HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours von Howell, V M, Haven, C J, Kahnoski, K, Khoo, S K, Petillo, D, Chen, J, Fleuren, G J, Robinson, B G, Delbridge, L W, Philips, J, Nelson, A E, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D J, Morreau, H, Teh, B T

Volltext

Clinical and genetic studies of Birt-Hogg-Dubé syndrome von Khoo, S K, Giraud, S, Kahnoski, K, Chen, J, Motorna, O, Nickolov, R, Binet, O, Lambert, D, Friedel, J, Lévy, R, Ferlicot, S, Wolkenstein, P, Hammel, P, Bergerheim, U, Hedblad, M-A, Bradley, M, Teh, B T, Nordenskjöld, M, Richard, S

Volltext

Hyperparathyroidism‐jaw tumour syndrome von Chen, J. D., Morrison, C., Zhang, C., Kahnoski, K., Carpten, J. D., Teh, B. T.

Volltext

Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP) von Villablanca, A, Calender, A, Forsberg, L, Höög, A, Cheng, J-D, Petillo, D, Bauters, C, Kahnoski, K, Ebeling, T, Salmela, P, Richardson, A-L, Delbridge, L, Meyrier, A, Proye, C, Carpten, J D, Teh, B T, Robinson, B G, Larsson, C

Volltext

Alterations of the Birt-Hogg-Dubé gene (BHD) in sporadic colorectal tumours von Kahnoski, K, Khoo, S K, Nassif, N T, Chen, J, Lobo, G P, Segelov, E, Teh, B T

Volltext

Inactivation of BHD in sporadic renal tumors von SOK KEAN KHOO, KAHNOSKI, Katherine, NORDENSKJÖLD, Magnus, BIN TEAN TEH, SUGIMURA, Jun, PETILLO, David, JINDONG CHEN, SHOCKLEY, Ken, LUDLOW, John, KNAPP, Robert, GIRAUD, Sophie, RICHARD, Stéphane

Volltext

Alterations of the Birt-Hogg-Dube gene von Kahnoski, K, Khoo, S.K, Nassif, N.T, Chen, J, Lobo, G.P, Segelov, E, Teh, B.T

Volltext

Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP) -: art. no. e32 von Villablanca, A, Calender, A, Forsberg, L, Höög, A, Cheng, JD, Petillo, D, Bauters, C, Kahnoski, K, Ebeling, T, Salmela, P

Volltext

Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome von Teh, B T, Howell, V M, Haven, C J, Kahnoski, K, Khoo, S K, Petillo, D, Chen, J, Fleuren, G J, Robinson, B G, Delbridge, L W, Philips, J, Nelson, A E, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D J, Morreau, H

Volltext

Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome von Teh, B T, Howell, V M, Haven, C J, Kahnoski, K, Khoo, S K, Petillo, D, Chen, J, Fleuren, G J, Robinson, B G, Delbridge, L W, Philips, J, Nelson, A E, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D J, Morreau, H

Volltext

Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome von Teh, B T, Howell, V M, Haven, C J, Kahnoski, K, Khoo, S K, Petillo, D, Chen, J, Fleuren, G J, Robinson, B G, Delbridge, L W, Philips, J, Nelson, A E, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D J, Morreau, H

Volltext

Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome von Teh, B T, Howell, V M, Haven, C J, Kahnoski, K, Khoo, S K, Petillo, D, Chen, J, Fleuren, G J, Robinson, B G, Delbridge, L W, Philips, J, Nelson, A E, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D J, Morreau, H

Volltext

Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome von Teh, B T, Howell, V M, Haven, C J, Kahnoski, K, Khoo, S K, Petillo, D, Chen, J, Fleuren, G J, Robinson, B G, Delbridge, L W, Philips, J, Nelson, A E, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D J, Morreau, H

Volltext

Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome von Teh, B T, Howell, V M, Haven, C J, Kahnoski, K, Khoo, S K, Petillo, D, Chen, J, Fleuren, G J, Robinson, B G, Delbridge, L W, Philips, J, Nelson, A E, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D J, Morreau, H

Volltext

Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome von Teh, B T, Howell, V M, Haven, C J, Kahnoski, K, Khoo, S K, Petillo, D, Chen, J, Fleuren, G J, Robinson, B G, Delbridge, L W, Philips, J, Nelson, A E, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D J, Morreau, H

Volltext

Clinical and genetic studies of Brit-Hogg-Dube syndrome (vol 39, pg 906, 2002) von Khoo, SK, Giraud, S, Kahnoski, K, Chen, J, Motorna, O, Nickolov, R, Binet, O, Lambert, D, Friedel, J, Levy, R, Ferlicot, S, Wolkenstein, P, Hammel, P, Bergerhein, U, Hedblad, MA, Bradley, M, Teh, BT, Nordenskjold, M, Richard, S

Volltext

Clinical and genetic studies of Brit-Hogg-Dube syndrome (vol 39, pg 906, 2002) von Khoo, SK, Giraud, S, Kahnoski, K, Chen, J, Motorna, O, Nickolov, R, Binet, O, Lambert, D, Friedel, J, Levy, R

Volltext

Comprehensive Molecular Characterization of Muscle-Invasive Bladder Cancer von Kim, Jaegil, Bellmunt, Joaquim, Cherniack, Andrew D., Hinoue, Toshinori, Hoadley, Katherine A., Gibb, Ewan A., Shukla, Sachet A., Sanchez-Vega, Francisco, Reuter, Victor E., Sadeghi, Sara, Pedamallu, Chandra Sekhar, Lu, Yiling, Klimczak, Leszek J., Zhang, Jiexin, Choo, Caleb, Leraas, Kristen M., Lichtenberg, Tara M., Schultz, Nicholaus, Getz, Gad, Mills, Gordon B., Al-Ahmadie, Hikmat, Alexopoulou, Iakovina, Ally, Adrian, Beaver, Allison, Bellmunt, Joaquim, Boice, Lori, Bootwalla, Moiz S., Bowen, Jay, Brooks, Denise, Broom, Bradley M., Bshara, Wiam, Bullman, Susan, Burks, Eric, Carvalho, Benilton S., Carvalho, Andre L., Castro, Mauro A.A., Chagas, Vinicius S., Cherniack, Andrew D., Cortessis, Victoria K., Czerniak, Bogdan A., Daneshmand, Siamak, Dhalla, Noreen, Egea, Sophie C., Engel, Jay, Felau, Ina, Gastier-Foster, Julie M., Getz, Gad, Gordenin, Dmitry A., Hansel, Donna E., Harr, Jodi, Hartmann, Arndt, Hinoue, Toshinori, Jones, Steven J.M., Kahnoski, Richard J., Kasaian, Katayoon, Lai, Phillip H., Lane, Brian R., Liu, Jia, Lolla, Laxmi, Lotan, Yair, Lu, Yiling, Lucchesi, Fabiano R., Mallery, David, Marra, Marco A., Mills, Gordon B., Mungall, Karen L., Ojesina, Akinyemi I., Parekh, Dipen J., Sekhar Pedamallu, Chandra, Pihl, Todd, Rathmell, W. Kimryn, Robertson, A. Gordon, Sadeghi, Sara, Saller, Charles, Salner, Andrew, Sanchez-Vega, Francisco, Scapulatempo-Neto, Cristovam, Schuckman, Anne K., Shukla, Sachet A., Simko, Jeff, Sipahimalani, Payal, Sorcini, Andrea, Stoehr, Robert, Su, Xiaoping, Tarnuzzer, Roy, Thiessen, Nina, Thorne, Leigh, Tse, Kane, Wach, Sven, Wang, Zhining, Weinstein, John N., Wise, Lisa, Wong, Tina, Wu, Ye, Zach, Leigh Anne, Zenklusen, Jean C., Zhang, Jiashan (Julia), Zhang, Jiexin, Zwarthoff, Ellen C., Weinstein, John N.

Volltext

A molecular classification of papillary renal cell carcinoma von YANG, Ximing J, TAN, Min-Han, KANAYAMA, Hiro-Omi, PUAY HOON TAN, BIN SING TEH, CHUNYAN LUAN, WANG, Kim, PINS, Michael, TRETIAKOVA, Maria, ANEMA, John, KAHNOSKI, Richard, NICOL, Theresa, KIM, Hyung L, STADLER, Walter, VOGELZANG, Nicholas G, AMATO, Robert, SELIGSON, David, FIGLIN, Robert, BELLDEGRUN, Arie, ROGERS, Craig G, BIN TEAN TEH, DITLEV, Jonathon A, BETTEN, Mark W, PNG, Carolina E, KORT, Eric J, FUTAMI, Kunihiko, FURGE, Kyle A, TAKAHASHI, Masayuki

Volltext

Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma von Machiela, Mitchell J., Hofmann, Jonathan N., Carreras-Torres, Robert, Brown, Kevin M., Johansson, Mattias, Wang, Zhaoming, Foll, Matthieu, Li, Peng, Rothman, Nathaniel, McKay, James D., Ye, Yuanqing, Henrion, Marc, Bruinsma, Fiona, Jordan, Susan, Severi, Gianluca, Hveem, Kristian, Vatten, Lars J., Larsson, Susanna C., Wolk, Alicja, Banks, Rosamonde E., Selby, Peter J., Easton, Douglas F., Pharoah, Paul, Andreotti, Gabriella, Freeman, Laura E. Beane, Albanes, Demetrius, Mannisto, Satu, Weinstein, Stephanie, Edwards, Todd E., Lipworth, Loren, Gapstur, Susan M., Stevens, Victoria L., Carol, Hallie, Freedman, Matthew L., Cho, Eunyoung, Kraft, Peter, Preston, Mark A., Wilson, Kathryn M., Gaziano, J. Michael, Sesso, Howard S., Freedman, Neal D., Huang, Wen-Yi, Anema, John G., Kahnoski, Richard J., Lane, Brian R., Noyes, Sabrina L., Petillo, David, Colli, Leandro M., Sampson, Joshua N., Besse, Celine, Blanche, Helene, Boland, Anne, Burdette, Laurie, Prokhortchouk, Egor, Skryabin, Konstantin G., Mijuskovic, Mirjana, Ognjanovic, Miodrag, Foretova, Lenka, Holcatova, Ivana, Janout, Vladimir, Mates, Dana, Mukeriya, Anush, Rascu, Stefan, Zaridze, David, Bencko, Vladimir, Cybulski, Cezary, Fabianova, Eleonora, Jinga, Viorel, Lissowska, Jolanta, Lubinski, Jan, Navratilova, Marie, Rudnai, Peter, Szeszenia-Dabrowska, Neonila, Benhamou, Simone, Cancel-Tassin, Geraldine, Cussenot, Olivier, Bueno-de-Mesquita, H. Bas, Canzian, Federico, Duell, Eric J., Sitaram, Raviprakash T., Peters, Ulrike, White, Emily, Anderson, Garnet L., Johnson, Lisa, Luo, Juhua, Buring, Julie, Lee, I-Min, Chow, Wong-Ho, Wood, Christopher, Eisen, Timothy, Larkin, James, Choueiri, Toni K., Lathrop, G. Mark, Teh, Bin Tean, Deleuze, Jean-Francois, Wu, Xifeng, Houlston, Richard S., Chanock, Stephen J., Scelo, Ghislaine, Purdue, Mark P.

Volltext