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Pharmacokinetic interaction between JBP485 and cephalexin in rats

Drug metabolism and disposition, 2010-06, Vol.38 (6), p.930

2010

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Peptide Cotransporter 1 in Intestine and Organic Anion Transporters in Kidney Are Targets of Interaction between JBP485 and Lisinopril in Rats

DRUG METABOLISM AND PHARMACOKINETICS, 2012, Vol.27 (2), p.232-241

2012

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Pharmacokinetics and Mechanism of Intestinal Absorption of JBP485 in Rats

DRUG METABOLISM AND PHARMACOKINETICS, 2010-01, Vol.25 (5), p.500-507

2010

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Inhibitory Effect of Zinc on the Absorption of JBP485 via the Gastrointestinal Oligopeptide Transporter (PEPT1) in Rats

DRUG METABOLISM AND PHARMACOKINETICS, 2011-01, Vol.26 (5), p.494-502

2011

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Hydroxyprolylserine derivatives JBP923 and JBP485 exhibit the antihepatitis activities after gastrointestinal absorption in rats

The Journal of pharmacology and experimental therapeutics, 2000-08, Vol.294 (2), p.510

2000

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Anoxic-epileptic seizures: observational study of epileptic seizures induced by syncopes

Archives of disease in childhood, 2005-12, Vol.90 (12), p.1283-1287

2005

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Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism

Journal of medical genetics, 2003-03, Vol.40 (3), p.183-187

2003

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Increased chromosomal radiosensitivity in breast cancer patients: a comparison of two assays

International journal of radiation biology, 1999, Vol.75 (1), p.1-10

SCOTT, D.

1999

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Gratification disorder (“infantile masturbation”): a review

Archives of disease in childhood, 2004-03, Vol.89 (3), p.225-226

2004

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Fauna and stratification of male orchid bees (Hymenoptera: Apidae) and their preference for odor baits in a forest fragment

Neotropical entomology, 2011-11, Vol.40 (6), p.639-646

2011

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Caregiver characteristics and economic cost of home-based care: a case study of Maun and Gumare villages in North West District, Botswana

Chronic illness, 2013-03, Vol.9 (1), p.3-15

2013

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Cardiac pacing for severe childhood neurally mediated syncope with reflex anoxic seizures

Heart (British Cardiac Society), 1999-12, Vol.82 (6), p.721-725

1999

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Cataplexy in the Prader–Willi syndrome

Archives of disease in childhood, 2002-08, Vol.87 (2), p.170-170

2002

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Adaptation of a South American malaria vector to laboratory colonization suggests faster-male evolution for mating ability

BMC evolutionary biology, 2004-05, Vol.4, p.12

2004

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Detection of Individual Differences in Radiation-Induced Apoptosis of Peripheral Blood Lymphocytes in Normal Individuals, Ataxia Telangiectasia Homozygotes and Heterozygotes, and Breast Cancer Patients after Radiotherapy

Radiation research, 2000-05, Vol.153 (5), p.570-578

2000

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The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)

Journal of medical genetics, 1995-11, Vol.32 (11), p.881-884

1995

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Analysis of Reproductive Isolation Between Sibling Species Anopheles albitarsis sensu stricto and Anopheles deaneorum, Two Malaria Vectors Belonging to the Albitarsis Complex (Diptera: Culicidae)

Journal of medical entomology, 2004-09, Vol.41 (5), p.888-893

2004

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The Prader-Willi syndrome

Archives of disease in childhood, 1994-01, Vol.70 (1), p.58-63

1994

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Clinical presentation, haematological indices and management of children with severe and uncomplicated malaria in Douala, Cameroon

Pakistan journal of biological sciences, 2008-10, Vol.11 (20), p.2401-2406

2008

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Heritability of chromosomal radiosensitivity in breast cancer patients: a pilot study with the lymphocyte micronucleus assay

International journal of radiation biology, 2000, Vol.76 (12), p.1617-1619

Burrill, J. B. P. Barber, S. A. Roberts, B. Bulman, D. Scott, W.

2000

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Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues

Journal of medical genetics, 1994-01, Vol.31 (1), p.41-44

1994

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"Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndrome

Journal of medical genetics, 1998-02, Vol.35 (2), p.94-98

1998

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Genetic aspects of tuberous sclerosis in the west of Scotland

Journal of medical genetics, 1989-01, Vol.26 (1), p.28-31

1989

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Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light

Cancer research (Chicago, Ill.), 1988-11, Vol.48 (21), p.6090-6096

1988

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Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families

Journal of neurology, neurosurgery and psychiatry, 1996-12, Vol.61 (6), p.616-620

1996

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Pharmacokinetic interaction between JBP485 and cephalexin in rats

Peptide Cotransporter 1 in Intestine and Organic Anion Transporters in Kidney Are Targets of Interaction between JBP485 and Lisinopril in Rats

Pharmacokinetics and Mechanism of Intestinal Absorption of JBP485 in Rats

Inhibitory Effect of Zinc on the Absorption of JBP485 via the Gastrointestinal Oligopeptide Transporter (PEPT1) in Rats

Hydroxyprolylserine derivatives JBP923 and JBP485 exhibit the antihepatitis activities after gastrointestinal absorption in rats

Anoxic-epileptic seizures: observational study of epileptic seizures induced by syncopes

Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism

Increased chromosomal radiosensitivity in breast cancer patients: a comparison of two assays

Gratification disorder (“infantile masturbation”): a review

Fauna and stratification of male orchid bees (Hymenoptera: Apidae) and their preference for odor baits in a forest fragment

Caregiver characteristics and economic cost of home-based care: a case study of Maun and Gumare villages in North West District, Botswana

Cardiac pacing for severe childhood neurally mediated syncope with reflex anoxic seizures

Cataplexy in the Prader–Willi syndrome

Adaptation of a South American malaria vector to laboratory colonization suggests faster-male evolution for mating ability

Detection of Individual Differences in Radiation-Induced Apoptosis of Peripheral Blood Lymphocytes in Normal Individuals, Ataxia Telangiectasia Homozygotes and Heterozygotes, and Breast Cancer Patients after Radiotherapy

The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)

Analysis of Reproductive Isolation Between Sibling Species Anopheles albitarsis sensu stricto and Anopheles deaneorum, Two Malaria Vectors Belonging to the Albitarsis Complex (Diptera: Culicidae)

The Prader-Willi syndrome

Clinical presentation, haematological indices and management of children with severe and uncomplicated malaria in Douala, Cameroon

Heritability of chromosomal radiosensitivity in breast cancer patients: a pilot study with the lymphocyte micronucleus assay

Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues

"Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndrome

Genetic aspects of tuberous sclerosis in the west of Scotland

Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light

Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families

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