Search research articles
Contact Us
Filters
Showing results (21-30 of 32) with videos related to
Page
of 4
Sort By:
Acta Neurobiologiae Experimentalis
|
January 1, 1996
Sphingosine stimulates calcium mobilization and modulates calcium signals evoked by thapsigargin in glioma C6 cells
P 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 phosphatidylserine
M Wiktorek-Wójcik, M Banasiak, M Czarny, et al.
FEBS Letters
|
February 17, 2000
Phospholipase D2: functional interaction with caveolin in low-density membrane microdomains
M 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 congenita
J 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 cells
A 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 cells
G 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 rostochiensis
A Wiśniewska, J Dąbrowska-Bronk, K Szafrański, et al.
Human Mutation
|
February 17, 2001
A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth disease
A 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 heterogeneity
M Czarny-Ratajczak, J Lohiniva, P Rogala, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Acta Neurobiologiae Experimentalis
|
January 1, 1996
Sphingosine stimulates calcium mobilization and modulates calcium signals evoked by thapsigargin in glioma C6 cells
P 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 phosphatidylserine
M Wiktorek-Wójcik, M Banasiak, M Czarny, et al.
FEBS Letters
|
February 17, 2000
Phospholipase D2: functional interaction with caveolin in low-density membrane microdomains
M 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 congenita
J 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 cells
A 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 cells
G 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 rostochiensis
A Wiśniewska, J Dąbrowska-Bronk, K Szafrański, et al.
Human Mutation
|
February 17, 2001
A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth disease
A 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 heterogeneity
M Czarny-Ratajczak, J Lohiniva, P Rogala, et al.
Page
of 4