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Results: 11 to 20 of 37

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Clinical and genetic correlates of aldosterone-to-renin ratio and relations to blood pressure in a community sample.
Newton-Cheh C, Guo CY, Gona P, Larson MG, Benjamin EJ, Wang TJ, Kathiresan S, O'Donnell CJ, Musone SL, Camargo AL, Drake JA, Levy D, Hirschhorn JN, Vasan RS
(2007) Hypertension 49: 846-56
MeSH Terms: Aged, Aldosterone, Blood Pressure, Chromosomes, Human, Pair 11, Female, Genetic Linkage, Genetic Variation, Haplotypes, Humans, Hypertension, Male, Middle Aged, Polymorphism, Single Nucleotide, Quantitative Trait, Heritable, Renin, Risk Factors
Added April 15, 2014
0 Communities
1 Members
0 Resources
16 MeSH Terms
Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.
Suarez BK, Duan J, Sanders AR, Hinrichs AL, Jin CH, Hou C, Buccola NG, Hale N, Weilbaecher AN, Nertney DA, Olincy A, Green S, Schaffer AW, Smith CJ, Hannah DE, Rice JP, Cox NJ, Martinez M, Mowry BJ, Amin F, Silverman JM, Black DW, Byerley WF, Crowe RR, Freedman R, Cloninger CR, Levinson DF, Gejman PV
(2006) Am J Hum Genet 78: 315-33
MeSH Terms: Adolescent, Adult, African Americans, Chromosome Mapping, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 8, Female, Genetic Linkage, Genetic Predisposition to Disease, Genome, Human, Humans, Male, Nerve Tissue Proteins, Neuregulin-1, Pedigree, Schizophrenia, Whites
Added February 22, 2016
0 Communities
1 Members
0 Resources
17 MeSH Terms
Genomewide linkage scan for quantitative trait loci underlying variation in age at menarche.
Guo Y, Shen H, Xiao P, Xiong DH, Yang TL, Guo YF, Long JR, Recker RR, Deng HW
(2006) J Clin Endocrinol Metab 91: 1009-14
MeSH Terms: Age Factors, Chromosome Mapping, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 22, Female, Genetic Markers, Genetic Variation, Genome, Human, Humans, Lod Score, Male, Menarche, Pedigree, Quantitative Trait Loci, Whites
Added December 10, 2013
0 Communities
1 Members
0 Resources
15 MeSH Terms
Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor.
Niemitz EL, Feinberg AP, Brandenburg SA, Grundy PE, DeBaun MR
(2005) Am J Hum Genet 77: 887-91
MeSH Terms: Beckwith-Wiedemann Syndrome, Child, Chromosomes, Human, Pair 11, DNA Methylation, Genotype, Humans, Wilms Tumor
Added November 27, 2013
1 Communities
1 Members
0 Resources
7 MeSH Terms
A genome-wide linkage scan for bone mineral density in an extended sample: evidence for linkage on 11q23 and Xq27.
Shen H, Zhang YY, Long JR, Xu FH, Liu YZ, Xiao P, Zhao LJ, Xiong DH, Liu YJ, Dvornyk V, Rocha-Sanchez S, Liu PY, Li JL, Conway T, Davies KM, Recker RR, Deng HW
(2004) J Med Genet 41: 743-51
MeSH Terms: Bone Density, Chromosomes, Human, Pair 11, Chromosomes, Human, X, Female, Genetic Linkage, Genome, Human, Genomics, Genotype, Humans, Lod Score, Male, Middle Aged, Pedigree
Added December 10, 2013
0 Communities
1 Members
0 Resources
13 MeSH Terms
Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome.
Niemitz EL, DeBaun MR, Fallon J, Murakami K, Kugoh H, Oshimura M, Feinberg AP
(2004) Am J Hum Genet 75: 844-9
MeSH Terms: Beckwith-Wiedemann Syndrome, Chromosomes, Human, Pair 11, Cyclin-Dependent Kinase Inhibitor p57, DNA Primers, Gene Deletion, Gene Expression, Haplotypes, Humans, In Situ Hybridization, Fluorescence, Karyotyping, Membrane Proteins, Nuclear Proteins, Potassium Channels, Voltage-Gated, Reverse Transcriptase Polymerase Chain Reaction
Added November 27, 2013
1 Communities
1 Members
0 Resources
14 MeSH Terms
A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14.
Silander K, Scott LJ, Valle TT, Mohlke KL, Stringham HM, Wiles KR, Duren WL, Doheny KF, Pugh EW, Chines P, Narisu N, White PP, Fingerlin TE, Jackson AU, Li C, Ghosh S, Magnuson VL, Colby K, Erdos MR, Hill JE, Hollstein P, Humphreys KM, Kasad RA, Lambert J, Lazaridis KN, Lin G, Morales-Mena A, Patzkowski K, Pfahl C, Porter R, Rha D, Segal L, Suh YD, Tovar J, Unni A, Welch C, Douglas JA, Epstein MP, Hauser ER, Hagopian W, Buchanan TA, Watanabe RM, Bergman RN, Tuomilehto J, Collins FS, Boehnke M
(2004) Diabetes 53: 821-9
MeSH Terms: Age of Onset, Aged, Base Sequence, Body Constitution, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 14, Chromosomes, Human, Pair 6, DNA Primers, Diabetes Mellitus, Type 2, Family, Female, Finland, Genetic Markers, Genetic Predisposition to Disease, Genome, Human, Humans, Male, Middle Aged, Siblings
Added October 1, 2014
0 Communities
1 Members
0 Resources
19 MeSH Terms
Growth suppression by acute promyelocytic leukemia-associated protein PLZF is mediated by repression of c-myc expression.
McConnell MJ, Chevallier N, Berkofsky-Fessler W, Giltnane JM, Malani RB, Staudt LM, Licht JD
(2003) Mol Cell Biol 23: 9375-88
MeSH Terms: Apoptosis, Base Sequence, Binding Sites, Cell Cycle, Cell Division, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 17, DNA, Complementary, DNA-Binding Proteins, Gene Expression, Genes, myc, Humans, Kruppel-Like Transcription Factors, Leukemia, Promyelocytic, Acute, Promoter Regions, Genetic, Promyelocytic Leukemia Zinc Finger Protein, Repressor Proteins, Transcription Factors, Translocation, Genetic, U937 Cells
Added March 5, 2014
0 Communities
1 Members
0 Resources
20 MeSH Terms
Confirmed locus on chromosome 11p and candidate loci on 6q and 8p for the triglyceride and cholesterol traits of combined hyperlipidemia.
Naoumova RP, Bonney SA, Eichenbaum-Voline S, Patel HN, Jones B, Jones EL, Amey J, Colilla S, Neuwirth CK, Allotey R, Seed M, Betteridge DJ, Galton DJ, Cox NJ, Bell GI, Scott J, Shoulders CC
(2003) Arterioscler Thromb Vasc Biol 23: 2070-7
MeSH Terms: Adult, Aged, Cholesterol, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 6, Chromosomes, Human, Pair 8, Female, Genetic Linkage, Humans, Hyperlipidemia, Familial Combined, Male, Middle Aged, Pedigree, Triglycerides
Added February 22, 2016
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1 Members
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14 MeSH Terms
MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site.
Slater DJ, Hilgenfeld E, Rappaport EF, Shah N, Meek RG, Williams WR, Lovett BD, Osheroff N, Autar RS, Ried T, Felix CA
(2002) Oncogene 21: 4706-14
MeSH Terms: Acute Disease, Base Sequence, Chromosome Breakage, Chromosome Mapping, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 3, Cytoskeletal Proteins, DNA Topoisomerases, Type II, DNA-Binding Proteins, GTP-Binding Proteins, Histone-Lysine N-Methyltransferase, Humans, In Situ Hybridization, Fluorescence, Infant, Leukemia, Myeloid, Leukemia, Myelomonocytic, Acute, Molecular Sequence Data, Myeloid-Lymphoid Leukemia Protein, Proto-Oncogenes, Septins, Transcription Factors, Translocation, Genetic, X Chromosome
Added March 5, 2014
0 Communities
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23 MeSH Terms