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J Schönling

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Letters in Applied Microbiology|February 24, 2015
Comparison of different methods for the recovery of DNA from spores of mycotoxin-producing moulds in spiked food samplesS Grube, J Schönling, A Prange
Human Molecular Genetics|December 1, 1993
Twenty different alleles at the locus D5S683 on 5q23-31J Schönling, N K Spurr, B Wirth
Journal of General Microbiology|July 1, 1991
Different promoters of SHV-2 and SHV-2a beta-lactamase lead to diverse levels of cefotaxime resistance in their bacterial producersA Podbielski, J Schönling, B Melzer, et al.
Zentralblatt Fur Bakteriologie : International Journal of Medical Microbiology|August 1, 1991
Molecular cloning and nucleotide sequence of a new plasmid-coded Klebsiella pneumoniae beta-lactamase gene (SHV-2a) responsible for high-level cefotaxime resistanceA Podbielski, J Schönling, B Melzer, et al.
Mycotoxin Research|April 23, 2013
Development of deoxynivalenol contents in relation to the PCR detection of potentially trichothecene producingFusarium spp. during storage of wheatB Birzele, A Prange, J Schönling, et al.
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism at the D12S371 locusA Leutner, J Schönling, N K Spurr, et al.
American Journal of Human Genetics|November 1, 1996
Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the diseaseE Hahnen, J Schönling, S Rudnik-Schöneborn, et al.
Journal of General Microbiology|March 1, 1991
Molecular characterization of a new plasmid-encoded SHV-type beta-lactamase (SHV-2 variant) conferring high-level cefotaxime resistance upon Klebsiella pneumoniaeA Podbielski, J Schönling, B Melzer, et al.
Human Molecular Genetics|May 1, 1997
Missense mutations in exon 6 of the survival motor neuron gene in patients with spinal muscular atrophy (SMA)E Hahnen, J Schönling, S Rudnik-Schöneborn, et al.
Human Molecular Genetics|October 1, 1995
Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individualsE Hahnen, R Forkert, C Marke, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Letters in Applied Microbiology|February 24, 2015
Comparison of different methods for the recovery of DNA from spores of mycotoxin-producing moulds in spiked food samplesS Grube, J Schönling, A Prange
Human Molecular Genetics|December 1, 1993
Twenty different alleles at the locus D5S683 on 5q23-31J Schönling, N K Spurr, B Wirth
Journal of General Microbiology|July 1, 1991
Different promoters of SHV-2 and SHV-2a beta-lactamase lead to diverse levels of cefotaxime resistance in their bacterial producersA Podbielski, J Schönling, B Melzer, et al.
Zentralblatt Fur Bakteriologie : International Journal of Medical Microbiology|August 1, 1991
Molecular cloning and nucleotide sequence of a new plasmid-coded Klebsiella pneumoniae beta-lactamase gene (SHV-2a) responsible for high-level cefotaxime resistanceA Podbielski, J Schönling, B Melzer, et al.
Mycotoxin Research|April 23, 2013
Development of deoxynivalenol contents in relation to the PCR detection of potentially trichothecene producingFusarium spp. during storage of wheatB Birzele, A Prange, J Schönling, et al.
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism at the D12S371 locusA Leutner, J Schönling, N K Spurr, et al.
American Journal of Human Genetics|November 1, 1996
Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the diseaseE Hahnen, J Schönling, S Rudnik-Schöneborn, et al.
Journal of General Microbiology|March 1, 1991
Molecular characterization of a new plasmid-encoded SHV-type beta-lactamase (SHV-2 variant) conferring high-level cefotaxime resistance upon Klebsiella pneumoniaeA Podbielski, J Schönling, B Melzer, et al.
Human Molecular Genetics|May 1, 1997
Missense mutations in exon 6 of the survival motor neuron gene in patients with spinal muscular atrophy (SMA)E Hahnen, J Schönling, S Rudnik-Schöneborn, et al.
Human Molecular Genetics|October 1, 1995
Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individualsE Hahnen, R Forkert, C Marke, et al.
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