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 mutations of butyrylcholine esterase identified from phenotypic abnormalities in Japan

Clinical chemistry (Baltimore, Md.), 1997-06, Vol.43 (6), p.924-929

1997

Volltextzugriff (PDF)

Lactate Dehydrogenase M subunit deficiency

Rinsho byori. The Japanese journal of clinical pathology, 2002-06, Vol.50 (6), p.571

Sudo, Kayoko

2002

Volltextzugriff (PDF)

Genetic and immunological analyses of patients with increased serum butyrylcholinesterase activity and its C5 variant form

Clinical chemistry and laboratory medicine, 2004-01, Vol.42 (9), p.991-996

2004

Volltextzugriff (PDF)

Characteristics of the complex between alkaline phosphatase and immunoglobulin A in human serum

Clinica chimica acta, 1985-08, Vol.150 (3), p.185-195

1985

Volltextzugriff (PDF)

Electrophoretic Analysis of a-Glycerophosphate Dehydrogenase and its Role in Metabolic Regulation

Electrophoresis '83, 2019, p.431-436

Originally published 1984, 2019

Volltextzugriff (PDF)

Human Butyrylcholinesterase L330I Mutation Belongs to a Fluoride-Resistant Gene, by Expression in Human Fetal Kidney Cells

Biochemical and biophysical research communications, 1997-11, Vol.240 (2), p.372-375

1997

Volltextzugriff (PDF)

Isoelectrophoretic Acidic Isoenzyme of Human Ribonuclease

Electrophoresis '83, 2019, p.401-408

Originally published 1984, 2019

Volltextzugriff (PDF)

Electrophoretic Separation of Tripeptide Aminopeptidase and its Distribution in Human Tissues

Electrophoresis '83, 2019, p.437-440

Originally published 1984, 2019

Volltextzugriff (PDF)

Lactate dehydrogenase M-subunit deficiency: a new type of hereditary exertional myopathy

Clinica chimica acta, 1988-03, Vol.173 (1), p.89-98

1988

Volltextzugriff (PDF)

A novel in-frame deletion mutation in a case of lactate dehydrogenase (LD) H subunit deficiency showing an atypical LD isoenzyme pattern in serum and erythrocytes

Clinical biochemistry, 1999-03, Vol.32 (2), p.137-141

1999

Volltextzugriff (PDF)

Three different point mutations in the butyrylcholinesterase gene of three Japanese subjects with a silent phenotype: Possible Japanese type alleles

Clinical biochemistry, 1996-04, Vol.29 (2), p.165-169

1996

Volltextzugriff (PDF)

Cholinesterase-producing hepatocellular carcinoma

Journal of hepatology, 1999-02, Vol.30 (2), p.348-349

1999

Volltextzugriff (PDF)

Butyrylcholinesterase Genes in Individuals with Abnormal Inhibition Numbers and with Trace Activity: One Common Mutation and Two Novel Silent Genes

Annals of clinical biochemistry, 1998-03, Vol.35 (2), p.302-310

1998

Volltextzugriff (PDF)

Genetic basis of the silent phenotype of serum butyrylcholinesterase in three compound heterozygotes

Clinica chimica acta, 1995-02, Vol.235 (1), p.41-57

1995

Volltextzugriff (PDF)

Molecular characterization of genetic mutation in human lactate dehydrogenase-A (M) deficiency

Biochemical and biophysical research communications, 1990-04, Vol.168 (2), p.677-682

1990

Volltextzugriff (PDF)

Effect of electrophoretic conditions on single strand conformation polymorphism (SSCP) pattern

Seibutsu-butsuri-kagaku, 1994, Vol.38 (2), p.95-101

1994

Volltextzugriff (PDF)

Analysis of LDH anomaly linked to IgG, IgA and IgM

Seibutsu-butsuri-kagaku, 1994, Vol.38 (4), p.249-252

1994

Volltextzugriff (PDF)

Analysis of LDH-H(B) unstable subunit variant gene using "Mismatched PCR" method

Seibutsu-butsuri-kagaku, 1992, Vol.36 (1), p.65-70

1992

Volltextzugriff (PDF)

Heterogeneity in the silent type serum cholinesterase variant

Seibutsu-butsuri-kagaku, 1987, Vol.31 (1), p.15-18

1987

Volltextzugriff (PDF)

A novel deletion mutation of lactate dehydrogenase A(M) gene in the fifth family with the enzyme deficiency

Human molecular genetics, 1994-05, Vol.3 (5), p.825-826

1994

Volltextzugriff (PDF)

Comparative study of binding affinity to lactate dehydrogenase of enzyme-linked immunoglobulin and anti-subunit antibody

Seibutsu-butsuri-kagaku, 1986, Vol.30 (3), p.223-228

1986

Volltextzugriff (PDF)

Analysis of genetic mutations in human lactate dehydrogenase-A(M) deficiency using DNA conformation polymorphism in combination with polyacrylamide gradient gel and silver staining

Biochemical and biophysical research communications, 1991-10, Vol.180 (2), p.1083-1090

1991

Volltextzugriff (PDF)

DNA analysis of slow type of electrophoretic lactate dehydrogenase B(H) variant

Seibutsu-butsuri-kagaku, 1994, Vol.38 (1), p.25-29

1994

Volltextzugriff (PDF)

Electrophoresis for analysis of genetic variants; polymerase chain reaction(PCR), mismatched PCR

Seibutsu-butsuri-kagaku, 1999-03, Vol.43 (1), p.1-7

1999

Volltextzugriff (PDF)

Premature termination mutations in two patients with deficiency of lactate dehydrogenase H(B) subunit

Clinical chemistry (Baltimore, Md.), 1994-08, Vol.40 (8), p.1567-1570

1994

Volltextzugriff (PDF)

1 – 25 von 83

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(56)
Mit Volltextzugriff
(61)

Publikationsform

Artikel
(80)
Buchkapitel
(3)

Sprache

Englisch
(79)
Japanisch
(7)

Erscheinungsjahr

n.n

Thema

Humans
(46)
Science & Technology
(44)
Life Sciences & Biomedicine
(41)
Male
(25)
Biological And Medical Sciences
(22)
Female
(16)
Medical Laboratory Technology
(16)
Base Sequence
(14)
L-Lactate Dehydrogenase - Deficiency
(14)
L-Lactate Dehydrogenase - Genetics
(14)
Mutation
(14)
Fundamental And Applied Biological Sciences. Psychology
(13)
Molecular Sequence Data
(13)
Polymerase Chain Reaction
(13)
Adult
(12)
Amino Acid Sequence
(11)
Isoenzymes
(10)
Aged
(9)
Biochemistry & Molecular Biology
(9)
Medical Sciences
(9)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Genetic mutations of butyrylcholine esterase identified from phenotypic abnormalities in Japan

Lactate Dehydrogenase M subunit deficiency

Genetic and immunological analyses of patients with increased serum butyrylcholinesterase activity and its C5 variant form

Characteristics of the complex between alkaline phosphatase and immunoglobulin A in human serum

Electrophoretic Analysis of a-Glycerophosphate Dehydrogenase and its Role in Metabolic Regulation

Human Butyrylcholinesterase L330I Mutation Belongs to a Fluoride-Resistant Gene, by Expression in Human Fetal Kidney Cells

Isoelectrophoretic Acidic Isoenzyme of Human Ribonuclease

Electrophoretic Separation of Tripeptide Aminopeptidase and its Distribution in Human Tissues

Lactate dehydrogenase M-subunit deficiency: a new type of hereditary exertional myopathy

A novel in-frame deletion mutation in a case of lactate dehydrogenase (LD) H subunit deficiency showing an atypical LD isoenzyme pattern in serum and erythrocytes

Three different point mutations in the butyrylcholinesterase gene of three Japanese subjects with a silent phenotype: Possible Japanese type alleles

Cholinesterase-producing hepatocellular carcinoma

Butyrylcholinesterase Genes in Individuals with Abnormal Inhibition Numbers and with Trace Activity: One Common Mutation and Two Novel Silent Genes

Genetic basis of the silent phenotype of serum butyrylcholinesterase in three compound heterozygotes

Molecular characterization of genetic mutation in human lactate dehydrogenase-A (M) deficiency

Effect of electrophoretic conditions on single strand conformation polymorphism (SSCP) pattern

Analysis of LDH anomaly linked to IgG, IgA and IgM

Analysis of LDH-H(B) unstable subunit variant gene using "Mismatched PCR" method

Heterogeneity in the silent type serum cholinesterase variant

A novel deletion mutation of lactate dehydrogenase A(M) gene in the fifth family with the enzyme deficiency

Comparative study of binding affinity to lactate dehydrogenase of enzyme-linked immunoglobulin and anti-subunit antibody

Analysis of genetic mutations in human lactate dehydrogenase-A(M) deficiency using DNA conformation polymorphism in combination with polyacrylamide gradient gel and silver staining

DNA analysis of slow type of electrophoretic lactate dehydrogenase B(H) variant

Electrophoresis for analysis of genetic variants; polymerase chain reaction(PCR), mismatched PCR

Premature termination mutations in two patients with deficiency of lactate dehydrogenase H(B) subunit

Suchergebnisse filtern