UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 666

Sortiert nach

Hfe and Hjv exhibit overlapping functions for iron signaling to hepcidin

Journal of molecular medicine (Berlin, Germany), 2015-05, Vol.93 (5), p.489-498

2015

Link zum Volltext

Verfügbarkeit prüfen

Bone morphogenetic protein (BMP)-responsive elements located in the proximal and distal hepcidin promoter are critical for its response to HJV/BMP/SMAD

Journal of molecular medicine (Berlin, Germany), 2009-05, Vol.87 (5), p.471-480

2009

Link zum Volltext

Verfügbarkeit prüfen

Hfe and Hjv exhibit overlapping functions for iron signaling to hepcidin

Journal of molecular medicine (Berlin, Germany), 2015-05, Vol.93 (5), p.489-498

2015

Link zum Volltext

Verfügbarkeit prüfen

Gene symbol: HFE2a (HJV). Disease: juvenile hemochromatosis

Human genetics, 2005-12, Vol.118 (3-4), p.545-546

2005

Link zum Volltext

Verfügbarkeit prüfen

Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene

Annals of hematology, 2009-10, Vol.88 (10), p.951-955

2009

Link zum Volltext

Verfügbarkeit prüfen

New HJV mutation in a patient with hyperferritinemia and H63D homozygosity for the HFE gene

International journal of hematology, 2007-11, Vol.86 (4), p.379-380

2007

Link zum Volltext

Verfügbarkeit prüfen

Genetic Variations of ferroportin-1(FPN1-8CG), TMPRSS6 (rs855791) and Hemojuvelin (I222N and G320V) Among a Cohort of Egyptian β-Thalassemia Major Patients

Indian journal of hematology & blood transfusion, 2023-04, Vol.39 (2), p.258-265

2023

Link zum Volltext

Verfügbarkeit prüfen

Two middle-age-onset hemochromatosis patients with heterozygous mutations in the hemojuvelin gene in a Chinese family

International journal of hematology, 2014-04, Vol.99 (4), p.487-492

2014

Link zum Volltext

Verfügbarkeit prüfen

Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population

BMC medical genetics, 2004-12, Vol.5 (1), p.29-29, Article 29

2004

Link zum Volltext

Verfügbarkeit prüfen

Hemojuvelin is a novel suppressor for Duchenne muscular dystrophy and age‐related muscle wasting

Journal of cachexia, sarcopenia and muscle, 2019-06, Vol.10 (3), p.557-573

2019

Link zum Volltext

Verfügbarkeit prüfen

DNA transfer into vascular smooth muscle using fusigenic Sendai virus (HVJ)-liposomes

Molecular and cellular biochemistry, 1997-07, Vol.172 (1-2), p.3-12

1997

Link zum Volltext

Verfügbarkeit prüfen

Tumour necrosis factor alpha downregulates human hemojuvelin expression via a novel response element within its promoter

Journal of biomedical science, 2012-09, Vol.19 (1), p.83-83

2012

Link zum Volltext

Verfügbarkeit prüfen

Is hemojuvelin a possible new player in iron metabolism in hemodialysis patients?

International urology and nephrology, 2012-12, Vol.44 (6), p.1805-1811

2012

Link zum Volltext

Verfügbarkeit prüfen

New HJV mutation in a patient with hyperferritinemia and H63D homozygosity for the HFE gene

International journal of hematology, 2007, Vol.86 (4), p.379-380

2007

Link zum Volltext

Verfügbarkeit prüfen

TMPRSS6 rs855791 polymorphism is associated with iron deficiency in a cohort of Sri Lankan pregnant women

The Egyptian journal of medical human genetics, 2022-12, Vol.23 (1), p.164

2022

Link zum Volltext

Verfügbarkeit prüfen

Genotypic and phenotypic spectra of hemojuvelin mutations in primary hemochromatosis patients: a systematic review

Orphanet journal of rare diseases, 2019-07, Vol.14 (1), p.171-171, Article 171

2019

Link zum Volltext

Verfügbarkeit prüfen

HIV-1-associated motor dysfunction as an outcome predictor only incompletely influenced by HAART

Journal of neurovirology, 2000-06, Vol.6 (3), p.246-246

2000

Link zum Volltext

Verfügbarkeit prüfen

CSF factors in HIV associated encephalopathy impair astroglial glutamate responses

Journal of neurovirology, 2000-06, Vol.6 (3), p.254-254

2000

Link zum Volltext

Verfügbarkeit prüfen

Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders

Journal of gastroenterology, 2010-11, Vol.45 (11), p.1163-1171

2010

Link zum Volltext

Verfügbarkeit prüfen

Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China

Orphanet journal of rare diseases, 2021-09, Vol.16 (1), p.398-398, Article 398

2021

Link zum Volltext

Verfügbarkeit prüfen

Positron emission tomography (PET) findings in HIV-1-associated minor motor disorder

Journal of neurovirology, 2000-06, Vol.6 (3), p.267-267

2000

Link zum Volltext

Verfügbarkeit prüfen

Magnetic resonance spectroscopy (MRS) findings in HIV-1-associated minor motor disorders (HIV-1 MMD)

Journal of neurovirology, 2000-06, Vol.6 (3), p.259-259

2000

Link zum Volltext

Verfügbarkeit prüfen

Localization of the iron-regulatory proteins hemojuvelin and transferrin receptor 2 to the basolateral membrane domain of hepatocytes

Histochemistry and cell biology, 2007-02, Vol.127 (2), p.221-226

2007

Link zum Volltext

Verfügbarkeit prüfen

Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes

Annals of hematology, 2009-03, Vol.88 (3), p.229-234

2009

Link zum Volltext

Verfügbarkeit prüfen

Vitamin A deficiency modulates iron metabolism independent of hemojuvelin (Hfe2) and bone morphogenetic protein 6 (Bmp6) transcript levels

Genes & nutrition, 2016, Vol.11 (1), p.1-1, Article 1

2016

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 666

Suche als RSS-Feed

Aktive Filter

SpracheTürkisch

ThemaBiochemistry & Molecular Biology

KollektionSpringer Nature - Complete Springer Journals

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(626)
Mit Volltextzugriff
(654)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Hfe and Hjv exhibit overlapping functions for iron signaling to hepcidin

Bone morphogenetic protein (BMP)-responsive elements located in the proximal and distal hepcidin promoter are critical for its response to HJV/BMP/SMAD

Hfe and Hjv exhibit overlapping functions for iron signaling to hepcidin

Gene symbol: HFE2a (HJV). Disease: juvenile hemochromatosis

Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene

New HJV mutation in a patient with hyperferritinemia and H63D homozygosity for the HFE gene

Genetic Variations of ferroportin-1(FPN1-8CG), TMPRSS6 (rs855791) and Hemojuvelin (I222N and G320V) Among a Cohort of Egyptian β-Thalassemia Major Patients

Two middle-age-onset hemochromatosis patients with heterozygous mutations in the hemojuvelin gene in a Chinese family

Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population

Hemojuvelin is a novel suppressor for Duchenne muscular dystrophy and age‐related muscle wasting

DNA transfer into vascular smooth muscle using fusigenic Sendai virus (HVJ)-liposomes

Tumour necrosis factor alpha downregulates human hemojuvelin expression via a novel response element within its promoter

Is hemojuvelin a possible new player in iron metabolism in hemodialysis patients?

New HJV mutation in a patient with hyperferritinemia and H63D homozygosity for the HFE gene

TMPRSS6 rs855791 polymorphism is associated with iron deficiency in a cohort of Sri Lankan pregnant women

Genotypic and phenotypic spectra of hemojuvelin mutations in primary hemochromatosis patients: a systematic review

HIV-1-associated motor dysfunction as an outcome predictor only incompletely influenced by HAART

CSF factors in HIV associated encephalopathy impair astroglial glutamate responses

Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders

Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China

Positron emission tomography (PET) findings in HIV-1-associated minor motor disorder

Magnetic resonance spectroscopy (MRS) findings in HIV-1-associated minor motor disorders (HIV-1 MMD)

Localization of the iron-regulatory proteins hemojuvelin and transferrin receptor 2 to the basolateral membrane domain of hepatocytes

Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes

Vitamin A deficiency modulates iron metabolism independent of hemojuvelin (Hfe2) and bone morphogenetic protein 6 (Bmp6) transcript levels

Aktive Filter

Suchergebnisse filtern