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- 2016
-
Mark
Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders
(
- Contribution to journal › Article
- 2014
-
Mark
A novel MT-CO2 m.8249G>A pathogenic variation and the MT-TW m.5521G>A mutation in patients with mitochondrial myopathy
(
- Contribution to journal › Article
- 2012
-
Mark
Friedreich's ataxia in patients with FXN p.R165P point mutation
2012) 16th Congress of the European-Federation-of-Neurological-Societies (EFNS) In European Journal of Neurology 19(Suppl 1). p.727-727(
- Contribution to journal › Published meeting abstract
- 2011
-
Mark
Clinical effect of point mutations in myelodysplastic syndromes
(
- Contribution to journal › Article
- 2006
-
Mark
Primaer cytomegalovirusinfektion og tromboflebitis/lungeemboli
(
- Contribution to journal › Article
-
Mark
Limited mutagenesis increases the stability of human carboxypeptidase U (TAFIa) and demonstrates the importance of CPU stability over proCPU concentration in down-regulating fibrinolysis
(
- Contribution to journal › Article
- 2003
-
Mark
Molecular Pharmacology and Structure Function Modelling of the Leukotriene B4 Receptor BLT1
2003)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Temperature-controlled structural alterations of an RNA thermometer
(
- Contribution to journal › Article
- 2002
-
Mark
Factor V and thrombotic disease: description of a janus-faced protein.
(
- Contribution to journal › Scientific review
-
Mark
Rates of nucleotide substitution, mutation at a locus, and the "beanbag" gene number in man
(
- Contribution to journal › Article
- 2001
-
Mark
Somatic mosaicism in hemophilia A: A fairly common event
(
- Contribution to journal › Article
- 2000
-
Mark
Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion
(
- Contribution to journal › Article
- 1999
-
Mark
Thrombophilia as a multigenic disease
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance and anticoagulant proteins in young adults with central retinal vein occlusion
(
- Contribution to journal › Article
-
Mark
The prothrombin gene G20210A mutation and the platelet glycoprotein IIIa polymorphism PlA2 in patients with central retinal vein occlusion
(
- Contribution to journal › Article
- 1998
-
Mark
Resistance to activated protein C, highly prevalent amongst users of oral contraceptives with venous thromboembolism
(
- Contribution to journal › Article
-
Mark
A new direct, fast and quantitative enzyme-linked ligandsorbent assay for measurement of free protein S antigen
(
- Contribution to journal › Article
-
Mark
Geographic distribution of the 20210 G to A prothrombin variant
(
- Contribution to journal › Article
- 1997
-
Mark
A novel thrombomodulin gene mutation in a patient suffering from sagittal sinus thrombosis
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance caused by a common factor V mutation has a single origin
(
- Contribution to journal › Article
-
Mark
The factor VR506Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
(
- Contribution to journal › Article
-
Mark
Evaluation of original and modified APC-resistance tests in unselected outpatients with clinically suspected thrombosis and in healthy controls
(
- Contribution to journal › Article
-
Mark
A common thrombomodulin amino acid dimorphism is associated with myocardial infarction
(
- Contribution to journal › Article
-
Mark
The factor VR5O6Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
(
- Contribution to journal › Article
- 1996
-
Mark
Four novel mutations in deficiency of coagulation factor XIII: Consequences to expression and structure of the A-subunit
(
- Contribution to journal › Article
-
Mark
Recurrent mutation Asn45-->Ser of glycoprotein IX in Bernard-Soulier syndrome
(
- Contribution to journal › Letter
-
Mark
Novel germline p16 mutation in familial malignant melanoma in southern Sweden
(
- Contribution to journal › Article
-
Mark
Elevated levels of prothrombin activation fragment 1 + 2 in plasma from patients with heterozygous Arg506 to Gln mutation in the factor V gene (APC-resistance) and/or inherited protein S deficiency
(
- Contribution to journal › Article
-
Mark
Resistance to activated protein C, the FV:Q506 allele, and venous thrombosis
(
- Contribution to journal › Scientific review
-
Mark
High prevalence of the FVR506Q mutation causing APC resistance in a region of southern Sweden with a high incidence of venous thrombosis.
(
- Contribution to journal › Letter
-
Mark
Factor V:Q506 mutation and anticardiolipin antibodies in systemic lupus erythematosus
(
- Contribution to journal › Article
-
Mark
Familial thrombophilia : clinical and molecular analysis of Swedish families with inherited resistance to activated protein C or protein S deficiency
1996) In Scandinavian journal of clinical and laboratory investigation. Supplementum 56(226). p.19-46(
- Contribution to journal › Scientific review
- 1995
-
Mark
The amino-terminal phosphorylation sites of C-MYC are frequently mutated in Burkitt's lymphoma lines but not in mouse plasmacytomas and rat immunocytomas
(
- Contribution to journal › Article
-
Mark
A new mutation in 16S rRNA of Escherichia coli conferring spectinomycin resistance
(
- Contribution to journal › Article
-
Mark
Resistance to activated protein C caused by a factor V gene mutation
(
- Contribution to journal › Article
-
Mark
Homozygous APC-resistance combined with inherited type I protein S deficiency in a young boy with severe thrombotic disease
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance : from phenotype to genotype and clinical practice
(
- Contribution to journal › Article
-
Mark
Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S
(
- Contribution to journal › Article
- 1994
-
Mark
Haemoglobin Koln as de novo mutations in Sweden : Diagnosis by PCR and specific enzymatic cleavage
(
- Contribution to journal › Article
-
Mark
Fusidic acid-resistant mutants define three regions in elongation factor G of Salmonella typhimurium
(
- Contribution to journal › Article
-
Mark
Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis
(
- Contribution to journal › Article
-
Mark
Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C
(
- Contribution to journal › Article
- 1993
-
Mark
Analysis of somatic mutation activity in multiple V kappa genes involved in the response to 2-phenyl-5-oxazolone
(
- Contribution to journal › Article