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...

Insulin resistance–associated hepatic iron overload

Gastroenterology (New York, N.Y. 1943), 1999-11, Vol.117 (5), p.1155-1163

1999

Volltextzugriff (PDF)

Phenotypic expression of HFE mutations: A French study of 1110 unrelated iron-overloaded patients and relatives

Gastroenterology (New York, N.Y. 1943), 1999-02, Vol.116 (2), p.372-377

1999

Volltextzugriff (PDF)

Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing Holoprosencephaly

Human molecular genetics, 1999-09, Vol.8 (9), p.1683-1689

1999

Volltextzugriff (PDF)

Effect of fish size and hydraulic regime on particulate organic matter dynamics in a recirculating aquaculture system: elemental carbon and nitrogen approach

Aquaculture, 2004-09, Vol.239 (1), p.179-198

2004

Volltextzugriff (PDF)

Serum paraoxonase activity and paraoxonase gene polymorphism in type 2 diabetic patients with or without vascular complications

Diabetes & metabolism, 2002-09, Vol.28 (4), p.297-304

2002

Volltextzugriff (PDF)

A genotypic study of 217 unrelated probands diagnosed as “genetic hemochromatosis” on “classical” phenotypic criteria

Journal of hepatology, 1999-04, Vol.30 (4), p.588-593

1999

Volltextzugriff (PDF)

Axonal transport of type III intermediate filament protein peripherin in intact and regenerating motor axons of the rat sciatic nerve

Journal of neuroscience research, 1994-10, Vol.39 (2), p.127-139

1994

Volltextzugriff (PDF)

Identification of an endogenous RNA transcribed from the antisense strand of the HFE gene

Human molecular genetics, 2001-08, Vol.10 (17), p.1859-1866

2001

Volltextzugriff (PDF)

Non-hyperfunctioning nodules from multinodular goiters : A minor role in pathogenesis for somatic activating mutations in the TSH-receptor and Gsα subunit genes

Journal of endocrinological investigation, 2001-05, Vol.24 (5), p.321-325

2001

Volltextzugriff (PDF)

Eukaryotic translation termination factor gene (ETF1/eRF1) maps at D5S500 in a commonly deleted region of chromosome 5q31 in malignant myeloid diseases

Cytogenetic and genome research, 2000-01, Vol.88 (1-2), p.82-86

2000

Volltextzugriff (PDF)

Particulate matter dynamics and transformations in a recirculating aquaculture system: application of stable isotope tracers in seabass rearing

Aquacultural engineering, 2004-10, Vol.31 (3-4), p.135-155

2004

Volltextzugriff (PDF)

Transferrin saturation and screening of genetic hemochromatosis

Clinical chemistry (Baltimore, Md.), 1998-02, Vol.44 (2), p.360-362

1998

Volltextzugriff (PDF)

Localization of seven new genes around the HLA-A locus

Human molecular genetics, 1993-01, Vol.2 (1), p.55-60

1993

Volltextzugriff (PDF)

A candidate gene for hemochromatosis : frequency of the C282Y and H63D mutations

Human genetics, 1997-10, Vol.100 (5-6), p.544-547

1997

Volltextzugriff (PDF)

Familial screening for genetic haemochromatosis by means of DNA markers

Journal of medical genetics, 1992-05, Vol.29 (5), p.320-322

1992

Volltextzugriff (PDF)

Analysis of 160 CF chromosomes : detection of a novel mutation in exon 20

Human genetics, 1993-04, Vol.91 (3), p.254-256

1993

Volltextzugriff (PDF)

Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutations

Molecular human reproduction, 2000-12, Vol.6 (12), p.1063-1067

2000

Volltextzugriff (PDF)

DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family

Human genetics, 1986-10, Vol.74 (2), p.113-120

1986

Volltextzugriff (PDF)

A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes

Immunogenetics (New York), 1992-02, Vol.35 (3), p.183-189

1992

Volltextzugriff (PDF)

Identification of 96 single nucleotide polymorphisms in eight genes involved in iron metabolism: efficiency of bioinformatic extraction compared with a systematic sequencing approach

Human genetics, 2001-10, Vol.109 (4), p.393-401

2001

Volltextzugriff (PDF)

Identification of a novel mutation in CFTR gene exon 8 (L375F) in a CUAVD phenotype

Human genetics, 1996-04, Vol.97 (4), p.548-549

1996

Volltextzugriff (PDF)

Structural analysis of CFTR gene in congenital bilateral absence of vas deferens

Clinical chemistry (Baltimore, Md.), 1995-06, Vol.41 (6 Pt 1), p.833-835

1995

Volltextzugriff (PDF)

Diagnostic génétique de l'hémochromatose

Hématologie, 2004-11, Vol.10 (6), p.447-452

2004

Volltextzugriff (PDF)

Haemochromatosis and HLA-H

Nature genetics, 1996-11, Vol.14 (3), p.251-252

1996

Volltextzugriff (PDF)

Low Penetrant Hemochromatosis Phenotype in Eight Families: No Evidence of Modifiers in the MHC Region

Blood cells, molecules, & diseases, 2001-03, Vol.27 (2), p.518-529

2001

Volltextzugriff (PDF)

1 – 25 von 2.701

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.705)
Mit Volltextzugriff
(2.033)

Publikationsform

5 weitere anzeigen...

Weniger anzeigen...

Sprache

3 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Humans
(328)
Sciences Biologiques Et Medicales
(291)
Sciences Medicales
(246)
Science & Technology
(241)
Life Sciences & Biomedicine
(177)
Humanities And Social Sciences
(154)
Male
(140)
Female
(137)
History
(104)
Adult
(100)
France
(97)
Middle Aged
(80)
Life Sciences
(77)
Biological And Medical Sciences
(73)
Physics
(72)
Generalites
(63)
Physical Sciences
(57)
Sciences Exactes Et Technologie
(57)
Aged
(56)
Sciences Biologiques Fondamentales Et Appliquees. Psychologie
(51)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(8)

Menü

Weitere Dienste

Einstellungen

Insulin resistance–associated hepatic iron overload

Phenotypic expression of HFE mutations: A French study of 1110 unrelated iron-overloaded patients and relatives

Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing Holoprosencephaly

Effect of fish size and hydraulic regime on particulate organic matter dynamics in a recirculating aquaculture system: elemental carbon and nitrogen approach

Serum paraoxonase activity and paraoxonase gene polymorphism in type 2 diabetic patients with or without vascular complications

A genotypic study of 217 unrelated probands diagnosed as “genetic hemochromatosis” on “classical” phenotypic criteria

Axonal transport of type III intermediate filament protein peripherin in intact and regenerating motor axons of the rat sciatic nerve

Identification of an endogenous RNA transcribed from the antisense strand of the HFE gene

Non-hyperfunctioning nodules from multinodular goiters : A minor role in pathogenesis for somatic activating mutations in the TSH-receptor and Gsα subunit genes

Eukaryotic translation termination factor gene (ETF1/eRF1) maps at D5S500 in a commonly deleted region of chromosome 5q31 in malignant myeloid diseases

Particulate matter dynamics and transformations in a recirculating aquaculture system: application of stable isotope tracers in seabass rearing

Transferrin saturation and screening of genetic hemochromatosis

Localization of seven new genes around the HLA-A locus

A candidate gene for hemochromatosis : frequency of the C282Y and H63D mutations

Familial screening for genetic haemochromatosis by means of DNA markers

Analysis of 160 CF chromosomes : detection of a novel mutation in exon 20

Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutations

DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family

A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes

Identification of 96 single nucleotide polymorphisms in eight genes involved in iron metabolism: efficiency of bioinformatic extraction compared with a systematic sequencing approach

Identification of a novel mutation in CFTR gene exon 8 (L375F) in a CUAVD phenotype

Structural analysis of CFTR gene in congenital bilateral absence of vas deferens

Diagnostic génétique de l'hémochromatose

Haemochromatosis and HLA-H

Low Penetrant Hemochromatosis Phenotype in Eight Families: No Evidence of Modifiers in the MHC Region

Suchergebnisse filtern