scholarly article | Q13442814 |
P50 | author | Carl D. Langefeld | Q102208371 |
Pamela J Hicks | Q111585264 | ||
Meredith A Bostrom | Q114332902 | ||
Barry Freedman | Q67485116 | ||
Cheryl A Winkler | Q87782749 | ||
Jasmin Divers | Q89813877 | ||
Donald W Bowden | Q92206005 | ||
Jeffrey B. Kopp | Q38359650 | ||
Yongmei Liu | Q67422669 | ||
P2093 | author name string | George W Nelson | |
Mary E Cunningham | |||
P2860 | cites work | Prognostic value of serum creatinine and effect of treatment of hypertension on renal function. Results from the hypertension detection and follow-up program. The Hypertension Detection and Follow-up Program Cooperative Group | Q69167761 |
Renal insufficiency in treated essential hypertension | Q69956789 | ||
Blood pressure and end-stage renal disease in men | Q71574790 | ||
Renal biopsy findings in presumed hypertensive nephrosclerosis | Q72173122 | ||
Association of the distal region of the ectonucleotide pyrophosphatase/phosphodiesterase 1 gene with type 2 diabetes in an African-American population enriched for nephropathy | Q80471061 | ||
A note on exact tests of Hardy-Weinberg equilibrium | Q24531633 | ||
A High-Density Admixture Map for Disease Gene Discovery in African Americans | Q24533390 | ||
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis | Q24643421 | ||
MYH9 is associated with nondiabetic end-stage renal disease in African Americans | Q24653027 | ||
Haploview: analysis and visualization of LD and haplotype maps | Q27860955 | ||
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis | Q28145757 | ||
Genotype-phenotype correlation in MYH9-related thrombocytopenia | Q33367809 | ||
Estimation of individual admixture: analytical and study design considerations | Q34394604 | ||
TRPC6 and FSGS: the latest TRP channelopathy | Q34622852 | ||
Long-term effects of renin-angiotensin system-blocking therapy and a low blood pressure goal on progression of hypertensive chronic kidney disease in African Americans | Q34774598 | ||
Familial clustering of chronic kidney disease | Q36842851 | ||
Actin up: regulation of podocyte structure and function by components of the actin cytoskeleton | Q36931220 | ||
Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study | Q37359254 | ||
Operating characteristics of prostate-specific antigen in men with an initial PSA level of 3.0 ng/ml or lower | Q39722492 | ||
The link between hypertension and nephrosclerosis | Q40586621 | ||
Clinical documentation of end-stage renal disease due to hypertension | Q40747330 | ||
Effect of ramipril vs amlodipine on renal outcomes in hypertensive nephrosclerosis: a randomized controlled trial | Q43626458 | ||
Hypertensive nephrosclerosis in African Americans versus Caucasians | Q44039626 | ||
Racial differences in the incidence of hypertensive end-stage renal disease (ESRD) are not entirely explained by differences in the prevalence of hypertension | Q44839105 | ||
Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population | Q45149880 | ||
Accuracy of the diagnosis of hypertensive nephrosclerosis in African Americans: a report from the African American Study of Kidney Disease (AASK) Trial. AASK Pilot Study Investigators | Q46250134 | ||
Renal function change in hypertensive members of the Multiple Risk Factor Intervention Trial. Racial and treatment effects. The MRFIT Research Group | Q46278015 | ||
The familial risk of end-stage renal disease in African Americans | Q46726027 | ||
Identification of podocin (NPHS2) gene mutations in African Americans with nondiabetic end-stage renal disease | Q46958377 | ||
Inaccuracy of clinical phenotyping parameters for hypertensive nephrosclerosis | Q64459160 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | arterial hypertension | Q41861 |
kidney disease | Q1054718 | ||
P304 | page(s) | 736-745 | |
P577 | publication date | 2009-01-28 | |
P1433 | published in | Kidney International | Q6404823 |
P1476 | title | Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans | |
P478 | volume | 75 |
Q28740367 | A genome-wide association search for type 2 diabetes genes in African Americans |
Q28943287 | A genome-wide association study for diabetic nephropathy genes in African Americans |
Q33540002 | A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level |
Q27022275 | APOL1 and nephropathy progression in populations of African ancestry |
Q51492603 | APOL1 variants and kidney disease in people of recent African ancestry. |
Q37467503 | Adrenergic beta-1 receptor genetic variation predicts longitudinal rate of GFR decline in hypertensive nephrosclerosis. |
Q24602407 | African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans |
Q35567885 | African origins and chronic kidney disease susceptibility in the human immunodeficiency virus era. |
Q33623998 | Analysis of coding variants identified from exome sequencing resources for association with diabetic and non-diabetic nephropathy in African Americans |
Q30501039 | Angiotensin II overcomes strain-dependent resistance of rapid CKD progression in a new remnant kidney mouse model |
Q24621889 | Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans |
Q35468728 | Apolipoprotein L1 nephropathy risk variants associate with HDL subfraction concentration in African Americans |
Q37809770 | Arrest of the true culprit and acquittal of the innocent? Genetic revelations charge APOL1 variants with kidney disease susceptibility |
Q55019060 | Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations. |
Q35675334 | Association of filtered sodium load with medullary volumes and medullary hypoxia in hypertensive African Americans as compared with whites |
Q34169649 | Association of polymorphisms in the klotho gene with severity of non-diabetic ESRD in African Americans |
Q36826342 | Association of the receptor for advanced glycation end-products (RAGE) gene polymorphisms in Malaysian patients with chronic kidney disease |
Q24606581 | Association of trypanolytic ApoL1 variants with kidney disease in African Americans |
Q37593685 | Blood pressure level and kidney disease progression: do we really need to go to 130/80 mm Hg? |
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Q33773661 | Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15. |
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Q45072634 | Diabetic Microvascular Disease: An Endocrine Society Scientific Statement |
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Q38192853 | Focal segmental glomerulosclerosis: towards a better understanding for the practicing nephrologist |
Q44562858 | Gene polymorphism of vascular endothelial growth factor -1154 G>A is associated with hypertensive nephropathy in a Hispanic population. |
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Q27024548 | Genetic and epigenetic factors influencing chronic kidney disease |
Q35675247 | Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy |
Q34018541 | Genetic basis of nondiabetic end-stage renal disease |
Q36925161 | Genetic contribution and associated pathophysiology in end-stage renal disease |
Q28657760 | Genetic variation and adaptation in Africa: implications for human evolution and disease |
Q33821365 | Genetics of focal segmental glomerulosclerosis and human immunodeficiency virus-associated collapsing glomerulopathy: the role of MYH9 genetic variation |
Q37781545 | Genome-Wide Association Studies in Nephrology Research |
Q46040078 | Genome-wide linkage analysis of serum creatinine in three isolated European populations. |
Q34803998 | Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study |
Q37802413 | Hereditary kidney diseases: highlighting the importance of classical Mendelian phenotypes |
Q38074565 | How benign is hematuria? Using genetics to predict prognosis |
Q26851271 | Hypertension and chronic kidney disease: controversies in pathogenesis and treatment |
Q34131899 | Hypertensive nephropathy: prevention and treatment recommendations |
Q33847247 | Inferring genetic ancestry: opportunities, challenges, and implications |
Q30248678 | Insights into kidney diseases from genome-wide association studies |
Q33828986 | Is collapsing C1q nephropathy another MYH9-associated kidney disease? A case report |
Q45377385 | Is there a genetic basis for health disparities in human immunodeficiency virus disease? |
Q33873191 | Kidney transplantation in a low-resource setting: Nigeria experience |
Q37045873 | Lifetime incidence of CKD stages 3-5 in the United States |
Q35128320 | MYH9 and APOL1 gene polymorphisms and the risk of CKD in patients with lupus nephritis from an admixture population |
Q34990741 | MYH9 genetic variants associated with glomerular disease: what is the role for genetic testing? |
Q38261393 | Macrophage migration inhibitory factor -173G/C gene polymorphism increases the risk of renal disease: a meta-analysis |
Q35745738 | Meta-analysis of genome-wide linkage scans for renal function traits |
Q24632288 | Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene |
Q38130063 | Nephrology in Africa--not yet uhuru |
Q35282729 | Non-AIDS-defining events among HIV-1-infected adults receiving combination antiretroviral therapy in resource-replete versus resource-limited urban setting |
Q89501822 | Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene |
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Q53093479 | Non-muscle myosin-IIA is critical for podocyte f-actin organization, contractility, and attenuation of cell motility. |
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Q41988586 | Pilot study of an association between a common variant in the non-muscle myosin heavy chain 9 (MYH9) gene and type 2 diabetic nephropathy in a Taiwanese population. |
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Q33748130 | Precipitation of kidney myosin IIA and IIB by freezing |
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