Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Gregory J. Hogan"'
Autor:
Valentina S. Vysotskaia, Gregory J. Hogan, Genevieve M. Gould, Xin Wang, Alex D. Robertson, Kevin R. Haas, Mark R. Theilmann, Lindsay Spurka, Peter V. Grauman, Henry H. Lai, Diana Jeon, Genevieve Haliburton, Matt Leggett, Clement S. Chu, Kevin Iori, Jared R. Maguire, Kaylene Ready, Eric A. Evans, Hyunseok P. Kang, Imran S. Haque
Publikováno v:
PeerJ, Vol 5, p e3046 (2017)
The past two decades have brought many important advances in our understanding of the hereditary susceptibility to cancer. Numerous studies have provided convincing evidence that identification of germline mutations associated with hereditary cancer
Externí odkaz:
https://doaj.org/article/2583b6401d394609b0e50fd51a04e636
Publikováno v:
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-13 (2018)
Abstract Background Noninvasive prenatal screening (NIPS) of common aneuploidies using cell-free DNA from maternal plasma is part of routine prenatal care and is widely used in both high-risk and low-risk patient populations. High specificity is need
Externí odkaz:
https://doaj.org/article/29f1a9ad1aa64382bcd4ecb370351db3
Autor:
Genevieve M Gould, Peter V Grauman, Mark R Theilmann, Lindsay Spurka, Irving E Wang, Laura M Melroy, Robert G Chin, Dustin H Hite, Clement S Chu, Jared R Maguire, Gregory J Hogan, Dale Muzzey
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-13 (2018)
Abstract Background Hereditary cancer screening (HCS) for germline variants in the 3′ exons of PMS2, a mismatch repair gene implicated in Lynch syndrome, is technically challenging due to homology with its pseudogene PMS2CL. Sequences of PMS2 and P
Externí odkaz:
https://doaj.org/article/ccfcf68da84140cda2157d12caa3e872
Autor:
David M. Kurtz, Sairah Ahmed, Cheuk Ka Tong, Matthew Mei, Cliff Ding, Ian W. Flinn, Peter A. Riedell, Gregory J. Hogan, Andre Schultz, Jacob J. Chabon, Helen E. Heslop, Aung Myo, Ash A. Alizadeh, Ivan D. Horak
Publikováno v:
Blood. 140:2378-2380
Autor:
Ryan C, Lynch, Christina, Poh, Chaitra S, Ujjani, Edus H, Warren, Stephen D, Smith, Mazyar, Shadman, Karolyn, Morris, Sydney, Lee, Heather, Rasmussen, Susan, Ottemiller, Megan, Shelby, Sarith, Keo, Kaitlin, Verni, David M, Kurtz, Ash A, Alizadeh, Jacob J, Chabon, Gregory J, Hogan, Andre, Schulz, Theodore A, Gooley, Jenna M, Voutsinas, Ajay K, Gopal
Publikováno v:
Blood advances.
The POLARIX trial demonstrated the superiority of polatuzumab vedotin (Pola) over vincristine in the R-CHOP regimen for large B-cell lymphomas, but it is unknown if Pola can be safely incorporated into intensified regimens (eg. DA-EPOCH-R) typically
Autor:
David M. Kurtz, Gregory J. Hogan, Andre Schultz, Katerina Kopeckova, Christian Kuffer, Derek Blair, Steve Wagner, Sandra Close, Maximilian Diehn, Jacob J. Chabon, Ash A. Alizadeh, Jason Westin
Publikováno v:
Blood. 140:3498-3499
Autor:
Mark Roschewski, David M. Kurtz, Jason Westin, Ryan C. Lynch, Charles Macaulay, Christian Kuffer, Gregory J. Hogan, Sandra Close, Jacob J. Chabon, Davide Rossi, Maximilian Diehn, Ash A. Alizadeh, Andre Schultz
Publikováno v:
Blood. 140:785-786
Publikováno v:
PLoS Biology, Vol 13, Iss 11, p e1002307 (2015)
Reprogramming of a gene's expression pattern by acquisition and loss of sequences recognized by specific regulatory RNA binding proteins may be a major mechanism in the evolution of biological regulatory programs. We identified that RNA targets of Pu
Externí odkaz:
https://doaj.org/article/f801b619ef1847ffa7a53787c1f7f26c
Publikováno v:
eLife, Vol 3 (2014)
During translation elongation, the ribosome ratchets along its mRNA template, incorporating each new amino acid and translocating from one codon to the next. The elongation cycle requires dramatic structural rearrangements of the ribosome. We show he
Externí odkaz:
https://doaj.org/article/6e33282401d741e08168d4b16492a00e
Publikováno v:
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-13 (2018)
BMC Medical Genomics
BMC Medical Genomics
Background Noninvasive prenatal screening (NIPS) of common aneuploidies using cell-free DNA from maternal plasma is part of routine prenatal care and is widely used in both high-risk and low-risk patient populations. High specificity is needed for cl