Zobrazeno 1 - 9
of 9
pro vyhledávání: '"A B Chowdry"'
Autor:
Joyce Y Tung, Chuong B Do, David A Hinds, Amy K Kiefer, J Michael Macpherson, Arnab B Chowdry, Uta Francke, Brian T Naughton, Joanna L Mountain, Anne Wojcicki, Nicholas Eriksson
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23473 (2011)
While the cost and speed of generating genomic data have come down dramatically in recent years, the slow pace of collecting medical data for large cohorts continues to hamper genetic research. Here we evaluate a novel online framework for obtaining
Externí odkaz:
https://doaj.org/article/6b0856aecd7845b09963675ce77be0ce
Autor:
Iain Comerford, Tracy M. Handel, Shaun R. McColl, Catherina L. Salanga, Melinda S. Hanes, Arnab B. Chowdry, Irina Kufareva
Publikováno v:
The Journal of biological chemistry, vol 290, iss 37
The chemokine CXCL12 and its G protein-coupled receptors CXCR4 and ACKR3 are implicated in cancer and inflammatory and autoimmune disorders and are targets of numerous antagonist discovery efforts. Here, we describe a series of novel, high affinity C
Autor:
Fernando R. Clemente, Jason DeChancie, K. N. Houk, T. M. Handel,† and, Hakan Gunaydin, Adam J.T. Smith, Arnab B. Chowdry, Xiyun Zhang
Publikováno v:
The Journal of Organic Chemistry. 73:889-899
The design of active sites has been carried out using quantum mechanical calculations to predict the rate-determining transition state of a desired reaction in presence of the optimal arrangement of catalytic functional groups (theozyme). Eleven vers
Autor:
Kimberly A. Reynolds, Mark Voorhies, Melinda S. Hanes, Tracy M. Handel, Navin Pokala, Arnab B. Chowdry
Publikováno v:
Journal of Computational Chemistry. 28:2378-2388
Recent advances in computational protein design have established it as a viable technique for the rational generation of stable protein sequences, novel protein folds, and even enzymatic activity. We present a new and object-oriented library of code,
Autor:
William A. Paznekas, C E Burgess, Laura Kasch, A E Wandstrat, Robert E. Shapiro, A B Chowdry, Ethylin Wang Jabs, M Schalling, Simeon A. Boyadjiev, Bernd Wollnik, J W Choi, Michael Lovett, G Zhang
Publikováno v:
Cytogenetic and Genome Research. 98:29-37
Oculodentodigital dysplasia (ODDD) is an autosomal dominant condition with congenital anomalies of the craniofacial and limb regions and neurodegeneration. Genetic anticipation for the dysmorphic and neurologic features has been inferred in a few fam
Autor:
Joyce Y. Tung, Chuong B. Do, David A. Hinds, Amy K. Kiefer, J. Michael Macpherson, Arnab B. Chowdry, Uta Francke, Brian T. Naughton, Joanna L. Naughton, Anne Wojcicki, Nicholas Eriksson
Publikováno v:
Nature Precedings
While the cost and speed of generating genomic data have come down dramatically in recent years, the slow pace of collecting medical data for large cohorts continues to hamper genetic research. Here we evaluate a novel online framework for amassing l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______984::78db6fb08164b25e57d031f5e3462581
http://hdl.handle.net/10101/npre.2011.6014.1
http://hdl.handle.net/10101/npre.2011.6014.1
Autor:
Arnab B. Chowdry, Anne Wojcicki, J. Michael Macpherson, Joyce Y. Tung, Uta Francke, Amy K. Kiefer, Joanna Naughton, Chuong B. Do, Brian Thomas Naughton, David A. Hinds, Nicholas Eriksson
Publikováno v:
Nature Precedings.
While the cost and speed of generating genomic data have come down dramatically in recent years, the slow pace of collecting medical data for large cohorts continues to hamper genetic research. Here we evaluate a novel online framework for amassing l
Autor:
Nicholas Eriksson, Brian Thomas Naughton, Arnab B. Chowdry, Anne Wojcicki, Amy K. Kiefer, Uta Francke, J. Michael Macpherson, Joyce Y. Tung, Joanna L. Mountain, David A. Hinds, Chuong B. Do
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 8, p e23473 (2011)
Nature Precedings
PLoS ONE, Vol 6, Iss 8, p e23473 (2011)
Nature Precedings
While the cost and speed of generating genomic data have come down dramatically in recent years, the slow pace of collecting medical data for large cohorts continues to hamper genetic research. Here we evaluate a novel online framework for obtaining
Autor:
Ethylin Wang Jabs, Ralph S. Lachman, Cristina M. Justice, Monzer Jabak, Simeon A. Boyadjiev, Johan Zwaan, Wafaa Eyaid, Arnab B. Chowdry, Victor A. McKusick, Alexander F. Wilson
Publikováno v:
Human genetics. 113(1)
We describe a new dysmorphic syndrome in an inbred Saudi Arabian family with 21 members. Five males and one female have similar craniofacial features including wide open calvarial sutures with large and late-closing anterior fontanels, frontal bossin