Research Topics
Species | Renhua LiSummaryAffiliation: The Jackson Laboratory Country: USA Publications
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Publications
Relationships of dietary fat, body composition, and bone mineral density in inbred mouse strain panelsRenhua Li
The Jackson Laboratory, Bar Harbor, Maine 04609, USA
Physiol Genomics 33:26-32. 2008..Sex has no net effect on areal BMD, but after accounting for body mass difference females have higher areal BMD. Leptin is affected by relative fat mass and has no net effect on areal BMD. IGF-I has a direct effect on areal BMD...
QTL mapping for genetic determinants of lipoprotein cholesterol levels in combined crosses of inbred mouse strainsHenning Wittenburg
The Jackson Laboratory, Bar Harbor, ME, USA
J Lipid Res 47:1780-90. 2006....
Quantitative trait loci that determine lipoprotein cholesterol levels in an intercross of 129S1/SvImJ and CAST/Ei inbred miceMalcolm A Lyons
The Jackson Laboratory, Bar Harbor, Maine 04609, USA
Physiol Genomics 17:60-8. 2004..Our analysis furthers the knowledge of the genetic control of lipoprotein levels and points to the importance of Hdlq10, which was detected repeatedly in multiple studies...
Association of a lithogenic Abcg5/Abcg8 allele on Chromosome 17 (Lith9) with cholesterol gallstone formation in PERA/EiJ miceHenning Wittenburg
The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine 04609, USA
Mamm Genome 16:495-504. 2005..Significantly higher mRNA expression of Abcg5 and Abcg8 in strain PERA compared with strains I/Ln and DBA/2 further substantiated that the PERA allele of Abcg5/Abcg8 was responsible for lithogenicity underlying Lith9...
Genetic contributors to lipoprotein cholesterol levels in an intercross of 129S1/SvImJ and RIIIS/J inbred miceMalcolm A Lyons
The Jackson Laboratory, Bar Harbor, Maine 04609, USA
Physiol Genomics 17:114-21. 2004..Overall, we detected eight QTLs for lipoprotein cholesterol concentrations on Chrs 1, 9, 12, and 17 (each two per chromosome), including a new QTL for non-HDL cholesterol, Nhdlq3, on Chr 17...
New quantitative trait loci that contribute to cholesterol gallstone formation detected in an intercross of CAST/Ei and 129S1/SvImJ inbred miceMalcolm A Lyons
Jackson Laboratory, Bar Harbor, Maine 04609, USA
Physiol Genomics 14:225-39. 2003..Our work continues to demonstrate the genetic complexity and to elucidate the pathophysiology of cholesterol gallstone formation. It should facilitate the development of new approaches for treating this common human disorder...
Quantitative trait loci for BMD in an SM/J by NZB/BlNJ intercross population and identification of Trps1 as a probable candidate geneNaoki Ishimori
The Jackson Laboratory, Bar Harbor, Maine 04609, USA
J Bone Miner Res 23:1529-37. 2008..This study shows the power of statistical modeling to resolve linked QTLs and the use of haplotype analysis in narrowing the list of candidates...
Quantitative trait locus mapping of genes that regulate phospholipid transfer activity in SM/J and NZB/BlNJ inbred miceRon Korstanje
The Jackson Laboratory, Bar Harbor, ME, USA
Arterioscler Thromb Vasc Biol 24:155-60. 2004..We performed quantitative trait locus (QTL) analysis to identify genomic loci regulating PLTP activity in mice...
Lith6: a new QTL for cholesterol gallstones from an intercross of CAST/Ei and DBA/2J inbred mouse strainsMalcolm A Lyons
The Jackson Laboratory, Bar Harbor, ME 04609, USA
J Lipid Res 44:1763-71. 2003....
Quantitative trait loci analysis for plasma HDL-cholesterol concentrations and atherosclerosis susceptibility between inbred mouse strains C57BL/6J and 129S1/SvImJNaoki Ishimori
The Jackson Laboratory, Bar Harbor, ME 04609, USA
Arterioscler Thromb Vasc Biol 24:161-6. 2004..To identify loci controlling these traits, we performed quantitative trait loci (QTL) analysis...
Single and interacting QTLs for cholesterol gallstones revealed in an intercross between mouse strains NZB and SMMalcolm A Lyons
The Jackson Laboratory, Bar Harbor, Maine 04609, USA
Mamm Genome 16:152-63. 2005..The QTLs identified herein largely contributed to gallstone formation rather than gallstone severity. Cloning the genes underlying these murine QTLs should facilitate prediction and cloning of the orthologous human genes...
FXR and ABCG5/ABCG8 as determinants of cholesterol gallstone formation from quantitative trait locus mapping in miceHenning Wittenburg
The Jackson Laboratory, Bar Harbor, Maine, USA
Gastroenterology 125:868-81. 2003..Cholesterol gallstone formation is a complex genetic trait. To identify additional cholesterol gallstone susceptibility loci, we performed a quantitative trait locus analysis using an intercross of PERA/Ei and I/LnJ inbred strains of mice...
Quantitative trait loci that determine plasma lipids and obesity in C57BL/6J and 129S1/SvImJ inbred miceNaoki Ishimori
The Jackson Laboratory, Bar Harbor, ME, USA
J Lipid Res 45:1624-32. 2004..0) interacting with Obq18 (chromosome 9, cM 65). Knowing the genes for these QTL will enhance our understanding of obesity and lipid metabolism...
Adult-onset Alopecia areata is a complex polygenic trait in the C3H/HeJ mouse modelJohn P Sundberg
The Jackson Laboratory, Bar Harbor, Maine 04609 1500, USA
J Invest Dermatol 123:294-7. 2004..These results indicate the necessity of integrating both gene association and genome-wide linkage studies in both mice and humans to understand the complex nature of these and other polygenic diseases...
Multiple trait measurements in 43 inbred mouse strains capture the phenotypic diversity characteristic of human populationsKaren L Svenson
The Jackson Laboratory, 600 Main St, Bar Harbor, ME 04609, USA
J Appl Physiol 102:2369-78. 2007..Data generated by this effort builds on the value of inbred mouse strains as a powerful tool for biomedical research...
NOD x 129.H2(g7) backcross delineates 129S1/SvImJ-derived genomic regions modulating type 1 diabetes development in miceEdward H Leiter
The Jackson Laboratory, Bar Harbor, ME, USA
Diabetes 58:1700-3. 2009..Our objective was to identify 129S1/SvJ non-MHC regions contributing type 1 diabetes resistance or susceptibility in backcross to NOD/LtJ...
Complex genetic architecture revealed by analysis of high-density lipoprotein cholesterol in chromosome substitution strains and F2 crossesIoannis M Stylianou
The Jackson Laboratory, Maine 04609, USA
Genetics 174:999-1007. 2006....
Identification of quantitative trait loci that modify the severity of hereditary spherocytosis in wan, a new mouse model of band-3 deficiencyLuanne L Peters
The Jackson Laboratory, Bar Harbor, ME 04609, USA
Blood 103:3233-40. 2004..The peak LOD score was obtained with a marker for Spnb1 encoding erythroid beta-spectrin, an obvious candidate gene...
Quantitative trait loci that determine BMD in C57BL/6J and 129S1/SvImJ inbred miceNaoki Ishimori
The Jackson Laboratory, Bar Harbor, Maine 04609, USA
J Bone Miner Res 21:105-12. 2006..To identify loci controlling BMD, we conducted a QTL analysis in a (B6 x 129) F2 population of mice. We report on additional QTLs and also narrow one QTL by combining the data from multiple crosses and through haplotype analysis...
Structural model analysis of multiple quantitative traitsRenhua Li
The Jackson Laboratory, Bar Harbor, Maine, USA
PLoS Genet 2:e114. 2006..The identification of causal networks sheds light on the nature of genetic heterogeneity and pleiotropy in complex genetic systems...
Using advanced intercross lines for high-resolution mapping of HDL cholesterol quantitative trait lociXiaosong Wang
The Jackson Laboratory, Bar Harbor, Maine 04609, USA
Genome Res 13:1654-64. 2003..All the major HDL QTLs in our study had homologous counterparts in humans, implying that their underlying genes regulate HDL in humans...
Influence of sex and diet on quantitative trait loci for HDL cholesterol levels in an SM/J by NZB/BlNJ intercross populationRon Korstanje
The Jackson Laboratory, 600 Main St, Bar Harbor, ME 04609, USA
J Lipid Res 45:881-8. 2004..The dependence of QTL effects on sex suggests an important role for the sex hormones in HDL regulation. We recommend that sex should be explicitly accounted for in future studies in the genetics of HDL regulation in both mice and humans...
Combining data from multiple inbred line crosses improves the power and resolution of quantitative trait loci mappingRenhua Li
The Jackson Laboratory, Bar Harbor, Maine 04609, USA
Genetics 169:1699-709. 2005..Moreover, combined-cross analysis can establish the allelic states of a QTL among a set of parental lines, thus providing critical information for narrowing QTL regions by haplotype analysis...
Distal Chr 4 harbors a genetic locus (Gct1) fundamental for spontaneous ovarian granulosa cell tumorigenesis in a mouse modelAnn M Dorward
The Jackson Laboratory, Bar Harbor, Maine, USA
Cancer Res 65:1259-64. 2005..Our data substantiate the evidence that Gct1 on Chr 4 is a fundamental oncogene for granulosa cell tumorigenesis in mice and has identified additional interacting autosomal loci that support tumor development...
Interacting QTLs for cholesterol gallstones and gallbladder mucin in AKR and SWR strains of miceHenning Wittenburg
Jackson Laboratory, Bar Harbor, Maine 04609, USA
Physiol Genomics 8:67-77. 2002..According to standard nomenclature, the gallstone QTL on chromosome 9 is named Lith5...
Genetic background modifies inner ear and eye phenotypes of jag1 heterozygous miceAmy E Kiernan
The Jackson Laboratory, Bar Harbor, Maine 04609, USA
Genetics 177:307-11. 2007..Genome scans of N2 backcross mice identified a significant modifier locus on chromosome 7, as well as a suggestive locus on chromosome 14. We also analyzed modifiers of an eye defect in Jag1del1 heterozygous mice from this same cross...
QTL associated with blood pressure, heart rate, and heart weight in CBA/CaJ and BALB/cJ miceFumihiro Sugiyama
The Jackson Laboratory, Bar Harbor, Maine 04609, USA
Physiol Genomics 10:5-12. 2002..Identification of the genes for these QTL should lead to a better understanding of the causes of essential hypertension...
Genetic analysis of resistance to Type-1 Diabetes in ALR/Lt mice, a NOD-related strain with defenses against autoimmune-mediated diabetogenic stressClayton E Mathews
The Jackson Laboratory, Bar Harbor, ME 04609, USA
Immunogenetics 55:491-6. 2003..Two additional ALR-contributed resistance loci may be ALR-specific and contribute to this strain's ability to dissipate free-radical stress...
Major locus on mouse chromosome 17 and minor locus on chromosome 9 are linked with alopecia areata in C3H/HeJ miceJohn P Sundberg
The Jackson Laboratory, Bar Harbor, Maine 04609 1500, USA
J Invest Dermatol 120:771-5. 2003..0) around D9Mit206, 20 cM from the centromere. The interval on mouse Chromosome 17 contains several orthologous genes potentially associated with human alopecia areata...
Quantitative trait loci that determine lipoprotein cholesterol levels in DBA/2J and CAST/Ei inbred miceMalcolm A Lyons
The Jackson Laboratory, Bar Harbor, ME 04609, USA
J Lipid Res 44:953-67. 2003....
Genetics of colitis susceptibility in IL-10-deficient mice: backcross versus F2 results contrasted by principal component analysisMichael Mahler
Institute for Laboratory Animal Science and Central Animal Facility, Medical School Hannover, Germany
Genomics 80:274-82. 2002..These findings show the complexity of inheritance underlying susceptibility to colitis and illustrate why detection of human inflammatory bowel disease loci has proven to be so difficult...
Genetic modulation of tau phosphorylation in the mouseJochen Brich
Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA
J Neurosci 23:187-92. 2003..Dab1 mutant mice provide an animal model for studying the relationships between ApoE receptors, tau hyperphosphorylation, and Alzheimer's disease...
Sex- and lineage-specific inheritance of depression-like behavior in the ratLeah C Solberg
Department of Psychiatry and Behavioral Science, Northwestern University Feinberg School of Medicine, 303 E Chicago Avenue, Chicago, Illinois 60611, USA
Mamm Genome 15:648-62. 2004..The presence of these loci across species suggests that these QTL may represent universal genetic factors contributing to mood disorders...
Genetic analysis of the stress-responsive adrenocortical axisLeah C Solberg
Department of Psychiatry and Behavioral Science, Northwestern University Feinberg School of Medicine, Chicago, USA
Physiol Genomics 27:362-9. 2006..This analysis confirms that three separate traits regulated by the HPA axis are controlled by multiple, but mainly nonoverlapping, QTLs...
Femur mechanical properties in the F2 progeny of an NZB/B1NJ x RF/J cross are regulated predominantly by genetic loci that regulate bone geometryJon E Wergedal
Musculoskeletal Disease Center, J L Pettis Memorial VA Medical Center, Loma Linda, CA 92357, USA
J Bone Miner Res 21:1256-66. 2006..Genetic analysis of an NZB/B1NJ x RF/J cross has identified QTLs for femur mechanical, geometric, and densitometric phenotypes. Most mechanical QTLs were associated with geometric QTLs, strongly suggesting common genetic regulation...
Kinesin family member 12 is a candidate polycystic kidney disease modifier in the cpk mouseMichal Mrug
Department of Medicine, University of Alabama at Birmingham, 740 Kaul Human Genetics Building, 720 20th Street South, Birmingham, AL 35294, USA
J Am Soc Nephrol 16:905-16. 2005..Therefore, the positional candidate gene, Kif12, fulfills the major criteria for QTL gene discovery established by the Complex Trait Consortium, and, thus, it is proposed that Kif12 is a cpk modifier gene...
Genetic variation in Glp1r expression influences the rate of gastric emptying in miceK Ganesh Kumar
Division of Experimental Obesity, Pennington Biomedical Research Center, Louisiana State University, 6400 Perkins Road, Baton Rouge, LA 70808 4124, USA
Am J Physiol Regul Integr Comp Physiol 294:R362-71. 2008..CAST-17 mice. Moreover, congenic mice displayed an impaired gastric emptying response to exendin-(9-39). These results suggest that genetic variation in Glp1r contributes to the strain differences in gastric emptying rate...
Discovery of 1-(3'-aminobenzisoxazol-5'-yl)-3-trifluoromethyl-N-[2-fluoro-4- [(2'-dimethylaminomethyl)imidazol-1-yl]phenyl]-1H-pyrazole-5-carboxyamide hydrochloride (razaxaban), a highly potent, selective, and orally bioavailable factor Xa inhibitorMimi L Quan
Discovery Chemistry, Pharmaceutical Research Institute, Bristol Myers Squibb Co, P O Box 5400, Princeton, New Jersey 08543 5400, USA
J Med Chem 48:1729-44. 2005....
