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M Czarny

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

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Acta Neurobiologiae Experimentalis|January 1, 1996
Sphingosine stimulates calcium mobilization and modulates calcium signals evoked by thapsigargin in glioma C6 cellsP Sabała, M Wiktorek, M Czarny, et al.
Chirurgia Narzadow Ruchu I Ortopedia Polska|August 3, 2001
[Osteochondrodysplasia determined genetically by a collagen type II gene mutation]M Czarny-Ratajczak, P Rogala, D Wolnik-Brzozowska, et al.
Biochemical and Biophysical Research Communications|February 12, 1998
Serine base exchange enzyme activity is modulated by sphingosine and other amphiphilic compounds: possible role of positive charge in increasing the synthesis of phosphatidylserineM Wiktorek-Wójcik, M Banasiak, M Czarny, et al.
FEBS Letters|February 17, 2000
Phospholipase D2: functional interaction with caveolin in low-density membrane microdomainsM Czarny, G Fiucci, Y Lavie, et al.
American Journal of Medical Genetics. Part A|August 10, 2005
Novel amino acid substitution in the Y-position of collagen type II causes spondyloepimetaphyseal dysplasia congenitaJ Sulko, M Czarny-Ratajczak, A Wozniak, et al.
Acta Biochimica Polonica|January 1, 1993
Effect of glucose and deoxyglucose on cytoplasmic concentration of free Ca2+ in Ehrlich ascites tumour: studies on single cellsA Czyz, V V Teplova, P Sabała, et al.
International Journal of Cancer|March 10, 2000
Changes in phospholipase D isoform activity and expression in multidrug-resistant human cancer cellsG Fiucci, M Czarny, Y Lavie, et al.
Transgenic Research|November 7, 2012
Analysis of tomato gene promoters activated in syncytia induced in tomato and potato hairy roots by Globodera rostochiensisA Wiśniewska, J Dąbrowska-Bronk, K Szafrański, et al.
Human Mutation|February 17, 2001
A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth diseaseA Kochanski, A Lofgren, H Jedrzejowska, et al.
American Journal of Human Genetics|September 21, 2001
A mutation in COL9A1 causes multiple epiphyseal dysplasia: further evidence for locus heterogeneityM Czarny-Ratajczak, J Lohiniva, P Rogala, et al.
Pageof 4

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

Sort By:
Pageof 4
Acta Neurobiologiae Experimentalis|January 1, 1996
Sphingosine stimulates calcium mobilization and modulates calcium signals evoked by thapsigargin in glioma C6 cellsP Sabała, M Wiktorek, M Czarny, et al.
Chirurgia Narzadow Ruchu I Ortopedia Polska|August 3, 2001
[Osteochondrodysplasia determined genetically by a collagen type II gene mutation]M Czarny-Ratajczak, P Rogala, D Wolnik-Brzozowska, et al.
Biochemical and Biophysical Research Communications|February 12, 1998
Serine base exchange enzyme activity is modulated by sphingosine and other amphiphilic compounds: possible role of positive charge in increasing the synthesis of phosphatidylserineM Wiktorek-Wójcik, M Banasiak, M Czarny, et al.
FEBS Letters|February 17, 2000
Phospholipase D2: functional interaction with caveolin in low-density membrane microdomainsM Czarny, G Fiucci, Y Lavie, et al.
American Journal of Medical Genetics. Part A|August 10, 2005
Novel amino acid substitution in the Y-position of collagen type II causes spondyloepimetaphyseal dysplasia congenitaJ Sulko, M Czarny-Ratajczak, A Wozniak, et al.
Acta Biochimica Polonica|January 1, 1993
Effect of glucose and deoxyglucose on cytoplasmic concentration of free Ca2+ in Ehrlich ascites tumour: studies on single cellsA Czyz, V V Teplova, P Sabała, et al.
International Journal of Cancer|March 10, 2000
Changes in phospholipase D isoform activity and expression in multidrug-resistant human cancer cellsG Fiucci, M Czarny, Y Lavie, et al.
Transgenic Research|November 7, 2012
Analysis of tomato gene promoters activated in syncytia induced in tomato and potato hairy roots by Globodera rostochiensisA Wiśniewska, J Dąbrowska-Bronk, K Szafrański, et al.
Human Mutation|February 17, 2001
A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth diseaseA Kochanski, A Lofgren, H Jedrzejowska, et al.
American Journal of Human Genetics|September 21, 2001
A mutation in COL9A1 causes multiple epiphyseal dysplasia: further evidence for locus heterogeneityM Czarny-Ratajczak, J Lohiniva, P Rogala, et al.
Pageof 4