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Diabetic Medicine : a Journal of the British Diabetic Association
|
April 25, 2009
A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients
M Shepherd, B Shields, S Ellard, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
September 5, 2002
Heterogeneity in young adult onset diabetes: aetiology alters clinical characteristics
K R Owen, M Shepherd, A Stride, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
November 4, 2015
tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy
T W Yew, L McCreight, K Colclough, et al.
Mutagenesis
|
November 1, 1991
The use of genetically engineered V79 Chinese hamster cultures expressing rat liver CYP1A1, 1A2 and 2B1 cDNAs in micronucleus assays
S Ellard, Y Mohammed, S Dogra, et al.
Nature Genetics
|
July 14, 1998
Mutations in the glucokinase gene of the fetus result in reduced birth weight
A T Hattersley, F Beards, E Ballantyne, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
July 31, 2012
Successful sulfonylurea treatment of a neonate with neonatal diabetes mellitus due to a novel missense mutation, p.P1199L, in the ABCC8 gene
O Oztekin, E Durmaz, S Kalay, et al.
Journal of Medical Genetics
|
May 15, 2003
Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis
P D Turnpenny, N Whittock, J Duncan, et al.
Human Mutation
|
September 12, 2000
Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG-->CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1 alpha) gene which causes maturity-onset diabetes of the young (MODY)
S Ellard, M P Bulman, T M Frayling, et al.
Diabetes, Obesity & Metabolism
|
October 9, 2007
Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period
A M Patch, S E Flanagan, C Boustred, et al.
Clinical and Laboratory Haematology
|
August 11, 2006
Large variation in t(11;14)(q13;q32) and t(14;18)(q32;q21) translocation product size is confirmed by sequence analysis of PCR products
C L Wickham, L W Harries, P Sarsfield, et al.
Page
of 15
Search research articles
Search
Showing results (31-40 of 144) with videos related to
Sort By:
Page
of 15
Diabetic Medicine : a Journal of the British Diabetic Association
|
April 25, 2009
A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients
M Shepherd, B Shields, S Ellard, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
September 5, 2002
Heterogeneity in young adult onset diabetes: aetiology alters clinical characteristics
K R Owen, M Shepherd, A Stride, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
November 4, 2015
tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy
T W Yew, L McCreight, K Colclough, et al.
Mutagenesis
|
November 1, 1991
The use of genetically engineered V79 Chinese hamster cultures expressing rat liver CYP1A1, 1A2 and 2B1 cDNAs in micronucleus assays
S Ellard, Y Mohammed, S Dogra, et al.
Nature Genetics
|
July 14, 1998
Mutations in the glucokinase gene of the fetus result in reduced birth weight
A T Hattersley, F Beards, E Ballantyne, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
July 31, 2012
Successful sulfonylurea treatment of a neonate with neonatal diabetes mellitus due to a novel missense mutation, p.P1199L, in the ABCC8 gene
O Oztekin, E Durmaz, S Kalay, et al.
Journal of Medical Genetics
|
May 15, 2003
Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis
P D Turnpenny, N Whittock, J Duncan, et al.
Human Mutation
|
September 12, 2000
Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG-->CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1 alpha) gene which causes maturity-onset diabetes of the young (MODY)
S Ellard, M P Bulman, T M Frayling, et al.
Diabetes, Obesity & Metabolism
|
October 9, 2007
Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period
A M Patch, S E Flanagan, C Boustred, et al.
Clinical and Laboratory Haematology
|
August 11, 2006
Large variation in t(11;14)(q13;q32) and t(14;18)(q32;q21) translocation product size is confirmed by sequence analysis of PCR products
C L Wickham, L W Harries, P Sarsfield, et al.
Page
of 15