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Scientific Reports
|
August 5, 2018
Coherent THz Emission Enhanced by Coherent Synchrotron Radiation Wakefield
S Di Mitri, A Perucchi, N Adhlakha, et al.
Nature
|
October 2, 2003
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
Stephen J Ansley, Jose L Badano, Oliver E Blacque, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 12, 2009
Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease
Loïc de Pontual, Norann A Zaghloul, Sophie Thomas, et al.
Genes & Development
|
July 3, 2004
Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport
Oliver E Blacque, Michael J Reardon, Chunmei Li, et al.
Nature Genetics
|
August 18, 2004
Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome
Yanli Fan, Muneer A Esmail, Stephen J Ansley, et al.
Nature Genetics
|
April 1, 2005
A manually curated functional annotation of the human X chromosome
H C Harsha, Shubha Suresh, Ramars Amanchy, et al.
Journal of Synchrotron Radiation
|
May 2, 2015
The FERMI free-electron lasers
E Allaria, L Badano, S Bassanese, et al.
Nature Genetics
|
April 4, 2006
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus
Corinne Stoetzel, Virginie Laurier, Erica E Davis, et al.
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Search research articles
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Showing results (81-90 of 88) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 88 results.
Scientific Reports
|
August 5, 2018
Coherent THz Emission Enhanced by Coherent Synchrotron Radiation Wakefield
S Di Mitri, A Perucchi, N Adhlakha, et al.
Nature
|
October 2, 2003
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
Stephen J Ansley, Jose L Badano, Oliver E Blacque, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 12, 2009
Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease
Loïc de Pontual, Norann A Zaghloul, Sophie Thomas, et al.
Genes & Development
|
July 3, 2004
Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport
Oliver E Blacque, Michael J Reardon, Chunmei Li, et al.
Nature Genetics
|
August 18, 2004
Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome
Yanli Fan, Muneer A Esmail, Stephen J Ansley, et al.
Nature Genetics
|
April 1, 2005
A manually curated functional annotation of the human X chromosome
H C Harsha, Shubha Suresh, Ramars Amanchy, et al.
Journal of Synchrotron Radiation
|
May 2, 2015
The FERMI free-electron lasers
E Allaria, L Badano, S Bassanese, et al.
Nature Genetics
|
April 4, 2006
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus
Corinne Stoetzel, Virginie Laurier, Erica E Davis, et al.
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of 9