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MBL2 and MASP2 gene polymorphisms in patients with hepatocellular carcinoma

Journal of viral hepatitis, 2008-05, Vol.15 (5), p.387-391

2008

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Uromodulin storage diseases: Clinical aspects and mechanisms

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

2004

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Polymorphisms in the MBL2 promoter correlated with risk of HIV-1 vertical transmission and AIDS progression

Genes and immunity, 2000-06, Vol.1 (5), p.346-348

2000

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ALS with variable phenotypes in a six-generation family caused by leu144phe mutation in the SOD1 gene

Journal of the neurological sciences, 2001-10, Vol.191 (1), p.11-18

2001

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Single-tube genotyping of MBL-2 polymorphisms using melting temperature analysis

Clinical and experimental medicine, 2002-07, Vol.2 (2), p.105-106

2002

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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

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Human beta defensin 1 gene: Six new variants

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

2000

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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

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Detection of MBL-2 gene expression in intestinal biopsies of celiac patients by in situ reverse transcription polymerase chain reaction

European journal of histochemistry, 2003, Vol.47 (2), p.177-180

2003

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Single tube melting temperature assay for rapid and sensitive detection of the most frequent hemocromatosis mutations, C282Y and H63D

Haematologica (Roma), 2000-09, Vol.85 (9), p.990

2000

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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

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Molecular analysis of uromodulin and SAH genes, positional candidates for autosomal dominant medullary cystic kidney disease linked to 16p12

Journal of nephrology, 2001-09, Vol.14 (5), p.392-396

2001

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Primary hyperoxaluria: genotype-phenotype correlation

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

2003

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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

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A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene

Human mutation, 2000-08, Vol.16 (2), p.180-180

2000

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Gene symbol: AGXT. Disease: primary hyperoxaluria type I

Human genetics, 1999-05, Vol.104 (5), p.441-441

1999

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Quantitative in situ detection of high-risk human papillomavirus in cytological specimens by SYBR Green I fluorescent labeling

Clinical and experimental medicine, 2002-05, Vol.2 (1), p.1-6

2002

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Effects of cAMP on Intercellular Coupling and Osteoblast Differentiation

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

2001

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Detection of AGXT gene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxaluria type 1

Clinical and experimental medicine, 2001-06, Vol.1 (2), p.99-104

2001

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

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

2002

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Localization and expression of two human b-defensins (HBD-1 and HBD-2) in intestinal biopsies of celiac patients

European journal of histochemistry, 2009-06, Vol.47 (4)

2009

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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

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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

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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

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Fluorescent in situ PCR allows sensitive three hours detection of human papilloma virus in cells and tissues

European journal of histochemistry, 1999, Vol.43 (2), p.155

1999

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MBL2 and MASP2 gene polymorphisms in patients with hepatocellular carcinoma

Uromodulin storage diseases: Clinical aspects and mechanisms

Polymorphisms in the MBL2 promoter correlated with risk of HIV-1 vertical transmission and AIDS progression

ALS with variable phenotypes in a six-generation family caused by leu144phe mutation in the SOD1 gene

Single-tube genotyping of MBL-2 polymorphisms using melting temperature analysis

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

Human beta defensin 1 gene: Six new variants

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

Detection of MBL-2 gene expression in intestinal biopsies of celiac patients by in situ reverse transcription polymerase chain reaction

Single tube melting temperature assay for rapid and sensitive detection of the most frequent hemocromatosis mutations, C282Y and H63D

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

Molecular analysis of uromodulin and SAH genes, positional candidates for autosomal dominant medullary cystic kidney disease linked to 16p12

Primary hyperoxaluria: genotype-phenotype correlation

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

A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene

Gene symbol: AGXT. Disease: primary hyperoxaluria type I

Quantitative in situ detection of high-risk human papillomavirus in cytological specimens by SYBR Green I fluorescent labeling

Effects of cAMP on Intercellular Coupling and Osteoblast Differentiation

Detection of AGXT gene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxaluria type 1

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

Localization and expression of two human b-defensins (HBD-1 and HBD-2) in intestinal biopsies of celiac patients

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

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

Fluorescent in situ PCR allows sensitive three hours detection of human papilloma virus in cells and tissues

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