Microsatellite instability in aberrant crypt foci from human colons.
Cancer research | 1996-12-01 | PMID 8968080
Heinen C D, Shivapurkar N, Tang Z and 2 more
Genes: APC
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.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 794 of 10600
IGF2 but not H19 shows loss of imprinting in human glioma.
Cancer research | 1996-12-01 | PMID 8968084
Uyeno S, Aoki Y, Nata M and 4 more
Genes: IGF2
Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas.
Cancer research | 1996-12-01 | PMID 8968085
Goggins M, Schutte M, Lu J and 8 more
Genes: BRCA2
Mismatch repair mutations override alkyltransferase in conferring resistance to temozolomide but not to 1,3-bis(2-chloroethyl)nitrosourea.
Cancer research | 1996-12-01 | PMID 8968088
Liu L, Markowitz S, Gerson S L
Genes: AGT
Identification of seven new BRCA1 germline mutations in Italian breast and breast/ovarian cancer families.
Cancer research | 1996-12-01 | PMID 8968102
Montagna M, Santacatterina M, Corneo B and 5 more
Genes: BRCA1
Microsatellite instability is associated with the histological features of the tumor in nonfamilial colorectal cancer.
Cancer research | 1996-12-01 | PMID 8968103
Risio M, Reato G, di Celle P F and 3 more
High levels of allele loss at the FHIT and ATM genes in non-comedo ductal carcinoma in situ and grade I tubular invasive breast cancers.
Cancer research | 1996-12-01 | PMID 8968105
Man S, Ellis I O, Sibbering M and 2 more
Genes: ATM, FHIT
Reversal of the in vivo metastatic phenotype of human tumor cells by an anti-CAPL (mts1) ribozyme.
Cancer research | 1996-12-01 | PMID 8968106
Maelandsmo G M, Hovig E, Skrede M and 7 more
Expanded CAG/CTG repeats in schizophrenia. A study of clinical correlates.
The British journal of psychiatry : the journal of mental science | 1996-12-01 | PMID 8968636
Cardno A G, Murphy K C, Jones L A and 9 more
Morbid risk of schizophrenia in first-degree relatives of white and African-Caribbean patients with psychosis.
The British journal of psychiatry : the journal of mental science | 1996-12-01 | PMID 8968638
Hutchinson G, Takei N, Fahy T A and 7 more
Combining extremely concordant sibpairs with extremely discordant sibpairs provides a cost effective way to linkage analysis of quantitative trait loci.
Genetic epidemiology | 1996-01-01 | PMID 8968712
Gu C, Todorov A, Rao D C
BRCA1 R841W: a strong candidate for a common mutation with moderate phenotype.
Genetic epidemiology | 1996-01-01 | PMID 8968716
Barker D F, Almeida E R, Casey G and 6 more
Genes: BRCA1
Commingling analysis of the distribution of a phenotype conditioned on two marker genotypes: application to plasma angiotensin-converting enzyme levels.
Genetic epidemiology | 1996-01-01 | PMID 8968718
Barrett J H, Foy C A, Grant P J
Genes: ACE
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.
Human molecular genetics | 1996-12-01 | PMID 8968737
Leclerc D, Campeau E, Goyette P and 7 more
Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome.
Human molecular genetics | 1996-12-01 | PMID 8968740
Dutly F, Schinzel A
ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.
Human molecular genetics | 1996-12-01 | PMID 8968741
Picketts D J, Higgs D R, Bachoo S and 3 more
Genes: ATRX, ATR
Homozygous and compound heterozygous mutations at the Werner syndrome locus.
Human molecular genetics | 1996-12-01 | PMID 8968742
Oshima J, Yu C E, Piussan C and 16 more
Genes: WRN
Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3' APC gene mutation.
Human molecular genetics | 1996-12-01 | PMID 8968744
Scott R J, Froggatt N J, Trembath R C and 3 more
Genes: APC, FAP
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiency.
Human molecular genetics | 1996-12-01 | PMID 8968745
Hong Y S, Kerr D S, Craigen W J and 4 more
An extended region of biallelic gene expression and rodent-human synteny downstream of the imprinted H19 gene on chromosome 11p15.5.
Human molecular genetics | 1996-12-01 | PMID 8968746
Yuan L, Qian N, Tycko B
Genes: TNNT3, IGF2
Delivery of a hammerhead ribozyme specifically down-regulates the production of fibrillin-1 by cultured dermal fibroblasts.
Human molecular genetics | 1996-12-01 | PMID 8968747
Kilpatrick M W, Phylactou L A, Godfrey M and 3 more
Genes: FBN1
Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E).
Human molecular genetics | 1996-12-01 | PMID 8968749
Bönnemann C G, Passos-Bueno M R, McNally E M and 8 more
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
Human molecular genetics | 1996-12-01 | PMID 8968750
Vainzof M, Passos-Bueno M R, Canovas M and 9 more
Molecular and biochemical analysis of protective protein/cathepsin A mutations: correlation with clinical severity in galactosialidosis.
Human molecular genetics | 1996-12-01 | PMID 8968752
Zhou X Y, van der Spoel A, Rottier R and 8 more
De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.
Human molecular genetics | 1996-12-01 | PMID 8968758
Ivanchuk S M, Myers S M, Eng C and 1 more
Genes: GDNF, RET
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway.
Human molecular genetics | 1996-12-01 | PMID 8968759
Brown K W, Villar A J, Bickmore W and 4 more
Genes: IGF2
Ataxia-telangiectasia: founder effect among north African Jews.
Human molecular genetics | 1996-12-01 | PMID 8968760
Gilad S, Bar-Shira A, Harnik R and 11 more
Genes: ATM
Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees.
Human molecular genetics | 1996-12-01 | PMID 8968761
Day D J, Speiser P W, Schulze E and 4 more
Polymorphisms of uncoupling protein (UCP) and beta 3 adrenoreceptor genes in obese people submitted to a low calorie diet.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity | 1996-12-01 | PMID 8968848
Fumeron F, Durack-Bown I, Betoulle D and 6 more
Polymorphism of the beta 3-adrenergic receptor gene in morbid obesity.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity | 1996-12-01 | PMID 8968849
Oksanen L, Mustajoki P, Kaprio J and 4 more
Additive effect of A-->G (-3826) variant of the uncoupling protein gene and the Trp64Arg mutation of the beta 3-adrenergic receptor gene on weight gain in morbid obesity.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity | 1996-12-01 | PMID 8968850
Clément K, Ruiz J, Cassard-Doulcier A M and 5 more
New hepatitis C virus (HCV) genotyping system that allows for identification of HCV genotypes 1a, 1b, 2a, 2b, 3a, 3b, 4, 5a, and 6a.
Journal of clinical microbiology | 1997-01-01 | PMID 8968908
Ohno O, Mizokami M, Wu R R and 6 more
Typing of porcine reproductive and respiratory syndrome viruses by a multiplex PCR assay.
Journal of clinical microbiology | 1997-01-01 | PMID 8968921
Gilbert S A, Larochelle R, Magar R and 2 more
Tet repressor-tetracycline interaction.
Journal of protein chemistry | 1996-10-01 | PMID 8968952
Kaszycki P, Guz A, Drwiega M and 1 more
Subacute sclerosing panencephalitis.
Seminars in pediatric neurology | 1996-12-01 | PMID 8969008
Gascon G G
Peroxisomal disorders.
Seminars in pediatric neurology | 1996-12-01 | PMID 8969011
Moser H W
B-haplotype control of CD4/CD8 subsets and TCR V beta usage in chicken T lymphocytes.
Veterinary immunology and immunopathology | 1996-10-01 | PMID 8969049
Ewald S J, Lien Y Y, Li L and 1 more
Localization of a conformational energy-coupling determinant near the C terminus of the beta subunit of the F1F0-ATPase.
The Journal of biological chemistry | 1996-12-27 | PMID 8969200
Schemidt R A, Brauning C K, Bouvier A and 1 more
Characterization of a high mobility group 1/2 homolog in yeast.
The Journal of biological chemistry | 1996-12-27 | PMID 8969238
Lu J, Kobayashi R, Brill S J
Creutzfeldt-Jakob disease in the United States, 1979-1994: using national mortality data to assess the possible occurrence of variant cases.
Emerging infectious diseases | 2000-01-01 | PMID 8969250
Holman R C, Khan A S, Belay E D and 1 more
Functional effects of mutating the closing GxA base-pair of a conserved hairpin loop in 23 S ribosomal RNA.
Journal of molecular biology | 1996-12-06 | PMID 8969293
Xu W, Murgola E J
A novel promoter motif for Caulobacter cell cycle-controlled DNA replication genes.
Journal of molecular biology | 1996-12-06 | PMID 8969294
Winzeler E, Shapiro L
Structure-function correlations of the insulin-linked polymorphic region.
Journal of molecular biology | 1996-12-06 | PMID 8969303
Catasti P, Chen X, Moyzis R K and 2 more
Quantitative conversion of glucose into glucose 6-phosphate by intact Escherichia coli cells.
Biotechnology and applied biochemistry | 1996-12-01 | PMID 8969452
van der Zee J R, Postma P W, Hellingwerf K J
The Bacillus subtilis genes for ribonucleotide reductase are similar to the genes for the second class I NrdE/NrdF enzymes of Enterobacteriaceae.
Microbiology (Reading, England) | 1996-11-01 | PMID 8969495
Scotti C, Valbuzzi A, Perego M and 2 more
The 52 degrees-55 degrees segment of the Bacillus subtilis chromosome: a region devoted to purine uptake and metabolism, and containing the genes cotA, gabP and guaA and the pur gene cluster within a 34960 bp nucleotide sequence.
Microbiology (Reading, England) | 1996-11-01 | PMID 8969499
Borriss R, Porwollik S, Schroeter R
The 25 degrees-36 degrees region of the Bacillus subtilis chromosome: determination of the sequence of a 146 kb segment and identification of 113 genes.
Microbiology (Reading, England) | 1996-11-01 | PMID 8969502
Yamane K, Kumano M, Kurita K
Phosphate-starvation-inducible proteins in Bacillus subtilis: a two-dimensional gel electrophoresis study.
Microbiology (Reading, England) | 1996-11-01 | PMID 8969513
Eymann C, Mach H, Harwood C R and 1 more
The acid tolerance response of Salmonella typhimurium provides protection against organic acids.
Microbiology (Reading, England) | 1996-11-01 | PMID 8969516
Baik H S, Bearson S, Dunbar S and 1 more
Genes: ATR
hymA (hypha-like metulae), a new developmental mutant of Aspergillus nidulans.
Microbiology (Reading, England) | 1996-11-01 | PMID 8969518
Karos M, Fischer R
The purB gene of Escherichia coli K-12 is located in an operon.
Microbiology (Reading, England) | 1996-11-01 | PMID 8969519
Green S M, Malik T, Giles I G and 1 more
Sequence variability of FrpB, a major iron-regulated outer-membrane protein in the pathogenic neisseriae.
Microbiology (Reading, England) | 1996-11-01 | PMID 8969523
van der Ley P, van der Biezen J, Sutmuller R and 2 more
RP4::Mu3A-mediated in vivo cloning and transfer of a chlorobiphenyl catabolic pathway.
Microbiology (Reading, England) | 1996-11-01 | PMID 8969525
Springael D, van Thor J, Goorissen H and 7 more
The cloned gene, Xa21, confers resistance to multiple Xanthomonas oryzae pv. oryzae isolates in transgenic plants.
Molecular plant-microbe interactions : MPMI | 1996-12-01 | PMID 8969533
Wang G L, Song W Y, Ruan D L and 2 more
Cerebrovascular disease, the apolipoprotein e4 allele, and cognitive decline in a community-based study of elderly men.
Stroke | 1996-12-01 | PMID 8969786
Kalmijn S, Feskens E J, Launer L J and 1 more
Genes: APOE
PCR/RFLP assay for copy number of mutant and wild-type alleles.
BioTechniques | 1996-12-01 | PMID 8969833
Finch J S, Bowden G T
Phenotypic changes and proliferation of adrenocortical cells during adrenal regeneration in rats.
Endocrine research | 1996-11-01 | PMID 8969888
Engeland W C, Gomez-Sanchez C E, Fitzgerald D A and 2 more
Phenotype of proliferating cells stimulated during compensatory adrenal growth.
Endocrine research | 1996-11-01 | PMID 8969889
Holzwarth M A, Gomez-Sanchez C E, Engeland W C
Nonclassical adrenal hyperplasia due to 21-hydroxylase-deficiency: does genotyping predict the clinical manifestation?
Endocrine research | 1996-11-01 | PMID 8969935
l'Allemand D, Keller E, Hoeppner W and 3 more
Capillary affinity gel electrophoresis. New tool for detection of the mutation on DNA.
Molecular biotechnology | 1996-10-01 | PMID 8970168
Baba Y
Clinical features of individuals with PI*SZ phenotype of alpha 1-antitrypsin deficiency. alpha 1-Antitrypsin Deficiency Registry Study Group.
American journal of respiratory and critical care medicine | 1996-12-01 | PMID 8970361
Turino G M, Barker A F, Brantly M L and 6 more
Apolipoprotein E phenotype frequency and cerebrospinal fluid concentration are not associated with Creutzfeldt-Jakob disease.
Archives of neurology | 1996-12-01 | PMID 8970451
Zerr I, Helmhold M, Poser S and 2 more
Basal ganglia volume and proximity to onset in presymptomatic Huntington disease.
Archives of neurology | 1996-12-01 | PMID 8970459
Aylward E H, Codori A M, Barta P E and 3 more
Two secondary structures for the RRE of HIV-1?
Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association | 1996-12-15 | PMID 8970465
Zhang M J, Dayton A I
Simultaneous detection of genetic and immunological markers in non-small cell lung cancer: prediction of metastatic potential of tumor.
Clinical & experimental metastasis | 1996-11-01 | PMID 8970579
Zborovskaya I, Gasparian A, Kitaeva M and 8 more
Adhesion properties, intermediate filaments and malignant behaviour of head and neck squamous cell carcinoma cells in vitro.
Clinical & experimental metastasis | 1996-11-01 | PMID 8970580
Tomson A M, Scholma J, Meijer B and 3 more
A review of inherited predisposition to melanoma.
Seminars in oncology | 1996-12-01 | PMID 8970585
Cannon-Albright L A, Kamb A, Skolnick M
Dysplastic nevi and other risk markers for melanoma.
Seminars in oncology | 1996-12-01 | PMID 8970587
Seykora J, Elder D
Rational approaches to resistance: using saquinavir.
AIDS (London, England) | 1996-11-01 | PMID 8970671
Boucher C
Changing therapy in HIV.
AIDS (London, England) | 1996-11-01 | PMID 8970673
Lange J M
HIV-2 infection in 12 European residents: virus characteristics and disease progression.
AIDS (London, England) | 1996-12-01 | PMID 8970685
van der Ende M E, Schutten M, Ly T D and 2 more
HIV-1 genetic diversity.
AIDS (London, England) | 1996-12-01 | PMID 8970707
McCutchan F E, Salminen M O, Carr J K and 1 more
HIV viral dynamics.
AIDS (London, England) | 1996-12-01 | PMID 8970715
Coffin J M
Summary of track A: basic science.
AIDS (London, England) | 1996-12-01 | PMID 8970716
Birx D L, VanCott T, Michael N and 6 more
The mammalian myosin heavy chain gene family.
Annual review of cell and developmental biology | 1996-01-01 | PMID 8970733
Weiss A, Leinwand L A
Detection of cone alpha transducin mRNA in human fetal cochlea: negative mutation analysis in Usher syndrome.
Hearing research | 1996-09-15 | PMID 8970808
Magovcevic I, Berson E L, Morton C C
Genes: GNAT2
Are vitamin D receptor polymorphisms associated with bone mineral density? A meta-analysis.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 1996-12-01 | PMID 8970884
Cooper G S, Umbach D M
Genes: VDR
Localization of the gene responsible for the op (osteopetrotic) defect in rats on chromosome 10.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 1996-12-01 | PMID 8970886
Remmers E F, Du Y, Ding Y P and 6 more
Genetic correlates of in vivo viral resistance to indinavir, a human immunodeficiency virus type 1 protease inhibitor.
Journal of virology | 1996-12-01 | PMID 8970946
Condra J H, Holder D J, Schleif W A and 20 more
Type, prevalence, and significance of core promoter/enhancer II mutations in hepatitis B viruses from immunosuppressed patients with severe liver disease.
Journal of virology | 1996-12-01 | PMID 8970951
Günther S, Piwon N, Iwanska A and 3 more
Genes: EBP
Resistance of human immunodeficiency virus type 1 to neutralization by natural antisera occurs through single amino acid substitutions that cause changes in antibody binding at multiple sites.
Journal of virology | 1996-12-01 | PMID 8970964
Watkins B A, Buge S, Aldrich K and 4 more
A single amino acid change in the glycoprotein of lymphocytic choriomeningitis virus is associated with the ability to cause growth hormone deficiency syndrome.
Journal of virology | 1996-12-01 | PMID 8970965
Teng M N, Borrow P, Oldstone M B and 1 more
Phenotypical characterization of lymphocytes infiltrating regressing papillomas.
Journal of virology | 1996-12-01 | PMID 8970967
Knowles G, O'Neil B W, Campo M S
Molecular characterization of replication-competent variants of adenovirus vectors and genome modifications to prevent their occurrence.
Journal of virology | 1996-12-01 | PMID 8970968
Hehir K M, Armentano D, Cardoza L M and 11 more
Analysis of the human env-specific cytotoxic T-lymphocyte (CTL) response in natural human immunodeficiency virus type 1 infection: low prevalence of broadly cross-reactive env-specific CTL.
Journal of virology | 1996-12-01 | PMID 8970969
Carmichael A, Jin X, Sissons P
Mutations within DR2 independently reduce the amount of both minus- and plus-strand DNA synthesized during duck hepatitis B virus replication.
Journal of virology | 1996-12-01 | PMID 8970995
Loeb D D, Tian R, Gulya K J
Intrapatient sequence variation of the gag gene of human immunodeficiency virus type 1 plasma virions.
Journal of virology | 1996-12-01 | PMID 8971017
Yoshimura F K, Diem K, Learn G H and 2 more
Variants able to cause growth hormone deficiency syndrome are present within the disease-nil WE strain of lymphocytic choriomeningitis virus.
Journal of virology | 1996-12-01 | PMID 8971029
Buesa-Gomez J, Teng M N, Oldstone C E and 2 more
Inhibition of generation of authentic genomic termini of herpes simplex virus type 1 DNA in temperature-sensitive mutant BHK-21 cells with a mutated CCG1/TAF(II)250 gene.
Journal of virology | 1996-12-01 | PMID 8971033
Umene K, Nishimoto T
Species-specific variants of GB virus A in captive monkeys .
Journal of virology | 1996-12-01 | PMID 8971037
Leary T P, Desai S M, Yamaguchi J and 4 more
Macrovascular disease is associated with increased plasma apolipoprotein A-IV levels in NIDDM.
Diabetes | 1997-01-01 | PMID 8971092
Vergès B L, Lagrost L, Vaillant G and 4 more
Genes: CETP
HLA-encoded genetic predisposition in IDDM: DR4 subtypes may be associated with different degrees of protection.
Diabetes | 1997-01-01 | PMID 8971095
Undlien D E, Friede T, Rammensee H G and 7 more
Brain MRI, lumbar CSF monoamine concentrations, and clinical descriptors of patients with spinocerebellar ataxia mutations.
Journal of neurology, neurosurgery, and psychiatry | 1996-12-01 | PMID 8971105
Higgins J J, Harvey-White J D, Nee L E and 3 more
Neuropsychological stability over two years in asymptomatic carriers of the Huntington's disease mutation.
Journal of neurology, neurosurgery, and psychiatry | 1996-12-01 | PMID 8971112
Campodonico J R, Codori A M, Brandt J
Human jejunal estrogen sulfotransferase and dehydroepiandrosterone sulfotransferase: immunochemical characterization of individual variation.
Drug metabolism and disposition: the biological fate of chemicals | 1996-12-01 | PMID 8971138
Her C, Szumlanski C, Aksoy I A and 1 more
A transforming growth factor beta type II receptor gene mutation common in sporadic cecum cancer with microsatellite instability.
Cancer research | 1996-12-15 | PMID 8971166
Togo G, Toda N, Kanai F and 6 more
Inhibition of angiogenesis in human glioblastomas by chromosome 10 induction of thrombospondin-1.
Cancer research | 1996-12-15 | PMID 8971176
Hsu S C, Volpert O V, Steck P A and 5 more
Independent regulation of invasion and anchorage-independent growth by different autophosphorylation sites of the macrophage colony-stimulating factor 1 receptor.
Cancer research | 1996-12-15 | PMID 8971179
Sapi E, Flick M B, Rodov S and 4 more
Transfection with human thioredoxin increases cell proliferation and a dominant-negative mutant thioredoxin reverses the transformed phenotype of human breast cancer cells.
Cancer research | 1996-12-15 | PMID 8971189
Gallegos A, Gasdaska J R, Taylor C W and 6 more
Multiple functions of fibroblast growth factors in vertebrate development.
Biochemical Society symposium | 1996-01-01 | PMID 8971338
Abud H E, Skinner J A, Cohn M J and 1 more