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Nathan E Hellman

Showing results (1-10 of 10) with videos related to

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Annual Review of Nutrition|June 11, 2002
Ceruloplasmin metabolism and functionNathan E Hellman, Jonathan D Gitlin
The Journal of Biological Chemistry|November 2, 2001
Biochemical analysis of a missense mutation in aceruloplasminemiaNathan E Hellman, Satoshi Kono, Hiroaki Miyajima, et al.
American Journal of Physiology. Renal Physiology|May 19, 2005
Activated extracellular signal-regulated kinases are necessary and sufficient to initiate tubulogenesis in renal tubular MDCK strain I cell cystsNathan E Hellman, Andres J Greco, Katherine K Rogers, et al.
Biochemical and Biophysical Research Communications|January 2, 2007
Intracellular signaling via ERK/MAPK completes the pathway for tubulogenic fibronectin in MDCK cellsZhao Liu, Andres J Greco, Nathan E Hellman, et al.
The Journal of Biological Chemistry|September 28, 2002
Mechanisms of copper incorporation into human ceruloplasminNathan E Hellman, Satoshi Kono, Grazia M Mancini, et al.
The Journal of Biological Chemistry|November 28, 2007
Matrix metalloproteinase 13 (MMP13) and tissue inhibitor of matrix metalloproteinase 1 (TIMP1), regulated by the MAPK pathway, are both necessary for Madin-Darby canine kidney tubulogenesisNathan E Hellman, June Spector, Jonathan Robinson, et al.
Human Molecular Genetics|September 17, 2009
Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6Marion Delous, Nathan E Hellman, Helori-Maël Gaudé, et al.
American Journal of Physiology. Renal Physiology|February 28, 2014
Novel MAPK-dependent and -independent tubulogenes identified via microarray analysis of 3D-cultured Madin-Darby canine kidney cellsMaria F Chacon-Heszele, Xiaofeng Zuo, Nathan E Hellman, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 13, 2010
The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretchNathan E Hellman, Yan Liu, Erin Merkel, et al.
Nature Genetics|June 15, 2007
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndromeMarion Delous, Lekbir Baala, Rémi Salomon, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Annual Review of Nutrition|June 11, 2002
Ceruloplasmin metabolism and functionNathan E Hellman, Jonathan D Gitlin
The Journal of Biological Chemistry|November 2, 2001
Biochemical analysis of a missense mutation in aceruloplasminemiaNathan E Hellman, Satoshi Kono, Hiroaki Miyajima, et al.
American Journal of Physiology. Renal Physiology|May 19, 2005
Activated extracellular signal-regulated kinases are necessary and sufficient to initiate tubulogenesis in renal tubular MDCK strain I cell cystsNathan E Hellman, Andres J Greco, Katherine K Rogers, et al.
Biochemical and Biophysical Research Communications|January 2, 2007
Intracellular signaling via ERK/MAPK completes the pathway for tubulogenic fibronectin in MDCK cellsZhao Liu, Andres J Greco, Nathan E Hellman, et al.
The Journal of Biological Chemistry|September 28, 2002
Mechanisms of copper incorporation into human ceruloplasminNathan E Hellman, Satoshi Kono, Grazia M Mancini, et al.
The Journal of Biological Chemistry|November 28, 2007
Matrix metalloproteinase 13 (MMP13) and tissue inhibitor of matrix metalloproteinase 1 (TIMP1), regulated by the MAPK pathway, are both necessary for Madin-Darby canine kidney tubulogenesisNathan E Hellman, June Spector, Jonathan Robinson, et al.
Human Molecular Genetics|September 17, 2009
Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6Marion Delous, Nathan E Hellman, Helori-Maël Gaudé, et al.
American Journal of Physiology. Renal Physiology|February 28, 2014
Novel MAPK-dependent and -independent tubulogenes identified via microarray analysis of 3D-cultured Madin-Darby canine kidney cellsMaria F Chacon-Heszele, Xiaofeng Zuo, Nathan E Hellman, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 13, 2010
The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretchNathan E Hellman, Yan Liu, Erin Merkel, et al.
Nature Genetics|June 15, 2007
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndromeMarion Delous, Lekbir Baala, Rémi Salomon, et al.
Pageof 1