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Endocrinology
|
October 1, 1988
HLA-DR gene expression in a proliferating human thyroid cell clone (12S)
R D Cone, M Platzer, L A Piccinini, et al.
Molecular Biology Reports
|
November 30, 1982
On the fine structure of rat liver ribosome small subunits
N A Kiselev, Stel'mashchuk VYa, E V Orlova, et al.
The Journal of General Virology
|
March 1, 1983
Studies on the SV40-like papovavirus SV40-GBM. I. Genomic analysis by restriction endonucleases and electron microscopy after propagation in CV-1 monkey cells
W Zimmermann, M Platzer, S Scherneck, et al.
Der Anaesthesist
|
May 25, 2011
[Tonsillotomy and adenotonsillectomy in childhood. Study on postoperative pain therapy]
M Platzer, R Likar, H Stettner, et al.
British Journal of Anaesthesia
|
March 19, 2011
Consecutive, prospective case series of a new method for ultrasound-guided supraclavicular approach to the brachiocephalic vein in children
C Breschan, M Platzer, R Jost, et al.
Molecular Phylogenetics and Evolution
|
June 29, 2011
Phylogeny, genetic variability and colour polymorphism of an emerging animal model: the short-lived annual Nothobranchius fishes from southern Mozambique
A Dorn, E Ng'oma, K Janko, et al.
International Journal of Radiation Oncology, Biology, Physics
|
July 27, 1999
Sequence analysis of the ATM gene in 20 patients with RTOG grade 3 or 4 acute and/or late tissue radiation side effects
U Oppitz, U Bernthaler, D Schindler, et al.
Human Molecular Genetics
|
September 1, 1997
Human renin binding protein: complete genomic sequence and association of an intronic T/C polymorphism with the prorenin level in males
A Knöll, H Schunkert, K Reichwald, et al.
Genes and Immunity
|
May 7, 2010
Both copy number and sequence variations affect expression of human DEFB4
M Groth, C Wiegand, K Szafranski, et al.
Journal of Medical Genetics
|
September 3, 2004
A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)
J Ramser, B Winnepenninckx, C Lenski, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 101) with videos related to
Sort By:
Page
of 11
Endocrinology
|
October 1, 1988
HLA-DR gene expression in a proliferating human thyroid cell clone (12S)
R D Cone, M Platzer, L A Piccinini, et al.
Molecular Biology Reports
|
November 30, 1982
On the fine structure of rat liver ribosome small subunits
N A Kiselev, Stel'mashchuk VYa, E V Orlova, et al.
The Journal of General Virology
|
March 1, 1983
Studies on the SV40-like papovavirus SV40-GBM. I. Genomic analysis by restriction endonucleases and electron microscopy after propagation in CV-1 monkey cells
W Zimmermann, M Platzer, S Scherneck, et al.
Der Anaesthesist
|
May 25, 2011
[Tonsillotomy and adenotonsillectomy in childhood. Study on postoperative pain therapy]
M Platzer, R Likar, H Stettner, et al.
British Journal of Anaesthesia
|
March 19, 2011
Consecutive, prospective case series of a new method for ultrasound-guided supraclavicular approach to the brachiocephalic vein in children
C Breschan, M Platzer, R Jost, et al.
Molecular Phylogenetics and Evolution
|
June 29, 2011
Phylogeny, genetic variability and colour polymorphism of an emerging animal model: the short-lived annual Nothobranchius fishes from southern Mozambique
A Dorn, E Ng'oma, K Janko, et al.
International Journal of Radiation Oncology, Biology, Physics
|
July 27, 1999
Sequence analysis of the ATM gene in 20 patients with RTOG grade 3 or 4 acute and/or late tissue radiation side effects
U Oppitz, U Bernthaler, D Schindler, et al.
Human Molecular Genetics
|
September 1, 1997
Human renin binding protein: complete genomic sequence and association of an intronic T/C polymorphism with the prorenin level in males
A Knöll, H Schunkert, K Reichwald, et al.
Genes and Immunity
|
May 7, 2010
Both copy number and sequence variations affect expression of human DEFB4
M Groth, C Wiegand, K Szafranski, et al.
Journal of Medical Genetics
|
September 3, 2004
A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)
J Ramser, B Winnepenninckx, C Lenski, et al.
Page
of 11