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M Ashcroft

Showing results (451-460 of 758) with videos related to

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Journal of Clinical Pharmacy and Therapeutics|November 5, 2015
Medication safety at the interface: evaluating risks associated with discharge prescriptions from mental health hospitalsR N Keers, S D Williams, J J Vattakatuchery, et al.
BMC Medicine|March 3, 2020
The effectiveness of frequent antibiotic use in reducing the risk of infection-related hospital admissions: results from two large population-based cohortsTjeerd Pieter van Staa, Victoria Palin, Yan Li, et al.
Journal of Affective Disorders|April 7, 2020
Fertility trends of women with serious mental illness in the United Kingdom 1992-2017: A primary care cohort study using the clinical practice research datalinkHolly Hope, Rosa Parisi, Darren M Ashcroft, et al.
Diabetologia|February 17, 2024
A loss-of-function mutation in KCNJ11 causing sulfonylurea-sensitive diabetes in early adult lifeNatascia Vedovato, Maria V Salguero, Siri Atma W Greeley, et al.
Plos One|February 27, 2016
Modelling Conditions and Health Care Processes in Electronic Health Records: An Application to Severe Mental Illness with the Clinical Practice Research DatalinkIvan Olier, David A Springate, Darren M Ashcroft, et al.
The Journal of Physiology|June 15, 1996
Endocytosis of secretory granules in mouse pancreatic beta-cells evoked by transient elevation of cytosolic calciumL Eliasson, P Proks, C Ammälä, et al.
FEBS Letters|July 29, 1996
Heteromeric channel formation and Ca(2+)-free media reduce the toxic effect of the weaver Kir 3.2 alleleS J Tucker, M Pessia, A J Moorhouse, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 14, 2018
Permanent neonatal diabetes: combining sulfonylureas with insulin may be an effective treatmentS Misra, N Vedovato, E Cliff, et al.
Diabetes, Obesity & Metabolism|October 9, 2007
Functional analysis of two Kir6.2 (KCNJ11) mutations, K170T and E322K, causing neonatal diabetesA I Tarasov, C A Girard, B Larkin, et al.
Diabetologia|March 11, 2003
Characterisation of new KATP-channel mutations associated with congenital hyperinsulinism in the Finnish populationF Reimann, H Huopio, M Dabrowski, et al.
Pageof 76

Showing results (451-460 of 758) with videos related to

Sort By:
Pageof 76
Journal of Clinical Pharmacy and Therapeutics|November 5, 2015
Medication safety at the interface: evaluating risks associated with discharge prescriptions from mental health hospitalsR N Keers, S D Williams, J J Vattakatuchery, et al.
BMC Medicine|March 3, 2020
The effectiveness of frequent antibiotic use in reducing the risk of infection-related hospital admissions: results from two large population-based cohortsTjeerd Pieter van Staa, Victoria Palin, Yan Li, et al.
Journal of Affective Disorders|April 7, 2020
Fertility trends of women with serious mental illness in the United Kingdom 1992-2017: A primary care cohort study using the clinical practice research datalinkHolly Hope, Rosa Parisi, Darren M Ashcroft, et al.
Diabetologia|February 17, 2024
A loss-of-function mutation in KCNJ11 causing sulfonylurea-sensitive diabetes in early adult lifeNatascia Vedovato, Maria V Salguero, Siri Atma W Greeley, et al.
Plos One|February 27, 2016
Modelling Conditions and Health Care Processes in Electronic Health Records: An Application to Severe Mental Illness with the Clinical Practice Research DatalinkIvan Olier, David A Springate, Darren M Ashcroft, et al.
The Journal of Physiology|June 15, 1996
Endocytosis of secretory granules in mouse pancreatic beta-cells evoked by transient elevation of cytosolic calciumL Eliasson, P Proks, C Ammälä, et al.
FEBS Letters|July 29, 1996
Heteromeric channel formation and Ca(2+)-free media reduce the toxic effect of the weaver Kir 3.2 alleleS J Tucker, M Pessia, A J Moorhouse, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 14, 2018
Permanent neonatal diabetes: combining sulfonylureas with insulin may be an effective treatmentS Misra, N Vedovato, E Cliff, et al.
Diabetes, Obesity & Metabolism|October 9, 2007
Functional analysis of two Kir6.2 (KCNJ11) mutations, K170T and E322K, causing neonatal diabetesA I Tarasov, C A Girard, B Larkin, et al.
Diabetologia|March 11, 2003
Characterisation of new KATP-channel mutations associated with congenital hyperinsulinism in the Finnish populationF Reimann, H Huopio, M Dabrowski, et al.
Pageof 76