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74篇 您的检索式：作者名="Ellard S"

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	题名	作者	年代	出处	被引量
1	A study of the aneugenic activity of trichlorfon detected by centromere-specific probes in human lymphoblastoid cell lines 显示文摘	DOHERTY A T ELLARD S PARRY E M	1996	Mutat Res1996，372，2：	1
2	Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes显示文摘	Macfarlane WM Frayling TM Ellard S	1999	J Clin Invest1999，104，9：	1
3	A typical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1 beta gene mutation显示文摘	Bingham C Ellard S van' t Hoff WG	2003	Kidney Int2003，63，5：	1
4	Missense mutations in the insulin promotion factor-1 gene predispose to type 2 diabetes显示文摘	Macfarlane W M Frayling T M Ellard S	1999	J Clin Invest1999，104，：	1
5	A high prevalence of glu- cokinase mutations in gestational diabetic subjects selected by clinical criteria显示文摘	Ellard S Beards F Allen LI	2000	Diabetologia2000，43，2：	1
6	The use of genetically engineered V79 Chinese hamster andAHH1 human lymphoblastoid Cultures expressing ratliverCYP1A1,1A2 and 2B1cDNAs in micronucleus assays显示文摘	Ellard S Mohammed S		0，，：	1
7	Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes显示文摘	Macfarlane WM Frayling TM Ellard S	1999	J Clin Invest1999，104，9：	1
8	The use of genetically engineered V79 Chinese lmter andAHH1 h lynlastoid Cules aressing ratliverCYP1A1, 1A2 and 2BlcDNAs in micronucleus assays 显示文摘	Ellard S Mohammed S	1991	Mtmgene1991，6，：	1
9	Improved genetic testing for monogenic diabetes using targeted next-generation sequencing显示文摘	Ellard S Lango Alien H De Franco E	2013	Diabetologia2013，56，9：	1
10	The use of genetically engineered V79 Chinese hamster and AHH-1 human lymphoblastoid cultures expressing rat liver CYP1A1,1A2 and 2B1 cDNAs in micronucleus assays显示文摘	Ellard S Mohammed S	1991	Mutagenesis1991，6，：	1
11	Mutations in the hepatocyte nuclear factor-1β gene are associated with familial hypoplastic glomerulocystic kidney disease显示文摘	Bingham C Bulman M P Ellard S	2001	Am J Hum Genet2001，68，：	1
12	Response to treatment with rosiglitazone in familial partial lipodystrophy due to a mutation in the LMNA gene显示文摘	Owen KR Donohoe M Ellard S	2003	Diabet Med2003，20，5：	1
13	Improved genetic testing for monogenic diabetes using targeted next-generation sequencing显示文摘	Ellard S Lango allen H De franco E	2013	Diabetologia2013，56，9：	1
14	Permanent neonatal diabetes in siblings with novel C109Y INS mutation transmitted by an unaffected parent with somatic mosaicism显示文摘	Bee YM Zhao Y Ellard S	2014	Pediatr Diabetes2014，15，4：	1
15	Identifying hepatic nuclear factor 1α mutations in children and young adults with a clinical diagnosis of type 1 diabetes显示文摘	Lambert AP Ellard S Allen LIS	2003	Diabetes Care2003，26，：	1
16	The laminopathies:a clinical review显示文摘	Rankin J Ellard S		0，，04：	1
17	Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes显示文摘	Macfarlane W M Frayling T M Ellard S	1999	J Clin Invest1999，104，：	1
18	Alagille syndrome: pathogenesis, diagnosis and management显示文摘	Turnpenny PD Ellard S	2012	Eur J Hum Genet2012，20，3：	1
19	Permanent neonatal diabetes caused by dominant,recessive,or compound heterozygous sur1 mutations with opposite functional effects显示文摘	Ellard S Flanagan SE Girard CA		0，，02：	1
20	Mutations in the hepatocyte nuclear factor-lbeta gene are associated with familial hypoplastic glomerulocystic kidney disease显示文摘	BINGHAM C BULMAN M P ELLARD S	2001	Am J Hum Genet2001，68，1：	1

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