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Developmental Biology
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September 1, 1981
Isolation of cloned genes differentially expressed at early and late stages of Drosophila embryonic development
G Scherer, J Telford, C Baldari, et al.
Nucleic Acids Research
|
July 10, 1987
Anonymous DNA sequence from chromosome 21 showing a three allele insertion/deletion RFLP (HGM 9 provisional no. D21S82)
G H Xiao, K H Grzeschik, G Scherer
Zeitschrift Fur Rheumatologie
|
September 1, 1980
[In vivo effect of oxyphenbutazone and prednisolone on the DNA metabolism of the Syrian hamster]
W Klein, F Kocsis, G Scherer, et al.
Nucleic Acids Research
|
July 10, 1987
PstI RFLP identified by an anonymous single copy genomic clone localized to chromosome 14 (HGM 9 provisional no. D14S14)
G H Xiao, K H Grzeschik, G Scherer
Electrophoresis
|
November 20, 1998
Genotyping metabolic polymorphisms in a cohort of Caucasians and single strand conformation polymorphism analysis of point mutations in human hprt exons 7 and 8
G Krause, F Garganta, P Kosytorz, et al.
Mutation Research
|
January 15, 2000
Spontaneous and chemically induced point mutations in HPRT cDNA of the metabolically competent human lymphoblastoid cell line, MCL-5
G Krause, F Garganta, H Vrieling, et al.
Nature
|
March 30, 1978
Nucleotide sequence of cro, cII and part of the O gene in phage lambda DNA
E Schwarz, G Scherer, G Hobom, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications
|
September 24, 1998
Determination of albumin adducts of (+)-anti-benzo[a]pyrene-diol-epoxide using an high-performance liquid chromatographic column switching technique for sample preparation and gas chromatography-mass spectrometry for the final detection
S Frank, T Renner, T Ruppert, et al.
Clinical Dysmorphology
|
August 24, 2000
SOX9 mutation in a previously published case of campomelic dysplasia without overt campomelia
U Friedrich, E Schaefer, P Meinecke, et al.
Nucleic Acids Research
|
July 11, 1990
Isolation and characterization of the human tyrosine aminotransferase gene
R Rettenmeier, E Natt, H Zentgraf, et al.
Page
of 21
Search research articles
Search
Showing results (41-50 of 209) with videos related to
Sort By:
Page
of 21
Developmental Biology
|
September 1, 1981
Isolation of cloned genes differentially expressed at early and late stages of Drosophila embryonic development
G Scherer, J Telford, C Baldari, et al.
Nucleic Acids Research
|
July 10, 1987
Anonymous DNA sequence from chromosome 21 showing a three allele insertion/deletion RFLP (HGM 9 provisional no. D21S82)
G H Xiao, K H Grzeschik, G Scherer
Zeitschrift Fur Rheumatologie
|
September 1, 1980
[In vivo effect of oxyphenbutazone and prednisolone on the DNA metabolism of the Syrian hamster]
W Klein, F Kocsis, G Scherer, et al.
Nucleic Acids Research
|
July 10, 1987
PstI RFLP identified by an anonymous single copy genomic clone localized to chromosome 14 (HGM 9 provisional no. D14S14)
G H Xiao, K H Grzeschik, G Scherer
Electrophoresis
|
November 20, 1998
Genotyping metabolic polymorphisms in a cohort of Caucasians and single strand conformation polymorphism analysis of point mutations in human hprt exons 7 and 8
G Krause, F Garganta, P Kosytorz, et al.
Mutation Research
|
January 15, 2000
Spontaneous and chemically induced point mutations in HPRT cDNA of the metabolically competent human lymphoblastoid cell line, MCL-5
G Krause, F Garganta, H Vrieling, et al.
Nature
|
March 30, 1978
Nucleotide sequence of cro, cII and part of the O gene in phage lambda DNA
E Schwarz, G Scherer, G Hobom, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications
|
September 24, 1998
Determination of albumin adducts of (+)-anti-benzo[a]pyrene-diol-epoxide using an high-performance liquid chromatographic column switching technique for sample preparation and gas chromatography-mass spectrometry for the final detection
S Frank, T Renner, T Ruppert, et al.
Clinical Dysmorphology
|
August 24, 2000
SOX9 mutation in a previously published case of campomelic dysplasia without overt campomelia
U Friedrich, E Schaefer, P Meinecke, et al.
Nucleic Acids Research
|
July 11, 1990
Isolation and characterization of the human tyrosine aminotransferase gene
R Rettenmeier, E Natt, H Zentgraf, et al.
Page
of 21