Association analysis of beta(2)-adrenergic receptor polymorphisms with hypertension in Japanese.
Hypertension (Dallas, Tex. : 1979) | 2001-02-01 | PMID 11230287
Kato N, Sugiyama T, Morita H and 4 more
Genes: ADRB2
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
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Publications
Page 1496 of 10600
Exclusion of the ACE D/I gene polymorphism as a determinant of endothelial dysfunction.
Hypertension (Dallas, Tex. : 1979) | 2001-02-01 | PMID 11230288
Rossi G P, Taddei S, Virdis A and 6 more
Genes: ACE
Reduced hypoxic pulmonary vascular remodeling by nitric oxide from the endothelium.
Hypertension (Dallas, Tex. : 1979) | 2001-02-01 | PMID 11230292
Ozaki M, Kawashima S, Yamashita T and 7 more
Twins in cardiovascular genetic research.
Hypertension (Dallas, Tex. : 1979) | 2001-02-01 | PMID 11230299
Luft F C
The future of hypertension therapy: sense, antisense, or nonsense?
Hypertension (Dallas, Tex. : 1979) | 2001-02-01 | PMID 11230300
Pachori A S, Huentelman M J, Francis S C and 3 more
Sodium-lithium countertransport activity is linked to chromosome 5 in baboons.
Hypertension (Dallas, Tex. : 1979) | 2001-02-01 | PMID 11230307
Kammerer C M, Cox L A, Mahaney M C and 2 more
Genome-wide linkage analysis of pulse pressure in Mexican Americans.
Hypertension (Dallas, Tex. : 1979) | 2001-02-01 | PMID 11230312
Atwood L D, Samollow P B, Hixson J E and 2 more
Brown Norway chromosome 13 confers protection from high salt to consomic Dahl S rat.
Hypertension (Dallas, Tex. : 1979) | 2001-02-01 | PMID 11230318
Cowley A W, Roman R J, Kaldunski M L and 4 more
C825T polymorphism of the G protein beta(3)-subunit and antihypertensive response to a thiazide diuretic.
Hypertension (Dallas, Tex. : 1979) | 2001-02-01 | PMID 11230366
Turner S T, Schwartz G L, Chapman A B and 1 more
Rotavirus strain diversity in Blantyre, Malawi, from 1997 to 1999.
Journal of clinical microbiology | 2001-03-01 | PMID 11230392
Cunliffe N A, Gondwe J S, Graham S M and 5 more
Genotyping of enterotoxigenic Clostridium perfringens fecal isolates associated with antibiotic-associated diarrhea and food poisoning in North America.
Journal of clinical microbiology | 2001-03-01 | PMID 11230399
Sparks S G, Carman R J, Sarker M R and 1 more
Genes: CPE
Frequency of acyclovir-resistant herpes simplex virus in clinical specimens and laboratory isolates.
Journal of clinical microbiology | 2001-03-01 | PMID 11230403
Shin Y K, Cai G Y, Weinberg A and 2 more
Diversity within reference strains of Corynebacterium matruchotii includes Corynebacterium durum and a novel organism.
Journal of clinical microbiology | 2001-03-01 | PMID 11230408
Barrett S L, Cookson B T, Carlson L C and 2 more
Phenotypic methods for determining genomovar status of the Burkholderia cepacia complex.
Journal of clinical microbiology | 2001-03-01 | PMID 11230429
Henry D A, Mahenthiralingam E, Vandamme P and 2 more
Isolation and characterization of a black-pigmented Corynebacterium sp. from a woman with spontaneous abortion.
Journal of clinical microbiology | 2001-03-01 | PMID 11230435
Shukla S K, Vevea D N, Frank D N and 2 more
Heterogeneity of Pneumocystis sterol profiles of samples from different sites in the same pair of lungs suggests coinfection by distinct organism populations.
Journal of clinical microbiology | 2001-03-01 | PMID 11230442
Amit Z, Kaneshiro E S
Phage types and genotypes of Shiga toxin-Producing Escherichia coli O157 in Finland.
Journal of clinical microbiology | 2001-03-01 | PMID 11230443
Saari M, Cheasty T, Leino K and 1 more
Rotavirus strains bearing genotype G9 or P[9] recovered from Brazilian children with diarrhea from 1997 to 1999.
Journal of clinical microbiology | 2001-03-01 | PMID 11230448
Santos N, Volotão E M, Soares C C and 6 more
Glutathione S-transferase polymorphisms and outcome of chemotherapy in childhood acute myeloid leukemia.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 2001-03-01 | PMID 11230469
Davies S M, Robison L L, Buckley J D and 5 more
Genes: GSTT1, GSTM1
Estimation of risk of inherited medullary thyroid carcinoma in apparent sporadic patients.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 2001-03-01 | PMID 11230481
Wiench M, Wygoda Z, Gubala E and 12 more
Genes: RET
Contrasting patterns of X-linked and autosomal nucleotide variation in Drosophila melanogaster and Drosophila simulans.
Molecular biology and evolution | 2001-03-01 | PMID 11230529
Andolfatto P
Living with genome instability: plant responses to telomere dysfunction.
Science (New York, N.Y.) | 2001-03-02 | PMID 11230697
Riha K, McKnight T D, Griffing L R and 1 more
Expression of p53 protein in T- and natural killer-cell lymphomas is associated with some clinicopathologic entities but rarely related to p53 mutations.
Human pathology | 2001-02-01 | PMID 11230707
Petit B, Leroy K, Kanavaros P and 5 more
Collagen type Ialpha1 and vitamin D receptor gene polymorphisms and bone mass in primary biliary cirrhosis.
Hepatology (Baltimore, Md.) | 2001-03-01 | PMID 11230734
Parés A, Guañabens N, Alvarez L and 11 more
Genes: VDR
Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1.
Hepatology (Baltimore, Md.) | 2001-03-01 | PMID 11230743
Persico M, Persico E, Bakker C T and 6 more
Interleukin 10 polymorphisms as predictors of sustained response in antiviral therapy for chronic hepatitis C infection.
Hepatology (Baltimore, Md.) | 2001-03-01 | PMID 11230752
Yee L J, Tang J, Gibson A W and 3 more
Genes: TNF
Mutational analysis of the structure and functions of hepatitis C virus RNA-dependent RNA polymerase.
Hepatology (Baltimore, Md.) | 2001-03-01 | PMID 11230755
Qin W, Yamashita T, Shirota Y and 3 more
Heterogeneity and plasticity of hepatocyte lineage cells.
Hepatology (Baltimore, Md.) | 2001-03-01 | PMID 11230756
Sell S
Nomenclature for antiviral-resistant human hepatitis B virus mutations in the polymerase region.
Hepatology (Baltimore, Md.) | 2001-03-01 | PMID 11230757
Stuyver L J, Locarnini S A, Lok A and 4 more
Interaction of estrogen replacement therapy with the thrombophilic 20210 G/A prothrombin gene mutation for atherothrombotic vascular disease: a cross-sectional study of 275 hyperlipidemic women.
Metabolism: clinical and experimental | 2001-03-01 | PMID 11230792
Glueck C J, Wang P, Fontaine R N and 2 more
Variations in the vitamin D-binding protein (Gc locus) and risk of type 2 diabetes mellitus in French Caucasians.
Metabolism: clinical and experimental | 2001-03-01 | PMID 11230793
Ye W Z, Dubois-Laforgue D, Bellanné-Chantelot C and 2 more
Genes: DBP
Trypanosoma cruzi: presence of the two major phylogenetic lineages and of several lesser discrete typing units (DTUs) in Chile and Paraguay.
Acta tropica | 2001-02-23 | PMID 11230822
Barnabé C, Neubauer K, Solari A and 1 more
Cu/Zn superoxide dismutase modulates phenotypic changes in cultured fibroblasts from human skin with chronic radiotherapy damage.
Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology | 2001-03-01 | PMID 11230895
Delanian S, Martin M, Bravard A and 2 more
Comparison of pulsed-field gel electrophoresis with random amplified polymorphic DNA for typing of Mycoplasma synoviae.
Veterinary microbiology | 2001-03-02 | PMID 11230924
Marois C, Dufour-Gesbert F, Kempf I
Receptor polymorphisms and diseases.
European journal of pharmacology | 2001-02-23 | PMID 11230990
Császár A, Abel T
Genes: TNF
The N-terminal domain of the Caulobacter crescentus CgtA protein does not function as a guanine nucleotide exchange factor.
FEBS letters | 2001-01-26 | PMID 11231024
Lin B, Maddock J R
Charcot-Marie-Tooth disease (CMT): distinctive phenotypic and genotypic features in CMT type 2.
Journal of the neurological sciences | 2001-02-15 | PMID 11231025
Gemignani F, Marbini A
Genes: MPZ
Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin gene.
Journal of the neurological sciences | 2001-02-15 | PMID 11231027
Nakagawa M, Matsuzaki T, Suehara M and 7 more
Association of alpha-2-macroglobulin deletion polymorphism with sporadic Alzheimer's disease in Koreans.
Journal of the neurological sciences | 2001-02-15 | PMID 11231028
Jhoo J H, Kim K W, Lee D Y and 6 more
Genes: APOE
Age of onset influences clinical features of chronic inflammatory demyelinating polyneuropathy.
Journal of the neurological sciences | 2001-02-15 | PMID 11231033
Hattori N, Misu K, Koike H and 4 more
NudE-L, a novel Lis1-interacting protein, belongs to a family of vertebrate coiled-coil proteins.
Mechanisms of development | 2001-03-01 | PMID 11231056
Sweeney K J, Prokscha A, Eichele G
Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf.
Mechanisms of development | 2001-03-01 | PMID 11231058
Hornyak T J, Hayes D J, Chiu L Y and 1 more
Generation of a prostate epithelial cell-specific Cre transgenic mouse model for tissue-specific gene ablation.
Mechanisms of development | 2001-03-01 | PMID 11231059
Wu X, Wu J, Huang J and 7 more
Increased XRALDH2 activity has a posteriorizing effect on the central nervous system of Xenopus embryos.
Mechanisms of development | 2001-03-01 | PMID 11231062
Chen Y, Pollet N, Niehrs C and 1 more
Genes: ATR
The tissue polarity gene nemo carries out multiple roles in patterning during Drosophila development.
Mechanisms of development | 2001-03-01 | PMID 11231065
Verheyen E M, Mirkovic I, MacLean S J and 3 more
Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: relation to expression and imprinting.
Mechanisms of development | 2001-03-01 | PMID 11231066
Weber M, Milligan L, Delalbre A and 4 more
Misexpression of IGF-I in the mouse lens expands the transitional zone and perturbs lens polarization.
Mechanisms of development | 2001-03-01 | PMID 11231069
Shirke S, Faber S C, Hallem E and 4 more
Molecular cloning and embryonic expression of Xenopus Six homeobox genes.
Mechanisms of development | 2001-03-01 | PMID 11231090
Ghanbari H, Seo H C, Fjose A and 1 more
Drosophila par-1 is required for oocyte differentiation and microtubule organization.
Current biology : CB | 2001-01-23 | PMID 11231123
Cox D N, Lu B, Sun T Q and 2 more
Self assembly of the transmembrane domain promotes signal transduction through the erythropoietin receptor.
Current biology : CB | 2001-01-23 | PMID 11231127
Kubatzky K F, Ruan W, Gurezka R and 6 more
Genes: GHR
SGS1 is required for telomere elongation in the absence of telomerase.
Current biology : CB | 2001-01-23 | PMID 11231130
Huang P, Pryde F E, Lester D and 4 more
Genes: RAD50, RAD51, RAD52, BLM, WRN
Dominant-negative mutant dynein allows spontaneous centrosome assembly, uncouples chromosome and centrosome cycles.
Current biology : CB | 2001-01-23 | PMID 11231132
Belecz I, Gonzalez C, Puro J and 1 more
Molecular evolution: Please release me, genetic code.
Current biology : CB | 2001-01-23 | PMID 11231144
Lehman N
The cyclin-dependent kinase inhibitor Roughex is involved in mitotic exit in Drosophila.
Current biology : CB | 2001-02-06 | PMID 11231149
Foley E, Sprenger F
Genes: APC
Synthetic lethality between mutation in Atm and DNA-PK(cs) during murine embryogenesis.
Current biology : CB | 2001-02-06 | PMID 11231155
Gurley K E, Kemp C J
Genes: ATM, ATR
Functional genomics: the worm scores a knockout.
Current biology : CB | 2001-02-06 | PMID 11231164
Kim S K
Atypical benign partial epilepsy/pseudo-Lennox syndrome.
Epileptic disorders : international epilepsy journal with videotape | 2000-01-01 | PMID 11231218
Hahn A
Benign epilepsies of childhood--distinct syndromes and overlap.
Epileptic disorders : international epilepsy journal with videotape | 2000-01-01 | PMID 11231223
Dulac O
The concept of hereditary impairment of brain maturation.
Epileptic disorders : international epilepsy journal with videotape | 2000-01-01 | PMID 11231224
Doose H, Neubauer B A, Petersen B
The genetics of rolandic epilepsy.
Epileptic disorders : international epilepsy journal with videotape | 2000-01-01 | PMID 11231229
Neubauer B A
Effects of mutations in mitochondrial cytochrome b in yeast and man. Deficiency, compensation and disease.
European journal of biochemistry | 2001-03-01 | PMID 11231266
Fisher N, Meunier B
Construction, separation and properties of hybrid hexamers of glutamate dehydrogenase in which five of the six subunits are contributed by the catalytically inert D165S.
European journal of biochemistry | 2001-03-01 | PMID 11231268
Hayden B M, Engel P C
Genes: DTNB
Identification and characterization of SEB, a novel protein that binds to the acute undifferentiated leukemia-associated protein SET.
European journal of biochemistry | 2001-03-01 | PMID 11231286
Minakuchi M, Kakazu N, Gorrin-Rivas M J and 4 more
Genes: SET
Structure-activity relationship of the p55 TNF receptor death domain and its lymphoproliferation mutants.
European journal of biochemistry | 2001-03-01 | PMID 11231290
De Wilde G, Murray-Rust J, Boone E and 6 more
Genes: TNF, FADD
A change in ionization of the NADP(H)-binding component (dIII) of proton-translocating transhydrogenase regulates both hydride transfer and nucleotide release.
European journal of biochemistry | 2001-03-01 | PMID 11231296
Rodrigues D J, Venning J D, Quirk P G and 1 more
Tyrosine phosphorylation-dependent activation of NF-kappa B. Requirement for p56 LCK and ZAP-70 protein tyrosine kinases.
European journal of biochemistry | 2001-03-01 | PMID 11231305
Livolsi A, Busuttil V, Imbert V and 2 more
Genes: LCK
Polymorphism of the androgen receptor gene is associated with male pattern baldness.
The Journal of investigative dermatology | 2001-03-01 | PMID 11231320
Ellis J A, Stebbing M, Harrap S B
"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivation.
The Journal of investigative dermatology | 2001-03-01 | PMID 11231323
Kruse R, Rütten A, Hosseiny-Malayeri H R and 5 more
Genes: MSH2, MLH1
Polymorphisms of the glucose transporter (GLUT1) gene are associated with diabetic nephropathy.
Kidney international | 2001-03-01 | PMID 11231353
Hodgkinson A D, Millward B A, Demaine A G
Novel method for simultaneous analysis of p53 and K-ras mutations and p53 protein expression in single histologic sections.
Archives of pathology & laboratory medicine | 2001-03-01 | PMID 11231481
Yamashita K, Yoshida T, Shinoda H and 1 more
An antisense-based functional genomics approach for identification of genes critical for growth of Candida albicans.
Nature biotechnology | 2001-03-01 | PMID 11231556
De Backer M D, Nelissen B, Logghe M and 10 more
Constitutive expression of Arabidopsis LEAFY or APETALA1 genes in citrus reduces their generation time.
Nature biotechnology | 2001-03-01 | PMID 11231561
Peña L, Martín-Trillo M, Juárez J and 3 more
A myosin II mutation uncouples ATPase activity from motility and shortens step size.
Nature cell biology | 2001-03-01 | PMID 11231583
Murphy C T, Rock R S, Spudich J A
Abacavir-lamivudine-zidovudine vs indinavir-lamivudine-zidovudine in antiretroviral-naive HIV-infected adults: A randomized equivalence trial.
JAMA | 2001-03-07 | PMID 11231744
Staszewski S, Keiser P, Montaner J and 14 more
Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus.
Archives of ophthalmology (Chicago, Ill. : 1960) | 2001-03-01 | PMID 11231769
Lois N, Holder G E, Bunce C and 2 more
Genes: ERG
Mutations in the CRB1 gene cause Leber congenital amaurosis.
Archives of ophthalmology (Chicago, Ill. : 1960) | 2001-03-01 | PMID 11231775
Lotery A J, Jacobson S G, Fishman G A and 10 more
Genes: CRB1
Whole-genome screening in ankylosing spondylitis: evidence of non-MHC genetic-susceptibility loci.
American journal of human genetics | 2001-04-01 | PMID 11231900
Laval S H, Timms A, Edwards S and 9 more
Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome).
American journal of human genetics | 2001-04-01 | PMID 11231901
Guichard C, Harricane M C, Lafitte J J and 5 more
Genes: DNAI1
A genetic factor for age-related cataract: identification and characterization of a novel galactokinase variant, "Osaka," in Asians.
American journal of human genetics | 2001-04-01 | PMID 11231902
Okano Y, Asada M, Fujimoto A and 10 more
Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency.
American journal of human genetics | 2001-04-01 | PMID 11231903
Binzak B A, Wevers R A, Moolenaar S H and 7 more
Genes: DMGDH
Effect of probucol in lecithin-cholesterol acyltransferase-deficient mice: inhibition of 2 independent cellular cholesterol-releasing pathways in vivo.
Arteriosclerosis, thrombosis, and vascular biology | 2001-03-01 | PMID 11231919
Tomimoto S, Tsujita M, Okazaki M and 6 more
Genes: LCAT
Lack of triglyceride-lowering properties of fish oil in apolipoprotein e-deficient mice.
Arteriosclerosis, thrombosis, and vascular biology | 2001-03-01 | PMID 11231920
Asset G, Baugé E, Fruchart J C and 1 more
Paraoxonase1-192 polymorphism modulates the nonfatal myocardial infarction risk associated with decreased HDLs.
Arteriosclerosis, thrombosis, and vascular biology | 2001-03-01 | PMID 11231922
Sentí M, Tomás M, Marrugat J and 1 more
Genes: PON1
Thrombomodulin promoter mutations, venous thrombosis, and varicose veins.
Arteriosclerosis, thrombosis, and vascular biology | 2001-03-01 | PMID 11231927
Le Flem L, Mennen L, Aubry M L and 4 more
Evidence for inflammatory bowel disease of a susceptibility locus on the X chromosome.
Gastroenterology | 2001-03-01 | PMID 11231937
Vermeire S, Satsangi J, Peeters M and 4 more
Genes: NPL
Continuous stimulation by normal luminal bacteria is essential for the development and perpetuation of colitis in Tg(epsilon26) mice.
Gastroenterology | 2001-03-01 | PMID 11231944
Veltkamp C, Tonkonogy S L, De Jong Y P and 5 more
Genes: MLN
A mutation of the Wilson disease protein, ATP7B, is degraded in the proteasomes and forms protein aggregates.
Gastroenterology | 2001-03-01 | PMID 11231950
Harada M, Sakisaka S, Terada K and 10 more
Molecular anatomy and pathophysiologic implications of drug resistance in hepatitis B virus infection.
Gastroenterology | 2001-03-01 | PMID 11231955
Doo E, Liang T J
Acute flares in chronic hepatitis B: the natural and unnatural history of an immunologically mediated liver disease.
Gastroenterology | 2001-03-01 | PMID 11231956
Perrillo R P
Compound heterozygous mutations in the gamma subunit gene of ENaC (1627delG and 1570-1G-->A) in one sporadic Japanese patient with a systemic form of pseudohypoaldosteronism type 1.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11231969
Adachi M, Tachibana K, Asakura Y and 4 more
A novel mutation in the calcium-sensing receptor gene in a Chinese subject with persistent hypercalcemia and hypocalciuria.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11231970
Jap T S, Wu Y C, Jenq S F and 1 more
Genes: CGA
Phenotypic heterogeneity in patients with familial partial lipodystrophy (dunnigan variety) related to the site of missense mutations in lamin a/c gene.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11231979
Garg A, Vinaitheerthan M, Weatherall P T and 1 more
Genes: LMNA
Relationship between angiotensin-converting enzyme gene polymorphism and insulin resistance in never-treated hypertensive patients.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11231997
Perticone F, Ceravolo R, Iacopino S and 6 more
Genes: ACE
Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11232002
Deneux C, Tardy V, Dib A and 5 more
Early-onset type 2 diabetes: metabolic and genetic characterization in the mexican population.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11232004
Aguilar-Salinas C A, Reyes-Rodríguez E, Ordóñez-Sánchez M L and 10 more
Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11232006
Vilain C, Rydlewski C, Duprez L and 7 more
Genes: PAX8
Loss of heterozygosity at the RET protooncogene locus in a case of multiple endocrine neoplasia type 2A.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11232007
Quadro L, Fattoruso O, Cosma M P and 4 more
Genes: RET
Three new mutations in the gene for the growth hormone (gh)-releasing hormone receptor in familial isolated gh deficiency type ib.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11232012
Salvatori R, Fan X, Phillips J A and 6 more
Genes: GHRHR, GHRH
The property of a novel v2 receptor mutant in a patient with nephrogenic diabetes insipidus.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11232028
Inaba S, Hatakeyama H, Taniguchi N and 1 more
Genes: AVP
Thyroid carcinoma usually occurs in patients with familial adenomatous polyposis in the absence of biallelic inactivation of the adenomatous polyposis coli gene.
The Journal of clinical endocrinology and metabolism | 2001-01-01 | PMID 11232035
Cetta F, Curia M C, Montalto G and 4 more
Genes: APC