › Letter

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