K. Olek

K. Olek, F. Bidlingmaier, L. Kochhan, 1990, Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie.

Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa.

E. Schwinger, A. Schinzel, M. Ludwig, 1991, Genomics.

A de novo Mutation in the Alpha-1-Antitrypsin Gene detected in a Case of disputed Paternity by DNA Sequence Analysis

K. Olek, J. Faber, S. Weidinger, 1992 .

Sequence data of the rare deficient alpha 1-antitrypsin variant PI Zaugsburg.

K. Olek, J. Faber, S. Weidinger, 1990, American journal of human genetics.

Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis.

S. Antonarakis, H. Kazazian, J. Oldenburg, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Recovery from hemophilia B Leyden: an androgen-responsive element in the factor IX promoter.

M. Crossley, K. Stowell, G. Brownlee, 1992, Science.

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition.

E G Tuddenham, S. Antonarakis, D. Cooper, 1994, Nucleic acids research.

Methylation levels at selected CpG sites in the factor VIII and FGFR3 genes, in mature female and male germ cells: implications for male-driven evolution.

J. Walter, M. Montag, J. Oldenburg, 1998, American journal of human genetics.

Hemophilia B caused by five different nondeletion mutations in the protease domain of factor IX.

H. Brackmann, K. Olek, K. Smith, 1992, Blood.

Haemophilia B: database of point mutations and short additions and deletions--second edition.

P. Reitsma, K. High, D. Lillicrap, 1991, Nucleic acids research.

Molecular defects in hemophilia A: identification and characterization of mutations in the factor VIII gene and family analysis.

R. Schwaab, H. Brackmann, K. Olek, 1989, Blood.

Haemophilia A: Carrier detection by DNA analysis

J. Oldenburg, R. Schwaab, H. Brackmann, 1988, Blut.

De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism.

J. Oldenburg, O. el-Maarri, S. Rost, 2000, Blood.

Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia A.

K. Zerres, J. Oldenburg, R. Schwaab, 1993, American journal of human genetics.

Haemophilia B: database of point mutations and short additions and deletions--third edition, 1992.

P. Reitsma, K. High, D. Lillicrap, 1992, Nucleic acids research.

Examination of postmortem animal interference to human remains using cross-species multiplex PCR

P. Schneider, M. Tsokos, K. Olek, 2006, Forensic science, medicine, and pathology.

Mitochondrial DNA and the origins of the domestic horse

M. Hurles, P. Forster, C. Renfrew, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Carnitine palmitoyltransferase II deficiency

K. Olek, S. Zierz, T. Wieser, 2003, Neurology.

Microdissection and microcloning of the long arm of human chromosome 7

L. Tsui, K. Grzeschik, M. Buchwald, 2004, Molecular Biology Reports.

Parental origin of factor IX gene mutations, and their distribution in the gene.

H. Brackmann, K. Olek, M. Ludwig, 1992, American journal of human genetics.

GENOTYPING BLAD, DUMPS AND κ-CSN LOCI IN HOLSTEIN YOUNG BULLS OF THE NATIONAL ANIMAL BREEDING CENTER OF IRAN

A. Nejati-Javaremi, K. Olek, G. Rahimi, 2006 .

Multiple paternity and sperm storage in captive Hermann's tortoises, Testudo hermanni boettgeri determined from amniotic fluid adhering to the eggshell.

C. Distler, K. Olek, W. M. Gerding, 2015, Molecular and cellular probes.

Isolation and characterization of microsatellite marker loci in the greylag goose (Anser anser)

K. Hirschenhauser, K. Olek, K. Foerster, 2008, Molecular ecology resources.

Polymorphic microsatellite markers in the spider Pholcus phalangioides isolated from a library enriched for CA repeats

K. Olek, G. Uhl, K. Rütten, 2001 .

Hypersarcosinemia with craniostenosis-syndactylism syndrome

K. Olek, P. Wardenbach, R. Minami, 1975, Human Genetics.

A G+3-to-T donor splice site mutation leads to skipping of exon 50 in von Willebrand factor mRNA.

R. Schwaab, H. Brackmann, K. Olek, 1994, Genomics.

MtDNA typing of single-sperm cells isolated by micromanipulation.

K. Olek, W. Huckenbeck, S. Forat, 2012, Forensic science international. Genetics.

Sequence variant of the human cathepsin G gene

W. Poller, K. Olek, K. Bartholomé, 1993, Human Genetics.

Correction: Methylation Markers for the Identification of Body Fluids and Tissues from Forensic Trace Evidence

R. Fimmers, R. Reinhardt, B. Huettel, 2016, PloS one.

Cystic fibrosis: typing 89 German families with linked DNA probes

K. Olek, A. Eigel, J. Horst, 1988, Human Genetics.

Mutations in haemophilia A

J. Oldenburg, R. Schwaab, H. Brackmann, 1993, British journal of haematology.

The cellular ratio of immune tolerance (immunoCRIT) is a definite marker for aggressiveness of solid tumors and may explain tumor dissemination patterns

T. Dickhaus, M. T. Hasan, E. Berns, 2013, Epigenetics.

Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker.

Y. Agid, K. Grzeschik, Y. Nakamura, 1989, Genomics.

A human single-copy DNA probe (DR 47) detects a Taq I RFLP on chromosome 9 (D9S5).

H. Orzechowski, K. Olek, A. Driesel, 1987, Nucleic acids research.

Microdissection and microcloning of human chromosome 7q22-32 region

A. Weith, K. Olek, R. Kaiser, 1990, Somatic cell and molecular genetics.

Myotonic dystrophy and limb girdle muscular dystrophy in one family

S. Beyenburg, K. Olek, S. Zierz, 1994, The clinical investigator.

The Influence of Baboon Liver Hemoperfusion on Serum Levels of Amino Acids and Free Fatty Acids in Patients with Acute Liver Failure

K. Olek, S. Uhlhaas, K. Gundermann, 1981 .

Comparison of a charcoal sorbent fiber with commercial charcoals for hemoperfusion.

K. Olek, S. Uhlhaas, K. Gundermann, 1983, Artificial organs.

A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease.

W. Poller, M. Kirchgesser, K. Olek, 1993, Genomics.

[Allele-specific sequencing].

V. Kalinin, K. Olek, W. Schmidt, 1995, Doklady Akademii nauk.

ΔC in Exon 18 of the von Willebrand Gene Is Uncommon in German vWD Type III Patients

R. Schwaab, H. Brackmann, K. Olek, 1993, Thrombosis and Haemostasis.

Compoond heterozygotes in hyperphenylalaninaemia

K. Olek, F. Trefz, K. Bartholomé, 2004, Human Genetics.

Free and conjugated CSF and plasma GABA in Huntington's chorea

H. Lange, K. Olek, S. Uhlhaas, 1986, Acta neurologica Scandinavica.

A New Charcoal Sorbent Fiber for Hemoperfusion

K. Olek, S. Uhlhaas, K. Gundermann, 1981 .

Chromosomal anchoring of linkage groups and identification of wing size QTL using markers and FISH probes derived from microdissected chromosomes in Nasonia (Pteromalidae: Hymenoptera)

M. Neusser, J. Gadau, K. Olek, 2004, Cytogenetic and Genome Research.

Diagnostic difficulties in glucokinase hyperinsulinism.

E. Mayatepek, T. Meissner, N. Cobo-Vuilleumier, 2009, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Sequence polymorphism in the human alpha-2-macroglobulin (A2M) gene

W. Poller, J. P. Faber, K. Olek, 1991, Nucleic Acids Res..

Sequence analysis of the cystic fibrosis gene in patients with disseminated bronchiectatic lung disease

K. Müller, W. Poller, K. Olek, 1991, Klinische Wochenschrift.

Maturity-onset diabetes of the young: an update.

K. Olek, 2006, Clinical laboratory.

Hemophilia B caused by five different nondeletion mutations in the protease domain of factor IX.

J. Birktoft, H. Brackmann, K. Olek, 1992, Blood.

protease domain of factor IX Hemophilia B caused by five different nondeletion mutations in the

H. Brackmann, K. Olek, S. Bajaj, 2011 .

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene.

D. Cooper, J. Gitschier, R. Schwaab, 1991, Nucleic Acids Research.

Haemophilia A: database of ncleotide substituttions, deletions, insertions and rearrangements of the factor VIII gene

S. Antonarakis, D. Cooper, H. Kazazian, 1991 .

Cystic fibrosis in Argentina: The frequency of the ΔF508 mutation

K. Olek, O. Pivetta, M. Luna, 1996, Human Genetics.

Statistical evaluation of a new method to detect carriers of phenylketonuria

K. Olek, P. Wardenbach, R. Minami, 1975, Humangenetik.

as a somatic mosaicism De novo factor VIII gene intron 22 inversion in a female carrier presents

J. Oldenburg, O. el-Maarri, S. Rost, 2013 .

Dihydropteridine reductase variation in man and the characid fish “Cheirodon axelrodi”: Evidence for a dimeric enzyme structure

K. Olek, P. Wardenbach, P. Kuhl, 2004, Human Genetics.

Assignment of a gene for human quinoid-dihydropteridine reductase (QDPR, EC 1.6.5.1) to chromosome 4

K. Olek, P. Wardenbach, P. Kuhl, 2004, Human Genetics.