Effect of inactivation of nuo and ackA-pta on redistribution of metabolic fluxes in Escherichia coli.
Biotechnology and bioengineering | 1999-11-05 | PMID 10486127
Yang Y T, Bennett G N, San K Y
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 1204 of 10600
Photoreceptor layer reconstruction in a rodent model of retinal degeneration.
Experimental neurology | 1999-09-01 | PMID 10486172
Kwan A S, Wang S, Lund R D
The IGF-I amino-terminal tripeptide glycine-proline-glutamate (GPE) is neuroprotective to striatum in the quinolinic acid lesion animal model of Huntington's disease.
Experimental neurology | 1999-09-01 | PMID 10486177
Alexi T, Hughes P E, van Roon-Mom W M and 4 more
Alternative splicing produces transcripts encoding four variants of mouse G-protein-coupled receptor kinase 6.
Genomics | 1999-09-01 | PMID 10486211
Moepps B, Vatter P, Frodl R and 4 more
Genes: GRK6, GRK1
Osteocalcin: genetic and physical mapping of the human gene BGLAP and its potential role in postmenopausal osteoporosis.
Genomics | 1999-09-01 | PMID 10486212
Raymond M H, Schutte B C, Torner J C and 2 more
Genes: BGLAP
LETM1, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, flanks the Wolf-Hirschhorn syndrome (WHS) critical region and is deleted in most WHS patients.
Genomics | 1999-09-01 | PMID 10486213
Endele S, Fuhry M, Pak S J and 2 more
Genes: LETM1
TTID: A novel gene at 5q31 encoding a protein with titin-like features.
Genomics | 1999-09-01 | PMID 10486214
Godley L A, Lai F, Liu J and 2 more
The ABCR gene in recessive and dominant Stargardt diseases: a genetic pathway in macular degeneration.
Genomics | 1999-09-01 | PMID 10486215
Zhang K, Kniazeva M, Hutchinson A and 3 more
Cloning, expression, and chromosomal mapping of the human 14-3-3gamma gene (YWHAG) to 7q11.23.
Genomics | 1999-09-01 | PMID 10486217
Horie M, Suzuki M, Takahashi E and 1 more
Genes: YWHAG
Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1 using historical recombinants in Libyan Jewish cystinuria patients.
Genomics | 1999-09-01 | PMID 10486219
Pras E, Kreiss Y, Frishberg Y and 3 more
Increased incidence and analysis of emperipolesis in megakaryocytes of the mouse mutant gunmetal.
Experimental and molecular pathology | 1999-08-01 | PMID 10486237
McGarry M P, Reddington M, Jackson C W and 3 more
Double-stranded RNA induces specific developmental defects in zebrafish embryos.
Biochemical and biophysical research communications | 1999-09-16 | PMID 10486270
Wargelius A, Ellingsen S, Fjose A
Tissue-specific somatic mosaicism in spinal and bulbar muscular atrophy is dependent on CAG-repeat length and androgen receptor--gene expression level.
American journal of human genetics | 1999-10-01 | PMID 10486315
Tanaka F, Reeves M F, Ito Y and 11 more
Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes.
American journal of human genetics | 1999-10-01 | PMID 10486316
Annunen S, Körkkö J, Czarny M and 22 more
Variegate porphyria in Western Europe: identification of PPOX gene mutations in 104 families, extent of allelic heterogeneity, and absence of correlation between phenotype and type of mutation.
American journal of human genetics | 1999-10-01 | PMID 10486317
Whatley S D, Puy H, Morgan R R and 5 more
Genes: PPOX
Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors.
American journal of human genetics | 1999-10-01 | PMID 10486318
Varley J M, McGown G, Thorncroft M and 7 more
Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1: distinct effects on biochemical and clinical phenotypes.
American journal of human genetics | 1999-10-01 | PMID 10486319
Schrijver I, Liu W, Brenn T and 2 more
Genes: EGF, FBN1
The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes.
American journal of human genetics | 1999-10-01 | PMID 10486320
Gayther S A, Russell P, Harrington P and 3 more
Genes: BRCA1, BRCA2
Temperature-sensitive RB mutations linked to incomplete penetrance of familial retinoblastoma in 12 families.
American journal of human genetics | 1999-10-01 | PMID 10486322
Otterson G A, Modi S, Nguyen K and 2 more
Distribution of two HIV-1-resistant polymorphisms (SDF1-3'A and CCR2-64I) in East Asian and world populations and its implication in AIDS epidemiology.
American journal of human genetics | 1999-10-01 | PMID 10486323
Su B, Jin L, Hu F and 12 more
Genes: CCR2
Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.
American journal of human genetics | 1999-10-01 | PMID 10486326
Jung M, Poepping I, Perrot A and 5 more
Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25.
American journal of human genetics | 1999-10-01 | PMID 10486328
Visapää I, Salonen R, Varilo T and 2 more
Linkage of familial schizophrenia to chromosome 13q32.
American journal of human genetics | 1999-10-01 | PMID 10486329
Brzustowicz L M, Honer W G, Chow E W and 4 more
A novel syndrome of episodic muscle weakness maps to xp22.3.
American journal of human genetics | 1999-10-01 | PMID 10486330
Ryan M M, Taylor P, Donald J A and 5 more
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci.
American journal of human genetics | 1999-10-01 | PMID 10486331
Hovatta I, Varilo T, Suvisaari J and 9 more
An empirical exploration of the (delta mu)2 genetic distance for 213 human microsatellite markers.
American journal of human genetics | 1999-10-01 | PMID 10486332
Cooper G, Amos W, Bellamy R and 4 more
Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentials.
American journal of human genetics | 1999-10-01 | PMID 10486334
Williams J T, Begleiter H, Porjesz B and 7 more
Transmission/disequilibrium tests for extended marker haplotypes.
American journal of human genetics | 1999-10-01 | PMID 10486335
Clayton D, Jones H
A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission.
American journal of human genetics | 1999-10-01 | PMID 10486336
Clayton D
Genes, demography, and life span: the contribution of demographic data in genetic studies on aging and longevity.
American journal of human genetics | 1999-10-01 | PMID 10486337
Yashin A I, De Benedictis G, Vaupel J W and 8 more
Heterogeneity in the Helicobacter pylori vacA and cagA genes: association with gastroduodenal disease in South Africa?
Gut | 1999-10-01 | PMID 10486355
Kidd M, Lastovica A J, Atherton J C and 1 more
N-acetyltransferase-2 polymorphism in Parkinson's disease: the Rotterdam study.
Journal of neurology, neurosurgery, and psychiatry | 1999-10-01 | PMID 10486401
Harhangi B S, Oostra B A, Heutink P and 3 more
Thermolabile methylenetetrahydrofolate reductase gene and the risk of cognitive impairment in those over 85.
Journal of neurology, neurosurgery, and psychiatry | 1999-10-01 | PMID 10486408
Gussekloo J, Heijmans B T, Slagboom P E and 3 more
Genes: MTHFR
Three-dimensional morphological analysis of isolated metopic synostosis.
The Anatomical record | 1999-10-01 | PMID 10486515
Zumpano M P, Carson B S, Marsh J L and 2 more
Positive regulation of Bacillus subtilis sigD by C-terminal truncated LacR at translational level.
FEBS letters | 1999-08-20 | PMID 10486575
Ogura M, Hirao S, Ohshiro Y and 1 more
Mitochondrial DNA repair pathways.
Mutation research | 1999-07-30 | PMID 10486588
Croteau D L, Stierum R H, Bohr V A
Intraindividual sequence diversity and a hierarchical approach to the study of mitochondrial DNA mutations.
Mutation research | 1999-07-30 | PMID 10486592
Chen J Z, Hebert P D
Terminal branch haplotype analysis: a novel approach to investigate newly arisen variants of mitochondrial DNA in natural populations.
Mutation research | 1999-07-30 | PMID 10486593
Chen J Z, Hebert P D
[Phenotypes of essential arterial hypertension in Caribbean women].
Archives des maladies du coeur et des vaisseaux | 1999-08-01 | PMID 10486645
Mpio I, Fauvel J P, Robert O and 3 more
High-throughput genotyping of factor V Leiden mutation by ultrathin-layer agarose gel electrophoresis.
Journal of chromatography. A | 1999-08-20 | PMID 10486761
Lengyel T, Sasvari-Szekely M, Guttman A
Molecular mechanisms of gonadotropin-releasing hormone receptor gene regulation.
Journal of the Society for Gynecologic Investigation | 2000-01-01 | PMID 10486777
Norwitz E R, Jeong K H, Chin W W
Genetic changes during the multistage pathogenesis of human papillomavirus positive and negative vulvar carcinomas.
Journal of the Society for Gynecologic Investigation | 2000-01-01 | PMID 10486784
Flowers L C, Wistuba I I, Scurry J and 5 more
[Thermal interhemispheric asymmetry of the brain in rats in a cataleptic state].
Zhurnal vysshei nervnoi deiatelnosti imeni I P Pavlova | 2000-01-01 | PMID 10486903
Petrova E V
Pathogenic and vaccine significance of toxin-coregulated pili of Vibrio cholerae E1 Tor.
Journal of biotechnology | 1999-08-20 | PMID 10486921
Attridge S R, Voss E, Manning P A
Developing dendritic cell polynucleotide vaccination for prostate cancer immunotherapy.
Journal of biotechnology | 1999-08-20 | PMID 10486925
Berlyn K A, Ponniah S, Stass S A and 8 more
Genes: APC
Characterization of porcine T lymphocytes and their immune response against viral antigens.
Journal of biotechnology | 1999-08-20 | PMID 10486931
Saalmüller A, Pauly T, Höhlich B J and 1 more
Genetic variation of three tetrameric tandem repeats in four distinct Israeli ethnic groups.
Journal of forensic sciences | 1999-09-01 | PMID 10486950
Amar A, Brautbar C, Motro U and 3 more
Interpreting DNA mixtures in structured populations.
Journal of forensic sciences | 1999-09-01 | PMID 10486951
Curran J M, Triggs C M, Buckleton J and 1 more
Spanish population data on the loci D13S317, D7S820, and D16S539 generated using silver staining (SilverSTR III Multiplex).
Journal of forensic sciences | 1999-09-01 | PMID 10486952
Entrala C, Lorente J A, Lorente M and 3 more
Swiss Caucasian population data for 13 STR loci using AmpFISTR profiler plus and cofiler PCR amplification kits.
Journal of forensic sciences | 1999-09-01 | PMID 10486953
Gehrig C, Hochmeister M, Borer U V and 2 more
Genes: FGA
STR HUMARA locus gene and genotype frequencies in Han and Bei populations in China.
Journal of forensic sciences | 1999-09-01 | PMID 10486954
Wu M Y, Zou L P, Shen B and 3 more
NaOH treatment to neutralize inhibitors of Taq polymerase.
Journal of forensic sciences | 1999-09-01 | PMID 10486956
Bourke M T, Scherczinger C A, Ladd C and 1 more
Gene and genotype frequencies for HLA-DQA1 in Caucasians and Mulattoes in Brazil.
Journal of forensic sciences | 1999-09-01 | PMID 10486957
Soares-Vieira J A, Billerbeck A E, Iwamura E S and 2 more
Chorionic villus sampling prior to pregnancy termination, a tool for forensic paternity testing.
Journal of forensic sciences | 1999-09-01 | PMID 10486960
Reshef A, Brauner P, Shpitzen M and 5 more
Genes: CPM
Sequence evolution of the CCR5 chemokine receptor gene in primates.
Molecular biology and evolution | 1999-09-01 | PMID 10486970
Zhang Y W, Ryder O A, Zhang Y P
Genes: CCR5
Multiple acquisitions via horizontal transfer of a group I intron in the mitochondrial cox1 gene during evolution of the Araceae family.
Molecular biology and evolution | 1999-09-01 | PMID 10486971
Cho Y, Palmer J D
Rate and directionality of mutations and effects of allele size constraints at anonymous, gene-associated, and disease-causing trinucleotide loci.
Molecular biology and evolution | 1999-09-01 | PMID 10486972
Deka R, Guangyun S, Smelser D and 3 more
Genome degradation is an ongoing process in Rickettsia.
Molecular biology and evolution | 1999-09-01 | PMID 10486973
Andersson J O, Andersson S G
Reduced nucleotide variability at an androgen-binding protein locus (Abpa) in house mice: evidence for positive natural selection.
Molecular biology and evolution | 1999-09-01 | PMID 10486974
Karn R C, Nachman M W
Apolipoprotein E polymorphism in non-diabetic patients with acute coronary syndrome.
Yonsei medical journal | 1999-08-01 | PMID 10487142
Kim I J, Hong B K, Lee B K and 7 more
Genes: CAD
Mutated nicotinic receptors responsible for autosomal dominant nocturnal frontal lobe epilepsy are more sensitive to carbamazepine.
Epilepsia | 1999-09-01 | PMID 10487182
Picard F, Bertrand S, Steinlein O K and 1 more
Herbicide resistance and supersensitivity in photosystem II.
Cellular and molecular life sciences : CMLS | 1999-08-15 | PMID 10487206
Oettmeier W
Insulin resistance and angiotensin converting enzyme polymorphism in Japanese hypertensive subjects.
Hypertension research : official journal of the Japanese Society of Hypertension | 1999-07-01 | PMID 10487323
Yamamoto J, Kageyama S, Sakurai T and 7 more
Genes: ACE
Angiotensinogen and angiotensin-converting enzyme genotypes, and day and night blood pressures in elderly Japanese hypertensives.
Hypertension research : official journal of the Japanese Society of Hypertension | 1999-07-01 | PMID 10487325
Kario K, Hoshide S, Umeda Y and 5 more
Genes: ACE
Serum phospholipid transfer protein activity and genetic variation of the PLTP gene.
Atherosclerosis | 1999-09-01 | PMID 10487493
Tahvanainen E, Jauhiainen M, Funke H and 3 more
Genes: PLTP
Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144.
Atherosclerosis | 1999-09-01 | PMID 10487497
Teh E M, Chisholm J W, Dolphin P J and 4 more
Genes: LCAT
Absence of association between genetic variation in the LIPC gene promoter and plasma lipoproteins in three Canadian populations.
Atherosclerosis | 1999-09-01 | PMID 10487498
Hegele R A, Harris S B, Brunt J H and 4 more
Genes: LIPC
Effects of troglitazone on atherogenic lipoprotein phenotype in coronary patients with insulin resistance.
Atherosclerosis | 1999-09-01 | PMID 10487503
Sunayama S, Watanabe Y, Ohmura H and 5 more
Conversion of C57Bl/6 mice from a tumor promotion-resistant to a -sensitive phenotype by enhanced ornithine decarboxylase expression.
Molecular carcinogenesis | 1999-09-01 | PMID 10487519
Guo Y, Zhao J, Sawicki J and 2 more
Transforming growth factor-beta responsiveness in DPC4/SMAD4-null cancer cells.
Molecular carcinogenesis | 1999-09-01 | PMID 10487520
Dai J L, Schutte M, Bansal R K and 3 more
Genes: SMAD4
Expression of mutant thyroid hormone nuclear receptors in human hepatocellular carcinoma cells.
Molecular carcinogenesis | 1999-09-01 | PMID 10487522
Lin K H, Shieh H Y, Chen S L and 1 more
Ki-ras activation in lung cells isolated from AC3F1 (A/J x C3H/HeJ) mice after treatment with aflatoxin B1.
Molecular carcinogenesis | 1999-09-01 | PMID 10487523
Donnelly P J, Massey T E
Cyclooxygenase knockout mice: models for elucidating isoform-specific functions.
Biochemical pharmacology | 1999-10-15 | PMID 10487525
Langenbach R, Loftin C, Lee C and 1 more
Genetic alterations on chromosome 17p associated with response to radiotherapy in bulky cervical cancer.
British journal of cancer | 1999-09-01 | PMID 10487620
Harima Y, Shirahama S, Harima K and 3 more
A polymorphism in the CYP17 gene is associated with male breast cancer.
British journal of cancer | 1999-09-01 | PMID 10487625
Young I E, Kurian K M, Annink C and 6 more
Intron variants of the p53 gene are associated with increased risk for ovarian cancer but not in carriers of BRCA1 or BRCA2 germline mutations.
British journal of cancer | 1999-09-01 | PMID 10487631
Wang-Gohrke S, Weikel W, Risch H and 13 more
Genes: BRCA1, BRCA2
A novel parathyroid hormone (PTH)/PTH-related peptide receptor mutation in Jansen's metaphyseal chondrodysplasia.
The Journal of clinical endocrinology and metabolism | 1999-09-01 | PMID 10487664
Schipani E, Langman C, Hunzelman J and 5 more
Genes: PTH
The thyroid hormone receptor-beta gene mutation R383H is associated with isolated central resistance to thyroid hormone.
The Journal of clinical endocrinology and metabolism | 1999-09-01 | PMID 10487671
Safer J D, O'Connor M G, Colan S D and 3 more
Genes: TRH
Suppression of insulin oversecretion by subcutaneous recombinant human insulin-like growth factor I in children with congenital hyperinsulinism due to defective beta-cell sulfonylurea receptor.
The Journal of clinical endocrinology and metabolism | 1999-09-01 | PMID 10487673
Katz L E, Ferry R J, Stanley C A and 3 more
Estrogen receptor polymorphism predicts the onset of natural and surgical menopause.
The Journal of clinical endocrinology and metabolism | 1999-09-01 | PMID 10487678
Weel A E, Uitterlinden A G, Westendorp I C and 6 more
HLA-DRB1*08, DRB1*03/DRB3*0101, and DRB3*0202 are susceptibility genes for Graves' disease in North American Caucasians, whereas DRB1*07 is protective.
The Journal of clinical endocrinology and metabolism | 1999-09-01 | PMID 10487684
Chen Q Y, Huang W, She J X and 3 more
Normal variation in leptin levels in associated with polymorphisms in the proopiomelanocortin gene, POMC.
The Journal of clinical endocrinology and metabolism | 1999-09-01 | PMID 10487685
Hixson J E, Almasy L, Cole S and 7 more
Genes: POMC
Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutations.
The Journal of clinical endocrinology and metabolism | 1999-09-01 | PMID 10487688
Duerr E M, Gimm O, Neuberg D S and 6 more
Genes: CUL2, VHL, RET
A novel mutation in the sodium/iodide symporter gene in the largest family with iodide transport defect.
The Journal of clinical endocrinology and metabolism | 1999-09-01 | PMID 10487695
Kosugi S, Bhayana S, Dean H J
Genes: AGA
A gene for congenital generalized lipodystrophy maps to human chromosome 9q34.
The Journal of clinical endocrinology and metabolism | 1999-09-01 | PMID 10487716
Garg A, Wilson R, Barnes R and 8 more
Genes: RXRA
Role of a white collar-1-white collar-2 complex in blue-light signal transduction.
The EMBO journal | 1999-09-15 | PMID 10487748
Talora C, Franchi L, Linden H and 2 more
The E6 protein of human papillomavirus type 16 binds to and inhibits co-activation by CBP and p300.
The EMBO journal | 1999-09-15 | PMID 10487758
Patel D, Huang S M, Baglia L A and 1 more
New mode of DNA binding of multi-zinc finger transcription factors: deltaEF1 family members bind with two hands to two target sites.
The EMBO journal | 1999-09-15 | PMID 10487759
Remacle J E, Kraft H, Lerchner W and 5 more
MEF-2 function is modified by a novel co-repressor, MITR.
The EMBO journal | 1999-09-15 | PMID 10487760
Sparrow D B, Miska E A, Langley E and 6 more
Genes: HDAC1
NuA4, an essential transcription adaptor/histone H4 acetyltransferase complex containing Esa1p and the ATM-related cofactor Tra1p.
The EMBO journal | 1999-09-15 | PMID 10487762
Allard S, Utley R T, Savard J and 6 more
Genes: ATM, TRRAP
Nucleolar localization signals of box H/ACA small nucleolar RNAs.
The EMBO journal | 1999-09-15 | PMID 10487763
Narayanan A, Lukowiak A, Jády B E and 4 more
A murine model of myocardial microvascular thrombosis.
The Journal of clinical investigation | 1999-09-01 | PMID 10487767
Christie P D, Edelberg J M, Picard M H and 6 more
A new animal model for relapsing polychondritis, induced by cartilage matrix protein (matrilin-1).
The Journal of clinical investigation | 1999-09-01 | PMID 10487773
Hansson A S, Heinegård D, Holmdahl R
Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemia.
The Journal of clinical investigation | 1999-09-01 | PMID 10487776
Norman D, Sun X M, Bourbon M and 3 more
Nuclear accumulation of mutated beta-catenin in hepatocellular carcinoma is associated with increased cell proliferation.
The American journal of pathology | 1999-09-01 | PMID 10487827
Nhieu J T, Renard C A, Wei Y and 3 more
The magnitude of brain lipid peroxidation correlates with the extent of degeneration but not with density of neuritic plaques or neurofibrillary tangles or with APOE genotype in Alzheimer's disease patients.
The American journal of pathology | 1999-09-01 | PMID 10487843
Montine T J, Markesbery W R, Zackert W and 3 more
Genes: APOE
Epstein-Barr virus (EBV) nuclear antigen (EBNA)-4 mutation in EBV-associated malignancies in three different populations.
The American journal of pathology | 1999-09-01 | PMID 10487851
Chu P G, Chang K L, Chen W G and 6 more
Overexpression of bax associated with mutations in the loop-sheet-helix motif of p53.
The American journal of pathology | 1999-09-01 | PMID 10487853
Huang C, Kohno N, Inufusa H and 3 more
Genetic analysis of prostatic atypical adenomatous hyperplasia (adenosis).
The American journal of pathology | 1999-09-01 | PMID 10487854
Doll J A, Zhu X, Furman J and 4 more
Regression trees for analysis of mutational spectra in nucleotide sequences.
Bioinformatics (Oxford, England) | 2000-01-01 | PMID 10487863
Berikov V B, Rogozin I B