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P Suzanne Hart

Showing results (21-30 of 32) with videos related to

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American Journal of Human Genetics|February 28, 2002
A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1Thomas C Hart, Yingze Zhang, Michael C Gorry, et al.
Bone|October 24, 2007
A 4 bp deletion mutation in DLX3 enhances osteoblastic differentiation and bone formation in vitroSun Jin Choi, In Sun Song, Ok Hee Ryu, et al.
The Journal of Biological Chemistry|February 25, 2005
Proteolysis of macrophage inflammatory protein-1alpha isoforms LD78beta and LD78alpha by neutrophil-derived serine proteasesOk Hee Ryu, Sun Jin Choi, Erhan Firatli, et al.
American Journal of Medical Genetics. Part A|March 3, 2012
Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading systemRafael Denadai, Cassio E Raposo-Amaral, Débora Bertola, et al.
Cells, Tissues, Organs|August 21, 2008
Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4J Timothy Wright, Thomas C Hart, P Suzanne Hart, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Chediak-Higashi syndrome with early developmental delay resulting from paternal heterodisomy of chromosome 1Irini Manoli, Gretchen Golas, Wendy Westbroek, et al.
European Journal of Human Genetics : EJHG|December 19, 2008
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/PSun J Choi, Mary L Marazita, P Suzanne Hart, et al.
American Journal of Human Genetics|August 12, 2009
Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failureMartina Zivná, Helena Hůlková, Marie Matignon, et al.
Clinical Journal of the American Society of Nephrology : CJASN|February 11, 2014
Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1Anthony J Bleyer, Stanislav Kmoch, Corinne Antignac, et al.
Blood|August 17, 2010
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3pMeral Gunay-Aygun, Yifat Zivony-Elboum, Fatma Gumruk, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|February 28, 2002
A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1Thomas C Hart, Yingze Zhang, Michael C Gorry, et al.
Bone|October 24, 2007
A 4 bp deletion mutation in DLX3 enhances osteoblastic differentiation and bone formation in vitroSun Jin Choi, In Sun Song, Ok Hee Ryu, et al.
The Journal of Biological Chemistry|February 25, 2005
Proteolysis of macrophage inflammatory protein-1alpha isoforms LD78beta and LD78alpha by neutrophil-derived serine proteasesOk Hee Ryu, Sun Jin Choi, Erhan Firatli, et al.
American Journal of Medical Genetics. Part A|March 3, 2012
Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading systemRafael Denadai, Cassio E Raposo-Amaral, Débora Bertola, et al.
Cells, Tissues, Organs|August 21, 2008
Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4J Timothy Wright, Thomas C Hart, P Suzanne Hart, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Chediak-Higashi syndrome with early developmental delay resulting from paternal heterodisomy of chromosome 1Irini Manoli, Gretchen Golas, Wendy Westbroek, et al.
European Journal of Human Genetics : EJHG|December 19, 2008
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/PSun J Choi, Mary L Marazita, P Suzanne Hart, et al.
American Journal of Human Genetics|August 12, 2009
Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failureMartina Zivná, Helena Hůlková, Marie Matignon, et al.
Clinical Journal of the American Society of Nephrology : CJASN|February 11, 2014
Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1Anthony J Bleyer, Stanislav Kmoch, Corinne Antignac, et al.
Blood|August 17, 2010
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3pMeral Gunay-Aygun, Yifat Zivony-Elboum, Fatma Gumruk, et al.
Pageof 4