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Your search keyword '"Liubchenko, Ludmila"' showing total 5 results
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5 results on '"Liubchenko, Ludmila"'

1. The International Testicular Cancer Linkage Consortium: A clinicopathologic descriptive analysis of 461 familial malignant testicular germ cell tumor kindred

Author

Mai, Phuong L., Friedlander, Michael, Tucker, Kathy, Phillips, Kelly-Anne, Hogg, David, Jewett, Michael A.S., Lohynska, Radka, Daugaard, Gedske, Richard, Stéphane, Bonaïti-Pellié, Catherine, Heidenreich, Axel, Albers, Peter, Bodrogi, Istvan, Geczi, Lajos, Olah, Edith, Daly, Peter A., Guilford, Parry, Fosså, Sophie D., Heimdal, Ketil, Liubchenko, Ludmila, Tjulandin, Sergei A., Stoll, Hans, Weber, Walter, Easton, Douglas F., Dudakia, Darshna, Huddart, Robert, Stratton, Michael R., Einhorn, Lawrence, Korde, Larissa, Nathanson, Katherine L., Bishop, D. Timothy, Rapley, Elizabeth A., and Greene, Mark H.

Published
2010
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2. The Y deletion gr/gr and susceptibility to testicular germ cell tumor

Author

Nathanson, Katherine L., Kanetsky, Peter A., Hawes, Rachel, Vaughn, David J., Letrero, Richard, Tucker, Kathy, Friedlander, Michael, Phillips, Kelly-Anne, Hogg, David, Jewett, Michael A.S., Lohynska, Radka, Daugaard, Gedske, Richard, Stephane, Chompret, Agnes, Bonaiti-Pellie, Catherine, Heidenreich, Axel, Olah, Edith, Geczi, Lajos, Bodrogi, Istvan, Ormiston, Wilma J., Daly, Peter A., Oosterhuis, J. Wolter, Gillis, Ad J.M., Looijenga, Leendert H.J., Guilford, Parry, Fossa, Sophie D., Heimdal, Ketil, Tjulandin, Sergei A., Liubchenko, Ludmila, Stoll, Hans, Weber, Walter, Rudd, Matthew, Huddart, Robert, Crockford, Gillian P., Forman, David, Oliver, D. Timothy, Einhorn, Lawrence, Weber, Barbara L., Kramer, Joan, McMaster, Mary, Greene, Mark H., Pike, Malcolm, Cortessis, Victoria, Chen, Chu, Schwartz, Stephen M., Bishop, D. Timothy, Easton, Douglas F., Stratton, Michael R., and Rapley, Elizabeth A.

Subjects
Germ cell tumors -- Research, Germ cell tumors -- Diagnosis, Germ cell tumors -- Risk factors, Human genetics -- Research, Biological sciences
Published
2005

3. Genome-wide linkage screen for testicular germ cell tumour susceptibility loci

Author

Crockford, Gillian P., Linger, Rachel, Hockley, Sarah, Dudakia, Darshna, Johnson, Lola, Huddart, Robert, Tucker, Kathy, Friedlander, Michael, Phillips, Kelly-Anne, Hogg, David, Jewett, Michael A.S., Lohynska, Radka, Daugaard, Gedske, Richard, Stéphane, Chompret, Agnes, Bonaïti-Pellié, Catherine, Heidenreich, Axel, Albers, Peter, Olah, Edith, Geczi, Lajos, Bodrogi, Istvan, Ormiston, Wilma J., Daly, Peter A., Guilford, Parry, Fosså, Sophie D., Heimdal, Ketil, Tjulandin, Sergei A., Liubchenko, Ludmila, Stoll, Hans, Weber, Walter, Forman, David, Oliver, Timothy, Einhorn, Lawrence, McMaster, Mary, Kramer, Joan, Greene, Mark H., Weber, Barbara L., Nathanson, Katherine L., Cortessis, Victoria, Easton, Douglas F., Bishop, D. Timothy, Stratton, Michael R., and Rapley, Elizabeth A.

Published
2006

4. Analysis of the DNDI gene in men with sporadic and familial testicular germ cell tumors

Author

Linger, Rachel, Dudakia, Darshna, Huddart, Robert, Tucker, Kathy, Friedlander, Michael, Phillips, Kelly-Anne, Hogg, David, Jewett, Michael A. S., Lohynska, Radka, Daugaard, Gedske, Richard, Stephane, Chompret, Agnes, Stoppa-Lyonnet, Dominique, Bonaiti-Pellie, Catherine, Heidenreich, Axel, Albers, Peter, Olah, Edith, Geczi, Lajos, Bodrogi, Istvan, Daly, Peter A., Guilford, Parry, Fossi, Sophie D., Heimdal, Ketil, Tjulandin, Sergei A., Liubchenko, Ludmila, Stoll, Hans, Weber, Walter, Einhorn, Lawrence, McMaster, Mary, Korde, Larissa, Greene, Mark H., Nathanson, Katherine L., Cortessis, Victoria, Easton, Douglas F., Bishop, D. Timothy, Stratton, Michael R., Rapley, Elizabeth A., and University of Groningen

Subjects
RISK, TER MUTATION, DEAD-END, SENSITIVE GEL-ELECTROPHORESIS, SUSCEPTIBILITY, TERATOMAS, CANCER
Abstract

A base substitution in the mouse DndI gene resulting in a truncated Dnd protein has been shown to be responsible for germ cell loss and the development of testicular germ cell tumors (TGCT) in the 129 strain of mice. We investigated the human orthologue of this gene in 263 patients (165 with a family history of TGCT and 98 without) and found a rare heterozygous variant, p. Glu86Ala, in a single case. This variant was not present in control chromosomes (0/4,132). Analysis of the variant in an additional 842 index TGCT cases (269 with a family history of TGCT and 573 without) did not reveal any additional instances. The variant, p. Glu86Ala, is within a known functional domain of DNDI and is highly conserved through evolution. Although the variant may be a rare polymorphism, a change at such a highly conserved residue is characteristic of a disease-causing variant. Whether it is disease-causing or not, mutations in DNDI make, at most, a very small contribution to TGCT susceptibility in adults and adolescents. (c) 2007 Wiley-Liss, Inc.

Published
2008

5. Analysis of the DND1 gene in men with sporadic and familial testicular germ cell tumors.

Author

Linger R, Dudakia D, Huddart R, Tucker K, Friedlander M, Phillips KA, Hogg D, Jewett MA, Lohynska R, Daugaard G, Richard S, Chompret A, Stoppa-Lyonnet D, Bonaïti-Pellié C, Heidenreich A, Albers P, Olah E, Geczi L, Bodrogi I, Daly PA, Guilford P, Fosså SD, Heimdal K, Tjulandin SA, Liubchenko L, Stoll H, Weber W, Einhorn L, McMaster M, Korde L, Greene MH, Nathanson KL, Cortessis V, Easton DF, Bishop DT, Stratton MR, and Rapley EA

Subjects
DNA Mutational Analysis, Family Health, Genetic Predisposition to Disease, Humans, Male, Mutation, Neoplasms, Germ Cell and Embryonal etiology, Polymerase Chain Reaction, Testicular Neoplasms etiology, Neoplasm Proteins genetics, Neoplasms, Germ Cell and Embryonal genetics, Testicular Neoplasms genetics
Abstract

A base substitution in the mouse Dnd1 gene resulting in a truncated Dnd protein has been shown to be responsible for germ cell loss and the development of testicular germ cell tumors (TGCT) in the 129 strain of mice. We investigated the human orthologue of this gene in 263 patients (165 with a family history of TGCT and 98 without) and found a rare heterozygous variant, p. Glu86Ala, in a single case. This variant was not present in control chromosomes (0/4,132). Analysis of the variant in an additional 842 index TGCT cases (269 with a family history of TGCT and 573 without) did not reveal any additional instances. The variant, p. Glu86Ala, is within a known functional domain of DND1 and is highly conserved through evolution. Although the variant may be a rare polymorphism, a change at such a highly conserved residue is characteristic of a disease-causing variant. Whether it is disease-causing or not, mutations in DND1 make, at most, a very small contribution to TGCT susceptibility in adults and adolescents., ((c) 2007 Wiley-Liss, Inc.)

Published
2008
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