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1.
Intensive lifestyle intervention in type 2 diabetes and risk of incident coronary artery disease for the common haptoglobin phenotypes: the Look AHEAD study.
Cardiovasc Diabetol
; 23(1): 82, 2024 02 24.
Article
in English
| MEDLINE | ID: mdl-38402400
2.
Molecular Insights into IQSEC2 Disease.
Int J Mol Sci
; 24(5)2023 Mar 05.
Article
in English
| MEDLINE | ID: mdl-36902414
3.
Daily Brief Heat Therapy Reduces Seizures in A350V IQSEC2 Mice and Is Associated with Correction of AMPA Receptor-Mediated Synaptic Dysfunction.
Int J Mol Sci
; 24(4)2023 Feb 15.
Article
in English
| MEDLINE | ID: mdl-36835332
4.
IQSEC2 mutation associated with epilepsy, intellectual disability, and autism results in hyperexcitability of patient-derived neurons and deficient synaptic transmission.
Mol Psychiatry
; 26(12): 7498-7508, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34535765
5.
Housing of A350V IQSEC2 pups at 37 °C ambient temperature prevents seizures and permits the development of social vocalizations in adulthood.
Int J Hyperthermia
; 38(1): 1495-1501, 2021.
Article
in English
| MEDLINE | ID: mdl-34666607
6.
Haptoglobin Phenotype Is Associated With High-Density Lipoprotein-Bound Hemoglobin Content and Coronary Endothelial Dysfunction in Patients With Mild Nonobstructive Coronary Artery Disease.
Arterioscler Thromb Vasc Biol
; 39(4): 774-786, 2019 04.
Article
in English
| MEDLINE | ID: mdl-30727751
7.
The Role of Haptoglobin Polymorphism in Cardiovascular Disease in the Setting of Diabetes.
Int J Mol Sci
; 22(1)2020 Dec 30.
Article
in English
| MEDLINE | ID: mdl-33396615
8.
IQSEC2-Associated Intellectual Disability and Autism.
Int J Mol Sci
; 20(12)2019 Jun 21.
Article
in English
| MEDLINE | ID: mdl-31234416
9.
Interaction Between the Haptoglobin Genotype and Vitamin E on Cardiovascular Disease in Diabetes.
Curr Diab Rep
; 17(6): 42, 2017 06.
Article
in English
| MEDLINE | ID: mdl-28451949
10.
Haptoglobin genotype-dependent differences in macrophage lysosomal oxidative injury.
J Biol Chem
; 289(23): 16313-25, 2014 Jun 06.
Article
in English
| MEDLINE | ID: mdl-24778180
11.
Molecular modeling of ARF6 dysregulation caused by mutations in IQSEC2.
J Biomol Struct Dyn
; 42(3): 1268-1279, 2024.
Article
in English
| MEDLINE | ID: mdl-37078745
12.
Haptoglobin phenotype and intensive glycemic control for coronary artery disease risk reduction in people with type two diabetes: The Veterans Affairs Diabetes Trial.
Am J Prev Cardiol
; 18: 100681, 2024 Jun.
Article
in English
| MEDLINE | ID: mdl-38800835
13.
Haptoglobin Phenotype and Intensive Glycemic Control for Coronary Artery Disease Risk Reduction in People With Type 2 Diabetes: The ADVANCE Study.
Diabetes Care
; 47(5): 835-843, 2024 May 01.
Article
in English
| MEDLINE | ID: mdl-38484336
14.
Vitamin E in the prevention of cardiovascular disease: the importance of proper patient selection.
J Lipid Res
; 54(9): 2307-14, 2013 Sep.
Article
in English
| MEDLINE | ID: mdl-23505320
15.
An enzyme linked immunosorbent assay (ELISA) for the determination of the human haptoglobin phenotype.
Clin Chem Lab Med
; 51(8): 1615-22, 2013 Aug.
Article
in English
| MEDLINE | ID: mdl-23492570
16.
The Relationship Between Time-Varying Achieved HbA1c and Risk of Coronary Events Depends on Haptoglobin Phenotype Among White and Black ACCORD Participants.
Diabetes Care
; 46(11): 1941-1948, 2023 11 01.
Article
in English
| MEDLINE | ID: mdl-37639669
17.
Relationship Between Time-Varying Achieved High-Density Lipoprotein Cholesterol and Risk of Coronary Events Depends on Haptoglobin Phenotype Within the ACCORD Lipid Study.
J Am Heart Assoc
; 12(19): e030288, 2023 10 03.
Article
in English
| MEDLINE | ID: mdl-37776200
18.
Is it time to screen for the haptoglobin genotype to assess the cardiovascular risk profile and vitamin E therapy responsiveness in patients with diabetes?
Curr Diab Rep
; 12(3): 274-9, 2012 Jun.
Article
in English
| MEDLINE | ID: mdl-22427005
19.
Haptoglobin genotype and its role in determining heme-iron mediated vascular disease.
Pharmacol Res
; 66(1): 1-6, 2012 Jul.
Article
in English
| MEDLINE | ID: mdl-22465143
20.
Characterization of spontaneous seizures and EEG abnormalities in a mouse model of the human A350V IQSEC2 mutation and identification of a possible target for precision medicine based therapy.
Epilepsy Res
; 182: 106907, 2022 05.
Article
in English
| MEDLINE | ID: mdl-35344748