Bibliotecas PUC-SP - Busca Integrada

Construction of a long-range physical map of the region containing the spinal muscular atrophy gene /

Por Carpten, John David
Publicado em 1994

High-resolution physical and transcript map of human chromosome 2p21 containing the sitosterolaemia locus

Por Lu, Kangmo, Lee, Mi-Hye, Carpten, John D, Sekhon, Mundeep, Patel, Shailendra B
Publicado em 2001

Confirmation study of prostate cancer risk variants at 8q24 in African Americans identifies a novel risk locus

Por Robbins, Christiane, Torres, Jada Benn, Hooker, Stanley, Bonilla, Carolina, Hernandez, Wenndy, Candreva, Angela, Ahaghotu, Chiledum, Kittles, Rick, Carpten, John
Publicado em 2007

Fine-mapping, mutation analyses, and structural mapping of cerebrotendinous xanthomatosis in U.S. pedigrees

Por Lee, Mi-Hye, Hazard, Starr, Carpten, John D., Yi, Sonia, Cohen, Jonathan, Gerhardt, Glenn T., Salen, Gerald, Patel, Shailendra B.
Publicado em 2001

Molecular subtype analysis determines the association of advanced breast cancer in Egypt with favorable biology

Por DuQuette Rachelle A, Hussain Khateeb H, Berghuis Bree, Gaber Salwa, Ishak Elia A, Tapia Coya, Salhia Bodour, Resau James, Carpten John
Publicado no BMC Women's Health (2011-09-01)

Family-Based Samples Can Play an Important Role in Genetic Association Studies

Por Lange, Ethan M., Sun, Jielin, Lange, Leslie A., Zheng, S. Lilly, Duggan, David, Carpten, John D., Gronberg, Henrik, Isaacs, William B., Xu, Jianfeng, Chang, Bao-Li
Publicado em 2008

The secreted glycoprotein lubricin protects cartilage surfaces and inhibits synovial cell overgrowth

Por Rhee, David K., Marcelino, Jose, Baker, MacArthur, Gong, Yaoqin, Smits, Patrick, Lefebvre, Véronique, Jay, Gregory D., Stewart, Matthew, Wang, Hongwei, Warman, Matthew L., Carpten, John D.
Publicado em 2005

Dynamic structure of the SPANX gene cluster mapped to the prostate cancer susceptibility locus HPCX at Xq27

Por Kouprina, Natalay, Pavlicek, Adam, Noskov, Vladimir N., Solomon, Greg, Otstot, John, Isaacs, William, Carpten, John D., Trent, Jeffrey M., Schleutker, Joanna, Barrett, J. Carl, Jurka, Jerzy, Larionov, Vladimir
Publicado em 2005

Comprehensive molecular profiling of 718 Multiple Myelomas reveals significant differences in mutation frequencies between African and European descent cases

Por Manojlovic, Zarko, Christofferson, Austin, Liang, Winnie S., Aldrich, Jessica, Washington, Megan, Wong, Shukmei, Rohrer, Daniel, Jewell, Scott, Kittles, Rick A., Derome, Mary, Auclair, Daniel, Craig, David Wesley, Keats, Jonathan, Carpten, John D.
Publicado em 2017

Germline Alterations of the RNASEL Gene, a Candidate HPC1 Gene at 1q25, in Patients and Families with Prostate Cancer

Por Rökman, Annika, Ikonen, Tarja, Seppälä, Eija H., Nupponen, Nina, Autio, Ville, Mononen, Nina, Bailey-Wilson, Joan, Trent, Jeffrey, Carpten, John, Matikainen, Mika P., Koivisto, Pasi A., Tammela, Teuvo L. J., Kallioniemi, Olli-P., Schleutker, Johanna
Publicado em 2002

Association between Ag1-CA Alleles and Severity of Autosomal Recessive Proximal Spinal Muscular Atrophy

Por DiDonato, Christine J., Morgan, Kenneth, Carpten, John D., Fuerst, Paul, Ingraham, Susan E., Prescott, Gary, McPherson, John D., Wirth, Brunhilde, Zerres, Klaus, Hurko, Orest, Wasmuth, John J., Mendell, Jerry R., Burghes, Arthur H. M., Simard, Louise R.
Publicado em 1994

Linkage Analyses at the Chromosome 1 Loci 1q24-25 (HPC1), 1q42.2-43 (PCAP), and 1p36 (CAPB) in Families with Hereditary Prostate Cancer

Por Berry, Rebecca, Schaid, Daniel J., Smith, Jeffrey R., French, Amy J., Schroeder, Jennifer J., McDonnell, Shannon K., Peterson, Brett J., Wang, Zheng-Yuan, Carpten, John D., Roberts, Steven G., Tester, David J., Blute, Michael L., Trent, Jeffrey M., Thibodeau, Stephen N.
Publicado em 2000

Association of a germline copy number variation at 2p24.3 and risk for aggressive prostate cancer

Por Liu, Wennuan, Sun, Jishan, Li, Ge, Zhu, Yi, Zhang, Scott, Kim, Seong-Tae, Sun, Jielin, Wiklund, Fredrik, Wiley, Kathleen, Isaacs, Sarah D., Stattin, Pär, Xu, Jianfeng, Duggan, David, Carpten, John D., Isaacs, William B., Grönberg, Henrik, Zheng, S. Lilly, Chang, Bao-Li
Publicado em 2009

Linkage and Association Studies of Prostate Cancer Susceptibility: Evidence for Linkage at 8p22-23

Por Xu, Jianfeng, Zheng, Siqun L., Hawkins, Gregory A., Faith, Dennis A., Kelly, Brian, Isaacs, Sarah D., Wiley, Kathleen E., Chang, Bao-li, Ewing, Charles M., Bujnovszky, Piroska, Carpten, John D., Bleecker, Eugene R., Walsh, Patrick C., Trent, Jeffrey M., Meyers, Deborah A., Isaacs, William B.
Publicado em 2001

Sequence variants at 22q13 are associated with prostate cancer risk

Por Sun, Jielin, Zheng, Siqun Lilly, Wiklund, Fredrik, Isaacs, Sarah D., Li, Ge, Wiley, Kathleen E., Kim, Seong-Tae, Zhu, Yi, Zhang, Zheng, Hsu, Fang-Chi, Turner, Aubrey R., Stattin, Pär, Liu, Wennuan, Kim, Jin Woo, Duggan, David, Carpten, John, Isaacs, William, Grönberg, Henrik, Xu, Jianfeng, Chang, Bao-Li
Publicado em 2009

Evaluation of Linkage and Association of HPC2/ELAC2 in Patients with Familial or Sporadic Prostate Cancer

Por Xu, Jianfeng, Zheng, Siqun L., Carpten, John D., Nupponen, Nina N., Robbins, Christiane M., Mestre, Juanita, Moses,4, Tracy Y., Faith, Dennis A., Kelly, Brian D., Isaacs, Sarah D., Wiley, Kathleen E., Ewing, Charles M., Bujnovszky, Piroska, Chang, Bao-li, Bailey-Wilson, Joan, Bleecker, Eugene R., Walsh, Patrick C., Trent, Jeffrey M., Meyers, Deborah A., Isaacs, William B.
Publicado em 2001

Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk

Por Chang, Bao-Li, Cramer, Scott D., Wiklund, Fredrik, Isaacs, Sarah D., Stevens, Victoria L., Sun, Jielin, Smith, Shelly, Pruett, Kristen, Romero, Lina M., Wiley, Kathleen E., Kim, Seong-Tae, Zhu, Yi, Zhang, Zheng, Hsu, Fang-Chi, Turner, Aubrey R., Adolfsson, Jan, Liu, Wennuan, Kim, Jin Woo, Duggan, David, Carpten, John, Zheng, S. Lilly, Rodriguez, Carmen, Isaacs, William B., Grönberg, Henrik, Xu, Jianfeng
Publicado em 2009

CACP, Encoding a Secreted Proteoglycan, Is Mutated in Camptodactyly- Arthropathy-Coxa Vara-Pericarditis Syndrome

Por Marcelino, Jose, Carpten, John D., Suwairi, Wafaa M., Gutierrez, Orlando M., Schwartz, Stuart, Robbins, Christiane, Sood, Raman, Makalowska, Izabela, Baxevanis, Andy, Johnstone, Brian, Laxer, Ronald M., Zemel, Lawrence, Kim, Chong Ae, Herd, J. Kenneth, Ihle, Johannes, Williams, Cal, Johnson, Mark, Raman, Vidya, Alonso, Luís Garcia, Brunoni, Decio, Gerstein, Amy, Papadopoulos, Nickolas, Bahabri, Sultan A., Trent, Jeffrey M., Warman, Matthew L.
Publicado em 1999

Promiscuous Mutations Activate the Non-Canonical NF-kB Pathway in Multiple Myeloma

Por Keats, Jonathan J., Fonseca, Rafael, Chesi, Marta, Schop, Roelandt, Baker, Angela, Chng, Wee-Joo, Van Wier, Scott, Tiedemann, Rodger, Shi, Chang-Xin, Sebag, Michael, Braggio, Esteban, Henry, Travis, Zhu, Yuan-Xiao, Fogle, Homer, Price-Troska, Tammy, Ahmann, Gregory, Mancini, Catherine, Brents, Leslie A., Kumar, Shaji, Greipp, Philip, Dispenzieri, Angela, Bryant, Barb, Mulligan, George, Bruhn, Laurakay, Barrett, Michael, Valdez, Riccardo, Trent, Jeff, Stewart, A. Keith, Carpten, John, Bergsagel, P. Leif
Publicado em 2007

Compelling Evidence for a Prostate Cancer Gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics

Por Camp, Nicola J., Cannon-Albright, Lisa A., Farnham, James M., Baffoe-Bonnie, Agnes B., George, Asha, Powell, Isaac, Bailey-Wilson, Joan E., Carpten, John D., Giles, Graham G., Hopper, John L., Severi, Gianluca, English, Dallas R., Foulkes, William D., Maehle, Lovise, Moller, Pal, Eeles, Ros, Easton, Douglas, Badzioch, Michael D., Whittemore, Alice S., Oakley-Girvan, Ingrid, Hsieh, Chih-Lin, Dimitrov, Latchezar, Xu, Jianfeng, Stanford, Janet L., Johanneson, Bo, Deutsch, Kerry, McIntosh, Laura, Ostrander, Elaine A., Wiley, Kathleen E., Isaacs, Sarah D., Walsh, Patrick C., Thibodeau, Stephen N., McDonnell, Shannon K., Hebbring, Scott, Schaid, Daniel J., Lange, Ethan M., Cooney, Kathleen A., Tammela, Teuvo L.J., Schleutker, Johanna, Paiss, Thomas, Maier, Christiane, Grönberg, Henrik, Wiklund, Fredrik, Emanuelsson, Monica, Isaacs, William B.
Publicado em 2007