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L Gorski

Showing results (41-50 of 94) with videos related to

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Genomics|August 1, 1997
Genomic organization of the faciogenital dysplasia (FGD1; Aarskog syndrome) geneN G Pasteris, J Buckler, A B Cadle, et al.
Human Molecular Genetics|July 1, 1993
Discordant phenotype of two overlapping deletions involving the PAX3 gene in chromosome 2q35N G Pasteris, B J Trask, S Sheldon, et al.
Current Biology : CB|December 1, 1996
Faciogenital dysplasia protein (FGD1) and Vav, two related proteins required for normal embryonic development, are upstream regulators of Rho GTPasesM F Olson, N G Pasteris, J L Gorski, et al.
The Journal of Biological Chemistry|June 23, 1998
Activation of G1 progression, JNK mitogen-activated protein kinase, and actin filament assembly by the exchange factor FGD1K Nagata, M Driessens, N Lamarche, et al.
Human Molecular Genetics|December 26, 2001
The Caenorhabditis elegans homolog of FGD1, the human Cdc42 GEF gene responsible for faciogenital dysplasia, is critical for excretory cell morphogenesisJ Gao, L Estrada, S Cho, et al.
Journal of Medical Genetics|March 1, 1989
Interstitial deletion of 2(q33q36) in a child with congenital abnormalitiesJ L Gorski, M Kiyne, W Uhlmann, et al.
Journal of Food Protection|December 17, 2005
Subtyping Listeria monocytogenes from bulk tank milk using automated repetitive element-based PCRJ S Van Kessel, J S Karns, L Gorski, et al.
Journal of the American Academy of Dermatology|May 1, 1989
Incontinentia pigmenti in a male infant with Klinefelter syndromeJ S Prendiville, J L Gorski, C K Stein, et al.
Journal of Materials Science. Materials in Medicine|April 17, 2008
Osteoblast behaviour on in situ photopolymerizable three-dimensional scaffolds based on D,L-lactide and epsilon-caprolactone: influence of pore volume, pore size and pore shapeHeidi A Declercq, Tomasz L Gorski, Etienne H Schacht, et al.
European Journal of Pediatrics|March 21, 2003
Acute extrapyramidal syndrome in mild ornithine transcarbamylase deficiency: metabolic stroke involving the caudate and putamen without metabolic decompensationC E Keegan, D M Martin, D J Quint, et al.
Pageof 10

Showing results (41-50 of 94) with videos related to

Sort By:
Pageof 10
Genomics|August 1, 1997
Genomic organization of the faciogenital dysplasia (FGD1; Aarskog syndrome) geneN G Pasteris, J Buckler, A B Cadle, et al.
Human Molecular Genetics|July 1, 1993
Discordant phenotype of two overlapping deletions involving the PAX3 gene in chromosome 2q35N G Pasteris, B J Trask, S Sheldon, et al.
Current Biology : CB|December 1, 1996
Faciogenital dysplasia protein (FGD1) and Vav, two related proteins required for normal embryonic development, are upstream regulators of Rho GTPasesM F Olson, N G Pasteris, J L Gorski, et al.
The Journal of Biological Chemistry|June 23, 1998
Activation of G1 progression, JNK mitogen-activated protein kinase, and actin filament assembly by the exchange factor FGD1K Nagata, M Driessens, N Lamarche, et al.
Human Molecular Genetics|December 26, 2001
The Caenorhabditis elegans homolog of FGD1, the human Cdc42 GEF gene responsible for faciogenital dysplasia, is critical for excretory cell morphogenesisJ Gao, L Estrada, S Cho, et al.
Journal of Medical Genetics|March 1, 1989
Interstitial deletion of 2(q33q36) in a child with congenital abnormalitiesJ L Gorski, M Kiyne, W Uhlmann, et al.
Journal of Food Protection|December 17, 2005
Subtyping Listeria monocytogenes from bulk tank milk using automated repetitive element-based PCRJ S Van Kessel, J S Karns, L Gorski, et al.
Journal of the American Academy of Dermatology|May 1, 1989
Incontinentia pigmenti in a male infant with Klinefelter syndromeJ S Prendiville, J L Gorski, C K Stein, et al.
Journal of Materials Science. Materials in Medicine|April 17, 2008
Osteoblast behaviour on in situ photopolymerizable three-dimensional scaffolds based on D,L-lactide and epsilon-caprolactone: influence of pore volume, pore size and pore shapeHeidi A Declercq, Tomasz L Gorski, Etienne H Schacht, et al.
European Journal of Pediatrics|March 21, 2003
Acute extrapyramidal syndrome in mild ornithine transcarbamylase deficiency: metabolic stroke involving the caudate and putamen without metabolic decompensationC E Keegan, D M Martin, D J Quint, et al.
Pageof 10