UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 29

Sortiert nach

Uromodulin storage diseases: Clinical aspects and mechanisms

American journal of kidney diseases, 2004-12, Vol.44 (6), p.987-999

2004

Volltextzugriff (PDF)

Effects of maturation on RNA transcription and protein expression of four MRP genes in human placenta and in BeWo cells

Biochemical and biophysical research communications, 2003-03, Vol.303 (1), p.259-265

2003

Volltextzugriff (PDF)

Effects of cAMP on Intercellular Coupling and Osteoblast Differentiation

Biochemical and biophysical research communications, 2001-04, Vol.282 (5), p.1138-1144

2001

Volltextzugriff (PDF)

The IgA nephropathy Biobank. An important starting point for the genetic dissection of a complex trait

BMC nephrology, 2005-12, Vol.6 (1), p.14-14, Article 14

2005

Volltextzugriff (PDF)

MBL2 genetic screening in patients with recurrent vaginal infections

American journal of reproductive immunology (1989), 2008-02, Vol.59 (2), p.146-151

2008

Volltextzugriff (PDF)

Secreted protein acidic and rich in cysteine (SPARC) gene polymorphism association with hepatocellular carcinoma in Italian patients

Journal of gastroenterology and hepatology, 2009-12, Vol.24 (12), p.1840-1846

2009

Volltextzugriff (PDF)

Association of interferon-γ +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients

Nephrology, dialysis, transplantation, 2006-05, Vol.21 (5), p.1317-1322

2006

Volltextzugriff (PDF)

Role of interferon-γ gene polymorphisms in susceptibility to IgA nephropathy : a family-based association study

European journal of human genetics : EJHG, 2006-04, Vol.14 (4), p.488-496

2006

Volltextzugriff (PDF)

Primary hyperoxaluria: genotype-phenotype correlation

Journal of nephrology, 2003-03, Vol.16 (2), p.297-309

2003

Volltextzugriff (PDF)

Mbl2 polymorphisms are involved in HIV-1 infection in brazilian perinatally infected children

AIDS (London), 2003-03, Vol.17 (5), p.779-780

2003

Volltextzugriff (PDF)

Genetic variant of C1GalT1 contributes to the susceptibility to IgA nephropathy

Journal of nephrology, 2009-01, Vol.22 (1), p.152-159

2009

Volltextzugriff (PDF)

Association of interferon-gamma +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients

Nephrology, dialysis, transplantation, 2006-05, Vol.21 (5), p.1317-1322

2006

Volltextzugriff (PDF)

ORIGINAL ARTICLE: MBL2 Genetic Screening in Patients with Recurrent Vaginal Infections

American journal of reproductive immunology (1989), 2008-02, Vol.59 (2), p.146-151

2008

Volltextzugriff (PDF)

AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria

Journal of the American Society of Nephrology, 2001-10, Vol.12 (10), p.2072-2079

2001

Volltextzugriff (PDF)

Extracellular NAD +: a novel autocrine/paracrine signal in osteoblast physiology

Biochemical and biophysical research communications, 2002-12, Vol.299 (3), p.424-431

2002

Volltextzugriff (PDF)

Comparative genomic sequence analysis coupled to chromatin immunoprecipitation: a screening procedure applied to search for regulatory elements at the RET locus

Physiological genomics, 2005-11, Vol.23 (3), p.269-274

2005

Volltextzugriff (PDF)

Rapid method for detection of extra (TA) in the promoter of the bilirubin-UDP-glucuronosyl transferase 1 gene associated with Gilbert syndrome

Clinical chemistry (Baltimore, Md.), 2000, Vol.46 (1), p.129-131

2000

Volltextzugriff (PDF)

Association of interferon-[gamma] +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients

Nephrology, dialysis, transplantation, 2006-05, Vol.21 (5), p.1317

2006

Volltextzugriff (PDF)

Molecular analysis of hyperoxaluria type 1 in italian patients reveals eight new mutations in the alanine : glyoxylate aminotransferase gene

Human genetics, 1999-06, Vol.104 (6), p.523-525

1999

Volltextzugriff (PDF)

Variant mannose-binding lectin alleles are associated with celiac disease

Immunogenetics (New York), 2002-11, Vol.54 (8), p.596-598

2002

Volltextzugriff (PDF)

Role of interferon- gene polymorphisms in susceptibility to IgA nephropathy: a family-based association study

European journal of human genetics : EJHG, 2006-04, Vol.14 (4), p.488-496

2006

Volltextzugriff (PDF)

Human beta defensin 1 gene: Six new variants

Human mutation, 2000-06, Vol.15 (6), p.582-583

2000

Volltextzugriff (PDF)

Flexibility of melting temperature assay for rapid detection of insertions, deletions, and single-point mutations of the AGXT gene responsible for type 1 primary hyperoxaluria

Clinical chemistry (Baltimore, Md.), 2000-11, Vol.46 (11), p.1842-1844

2000

Volltextzugriff (PDF)

(A,G)-Oligonucleotides Form Extraordinary Stable Triple Helices with a Critical R·Y Sequence of the Murine c-Ki-ras Promoter and Inhibit Transcription in Transfected NIH 3T3 Cells

Biochemistry (Easton), 1996-12, Vol.35 (50), p.16361-16369

1996

Volltextzugriff (PDF)

Polymorphisms in the promoter region and at codon 54 of the MBL2 gene are not associated with IgA nephropathy

Nephrology, dialysis, transplantation, 2001-04, Vol.16 (4), p.759-764

2001

Volltextzugriff (PDF)

1 – 25 von 29

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(29)
Mit Volltextzugriff
(28)

Publikationsform

Artikel
(29)

Sprache

Englisch
(29)
Japanisch
(3)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Uromodulin storage diseases: Clinical aspects and mechanisms

Effects of maturation on RNA transcription and protein expression of four MRP genes in human placenta and in BeWo cells

Effects of cAMP on Intercellular Coupling and Osteoblast Differentiation

The IgA nephropathy Biobank. An important starting point for the genetic dissection of a complex trait

MBL2 genetic screening in patients with recurrent vaginal infections

Secreted protein acidic and rich in cysteine (SPARC) gene polymorphism association with hepatocellular carcinoma in Italian patients

Association of interferon-γ +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients

Role of interferon-γ gene polymorphisms in susceptibility to IgA nephropathy : a family-based association study

Primary hyperoxaluria: genotype-phenotype correlation

Mbl2 polymorphisms are involved in HIV-1 infection in brazilian perinatally infected children

Genetic variant of C1GalT1 contributes to the susceptibility to IgA nephropathy

Association of interferon-gamma +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients

ORIGINAL ARTICLE: MBL2 Genetic Screening in Patients with Recurrent Vaginal Infections

AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria

Extracellular NAD +: a novel autocrine/paracrine signal in osteoblast physiology

Comparative genomic sequence analysis coupled to chromatin immunoprecipitation: a screening procedure applied to search for regulatory elements at the RET locus

Rapid method for detection of extra (TA) in the promoter of the bilirubin-UDP-glucuronosyl transferase 1 gene associated with Gilbert syndrome

Association of interferon-[gamma] +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients

Molecular analysis of hyperoxaluria type 1 in italian patients reveals eight new mutations in the alanine : glyoxylate aminotransferase gene

Variant mannose-binding lectin alleles are associated with celiac disease

Role of interferon- gene polymorphisms in susceptibility to IgA nephropathy: a family-based association study

Human beta defensin 1 gene: Six new variants

Flexibility of melting temperature assay for rapid detection of insertions, deletions, and single-point mutations of the AGXT gene responsible for type 1 primary hyperoxaluria

(A,G)-Oligonucleotides Form Extraordinary Stable Triple Helices with a Critical R·Y Sequence of the Murine c-Ki-ras Promoter and Inhibit Transcription in Transfected NIH 3T3 Cells

Polymorphisms in the promoter region and at codon 54 of the MBL2 gene are not associated with IgA nephropathy

Suchergebnisse filtern