Karen E Cosgrove
Karen E Cosgrove
Vahvistettu sähköpostiosoite verkkotunnuksessa
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
M Bitner-Glindzicz, KJ Lindley, P Rutland, D Blaydon, VV Smith, PJ Milla, ...
Nature genetics 26 (1), 56-60, 2000
Hyperinsulinism in infancy: from basic science to clinical disease
MJ Dunne, KE Cosgrove, RM Shepherd, A Aynsley-Green, KJ Lindley
Physiological Reviews 84 (1), 239-275, 2004
A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.
T Otonkoski, C Ammälä, H Huopio, GJ Cote, J Chapman, K Cosgrove, ...
Diabetes 48 (2), 408-415, 1999
Therapies and outcomes of congenital hyperinsulinism‐induced hypoglycaemia
I Banerjee, M Salomon‐Estebanez, P Shah, J Nicholson, KE Cosgrove, ...
Diabetic Medicine 36 (1), 9-21, 2019
Abnormal neurodevelopmental outcomes are common in children with transient congenital hyperinsulinism
HB Avatapalle, I Banerjee, S Shah, M Pryce, J Nicholson, L Rigby, ...
Frontiers in endocrinology 4, 60, 2013
The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism
I Banerjee, M Skae, SE Flanagan, L Rigby, L Patel, M Didi, J Blair, ...
European journal of endocrinology 164 (5), 733-740, 2011
Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity
S Tornovsky, A Crane, KE Cosgrove, K Hussain, J Lavie, M Heyman, ...
The Journal of Clinical Endocrinology & Metabolism 89 (12), 6224-6234, 2004
Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic β-cell adenosine triphosphate-sensitive potassium channels
K Hussain, KE Cosgrove, RM Shepherd, A Luharia, VV Smith, S Kassem, ...
The Journal of Clinical Endocrinology & Metabolism 90 (7), 4376-4382, 2005
Glucose modulation of insulin mRNA levels is dependent on transcription factor PDX-1 and occurs independently of changes in intracellular Ca2+.
WM Macfarlane, RM Shepherd, KE Cosgrove, RF James, MJ Dunne, ...
Diabetes 49 (3), 418-423, 2000
Engineering a glucose-responsive human insulin-secreting cell line from islets of Langerhans isolated from a patient with persistent hyperinsulinemic hypoglycemia of infancy
WM MacFarlane, JC Chapman, RM Shepherd, MN Hashmi, N Kamimura, ...
Journal of Biological Chemistry 274 (48), 34059-34066, 1999
PAX4 enhances beta-cell differentiation of human embryonic stem cells
CG Liew, NN Shah, SJ Briston, RM Shepherd, CP Khoo, MJ Dunne, ...
PLoS One 3 (3), e1783, 2008
Hyperinsulinism of Infancy: The Regulated Release of Insulin by KATP Channel—Independent Pathways
SG Straub, KE Cosgrove, C Ämmälä, RM Shepherd, RE O'Brien, ...
Diabetes 50 (2), 329-339, 2001
Potassium channels, sulphonylurea receptors and control of insulin release
MJ Dunne, KE Cosgrove, RM Shepherd, C Ämmälä
Trends in Endocrinology & Metabolism 10 (4), 146-152, 1999
Human embryonic stem cells: possibilities for human cell transplantation
C Liew, H Moore, L Ruban, N Shah, K Cosgrove, M Dunne, P Andrews
Annals of medicine 37 (7), 521-532, 2005
Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time
M Salomon-Estebanez, SE Flanagan, S Ellard, L Rigby, L Bowden, ...
Orphanet journal of rare diseases 11, 1-11, 2016
Hyperinsulinism of infancy: towards an understanding of unregulated insulin release
RM Shepherd, KE Cosgrove, RE O'Brien, PD Barnes, C Ämmälä, ...
Archives of Disease in Childhood-Fetal and Neonatal Edition 82 (2), F87-F97, 2000
Integrating genetic and imaging investigations into the clinical management of congenital hyperinsulinism
I Banerjee, B Avatapalle, R Padidela, A Stevens, KE Cosgrove, ...
Clinical endocrinology 78 (6), 803-813, 2013
BPDZ 154 Activates Adenosine 5′-Triphosphate-Sensitive Potassium Channels: In Vitro Studies Using Rodent Insulin-Secreting Cells and Islets Isolated from …
KE Cosgrove, MH Antoine, AT Lee, PD Barnes, P De Tullio, P Clayton, ...
The Journal of Clinical Endocrinology & Metabolism 87 (11), 4860-4868, 2002
Enhanced islet cell nucleomegaly defines diffuse congenital hyperinsulinism in infancy but not other forms of the disease
B Han, M Newbould, G Batra, E Cheesman, RJ Craigie, Z Mohamed, ...
American journal of clinical pathology 145 (6), 757-768, 2016
Network analysis: a new approach to study endocrine disorders
A Stevens, C De Leonibus, D Hanson, AW Dowsey, A Whatmore, S Meyer, ...
Journal of molecular endocrinology 52 (1), R79-R93, 2014
Järjestelmä ei voi suorittaa toimenpidettä nyt. Yritä myöhemmin uudelleen.
Artikkelit 1–20