Berg LP - Search Results

1

Aberrant RNA splicing of the protein C and protein S genes in healthy individuals.

Berg LP, Soria JM, Formstone CJ, Morell M, Kakkar VV, Estivill X, Sala N, Cooper DN. Berg LP, et al. Blood Coagul Fibrinolysis. 1996 Sep;7(6):625-31. doi: 10.1097/00001721-199609000-00008. Blood Coagul Fibrinolysis. 1996. PMID: 8899152

2

Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategy.

Formstone CJ, Wacey AI, Berg LP, Rahman S, Bevan D, Rowley M, Voke J, Bernardi F, Legnani C, Simioni P, Girolami A, Tuddenham EG, Kakkar VV, Cooper DN. Formstone CJ, et al. Among authors: berg lp. Blood. 1995 Oct 1;86(7):2632-41. Blood. 1995. PMID: 7545463 Free article.

3

Polymorphic variation in the human protein C (PROC) gene promoter can influence transcriptional efficiency in vitro.

Scopes D, Berg LP, Krawczak M, Kakkar VV, Cooper DN. Scopes D, et al. Among authors: berg lp. Blood Coagul Fibrinolysis. 1995 Jun;6(4):317-21. doi: 10.1097/00001721-199506000-00004. Blood Coagul Fibrinolysis. 1995. PMID: 7548679

4

Ectopic (illegitimate) transcription: new possibilities for the analysis and diagnosis of human genetic disease.

Cooper DN, Berg LP, Kakkar VV, Reiss J. Cooper DN, et al. Among authors: berg lp. Ann Med. 1994 Feb;26(1):9-14. doi: 10.3109/07853899409147321. Ann Med. 1994. PMID: 8166994 Free article. Review.

5

Combined factor VIII/factor XI deficiency may cause intra-familial clinical variability in haemophilia A among Ashkenazi Jews.

Berg LP, Varon D, Martinowitz U, Wieland K, Kakkar VV, Cooper DN. Berg LP, et al. Blood Coagul Fibrinolysis. 1994 Feb;5(1):59-62. doi: 10.1097/00001721-199402000-00009. Blood Coagul Fibrinolysis. 1994. PMID: 8180339

6

Ectopic transcript analysis indicates that allelic exclusion is an important cause of type I protein C deficiency in patients with nonsense and frameshift mutations in the PROC gene.

Soria JM, Berg LP, Fontcuberta J, Kakkar VV, Estivill X, Cooper DN, Sala N. Soria JM, et al. Among authors: berg lp. Thromb Haemost. 1996 Jun;75(6):870-6. Thromb Haemost. 1996. PMID: 8822578

7

De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: demonstration of exon skipping by ectopic transcript analysis.

Berg LP, Grundy CB, Thomas F, Millar DS, Green PJ, Slomski R, Reiss J, Kakkar VV, Cooper DN. Berg LP, et al. Genomics. 1992 Aug;13(4):1359-61. doi: 10.1016/0888-7543(92)90070-9. Genomics. 1992. PMID: 1505975

8

Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNA.

Berg LP, Wieland K, Millar DS, Schlösser M, Wagner M, Kakkar VV, Reiss J, Cooper DN. Berg LP, et al. Hum Genet. 1990 Oct;85(6):655-8. doi: 10.1007/BF00193593. Hum Genet. 1990. PMID: 2121641

9

Molecular genetic analysis of a novel form of haemophilia A characterized by the variable expression of factor VIII.

Wieland K, Berg LP, Kakkar VV, Cooper DN, Martinowitz U. Wieland K, et al. Among authors: berg lp. Thromb Res. 1990 Sep 1;59(5):871-7. doi: 10.1016/0049-3848(90)90400-7. Thromb Res. 1990. PMID: 2122548 No abstract available.

10

Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophilia.

Berg LP, Scopes DA, Alhaq A, Kakkar VV, Cooper DN. Berg LP, et al. Hum Mol Genet. 1994 Dec;3(12):2147-52. doi: 10.1093/hmg/3.12.2147. Hum Mol Genet. 1994. PMID: 7881411

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