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...

Influence of nitric oxide signaling mechanisms in cancer

International journal of immunopathology and pharmacology, 2022-10, Vol.36, p.3946320221135454-3946320221135454

2022

Volltextzugriff (PDF)

Therapeutic goals in the treatment of Fabry disease

Genetics in medicine, 2010-11, Vol.12 (11), p.713-720

2010

Volltextzugriff (PDF)

Effects of enzyme replacement therapy in Fabry disease—A comprehensive review of the medical literature

Genetics in medicine, 2010-11, Vol.12 (11), p.668-679

2010

Volltextzugriff (PDF)

Manifestaciones oftalmológicas en pacientes mexicanos con enfermedad de Fabry

Archivos de la Sociedad Española de Oftalmología, 2012-11, Vol.87 (11), p.373-375

2012

Volltextzugriff (PDF)

Determination of SCN1A genetic variants in Mexican patients with refractory epilepsy and Dravet syndrome

Genetics and molecular research, 2017-05, Vol.16 (2), p.1

2017

Volltextzugriff (PDF)

Contribution of GSTM1, GSTT1, and MTHFR polymorphisms to end-stage renal disease of unknown etiology in Mexicans

Indian journal of nephrology, 2013-11, Vol.23 (6), p.438-443

2013

Volltextzugriff (PDF)

Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion

American journal of medical genetics. Part A, 2012-06, Vol.158A (6), p.1498-1502

2012

Volltextzugriff (PDF)

Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum

Journal of molecular medicine (Berlin, Germany), 2000-01, Vol.78 (5), p.282-286

2000

Volltextzugriff (PDF)

A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

British journal of dermatology (1951), 2005-12, Vol.153 (6), p.1216-1219

2005

Volltextzugriff (PDF)

Clinical features of Mexican patients with Mucopolysaccharidosis type I

Genetics and molecular research, 2017-09, Vol.16 (3), p.1

2017

Volltextzugriff (PDF)

Inherited hypertrichoses

Clinical genetics, 2002-05, Vol.61 (5), p.321-329

2002

Volltextzugriff (PDF)

Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients

American journal of human genetics, 1996-05, Vol.58 (5), p.998-1007

1996

Volltextzugriff (PDF)

Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia

Blood cells, molecules, & diseases, 2005-07, Vol.35 (1), p.66-69

2005

Volltextzugriff (PDF)

Apolipoprotein E genotypes in Mexican patients with Parkinson's disease

Disease markers, 2009, Vol.27 (5), p.225-230

2009

Volltextzugriff (PDF)

Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability

Clinical genetics, 2018-06, Vol.93 (6), p.1229-1233

2018

Volltextzugriff (PDF)

A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus : high-resolution mapping and genomic structure

Journal of molecular medicine (Berlin, Germany), 2000, Vol.78 (1), p.36-46

2000

Volltextzugriff (PDF)

Y-linked haplotypes in Amerindian chromosomes from Mexican populations: Genetic evidence to the dual origin of the Huichol tribe

Legal medicine (Tokyo, Japan), 2006-07, Vol.8 (4), p.220-225

2006

Volltextzugriff (PDF)

Cytochrome P4501A1 polymorphism is associated with susceptibility to acute lymphoblastic leukemia in adult Mexican patients

Blood cells, molecules, & diseases, 2004-11, Vol.33 (3), p.326-329

2004

Volltextzugriff (PDF)

Urinary Glycosaminoglycan Excretion in Healthy Subjects and in Patients with Mucopolysaccharidoses

Archives of medical research, 2000-09, Vol.31 (5), p.505-510

2000

Volltextzugriff (PDF)

Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1

Nature genetics, 1995-06, Vol.10 (2), p.202-207

1995

Volltextzugriff (PDF)

SNPs in human β-defensin 1 gene (DEFB1): frequencies in a Mexican population and new PCR-RFLPs assays

International Journal of Immunogenetics, 2006-10, Vol.33 (5), p.339-342

2006

Volltextzugriff (PDF)

Association of ss-Defensin 1 Single Nucleotide Polymorphisms with Atopic Dermatitis

International Archives of Allergy and Immunology, 2007-02, Vol.142 (3), p.211-218

2007

Volltextzugriff (PDF)

Association of the 677C1T Polymorphism in the MTHFR Gene with Colorectal Cancer in Mexican Patients

Cancer genomics & proteomics, 2009-06, Vol.6 (3), p.183-188

2009

Volltextzugriff (PDF)

GENE CORNER: A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

British journal of dermatology (1951), 2005-12, Vol.153 (6), p.1216-1219

2005

Volltextzugriff (PDF)

Allele frequency distributions of six Amp-FLPS (D1S80, APO-B, VWA, TH01, CSF1PO and HPRTB) in a Mexican population

Forensic science international, 1999-11, Vol.105 (2), p.125-129

1999

Volltextzugriff (PDF)

1 – 25 von 538

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(356)
Mit Volltextzugriff
(325)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Influence of nitric oxide signaling mechanisms in cancer

Therapeutic goals in the treatment of Fabry disease

Effects of enzyme replacement therapy in Fabry disease—A comprehensive review of the medical literature

Manifestaciones oftalmológicas en pacientes mexicanos con enfermedad de Fabry

Determination of SCN1A genetic variants in Mexican patients with refractory epilepsy and Dravet syndrome

Contribution of GSTM1, GSTT1, and MTHFR polymorphisms to end-stage renal disease of unknown etiology in Mexicans

Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion

Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum

A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

Clinical features of Mexican patients with Mucopolysaccharidosis type I

Inherited hypertrichoses

Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients

Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia

Apolipoprotein E genotypes in Mexican patients with Parkinson's disease

Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability

A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus : high-resolution mapping and genomic structure

Y-linked haplotypes in Amerindian chromosomes from Mexican populations: Genetic evidence to the dual origin of the Huichol tribe

Cytochrome P4501A1 polymorphism is associated with susceptibility to acute lymphoblastic leukemia in adult Mexican patients

Urinary Glycosaminoglycan Excretion in Healthy Subjects and in Patients with Mucopolysaccharidoses

Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1

SNPs in human β-defensin 1 gene (DEFB1): frequencies in a Mexican population and new PCR-RFLPs assays

Association of ss-Defensin 1 Single Nucleotide Polymorphisms with Atopic Dermatitis

Association of the 677C1T Polymorphism in the MTHFR Gene with Colorectal Cancer in Mexican Patients

GENE CORNER: A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

Allele frequency distributions of six Amp-FLPS (D1S80, APO-B, VWA, TH01, CSF1PO and HPRTB) in a Mexican population

Suchergebnisse filtern