Identification of an enhancer and an alternative promoter in the first intron of the alpha-fetoprotein gene.
Nucleic acids research | 2000-10-01 | PMID 11000266
Scohy S, Gabant P, Szpirer C and 1 more
Genes: AFP
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 1406 of 10600
Mode of action and application of Scorpion primers to mutation detection.
Nucleic acids research | 2000-10-01 | PMID 11000267
Thelwell N, Millington S, Solinas A and 2 more
CArG binding factor A (CBF-A) is involved in transcriptional regulation of the rat Ha-ras promoter.
Nucleic acids research | 2000-10-01 | PMID 11000268
Mikheev A M, Mikheev S A, Zhang Y and 2 more
An alternate form of Ku80 is required for DNA end-binding activity in mammalian mitochondria.
Nucleic acids research | 2000-10-01 | PMID 11000272
Coffey G, Campbell C
Histone H2A.Z has a conserved function that is distinct from that of the major H2A sequence variants.
Nucleic acids research | 2000-10-01 | PMID 11000274
Jackson J D, Gorovsky M A
Gonadal pathology in triploidy.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society | 2000-01-01 | PMID 11000332
McFadden D E, Pantzar J T, Jevon G P
Familial Wilms' tumor with neural elements: characterization by histology, immunohistochemistry, and genetic analysis.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society | 2000-01-01 | PMID 11000334
Hussong J W, Perkins S L, Huff V and 4 more
Study of the malformation of ductal plate of the liver in Meckel syndrome and review of other syndromes presenting with this anomaly.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society | 2000-01-01 | PMID 11000335
Sergi C, Adam S, Kahl P and 1 more
Dopamine characteristics in different rat genotypes: the relation to absence epilepsy.
Neuroscience research | 2000-10-01 | PMID 11000443
de Bruin N M, van Luijtelaar E L, Jansen S J and 2 more
Functional differences between splice variants of the murine 5-HT(3A) receptor: possible role for phosphorylation.
Brain research. Molecular brain research | 2000-09-30 | PMID 11000482
Hubbard P C, Thompson A J, Lummis S C
Usefulness of human papilloma virus testing in the screening of cervical cancer precursor lesions: a retrospective study in 314 cases.
European journal of obstetrics, gynecology, and reproductive biology | 2000-11-01 | PMID 11000508
Infantolino C, Fabris P, Infantolino D and 4 more
A diabetes insipidus vasopressin prohormone altered outside the central core of neurophysin accumulates in the endoplasmic reticulum.
Molecular and cellular endocrinology | 2000-09-25 | PMID 11000520
Nijenhuis M, Zalm R, Burbach J P
Ret oncogene signal transduction via a IRS-2/PI 3-kinase/PKB and a SHC/Grb-2 dependent pathway: possible implication for transforming activity in NIH3T3 cells.
Molecular and cellular endocrinology | 2000-09-25 | PMID 11000521
Hennige A M, Lammers R, Arlt D and 6 more
Splice site mutation in the type VII collagen gene (COL7A1) in a Taiwanese family with recessive dystrophic epidermolysis bullosa.
Journal of the Formosan Medical Association = Taiwan yi zhi | 2000-09-01 | PMID 11000732
Lin G T, Chen S K, Liu C S and 1 more
HLA-DQB1 genotyping with simple automated DNA sequencing and single-strand conformation polymorphism analysis.
Journal of the Formosan Medical Association = Taiwan yi zhi | 2000-09-01 | PMID 11000733
Yang C H, Lee C L, Pai C Y
Identification of a vesicular glutamate transporter that defines a glutamatergic phenotype in neurons.
Nature | 2000-09-14 | PMID 11001057
Takamori S, Rhee J S, Rosenmund C and 1 more
Neither IL-1beta, IL-1 receptor antagonist, nor TNF-alpha polymorphisms are associated with susceptibility to COPD.
Respiratory medicine | 2000-09-01 | PMID 11001075
Ishii T, Matsuse T, Teramoto S and 6 more
Genes: TNF
Do idebenone and vitamin therapy shorten the time to achieve visual recovery in Leber hereditary optic neuropathy?
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society | 2000-09-01 | PMID 11001192
Mashima Y, Kigasawa K, Wakakura M and 1 more
Alpha1-antitrypsin in serum determined by capillary isoelectric focusing.
Electrophoresis | 2000-09-01 | PMID 11001231
Lupi A, Viglio S, Luisetti M and 5 more
DNA damage promotes mistyping in the allele specific oligonucleotide probing analysis of forensic samples.
Electrophoresis | 2000-08-01 | PMID 11001311
Fattorini P, Cossutta F, Giulianini P and 2 more
Capillary electrophoretic analysis of wild type and mutant Proteus penneri outer membrane proteins.
Electrophoresis | 2000-08-01 | PMID 11001319
Kustos I, Tóth V, Kocsis B and 3 more
Genes: OMP
Induction of monoclonal antibody with predefined ELNKWA epitope specificity by epitope vaccine.
Hybridoma | 2000-08-01 | PMID 11001409
Xiao Y, Dong X N, Chen Y H
Routing of the aquaporin-2 water channel in health and disease.
European journal of cell biology | 2000-08-01 | PMID 11001488
Deen P M, van Balkom B W, Kamsteeg E J
Genes: AQP2
Defining CD95 as a tumor suppressor gene.
Journal of molecular medicine (Berlin, Germany) | 2000-01-01 | PMID 11001528
Müschen M, Warskulat U, Beckmann M W
The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor gamma2 gene is not associated with postprandial responses to glucose or fat tolerance tests in young healthy subjects: the European Atherosclerosis Research Study II.
Journal of molecular medicine (Berlin, Germany) | 2000-01-01 | PMID 11001532
Poirier O, Nicaud V, Cambien F and 1 more
A genetic model: analysis and application to MAXSAT.
Evolutionary computation | 2000-01-01 | PMID 11001553
Bertoni A, Campadelli P, Carpentieri M and 1 more
Adaptive linkage crossover.
Evolutionary computation | 2000-01-01 | PMID 11001555
Salman A A, Mehrotra K, Mohan C K
Localization of a small genomic region associated with elevated ACE.
American journal of human genetics | 2000-11-01 | PMID 11001581
Zhu X, McKenzie C A, Forrester T and 7 more
Genes: ACE
Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.
American journal of human genetics | 2000-11-01 | PMID 11001582
Stöber G, Saar K, Rüschendorf F and 8 more
Isolation of a cDNA representing the Fanconi anemia complementation group E gene.
American journal of human genetics | 2000-11-01 | PMID 11001585
de Winter J P, Léveillé F, van Berkel C G and 17 more
Genes: FANCE, FANCA, FANCC, FANCF, FANCG
Metabolic flux balance analysis and the in silico analysis of Escherichia coli K-12 gene deletions.
BMC bioinformatics | 2000-01-01 | PMID 11001586
Edwards J S, Palsson B O
Anovel catalase mutation (a GA insertion) causes the Hungarian type of acatalasemia.
Blood cells, molecules & diseases | 2000-04-01 | PMID 11001624
Góth L, Shemirani A, Kalmár T
Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity.
Blood cells, molecules & diseases | 2000-04-01 | PMID 11001626
Papanikolaou G, Politou M, Terpos E and 3 more
Genes: HFE
Characterization of an unusual tRNA-like sequence found inserted in a Neurospora retroplasmid.
Nucleic acids research | 2000-07-01 | PMID 11001704
Mohr S, Wanner L A, Bertrand H and 1 more
Genes: GC
Deconstructing myotonic dystrophy.
Science (New York, N.Y.) | 2000-09-08 | PMID 11001736
Tapscott S J
Genes: DMPK
Immunology. RNA editing AIDs antibody diversification?
Science (New York, N.Y.) | 2000-09-08 | PMID 11001738
Neuberger M S, Scott J
Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathways.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001791
Vockley J, Rinaldo P, Bennett M J and 2 more
Molecular heterosis: a review.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001792
Comings D E, MacMurray J P
Genes: DRD1, DRD2, DRD3, DRD4, ESR1, HBB, PNMT
Molecular basis of disorders of human galactose metabolism: past, present, and future.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001796
Novelli G, Reichardt J K
Genes: GALE, GALT
Genetic determinants of Graves disease.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001797
Chistyakov D A, Savost'anov K V, Turakulov R I and 1 more
Genes: CTLA4, TSHR
Nonexpressing homozygotes for C282Y hemochromatosis: minority or majority of cases?
Molecular genetics and metabolism | 2000-01-01 | PMID 11001800
Adams P C
Genes: HFE
Corneal crystals in nephropathic cystinosis: natural history and treatment with cysteamine eyedrops.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001803
Gahl W A, Kuehl E M, Iwata F and 2 more
Genes: CTNS
Smith-Lemli-Opitz syndrome: the first malformation syndrome associated with defective cholesterol synthesis.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001806
Battaile K P, Steiner R D
Genes: DHCR7
RSH/Smith-Lemli-Opitz syndrome: a multiple congenital anomaly/mental retardation syndrome due to an inborn error of cholesterol biosynthesis.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001807
Porter F D
Genes: DHCR7
Liver disease in pregnancy and fetal fatty acid oxidation defects.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001809
Ibdah J A, Yang Z, Bennett M J
Developmental changes in the expression of neuronal ceroid lipofuscinoses-linked proteins.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001810
Suopanki J, Partanen S, Ezaki J and 3 more
Genes: NCL, PPT1
Neuronal ceroid lipofuscinoses and possible pathogenic mechanism.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001811
Zhong N
Genes: NCL
Mutations in the lysyl hydroxylase 1 gene that result in enzyme deficiency and the clinical phenotype of Ehlers-Danlos syndrome type VI.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001813
Yeowell H N, Walker L C
Osteogenesis imperfecta: prospects for molecular therapeutics.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001814
Forlino A, Marini J C
Kidney development: regulatory molecules crucial to both mice and men.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001832
Bates C M
Genes: GDNF, PAX2, RET
Deletions of 9p and the quest for a conserved mechanism of sex determination.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001833
Ottolenghi C, McElreavey K
Genes: DMRT1, SRY
Bilirubin oxidation in brain.
Molecular genetics and metabolism | 2000-01-01 | PMID 11001835
Hansen T W
Effects of extracellular matrix on phenotype modulation and MAPK transduction of rat aortic smooth muscle cells in vitro.
Experimental and molecular pathology | 2000-10-01 | PMID 11001858
Qin H, Ishiwata T, Wang R and 4 more
Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia.
Blood | 2000-10-01 | PMID 11001877
Dale D C, Person R E, Bolyard A A and 9 more
Factor V Leiden mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome and portal vein thrombosis: results of a case-control study.
Blood | 2000-10-01 | PMID 11001884
Janssen H L, Meinardi J R, Vleggaar F P and 9 more
Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia.
Blood | 2000-10-01 | PMID 11001900
Balogh I, Szôke G, Kárpáti L and 7 more
Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation.
Blood | 2000-10-01 | PMID 11001902
Asselta R, Duga S, Simonic T and 5 more
A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing.
Blood | 2000-10-01 | PMID 11001903
Margaglione M, Santacroce R, Colaizzo D and 8 more
Concept of lymphoid versus myeloid dendritic cell lineages revisited: both CD8alpha(-) and CD8alpha(+) dendritic cells are generated from CD4(low) lymphoid-committed precursors.
Blood | 2000-10-01 | PMID 11001905
Martín P, del Hoyo G M, Anjuère F and 4 more
Identification of critical antigen-specific mechanisms in the development of immune thrombocytopenic purpura in mice.
Blood | 2000-10-01 | PMID 11001906
Nieswandt B, Bergmeier W, Rackebrandt K and 2 more
Isotype switch variants reveal clonally related subpopulations in diffuse large B-cell lymphoma.
Blood | 2000-10-01 | PMID 11001910
Ottensmeier C H, Stevenson F K
An IL6 promoter polymorphism is associated with a lifetime risk of development of Kaposi sarcoma in men infected with human immunodeficiency virus.
Blood | 2000-10-01 | PMID 11001912
Foster C B, Lehrnbecher T, Samuels S and 9 more
Genes: TNF
Identification of the dombrock blood group glycoprotein as a polymorphic member of the ADP-ribosyltransferase gene family.
Blood | 2000-10-01 | PMID 11001920
Gubin A N, Njoroge J M, Wojda U and 4 more
Two imprinted gene mutations: three phenotypes.
Human molecular genetics | 2000-09-22 | PMID 11001929
Cattanach B M, Peters J, Ball S and 1 more
Genes: GNAS
The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease.
Human molecular genetics | 2000-09-22 | PMID 11001930
Lambert J C, Goumidi L, Vrièze F W and 13 more
Genes: LBP
Alzheimer's disease-associated presenilin 2 interacts with DRAL, an LIM-domain protein.
Human molecular genetics | 2000-09-22 | PMID 11001931
Tanahashi H, Tabira T
Structural and functional analysis of mutations in alkaptonuria.
Human molecular genetics | 2000-09-22 | PMID 11001939
Rodríguez J M, Timm D E, Titus G P and 5 more
Identification of cyclic ADP-ribose-dependent mechanisms in pancreatic muscarinic Ca(2+) signaling using CD38 knockout mice.
The Journal of biological chemistry | 2001-01-05 | PMID 11001947
Fukushi Y, Kato I, Takasawa S and 8 more
Scavenger receptor class B, type I-mediated [3H]cholesterol efflux to high and low density lipoproteins is dependent on lipoprotein binding to the receptor.
The Journal of biological chemistry | 2000-09-29 | PMID 11001950
Gu X, Kozarsky K, Krieger M
Cancer risk in families with hereditary prostate carcinoma.
Cancer | 2000-09-15 | PMID 11002228
Grönberg H, Bergh A, Damber J E and 1 more
Growth phenotypes of cytomegalovirus isolates do not correlate with glycoprotein B, major immediate early genotypes or antiviral sensitivity.
Journal of medical virology | 2000-10-01 | PMID 11002239
Mousavi-Jazi M, Sundqvist V A, Linde A and 2 more
Replication-defective mutants of mouse cytomegalovirus protect against wild-type virus challenge.
Journal of medical virology | 2000-10-01 | PMID 11002240
Gill T A, Morley P J, Sweet C
Genetic relatedness of hepatitis A virus isolates during a community-wide outbreak.
Journal of medical virology | 2000-10-01 | PMID 11002242
Robertson B H, Averhoff F, Cromeans T L and 8 more
Detection of mutations in hepatitis B virus enhancer 2/core promoter and X protein regions in patients with fatal hepatitis B virus infection.
Journal of medical virology | 2000-10-01 | PMID 11002245
Honda A, Yokosuka O, Suzuki K and 1 more
Hepatitis B virus X gene variability in French-born patients with chronic hepatitis and hepatocellular carcinoma.
Journal of medical virology | 2000-10-01 | PMID 11002246
Venard V, Corsaro D, Kajzer C and 2 more
Effect of interferon treatment on serum 2',5'-oligoadenylate synthetase levels in hepatitis C-infected patients.
Journal of medical virology | 2000-10-01 | PMID 11002247
Murashima S, Kumashiro R, Ide T and 7 more
Prospective follow-up of patients with GBV-C/HGV infection: specific mutational patterns, clinical outcome, and genetic diversity.
Journal of medical virology | 2000-10-01 | PMID 11002248
Sarrazin C, Rüster B, Lee J H and 3 more
Prevalence and genetic diversity of human caliciviruses (HuCVs) in Mexican children.
Journal of medical virology | 2000-10-01 | PMID 11002251
Farkas T, Jiang X, Guerrero M L and 6 more
Reactivation of acyclovir-resistant thymidine kinase-deficient herpes simplex virus harbouring single base insertion within a 7 Gs homopolymer repeat of the thymidine kinase gene.
Journal of medical virology | 2000-10-01 | PMID 11002255
Morfin F, Thouvenot D, Aymard M and 1 more
Single genotype of measles virus is dominant whereas several genotypes of mumps virus are co-circulating.
Journal of medical virology | 2000-10-01 | PMID 11002259
Takahashi M, Nakayama T, Kashiwagi Y and 6 more
Mouse mutant "rib-vertebrae" (rv): a defect in somite polarity.
Developmental dynamics : an official publication of the American Association of Anatomists | 2000-10-01 | PMID 11002339
Nacke S, Schäfer R, Habré de Angelis M and 1 more
Mechanism for uptake of silica particles by monocytic U937 cells.
Human & experimental toxicology | 2000-07-01 | PMID 11002391
Hetland G, Namork E, Schwarze P E and 1 more
Hormesis: a stress response in cells exposed to low levels of heavy metals.
Human & experimental toxicology | 2000-07-01 | PMID 11002392
Damelin L H, Vokes S, Whitcutt J M and 2 more
Papillon-Lefèvre syndrome: analysis of HLA antigens.
Oral diseases | 2000-09-01 | PMID 11002409
Nitta H, Kato H, Umeda M and 2 more
Activation of the NF-kappaB pathway by caspase 8 and its homologs.
Oncogene | 2000-09-14 | PMID 11002417
Chaudhary P M, Eby M T, Jasmin A and 3 more
Genes: FADD
Role of heteroduplex joints in the functional interactions between human Rad51 and wild-type p53.
Oncogene | 2000-09-14 | PMID 11002423
Süsse S, Janz C, Janus F and 2 more
Interference with the constitutive activation of ERK1 and ERK2 impairs EWS/FLI-1-dependent transformation.
Oncogene | 2000-09-14 | PMID 11002425
Silvany R E, Eliazer S, Wolff N C and 1 more
Deletion and tandem duplication of exons 2 - 7 in the epidermal growth factor receptor gene of a human malignant glioma.
Oncogene | 2000-09-14 | PMID 11002427
Fenstermaker R A, Ciesielski M J
Genes: EGFR
[N-acetyltransferase genetic polymorphism and its role in the development of neoplastic disease].
Medycyna pracy | 2000-01-01 | PMID 11002474
Lutz W
Genes: NAT2, NAT1
The p53 codon 72 polymorphism in black South African women and the risk of cervical cancer.
BJOG : an international journal of obstetrics and gynaecology | 2000-09-01 | PMID 11002963
Pegoraro R, Moodley J, Naiker S and 2 more
Genetic variation in the beta-3-adrenergic receptor in essential hypertension.
Life sciences | 2000-06-16 | PMID 11003049
Pamies-Andreu E, García-Lozano R, Palmero-Palmero C and 5 more
Covalent modification of subtilisin Bacillus lentus cysteine mutants with enantiomerically pure chiral auxiliaries causes remarkable changes in activity.
Bioorganic & medicinal chemistry | 2000-08-01 | PMID 11003141
Dickman M, Jones J B
Allelic variation in the GABA A receptor gamma2 subunit is associated with genetic susceptibility to ethanol-induced motor incoordination and hypothermia, conditioned taste aversion, and withdrawal in BXD/Ty recombinant inbred mice.
Alcoholism, clinical and experimental research | 2000-09-01 | PMID 11003197
Hood H M, Buck K J
Nicotinic receptor pore mutations create a sensitive inhibitory site for ethanol.
Alcoholism, clinical and experimental research | 2000-09-01 | PMID 11003201
Forman S A, Zhou Q
Effects of pasture allowance on the yield and composition of milk from cows of different beta-lactoglobulin phenotypes.
Journal of dairy science | 2000-09-01 | PMID 11003240
Auldist M J, Thomson N A, Mackle T R and 2 more
Single-strand conformational polymorphism and sequence polymorphism of Mhc-DRB in Latxa and Karrantzar sheep: implications for Caprinae phylogeny.
Immunogenetics | 2000-09-01 | PMID 11003382
Jugo B M, Vicario A
MHC diversity in Caucasians, investigated using highly heterogeneous noncoding sequence motifs at the DQB1 locus including a retroviral long terminal repeat element, and its comparison to nonhuman primate homologues.
Immunogenetics | 2000-09-01 | PMID 11003383
Donner H, Tönjes R R, Bontrop R E and 3 more
Prognostic value of mitotic metaphase rate in oesophageal cancer.
The European journal of surgery = Acta chirurgica | 2000-08-01 | PMID 11003429
Yasunaga M, Tabira Y, Imaoka S and 1 more
The entire nucleotide sequences of two distinct TT virus (TTV) isolates (TJN01 and TJN02) remotely related to the original TTV isolates.
Archives of virology | 2000-01-01 | PMID 11003468
Ukita M, Okamoto H, Nishizawa T and 5 more
Molecular analyses of European A, B and P type sources of Beet necrotic yellow vein virus and detection of the rare P type in Kazakhstan.
Archives of virology | 2000-01-01 | PMID 11003469
Koenig R, Lennefors B L