Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Joseph Boland"'
Autor:
Robert D. Burk, Joseph Boland, Meredith Yeager, Michael Cullen, Jason Mitchell, Nicolas Wentzensen, Michael Dean, David Roberson, Enrique Alvirez, Eduardo Gharzouzi, Mark Schiffman, Lena Diaw, Lisa Mirabello, Hong Lou, Edmundo Torres-Gonzalez, Lisa Garland, Weiyin Zhou, Mia Steinberg, Anaseidy Albanez, Sara Bass
Publikováno v:
Cancer Res
Human papillomavirus (HPV) 16 displays substantial sequence variation; four HPV16 lineages (A, B, C, and D) have been described as well as multiple sublineages. To identify molecular events associated with HPV16 carcinogenesis, we evaluated viral var
Autor:
Edmundo Torres-Gonzalez, Lisa Mirabello, Enrique Alvirez, Mark Schiffman, Anaseidy Albanez, Sara Bass, Jason Mitchell, Michael Cullen, Lisa Garland, Hong Lou, Nicolas Wentzensen, Eduardo Gharzouzi, Weiyin Zhou, Michael Dean, David Roberson, Mia Steinberg, Lena Diaw, Robert D. Burk, Joseph Boland, Meredith Yeager
Human papillomavirus (HPV) 16 displays substantial sequence variation; four HPV16 lineages (A, B, C, D) have been described, as well as multiple sub-lineages. To identify molecular events associated with HPV16 carcinogenesis we evaluated viral variat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6c98030f9a68dfcc34b4d5f3f470e3a
Autor:
S Bass, Alexander Pemov, Settara C. Chandrasekharappa, Abdel G. Elkahloun, Douglas R. Stewart, Hua Li, Jim C. Mullikin, Nancy F. Hansen, Stephen W. Hartley, Joseph Boland, Jun Wei, Brigitte C. Widemann, Javed Khan, Sivasish Sindiri, Margaret R. Wallace, Rajesh Patidar
Publikováno v:
Oncogene. 36:3168-3177
Neurofibromatosis type 1 (NF1) is a common tumor-predisposition disorder due to germline mutations in the tumor suppressor gene NF1 A virtually pathognomonic finding of NF1 is the plexiform neurofibroma (PN), a benign, likely congenital tumor that ar
Autor:
Wen-Qing Li, Stephen J. Chanock, Michael Cullen, Alisa M. Goldstein, Laurie Burdette, Dilys M. Parry, Norbert J. Liebsch, Paula L. Hyland, Meredith Yeager, Melissa Rotunno, David A. Alcorta, Joseph Boland, Ji He, Bari J. Ballew, Xiaohong R. Yang, Jason Mitchell, David Roberson, Jianxin Shi, Sara Bass, Michael J. Kelley
Publikováno v:
Human Genetics. 133:1289-1297
Chordoma is a rare bone cancer that is believed to originate from notochordal remnants. We previously identified germline T duplication as a major susceptibility mechanism in several chordoma families. Recently, a common genetic variant in T (rs23050
Autor:
Jarmo Virtamo, Laura Burdett, Robert N. Hoover, Gilles Thomas, Kevin B. Jacobs, Kerry A. Pettigrew, Zhaoming Wang, W. Ryan Diver, Geraldine Cancel-Tassin, Laufey T. Amundadottir, Sonja I. Berndt, Irene Collins, Hemang Parikh, Jinping Jia, Stephen J. Chanock, Olivier Cussenot, Demetrius Albanes, Joshua N. Sampson, Thomas J. Albert, Sarah E. Daugherty, Amy Hutchinson, Kristian Hveem, Lars J. Vatten, Heather Spencer Feigelson, Meredith Yeager, Antoine Valeri, Inger Njølstad, Michael J. Thun, Joseph Boland, Liqun Qi, Michael Cullen, Nilanjan Chatterjee, David J. Hunter, Richard B. Hayes
Publikováno v:
Human Genetics
Measurements of serum prostate-specific antigen (PSA) protein levels form the basis for a widely used test to screen men for prostate cancer. Germline variants in the gene that encodes the PSA protein (KLK3) have been shown to be associated with both
Autor:
Ana Patiño-García, Lisa Mirabello, Xijun Zhang, Aurelie Vogt, Joseph Boland, Richard Gorlick, Luis Sierrasesúmaga, Fernando Lecanda, Jay S. Wunder, Donald A. Barkauskas, Phuong L. Mai, Irene L. Andrulis, Nalan Gokgoz, Kristine Jones, Meredith Yeager, Sharon A. Savage, Stephen J. Chanock, Chand Khanna, Julie M. Gastier-Foster
Publikováno v:
Journal of the National Cancer Institute. 107(7)
The etiologic contribution of germline genetic variation to sporadic osteosarcoma is not well understood. Osteosarcoma is a sentinel cancer of Li-Fraumeni syndrome (LFS), in which approximately 70% of families meeting the classic criteria have germli
Autor:
Eric Legius, Javed Khan, Settara C. Chandrasekharappa, Alexander Pemov, Nancy F. Hansen, Douglas R. Stewart, Brigitte C. Widemann, Christine Higham, Joseph Boland, Rajesh Patidar, Eva Dombi, Margaret R. Wallace, James C. Mullikin
Publikováno v:
Cancer Research. 77:1456-1456
BACKGROUND: Neurofibromatosis type 1 (NF1) is a genetic tumor predisposition disorder caused by germline mutations in tumor suppressor NF1. Plexiform neurofibromas (PN) are benign tumors that arise prenatally or early in childhood and affect 30-50% o
Autor:
Sharon A. Savage, Joseph Boland, Leonard I. Zon, Lea Jessop, Jessica M. Humphries, Belynda Hicks, Meredith Yeager, Laurie Burdett, Ji He, Timothy G. Myers, Steven R. Ellis, Lisa Mirabello, Blanche P. Alter, Neelam Giri, Alison M. Taylor, Elizabeth R. Macari, Bari J. Ballew, Katherine E. McGrath
Diamond-Blackfan anemia (DBA) is a cancer-prone inherited bone marrow failure syndrome. Approximately half of DBA patients have a germ-line mutation in a ribosomal protein gene. We used whole-exome sequencing to identify disease-causing genes in 2 la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c8efc2dacb04143f57ac3b903558bf3
https://europepmc.org/articles/PMC4125351/
https://europepmc.org/articles/PMC4125351/
Autor:
Bin Zhu, Sharon A. Savage, Weiyin Zhou, Lisa Mirabello, Frank X. Donovan, Belynda Hicks, Meredith Yeager, Steven R. Ellis, Mingyi Wang, Blanche P. Alter, Settara C. Chandrasekharappa, Neelam Giri, Seth A. Brodie, Kristine Jones, Payal P. Khincha, Joseph Boland
Publikováno v:
Blood. 128:1495-1495
Introduction: Diamond-Blackfan anemia (DBA) is a rare inherited bone marrow failure syndrome (IBMFS) characterized by erythroid hypoplasia. It is associated with a number of congenital anomalies and a high risk of developing specific cancers. DBA is
Autor:
Sharon A. Savage, Meredith Yeager, Neelam Giri, Kevin B. Jacobs, Bari J. Ballew, Joseph Boland, Laurie Burdett, Blanche P. Alter
Dyskeratosis congenita (DC) is an inherited bone marrow failure and cancer predisposition syndrome caused by aberrant telomere biology. The classic triad of dysplastic nails, abnormal skin pigmentation, and oral leukoplakia is diagnostic of DC, but s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c392bf881a4e63b3438192aea6394d1
https://europepmc.org/articles/PMC3600110/
https://europepmc.org/articles/PMC3600110/