UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 26

Sortiert nach

Characterization of the genetic profile of CYP2C19 in two South African populations

Pharmacogenomics, 2010-08, Vol.11 (8), p.1095-1103

2010

Link zum Volltext

Verfügbarkeit prüfen

A pharmacogenetic study of CD4 recovery in response to HIV antiretroviral therapy in two South African population groups

Journal of human genetics, 2009-05, Vol.54 (5), p.261-265

2009

Link zum Volltext

Verfügbarkeit prüfen

The Glu298Asp variant of the endothelial nitric oxide synthase gene is associated with an increased risk for abruptio placentae in pre-eclampsia

Journal of human genetics, 2005-09, Vol.50 (8), p.415-419

2005

Link zum Volltext

Verfügbarkeit prüfen

Altered plasma neurokinin B levels in patients with pre-eclampsia

Archives of gynecology and obstetrics, 2007-08, Vol.276 (2), p.151-157

2007

Link zum Volltext

Verfügbarkeit prüfen

Prediction of Preeclampsia – A Workshop Report

Placenta, 2008-03, Vol.29 (Suppl A), p.83-85

2008

Link zum Volltext

Verfügbarkeit prüfen

Parallel assessment of circulatory fetal DNA and corticotropin-releasing hormone mRNA in early- and late-onset preeclampsia

Clinical chemistry (Baltimore, Md.), 2005-09, Vol.51 (9), p.1730-1733

2005

Link zum Volltext

Verfügbarkeit prüfen

Analysis of plasma elastase levels in early and late onset preeclampsia

Archives of gynecology and obstetrics, 2006-01, Vol.273 (4), p.239-242

2006

Link zum Volltext

Verfügbarkeit prüfen

Altered circulating neurokinin B (NKB) levels are not due to sequence variants in the encoding genes

European journal of obstetrics & gynecology and reproductive biology, 2008-09, Vol.140 (1), p.135-136

2008

Link zum Volltext

Verfügbarkeit prüfen

Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria

Human molecular genetics, 1999-08, Vol.8 (8), p.1517-1522

1999

Link zum Volltext

Verfügbarkeit prüfen

Circulatory nucleosome levels are significantly increased in early and late-onset preeclampsia

Prenatal diagnosis, 2005-08, Vol.25 (8), p.700-703

2005

Link zum Volltext

Verfügbarkeit prüfen

Third trimester plasma neurokinin B levels in women with and without preeclampsia

The journal of maternal-fetal & neonatal medicine, 2008-01, Vol.21 (2), p.95-100

2008

Link zum Volltext

Verfügbarkeit prüfen

Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction

European journal of obstetrics & gynecology and reproductive biology, 2001-08, Vol.97 (2), p.174-177

2001

Link zum Volltext

Verfügbarkeit prüfen

The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4-phosphate 5-kinase

Nature genetics, 1996-10, Vol.14 (2), p.157-162

1996

Link zum Volltext

Verfügbarkeit prüfen

Minimal Alteration in the Ratio of Circulatory Fetal DNA to Fetal Corticotropin-Releasing Hormone mRNA Level in Preeclampsia

Fetal diagnosis and therapy, 2006-04, Vol.21 (3), p.246-249

2006

Link zum Volltext

Verfügbarkeit prüfen

Mutation −59c→t in Repeat 2 of the LDL Receptor Promoter: Reduction in Transcriptional Activity and Possible Allelic Interaction in a South African Family with Familial Hypercholesterolaemia

Human molecular genetics, 1999-10, Vol.8 (11), p.2025-2030

1999

Link zum Volltext

Verfügbarkeit prüfen

Reply to "Frataxin fracas"

Nature genetics, 1997-04, Vol.15 (4), p.338-338

1997

Link zum Volltext

Verfügbarkeit prüfen

Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry

Clinical genetics, 1999-05, Vol.55 (5), p.340-345

1999

Link zum Volltext

Verfügbarkeit prüfen

Analysis of two mutations in the mthfr gene associated with mild hyperhomocysteinaemia: Heterogeneous distribution in the South African population

South African medical journal, 2002-06, Vol.92 (6), p.464-467

2002

Link zum Volltext

Verfügbarkeit prüfen

Genetic and physical mapping studies of the friereich's ataxia (frda) locus and mutational analysis of a novel candidate, stm7

Hillermann, Renate

1997

Link zum Volltext

Verfügbarkeit prüfen

Mutations in prothrombin and factor V genes do not contribute significantly to placental vasculopathy in a high-risk patient cohort in South Africa

South African medical journal, 2002-07, Vol.92 (7), p.526-527

2002

Link zum Volltext

Verfügbarkeit prüfen

Friedreich's ataxia: a defect in signal transduction?

Human molecular genetics, 1995-08, Vol.4 (8), p.1411-1419

1995

Link zum Volltext

Verfügbarkeit prüfen

Human glial cell line-derived neurotrophic factor (GDNF) maps to chromosome 5

Human genetics, 1995-12, Vol.96 (6), p.671-673

1995

Link zum Volltext

Verfügbarkeit prüfen

Exon–Intron Structure of a 2.7-kb Transcript of the STM7 Gene with Phosphatidylinositol-4-phosphate 5-Kinase Activity

Genomics (San Diego, Calif.), 1997-05, Vol.42 (1), p.170-172

1997

Link zum Volltext

Verfügbarkeit prüfen

The SHB Adaptor Protein Maps to Human Chromosome 9

Genomics (San Diego, Calif.), 1994-12, Vol.24 (3), p.615-617

1994

Link zum Volltext

Verfügbarkeit prüfen

Lipoprotein(A) determination and risk of cardiovascular disease in South African patients with familial hypercholesterolaemia

South African medical journal, 2000-04, Vol.90 (4), p.374-378

2000

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 26

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(24)
Mit Volltextzugriff
(25)

Publikationsform

Artikel
(25)
Dissertationen
(1)

Sprache

Englisch
(26)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Characterization of the genetic profile of CYP2C19 in two South African populations

A pharmacogenetic study of CD4 recovery in response to HIV antiretroviral therapy in two South African population groups

The Glu298Asp variant of the endothelial nitric oxide synthase gene is associated with an increased risk for abruptio placentae in pre-eclampsia

Altered plasma neurokinin B levels in patients with pre-eclampsia

Prediction of Preeclampsia – A Workshop Report

Parallel assessment of circulatory fetal DNA and corticotropin-releasing hormone mRNA in early- and late-onset preeclampsia

Analysis of plasma elastase levels in early and late onset preeclampsia

Altered circulating neurokinin B (NKB) levels are not due to sequence variants in the encoding genes

Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria

Circulatory nucleosome levels are significantly increased in early and late-onset preeclampsia

Third trimester plasma neurokinin B levels in women with and without preeclampsia

Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction

The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4-phosphate 5-kinase

Minimal Alteration in the Ratio of Circulatory Fetal DNA to Fetal Corticotropin-Releasing Hormone mRNA Level in Preeclampsia

Mutation −59c→t in Repeat 2 of the LDL Receptor Promoter: Reduction in Transcriptional Activity and Possible Allelic Interaction in a South African Family with Familial Hypercholesterolaemia

Reply to "Frataxin fracas"

Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry

Analysis of two mutations in the mthfr gene associated with mild hyperhomocysteinaemia: Heterogeneous distribution in the South African population

Genetic and physical mapping studies of the friereich's ataxia (frda) locus and mutational analysis of a novel candidate, stm7

Mutations in prothrombin and factor V genes do not contribute significantly to placental vasculopathy in a high-risk patient cohort in South Africa

Friedreich's ataxia: a defect in signal transduction?

Human glial cell line-derived neurotrophic factor (GDNF) maps to chromosome 5

Exon–Intron Structure of a 2.7-kb Transcript of the STM7 Gene with Phosphatidylinositol-4-phosphate 5-Kinase Activity

The SHB Adaptor Protein Maps to Human Chromosome 9

Lipoprotein(A) determination and risk of cardiovascular disease in South African patients with familial hypercholesterolaemia

Suchergebnisse filtern