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Scandinavian Journal of Rheumatology
|
March 7, 2015
Autosomal recessive transmission of TRAPS in a family with a novel TNFRSF1A mutation
K K Y Wong, J Jackson, R Whidborne, et al.
Molecular Pharmacology
|
June 16, 2001
Fast and slow gating of CLC-1: differential effects of 2-(4-chlorophenoxy) propionic acid and dominant negative mutations
E C Aromataris, G Y Rychkov, B Bennetts, et al.
Journal of Hematotherapy
|
October 1, 1996
Myeloma stem cells in autografting in multiple myeloma
L B To, N Horvath, P Dyson, et al.
The Journal of Physiology
|
June 1, 1997
pH-dependent interactions of Cd2+ and a carboxylate blocker with the rat C1C-1 chloride channel and its R304E mutant in the Sf-9 insect cell line
G Y Rychkov, D S Astill, B Bennetts, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
September 24, 2005
The association of aldose reductase gene (AKR1B1) polymorphisms with diabetic neuropathy in adolescents
K C Donaghue, S H Margan, A K F Chan, et al.
Metabolism: Clinical and Experimental
|
June 9, 2001
Modulation by blood glucose levels of activity and concentration of paraoxonase in young patients with type 1 diabetes mellitus
O Kordonouri, R W James, B Bennetts, et al.
Journal of Inherited Metabolic Disease
|
May 20, 2005
OPA3 mutation screening in patients with unexplained 3-methylglutaconic aciduria
K Neas, B Bennetts, K Carpenter, et al.
Molecular Psychiatry
|
July 26, 2002
Anorexia nervosa (restrictive subtype) is associated with a polymorphism in the novel norepinephrine transporter gene promoter polymorphic region
R E Urwin, B Bennetts, B Wilcken, et al.
Pathology
|
May 19, 2001
The application of a PCR technique for the detection of immunoglobulin heavy chain gene rearrangements in fresh or paraffin-embedded skin tissue
J Hughes, S Weston, B Bennetts, et al.
Prenatal Diagnosis
|
December 18, 2001
Karyotype, phenotype and parental origin in 19 cases of triploidy
A Daniel, Z Wu, B Bennetts, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Scandinavian Journal of Rheumatology
|
March 7, 2015
Autosomal recessive transmission of TRAPS in a family with a novel TNFRSF1A mutation
K K Y Wong, J Jackson, R Whidborne, et al.
Molecular Pharmacology
|
June 16, 2001
Fast and slow gating of CLC-1: differential effects of 2-(4-chlorophenoxy) propionic acid and dominant negative mutations
E C Aromataris, G Y Rychkov, B Bennetts, et al.
Journal of Hematotherapy
|
October 1, 1996
Myeloma stem cells in autografting in multiple myeloma
L B To, N Horvath, P Dyson, et al.
The Journal of Physiology
|
June 1, 1997
pH-dependent interactions of Cd2+ and a carboxylate blocker with the rat C1C-1 chloride channel and its R304E mutant in the Sf-9 insect cell line
G Y Rychkov, D S Astill, B Bennetts, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
September 24, 2005
The association of aldose reductase gene (AKR1B1) polymorphisms with diabetic neuropathy in adolescents
K C Donaghue, S H Margan, A K F Chan, et al.
Metabolism: Clinical and Experimental
|
June 9, 2001
Modulation by blood glucose levels of activity and concentration of paraoxonase in young patients with type 1 diabetes mellitus
O Kordonouri, R W James, B Bennetts, et al.
Journal of Inherited Metabolic Disease
|
May 20, 2005
OPA3 mutation screening in patients with unexplained 3-methylglutaconic aciduria
K Neas, B Bennetts, K Carpenter, et al.
Molecular Psychiatry
|
July 26, 2002
Anorexia nervosa (restrictive subtype) is associated with a polymorphism in the novel norepinephrine transporter gene promoter polymorphic region
R E Urwin, B Bennetts, B Wilcken, et al.
Pathology
|
May 19, 2001
The application of a PCR technique for the detection of immunoglobulin heavy chain gene rearrangements in fresh or paraffin-embedded skin tissue
J Hughes, S Weston, B Bennetts, et al.
Prenatal Diagnosis
|
December 18, 2001
Karyotype, phenotype and parental origin in 19 cases of triploidy
A Daniel, Z Wu, B Bennetts, et al.
Page
of 3