UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Mycoplasma pneumoniae Compared to Streptococcus pneumoniae Avoids Induction of Proinflammatory Epithelial Cell Responses despite Robustly Inducing TLR2 Signaling

Infection and immunity, 2022-08, Vol.90 (8), p.e0012922-e0012922

2022

Volltextzugriff (PDF)

Brain-derived Neurotrophic Factor (BDNF) and gray matter volume in bipolar disorder

European psychiatry, 2017-02, Vol.40, p.33-37

2017

Volltextzugriff (PDF)

Distinct SagA from Hospital-Associated Clade A1 Enterococcus faecium Strains Contributes to Biofilm Formation

Applied and Environmental Microbiology, 2015-10, Vol.81 (19), p.6873-6882

2015

Volltextzugriff (PDF)

Comparative study of five different DNA fingerprint techniques for molecular typing of Streptococcus pneumoniae strains

Journal of Clinical Microbiology, 1995-06, Vol.33 (6), p.1606-1612

1995

Volltextzugriff (PDF)

PerR controls peroxide- and iron-responsive expression of oxidative stress defense genes in Helicobacter hepaticus

European journal of microbiology & immunology, 2011-09, Vol.1 (3), p.215-222

2011

Volltextzugriff (PDF)

The Streptococcal Lipoprotein Rotamase A (SlrA) Is a Functional Peptidyl-prolyl Isomerase Involved in Pneumococcal Colonization

The Journal of biological chemistry, 2006-01, Vol.281 (2), p.968-976

2006

Volltextzugriff (PDF)

Molecular basis of androgen insensitivity

The Journal of steroid biochemistry and molecular biology, 1996-08, Vol.58 (5), p.569-575

1996

Volltextzugriff (PDF)

Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: characteristics of three unusual haplotypes

Human genetics, 2002-10, Vol.111 (4-5), p.405-410

2002

Volltextzugriff (PDF)

Carriership of a defective tenascin-X gene in steroid 21-hydroxylase deficiency patients: TNXB –TNXA hybrids in apparent large-scale gene conversions

Human molecular genetics, 2002-10, Vol.11 (21), p.2581-2590

2002

Volltextzugriff (PDF)

The Role of the Ferric Uptake Regulator (Fur) in Regulation of Helicobacter pylori Iron Uptake

Helicobacter (Cambridge, Mass.), 2002-08, Vol.7 (4), p.237-244

2002

Volltextzugriff (PDF)

A practical approach to the detection of androgen receptor gene mutations and pedigree analysis in families with X-linked androgen insensitivity

Pediatric research, 1994-08, Vol.36 (2), p.227-234

1994

Volltextzugriff (PDF)

Identification and Characterization of a Novel Outer Membrane Protein (OMP J) of Moraxella catarrhalis That Exists in Two Major Forms

Journal of Bacteriology, 2005-12, Vol.187 (23), p.7977-7984

2005

Volltextzugriff (PDF)

Vitamin D metabolism in breast-fed infants and their mothers

Pediatric research, 1989-06, Vol.25 (6), p.623-628

1989

Volltextzugriff (PDF)

A novel pathogenic taxon of the Mycobacterium tuberculosis complex, Canetti: characterization of an exceptional isolate from Africa

International journal of systematic bacteriology, 1997-10, Vol.47 (4), p.1236-1245

1997

Volltextzugriff (PDF)

A rare TaqI polymorphism in a human complement C4 gene is caused by an additional restriction site in the first intron

Immunology letters, 1992-10, Vol.34 (2), p.93-97

1992

Volltextzugriff (PDF)

CYP21 and CYP21P variability in steroid 21-hydroxylase deficiency patients and in the general population in the Netherlands

European journal of human genetics : EJHG, 2000-11, Vol.8 (11), p.827-836

2000

Volltextzugriff (PDF)

The peptidyl-prolyl isomerase SlrA contributes to virulence and adherence of Streptococcus pneumoniae

Pneumologie, 2006, Vol.60 (2)

2006

Volltextzugriff (PDF)

Plasma 1.25-Dihydroxyvitamin D Concentrations in Preterm Infants

Acta Paediatrica, 1985-07, Vol.74 (4), p.549-554

1985

Volltextzugriff (PDF)

Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt‐losing congenital adrenal hyperplasia caused by steroid 21‐hydroxylase deficiency

Clinical endocrinology (Oxford), 1998-12, Vol.49 (6), p.815-822

1998

Volltextzugriff (PDF)

The PvuII restriction site in the second intron of the human steroid 21-hydroxylase gene CYP21 is polymorphic

Clinical genetics, 1995-08, Vol.48 (2), p.109-110

1995

Volltextzugriff (PDF)

Family studies of the steroid 21-hydroxylase and complement C4 genes define 11 haplotypes in classical congenital adrenal hyperplasia in the Netherlands

European journal of pediatrics, 1992-12, Vol.151 (12), p.885-892

1992

Volltextzugriff (PDF)

Adrenogenital syndrome. II. Molecular biology

Tijdschrift voor kindergeneeskunde, 1991-02, Vol.59 (1), p.1-8

1991

Volltextzugriff (PDF)

Adrenogenital syndrome. I. Introduction, enzymology and heredity

Tijdschrift voor kindergeneeskunde, 1989-08, Vol.57 (4), p.129-135

1989

Volltextzugriff (PDF)

Interlaboratory Variation of Vitamin D Metabolite Measurements

Clinical chemistry and laboratory medicine, 1982, Vol.20 (10), p.753-756

1982

Volltextzugriff (PDF)

Interlaboratory variation of vitamin D1) metabolite measurements

Journal of clinical chemistry and clinical biochemistry, 1982-10, Vol.20 (10), p.753

1982

Volltextzugriff (PDF)

1 – 25 von 282

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(254)
Mit Volltextzugriff
(229)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(160)
Life Sciences & Biomedicine
(138)
Humans
(97)
Animals
(51)
Mice
(39)
Hematology
(35)
Female
(33)
Biological And Medical Sciences
(30)
Male
(29)
Mutation
(24)
Adult
(23)
Immunology
(23)
Fundamental And Applied Biological Sciences. Psychology
(22)
Microbiology
(18)
Cell Biology
(17)
Engineering
(17)
Bone Marrow
(16)
Inflammation
(16)
Middle Aged
(16)
Technology
(16)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Blood
(32)
Blood Advances
(7)
Haematologica
(7)
Hemasphere
(6)
Leukemia
(6)
Plos One
(6)
The Journal Of Immunology
(6)
The journal Of Immunology/the journal Of Immunology
(5)
Water Science And Technology
(5)
Cancer Research
(4)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Mycoplasma pneumoniae Compared to Streptococcus pneumoniae Avoids Induction of Proinflammatory Epithelial Cell Responses despite Robustly Inducing TLR2 Signaling

Brain-derived Neurotrophic Factor (BDNF) and gray matter volume in bipolar disorder

Distinct SagA from Hospital-Associated Clade A1 Enterococcus faecium Strains Contributes to Biofilm Formation

Comparative study of five different DNA fingerprint techniques for molecular typing of Streptococcus pneumoniae strains

PerR controls peroxide- and iron-responsive expression of oxidative stress defense genes in Helicobacter hepaticus

The Streptococcal Lipoprotein Rotamase A (SlrA) Is a Functional Peptidyl-prolyl Isomerase Involved in Pneumococcal Colonization

Molecular basis of androgen insensitivity

Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: characteristics of three unusual haplotypes

Carriership of a defective tenascin-X gene in steroid 21-hydroxylase deficiency patients: TNXB –TNXA hybrids in apparent large-scale gene conversions

The Role of the Ferric Uptake Regulator (Fur) in Regulation of Helicobacter pylori Iron Uptake

A practical approach to the detection of androgen receptor gene mutations and pedigree analysis in families with X-linked androgen insensitivity

Identification and Characterization of a Novel Outer Membrane Protein (OMP J) of Moraxella catarrhalis That Exists in Two Major Forms

Vitamin D metabolism in breast-fed infants and their mothers

A novel pathogenic taxon of the Mycobacterium tuberculosis complex, Canetti: characterization of an exceptional isolate from Africa

A rare TaqI polymorphism in a human complement C4 gene is caused by an additional restriction site in the first intron

CYP21 and CYP21P variability in steroid 21-hydroxylase deficiency patients and in the general population in the Netherlands

The peptidyl-prolyl isomerase SlrA contributes to virulence and adherence of Streptococcus pneumoniae

Plasma 1.25-Dihydroxyvitamin D Concentrations in Preterm Infants

Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt‐losing congenital adrenal hyperplasia caused by steroid 21‐hydroxylase deficiency

The PvuII restriction site in the second intron of the human steroid 21-hydroxylase gene CYP21 is polymorphic

Family studies of the steroid 21-hydroxylase and complement C4 genes define 11 haplotypes in classical congenital adrenal hyperplasia in the Netherlands

Adrenogenital syndrome. II. Molecular biology

Adrenogenital syndrome. I. Introduction, enzymology and heredity

Interlaboratory Variation of Vitamin D Metabolite Measurements

Interlaboratory variation of vitamin D1) metabolite measurements

Suchergebnisse filtern