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L Badano

Showing results (81-90 of 88) with videos related to

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Scientific Reports|August 5, 2018
Coherent THz Emission Enhanced by Coherent Synchrotron Radiation WakefieldS Di Mitri, A Perucchi, N Adhlakha, et al.
Nature|October 2, 2003
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndromeStephen 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 diseaseLoïc 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 transportOliver 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 syndromeYanli Fan, Muneer A Esmail, Stephen J Ansley, et al.
Nature Genetics|April 1, 2005
A manually curated functional annotation of the human X chromosomeH C Harsha, Shubha Suresh, Ramars Amanchy, et al.
Journal of Synchrotron Radiation|May 2, 2015
The FERMI free-electron lasersE 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 locusCorinne Stoetzel, Virginie Laurier, Erica E Davis, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 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 WakefieldS Di Mitri, A Perucchi, N Adhlakha, et al.
Nature|October 2, 2003
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndromeStephen 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 diseaseLoïc 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 transportOliver 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 syndromeYanli Fan, Muneer A Esmail, Stephen J Ansley, et al.
Nature Genetics|April 1, 2005
A manually curated functional annotation of the human X chromosomeH C Harsha, Shubha Suresh, Ramars Amanchy, et al.
Journal of Synchrotron Radiation|May 2, 2015
The FERMI free-electron lasersE 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 locusCorinne Stoetzel, Virginie Laurier, Erica E Davis, et al.
Pageof 9