Molecular basis of the Cd36 chromosomal deletion underlying SHR defects in insulin action and fatty acid metabolism

Role of Insulin Resistance in Human Disease

1988 • 12,099 citations

A molecular timescale for vertebrate evolution

1998 • 1,945 citations

The deadly quartet. Upper-body obesity, glucose intolerance, hypertriglyceridemia, and hypertension

1989 • 1,560 citations

A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

1992 • 1,126 citations

Role of Insulin Resistance in Human Disease (Syndrome X): An Expanded Definition

1993 • 878 citations

Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats

1999 • 739 citations

Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome.

1995 • 236 citations

Transgenic rescue of defective Cd36 ameliorates insulin resistance in spontaneously hypertensive rats

2001 • 202 citations

The fourth Musketeer ? from Alexandre Dumas to Claude Bernard

1995 • 187 citations

Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains.

1995 • 162 citations

Quantitative trait loci for cellular defects in glucose and fatty acid metabolism in hypertensive rats

1997 • 147 citations

Structural organization of the gene for human CD36 glycoprotein.

1994 • 139 citations

Resistance to Insulin-Stimulated Glucose Uptake in Adipocytes Isolated From Spontaneously Hypertensive Rats

1989 • 126 citations

Pathological Consequences of Sequence Duplications in the Human Genome

1998 • 112 citations

Identification of Genes from a 500-kb Region at 7q11.23 That Is Commonly Deleted in Williams Syndrome Patients

1996 • 110 citations

Genetics of Cd36 and the clustering of multiple cardiovascular risk factors in spontaneous hypertension

1999 • 107 citations

Defects of Insulin Action on Fatty Acid and Carbohydrate Metabolism in Familial Combined Hyperlipidemia

1997 • 100 citations

The molecular clock ticks regularly in muroid rodents and hamsters

1992 • 93 citations

Quantitative trait loci influencing cholesterol and phospholipid phenotypes map to chromosomes that contain genes regulating blood pressure in the spontaneously hypertensive rat.

1996 • 85 citations

Lipid metabolism in spontaneously hypertensive rats (SHR)

1977 • 84 citations

The sequence organization of the long arm pseudoautosomal region of the human sex chromosomes

1994 • 71 citations

Cd36 and molecular mechanisms of insulin resistance in the stroke-prone spontaneously hypertensive rat.

2000 • 57 citations

Topoisomerase I and II Consensus Sequences in a 17-kb Deletion Junction of the COL4A5 and COL4A6 Genes and Immunohistochemical Analysis of Esophageal Leiomyomatosis Associated with Alport Syndrome

1998 • 54 citations

Insulin Resistance in Spontaneously Hypertensive Rats: Difference in Interpretation Based on Insulin Infusion Rate or on Plasma Insulin in Glucose Clamp Studies

1993 • 40 citations

A LINE element is present at the site of a 300-kb deletion starting in intron 10 of the PAX6 gene in a case of familial aniridia

1996 • 26 citations

Detection of tandem duplications and implications for linkage analysis.

1994 • 22 citations

Non-radioactive detection of 17p11.2 duplication in CMT1A: a study of 78 patients.

1994 • 14 citations

Deletion in the beige gene of the beige rat owing to recombination between LINE1s

1999 • 12 citations