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...

Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk

Journal of medical genetics, 2006-12, Vol.43 (12), p.943-949

2006

Volltextzugriff (PDF)

Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project

Clinical genetics, 2010-06, Vol.77 (6), p.572-580

2010

Volltextzugriff (PDF)

Update and Analysis of the University College London Low Density Lipoprotein Receptor Familial Hypercholesterolemia Database

Annals of human genetics, 2008-07, Vol.72 (4), p.485-498

2008

Volltextzugriff (PDF)

Host Systems for the Production of Recombinant Spider Silk

Trends in biotechnology (Regular ed.), 2021-06, Vol.39 (6), p.560-573

2021

Volltextzugriff (PDF)

A demonstration of the use of ultra-performance liquid chromatography–mass spectrometry [UPLC/MS] in the determination of amphetamine-type substances and ketamine for forensic and toxicological analysis

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2006-05, Vol.836 (1), p.111-115

2006

Volltextzugriff (PDF)

Analysis of mutations causing familial hypercholesterolaemia in black South African patients of different ancestry

SAMJ: South African Medical Journal, 2017-02, Vol.107 (2), p.145-148

2017

Volltextzugriff (PDF)

A risk-based methodology for establishing landslide exclusion zones in operating open pit mines

International journal of rock mechanics and mining sciences (Oxford, England : 1997), 2017-12, Vol.100, p.100-107

2017

Volltextzugriff (PDF)

Common Adiponectin Gene Variants Show Different Effects on Risk of Cardiovascular Disease and Type 2 Diabetes in European Subjects

Annals of human genetics, 2007-07, Vol.71 (4), p.453-466

2007

Volltextzugriff (PDF)

Blood, sweat, and tears: extraterrestrial regolith biocomposites with in vivo binders

Materials today bio, 2021-09, Vol.12, p.100136, Article 100136

2021

Volltextzugriff (PDF)

Development of a high-resolution melting method for mutation detection in familial hypercholesterolaemia patients

Annals of clinical biochemistry, 2010-01, Vol.47 (Pt 1), p.44-55

2010

Volltextzugriff (PDF)

Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor binding

Arteriosclerosis, thrombosis, and vascular biology, 2008-10, Vol.28 (10), p.1866-1871

2008

Volltextzugriff (PDF)

Matrix Effect and Cross-Reactivity of Select Amphetamine-Type Substances, Designer Analogues, and Putrefactive Amines using the Bio-Quant Direct ELISA Presumptive Assays for Amphetamine and Methamphetamine

Journal of analytical toxicology, 2007-05, Vol.31 (4), p.208-213

2007

Volltextzugriff (PDF)

Identification of patients with familial hypercholesterolaemia (FH) through the application of genetic testing in young mi patients from the MINAP register

Atherosclerosis, 2011-10, Vol.218 (2), p.e5-e5

2011

Volltextzugriff (PDF)

Synthetic biology approaches to actinomycete strain improvement

FEMS microbiology letters, 2021-06, Vol.368 (10), p.1

2021

Volltextzugriff (PDF)

Analysis of the proc gene in patients with type 2 diabetes and low levels of activated protein c

Atherosclerosis, 2012-12, Vol.225 (2), p.e5-e5

2012

Volltextzugriff (PDF)

Organometallic Complexes for Nonlinear Optics. 22. Quadratic and Cubic Hyperpolarizabilities of trans-Bis(bidentate phosphine)ruthenium σ-Arylvinylidene and σ-Arylalkynyl Complexes

Organometallics, 2001-10, Vol.20 (22), p.4664-4675

2001

Volltextzugriff (PDF)

Low-density lipoprotein receptor gene (LDLR) world-wide website in familial hypercholesterolaemia: update, new features and mutation analysis

Atherosclerosis, 2001, Vol.154 (1), p.243-246

2001

Volltextzugriff (PDF)

Multiplex MassARRAY spectrometry (iPLEX) produces a fast and economical test for 56 familial hypercholesterolaemia-causing mutations

Clinical genetics, 2008-11, Vol.74 (5), p.463-468

2008

Volltextzugriff (PDF)

Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemia

Clinical genetics, 2007-06, Vol.71 (6), p.561-568

2007

Volltextzugriff (PDF)

Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia

Human mutation, 1997, Vol.10 (2), p.116-127

1997

Volltextzugriff (PDF)

Organometallic Complexes for Nonlinear Optics. 8. Syntheses and Molecular Quadratic Hyperpolarizabilities of Systematically Varied (Triphenylphosphine)gold σ-Arylacetylides: X-ray Crystal Structures of Au(C⋮CR)(PPh3) (R = 4-C6H4NO2, 4,4‘-C6H4C6H4NO2)

Organometallics, 1996-12, Vol.15 (26), p.5738-5745

1996

Volltextzugriff (PDF)

P725Molecular genetics of familial hypercholesterolemia in Israel revisited

European heart journal, 2019-10, Vol.40 (Supplement_1)

2019

Volltextzugriff (PDF)

Organometallic Complexes for Nonlinear Optics. 4. Cubic Hyperpolarizabilities of (Cyclopentadienyl)bis(phosphine)ruthenium .sigma.-Arylacetylides

Organometallics, 1995-12, Vol.14 (12), p.5493-5495

1995

Volltextzugriff (PDF)

Organometallic Complexes for Nonlinear Optics. 2. Syntheses, Electrochemical Studies, Structural Characterization, and Computationally-Derived Molecular Quadratic Hyperpolarizabilities of Ruthenium .sigma.-Arylacetylides: X-ray Crystal Structures of Ru(C.tplbond.CPh)(PMe3)2(.eta.-C5H5) and Ru(C.tplbond.CC6H4NO2-4)(L)2(.eta.-C5H5) (L = PPh3, PMe3)

Organometallics, 1995-08, Vol.14 (8), p.3970-3979

1995

Volltextzugriff (PDF)

Analysis of mutations causing familial hypercholesterolaemia in black South African patients of different ancestry

South African medical journal, 2017-02, Vol.107 (2), p.145-148

2017

Volltextzugriff (PDF)

1 – 25 von 200

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(172)
Mit Volltextzugriff
(163)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(113)
Life Sciences & Biomedicine
(87)
Humans
(62)
Biological And Medical Sciences
(39)
Medical Sciences
(33)
Physical Sciences
(32)
Chemistry
(29)
Female
(27)
Male
(26)
Mutation
(20)
Receptors, Ldl - Genetics
(20)
Middle Aged
(19)
Hyperlipoproteinemia Type Ii - Genetics
(17)
Animals
(16)
Fundamental And Applied Biological Sciences. Psychology
(14)
Chemistry, Organic
(13)
Genetics & Heredity
(13)
Adult
(12)
Immunology
(12)
Aged
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk

Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project

Update and Analysis of the University College London Low Density Lipoprotein Receptor Familial Hypercholesterolemia Database

Host Systems for the Production of Recombinant Spider Silk

A demonstration of the use of ultra-performance liquid chromatography–mass spectrometry [UPLC/MS] in the determination of amphetamine-type substances and ketamine for forensic and toxicological analysis

Analysis of mutations causing familial hypercholesterolaemia in black South African patients of different ancestry

A risk-based methodology for establishing landslide exclusion zones in operating open pit mines

Common Adiponectin Gene Variants Show Different Effects on Risk of Cardiovascular Disease and Type 2 Diabetes in European Subjects

Blood, sweat, and tears: extraterrestrial regolith biocomposites with in vivo binders

Development of a high-resolution melting method for mutation detection in familial hypercholesterolaemia patients

Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor binding

Matrix Effect and Cross-Reactivity of Select Amphetamine-Type Substances, Designer Analogues, and Putrefactive Amines using the Bio-Quant Direct ELISA Presumptive Assays for Amphetamine and Methamphetamine

Identification of patients with familial hypercholesterolaemia (FH) through the application of genetic testing in young mi patients from the MINAP register

Synthetic biology approaches to actinomycete strain improvement

Analysis of the proc gene in patients with type 2 diabetes and low levels of activated protein c

Organometallic Complexes for Nonlinear Optics. 22. Quadratic and Cubic Hyperpolarizabilities of trans-Bis(bidentate phosphine)ruthenium σ-Arylvinylidene and σ-Arylalkynyl Complexes

Low-density lipoprotein receptor gene (LDLR) world-wide website in familial hypercholesterolaemia: update, new features and mutation analysis

Multiplex MassARRAY spectrometry (iPLEX) produces a fast and economical test for 56 familial hypercholesterolaemia-causing mutations

Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemia

Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia

Organometallic Complexes for Nonlinear Optics. 8. Syntheses and Molecular Quadratic Hyperpolarizabilities of Systematically Varied (Triphenylphosphine)gold σ-Arylacetylides: X-ray Crystal Structures of Au(C⋮CR)(PPh3) (R = 4-C6H4NO2, 4,4‘-C6H4C6H4NO2)

P725Molecular genetics of familial hypercholesterolemia in Israel revisited

Organometallic Complexes for Nonlinear Optics. 4. Cubic Hyperpolarizabilities of (Cyclopentadienyl)bis(phosphine)ruthenium .sigma.-Arylacetylides

Analysis of mutations causing familial hypercholesterolaemia in black South African patients of different ancestry

Suchergebnisse filtern