UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 63

Sortiert nach

Leydig cell hypoplasia due to inactivation of luteinizing hormone receptor by a novel homozygous nonsense truncation mutation in the seventh transmembrane domain

Molecular and cellular endocrinology, 2005-01, Vol.229 (1), p.57-64

2005

Volltextzugriff (PDF)

Congenital adrenal hyperplasia : Molecular genetics and alternative approaches to treatment

Advances in pediatrics, 1995, Vol.42 (1), p.113-143

1995

Volltextzugriff (PDF)

Pathological and biochemical studies of fetal Krabbe disease

Brain & development (Tokyo. 1979), 1994-11, Vol.16 (6), p.480-484

1994

Volltextzugriff (PDF)

Familial congenital diaphragmatic hernia is an autosomal recessive variant

Journal of pediatric surgery, 1989-09, Vol.24 (9), p.860-864

1989

Volltextzugriff (PDF)

Type 1 Gaucher Disease: Phenotypic Expression and Natural History in Japanese Patients

Blood cells, molecules, & diseases, 1998-03, Vol.24 (1), p.73-81

1998

Volltextzugriff (PDF)

Genetic Heterogeneity of Adrenocorticotropin (ACTH) Resistance Syndromes: Identification of a Novel Mutation of the ACTH Receptor Gene in Hereditary Glucocorticoid Deficiency

Molecular genetics and metabolism, 1998-08, Vol.64 (4), p.256-265

1998

Volltextzugriff (PDF)

Coincidence of seizure susceptibility to caffeine and to the benzodiazepine inverse agonist, DMCM, in SWR and CBA inbred mice

Pharmacology, biochemistry and behavior, 1987-02, Vol.26 (2), p.381-387

1987

Volltextzugriff (PDF)

Intestinal transport of manganese from human milk, bovine milk and infant formula in rats

Life sciences (1973), 1984-12, Vol.35 (24), p.2415-2419

1984

Volltextzugriff (PDF)

Glucose tolerance and plasma lipid distributions in rats fed a high-sucrose, high-cholesterol, low-chromium diet

Metabolism, clinical and experimental, 1985-12, Vol.34 (12), p.1086-1093

1985

Volltextzugriff (PDF)

Interstrain variation in acute toxic response to caffeine among inbred mice

Pharmacology, biochemistry and behavior, 1984-04, Vol.20 (4), p.567-573

1984

Volltextzugriff (PDF)

Different genes specify hyporesponsiveness to seizures induced by caffeine and the benzodiazepine inverse agonist, DMCM

Pharmacology, biochemistry and behavior, 1987-07, Vol.27 (3), p.451-456

1987

Volltextzugriff (PDF)

Androgen receptors in ventral prostate glands of zinc deficient rats

Life sciences (1973), 1986-01, Vol.38 (4), p.351-356

1986

Volltextzugriff (PDF)

Differential antagonism of the behavioral depressant and hypothermic effects of 5′-(N-ethylcarboxamide) adenosine by theobromine

Pharmacology, biochemistry and behavior, 1986-10, Vol.25 (4), p.769-773

1986

Volltextzugriff (PDF)

Inherent hyporesponsiveness to methylxanthine-induced behavioral changes associated with supersensitivity to 5'-N-ethylcarboxamidoadenosine (NECA)

Pharmacology, biochemistry and behavior, 1986-12, Vol.25 (6), p.1271-1277

1986

Volltextzugriff (PDF)

Complex genetic determinants of susceptibility to methylxanthine-induced locomotor activity changes

Pharmacology, biochemistry and behavior, 1986-05, Vol.24 (5), p.1333-1341

1986

Volltextzugriff (PDF)

Idiopathic intracranial hypertension in cystinosis

The Journal of pediatrics, 2004-11, Vol.145 (5), p.673-678

2004

Volltextzugriff (PDF)

Absence of a 23 KD protein in testes of testicular feminization rat

Life sciences (1973), 1987-06, Vol.40 (22), p.2169-2173

1987

Volltextzugriff (PDF)

A single gene difference determines relative susceptibility to caffeine-induced lethality in SWR and CBA inbred mice

Pharmacology, biochemistry and behavior, 1985-08, Vol.23 (2), p.275-278

1985

Volltextzugriff (PDF)

Inheritance of amphetamine-induced thermoregulatory responses in inbred mice

Pharmacology, biochemistry and behavior, 1985-01, Vol.23 (3), p.373-377

1985

Volltextzugriff (PDF)

Application of transcriptional and biological network analyses in mouse germ-cell transcriptomes

Genomics (San Diego, Calif.), 2006-07, Vol.88 (1), p.18-33

2006

Volltextzugriff (PDF)

Analysis of mouse germ-cell transcriptome at different stages of spermatogenesis by SAGE: Biological significance

Genomics (San Diego, Calif.), 2004-12, Vol.84 (6), p.971-981

2004

Volltextzugriff (PDF)

The complexity of antisense transcription revealed by the study of developing male germ cells

Genomics (San Diego, Calif.), 2006-06, Vol.87 (6), p.681-692

2006

Volltextzugriff (PDF)

Fluorescence micro disc electrophoresis in sodium dodecyl sulfate : A simple and sensitive method applicable for routine laboratory analysis

Journal of chromatography, 1980-02, Vol.181 (2), p.259-265

1980

Volltextzugriff (PDF)

Autosomal recessively inherited electrolyte excretory defect in the parotid of the “cribriform degeneration” mouse mutant — possible analogy to cystic fibrosis

Life sciences (1973), 1974-08, Vol.15 (4), p.803-810

1974

Volltextzugriff (PDF)

Polyamine conjugates and total polyamine concentrations in human amniotic fluid

Clinica chimica acta, 1979-02, Vol.91 (3), p.233-241

1979

Volltextzugriff (PDF)

1 – 25 von 63

Suche als RSS-Feed

Aktive Filter

KollektionElsevier ScienceDirect Journals Complete

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(63)
Mit Volltextzugriff
(62)

Publikationsform

Artikel
(63)

Sprache

Englisch
(63)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Leydig cell hypoplasia due to inactivation of luteinizing hormone receptor by a novel homozygous nonsense truncation mutation in the seventh transmembrane domain

Congenital adrenal hyperplasia : Molecular genetics and alternative approaches to treatment

Pathological and biochemical studies of fetal Krabbe disease

Familial congenital diaphragmatic hernia is an autosomal recessive variant

Type 1 Gaucher Disease: Phenotypic Expression and Natural History in Japanese Patients

Genetic Heterogeneity of Adrenocorticotropin (ACTH) Resistance Syndromes: Identification of a Novel Mutation of the ACTH Receptor Gene in Hereditary Glucocorticoid Deficiency

Coincidence of seizure susceptibility to caffeine and to the benzodiazepine inverse agonist, DMCM, in SWR and CBA inbred mice

Intestinal transport of manganese from human milk, bovine milk and infant formula in rats

Glucose tolerance and plasma lipid distributions in rats fed a high-sucrose, high-cholesterol, low-chromium diet

Interstrain variation in acute toxic response to caffeine among inbred mice

Different genes specify hyporesponsiveness to seizures induced by caffeine and the benzodiazepine inverse agonist, DMCM

Androgen receptors in ventral prostate glands of zinc deficient rats

Differential antagonism of the behavioral depressant and hypothermic effects of 5′-(N-ethylcarboxamide) adenosine by theobromine

Inherent hyporesponsiveness to methylxanthine-induced behavioral changes associated with supersensitivity to 5'-N-ethylcarboxamidoadenosine (NECA)

Complex genetic determinants of susceptibility to methylxanthine-induced locomotor activity changes

Idiopathic intracranial hypertension in cystinosis

Absence of a 23 KD protein in testes of testicular feminization rat

A single gene difference determines relative susceptibility to caffeine-induced lethality in SWR and CBA inbred mice

Inheritance of amphetamine-induced thermoregulatory responses in inbred mice

Application of transcriptional and biological network analyses in mouse germ-cell transcriptomes

Analysis of mouse germ-cell transcriptome at different stages of spermatogenesis by SAGE: Biological significance

The complexity of antisense transcription revealed by the study of developing male germ cells

Fluorescence micro disc electrophoresis in sodium dodecyl sulfate : A simple and sensitive method applicable for routine laboratory analysis

Autosomal recessively inherited electrolyte excretory defect in the parotid of the “cribriform degeneration” mouse mutant — possible analogy to cystic fibrosis

Polyamine conjugates and total polyamine concentrations in human amniotic fluid

Aktive Filter

Suchergebnisse filtern