Positional identification of variants of Adamts16 linked to inherited hypertension
暂无分享,去创建一个
Bryan Frank | C. Bouchard | A. Chakravarti | T. Rice | R. Cooper | D. Rao | T. Rankinen | L. Pérusse | G. Ehret | S. Ganesh | A. Weder | N. Lee | M. Garrett | Truong Luu | B. Joe | K. Gopalakrishnan | S. Apte | Edward J. Toland | J. Rapp | Ashley A O'Connor | P. Farms | Ezhilarasi Manickavasagam | Y. Saad | D. Coe | S. Yerga‐Woolwine | E. Toland | Ovokeraye H. Achinike | D. Rao | Kathirvel Gopalakrishnan | Shane Yerga‐Woolwine | Phyllis Farms | R. Cooper
[1] Elias I. Traboulsi,et al. Functional analysis of an ADAMTS10 signal peptide mutation in Weill‐Marchesani syndrome demonstrates a long‐range effect on secretion of the full‐length enzyme , 2008, Human mutation.
[2] B. Browning,et al. Haplotypic analysis of Wellcome Trust Case Control Consortium data , 2008, Human Genetics.
[3] C. Bouchard,et al. Effect of Endothelin 1 Genotype on Blood Pressure Is Dependent on Physical Activity or Fitness Levels , 2007, Hypertension.
[4] C. De Geyter,et al. FSH stimulates the expression of the ADAMTS-16 protease in mature human ovarian follicles. , 2007, Molecular human reproduction.
[5] Simon C. Potter,et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.
[6] A. Cowley. The genetic dissection of essential hypertension , 2006, Nature Reviews Genetics.
[7] M. Noor,et al. Speciation genetics: evolving approaches , 2006, Nature Reviews Genetics.
[8] Philipp W. Raess,et al. Positional cloning of Sorcs1, a type 2 diabetes quantitative trait locus , 2006, Nature Genetics.
[9] I. Hajjar,et al. Hypertension: trends in prevalence, incidence, and control. , 2006, Annual review of public health.
[10] C. Flannery. MMPs and ADAMTSs: functional studies. , 2006, Frontiers in bioscience : a journal and virtual library.
[11] L. Pegg,et al. ADAMTS-4 (aggrecanase-1): N-terminal activation mechanisms. , 2005, Archives of biochemistry and biophysics.
[12] N. Lee,et al. Genomic approaches for reconstructing gene networks. , 2005, Pharmacogenomics.
[13] Razvan Sultana,et al. Transcriptional profiling with a blood pressure QTL interval-specific oligonucleotide array. , 2005, Physiological genomics.
[14] Per Eriksson,et al. Positional identification of TNFSF4, encoding OX40 ligand, as a gene that influences atherosclerosis susceptibility , 2005, Nature Genetics.
[15] H. Meng,et al. Locating a Blood Pressure Quantitative Trait Locus Within 117 kb on the Rat Genome: Substitution Mapping and Renal Expression Analysis , 2005, Hypertension.
[16] K. Reynolds,et al. Global burden of hypertension: analysis of worldwide data , 2005, The Lancet.
[17] S. Apte,et al. Discovery and Characterization of a Novel, Widely Expressed Metalloprotease, ADAMTS10, and Its Proteolytic Activation* , 2004, Journal of Biological Chemistry.
[18] A. Pertsemlidis,et al. Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus. , 2004, Immunity.
[19] R. Leduc,et al. Identification of Prodomain Determinants Involved in ADAMTS-1 Biosynthesis* , 2004, Journal of Biological Chemistry.
[20] Ping Wang,et al. Proprotein Convertase Furin Interacts with and Cleaves Pro-ADAMTS4 (Aggrecanase-1) in the trans-Golgi Network* , 2004, Journal of Biological Chemistry.
[21] O. Martínez. Spurious linkage between markers in QTL mapping , 1996, Molecular Breeding.
[22] M. Garrett,et al. Substitution mapping of a blood pressure quantitative trait locus to a 2.73 Mb region on rat chromosome 1 , 2003, Journal of hypertension.
[23] Douglas A. Hosack,et al. Identifying biological themes within lists of genes with EASE , 2003, Genome Biology.
[24] R. Leduc,et al. Characterization of ADAMTS-9 and ADAMTS-20 as a Distinct ADAMTS Subfamily Related to Caenorhabditis elegans GON-1* , 2003, The Journal of Biological Chemistry.
[25] T. Sugiura. Baculoviral expression of correctly processed ADAMTS proteins fused with the human IgG-Fc region. , 2003, Journal of biotechnology.
[26] N. Schork,et al. A genome-wide linkage analysis investigating the determinants of blood pressure in whites and African Americans. , 2003, American journal of hypertension.
[27] Jens Holmberg,et al. Positional identification of Ncf1 as a gene that regulates arthritis severity in rats , 2003, Nature Genetics.
[28] J. Nadeau,et al. Finding Genes That Underlie Complex Traits , 2002, Science.
[29] M. Garrett,et al. Two closely linked interactive blood pressure QTL on rat chromosome 5 defined using congenic Dahl rats. , 2002, Physiological genomics.
[30] Víctor Quesada,et al. Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains. , 2002, Gene.
[31] Robert J. Unwin,et al. Human Hypertension Caused by Mutations in WNK Kinases , 2001, Science.
[32] Ali G. Gharavi,et al. Molecular Mechanisms of Human Hypertension , 2001, Cell.
[33] M. Garrett,et al. Multiple blood pressure QTL on rat chromosome 1 defined by Dahl rat congenic strains. , 2001, Physiological genomics.
[34] B. Tang,et al. ADAMTS: a novel family of extracellular matrix proteases. , 2001, The international journal of biochemistry & cell biology.
[35] C. Bouchard,et al. Genome-Wide Linkage Analysis of Systolic and Diastolic Blood Pressure: The Québec Family Study , 2000, Circulation.
[36] P. Sigler,et al. Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy. , 2000, Science.
[37] C. Bouchard,et al. Genome-Wide Linkage Analysis of Systolic and Diastolic Blood Pressure , 2000 .
[38] S. O’Rahilly,et al. Dominant negative mutations in human PPARγ associated with severe insulin resistance, diabetes mellitus and hypertension , 1999, Nature.
[39] A. Winterpacht,et al. Isolation, characterization, and mapping of a zinc finger gene, ZFP95, containing both a SCAN box and an alternatively spliced KRAB A domain. , 1999, Genomics.
[40] M. Garrett,et al. Localization of a blood pressure QTL on rat chromosome 1 using Dahl rat congenic strains. , 1999, Physiological genomics.
[41] M. Garrett,et al. Genome scan and congenic strains for blood pressure QTL using Dahl salt-sensitive rats. , 1998, Genome research.
[42] A. Kong,et al. Linkage mapping in experimental crosses: the robustness of single-gene models. , 1997, Genetics.
[43] C. Bouchard. Genetic epidemiology, association, and sib-pair linkage: results from the Quebec Family Study , 1996 .
[44] G. Bray,et al. Molecular and genetic aspects of obesity , 1996 .
[45] L. Schild,et al. Hypertension caused by a truncated epithelial sodium channel γ subunit: genetic heterogeneity of Liddle syndrome , 1995, Nature Genetics.
[46] T. Mune,et al. Human hypertension caused by mutations in the kidney isozyme of 11β–hydroxysteroid dehydrogenase , 1995, Nature Genetics.
[47] L. Schild,et al. A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[48] Morris Schambelan,et al. Liddle's syndrome: heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel , 1994, Cell.
[49] C. Haley,et al. A simple regression method for mapping quantitative trait loci in line crosses using flanking markers , 1992, Heredity.
[50] J. Lalouel,et al. A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension , 1992, Nature.
[51] R. Buñag,et al. Tail‐Cuff Blood Pressure Measurement without External Preheating in Awake Rats , 1982, Hypertension.