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 917 of 10600

Genotype and environment interact to control dormancy and differential expression of the VIVIPAROUS 1 homologue in embryos of Avena fatua.
The Plant journal : for cell and molecular biology | 1997-10-01 | PMID 9375401
Jones H D, Peters N C, Holdsworth M J
Internal AU-rich elements modulate activity of two competing 3' splice sites in plant nuclei.
The Plant journal : for cell and molecular biology | 1997-10-01 | PMID 9375404
Merritt H, McCullough A J, Schuler M A
Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16.
Investigative ophthalmology & visual science | 1997-11-01 | PMID 9375568
Sidjanin D J, Grimes P A, Pretsch W and 3 more
The Caenorhabditis elegans avermectin resistance and anesthetic response gene unc-9 encodes a member of a protein family implicated in electrical coupling of excitable cells.
Journal of neurochemistry | 1997-12-01 | PMID 9375655
Barnes T M, Hekimi S
Alpha-secretase-derived product of beta-amyloid precursor protein is decreased by presenilin 1 mutations linked to familial Alzheimer's disease.
Journal of neurochemistry | 1997-12-01 | PMID 9375682
Ancolio K, Marambaud P, Dauch P and 1 more
Genes: APP
Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome.
American journal of medical genetics | 1997-11-12 | PMID 9375719
Tolarova M M, Harris J A, Ordway D E and 1 more
Fragile X syndrome and deletions in FMR1: new case and review of the literature.
American journal of medical genetics | 1997-11-12 | PMID 9375726
Hammond L S, Macias M M, Tarleton J C and 1 more
Genes: FMR1
A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomes.
American journal of medical genetics | 1997-11-12 | PMID 9375728
Crolla J A, Howard P, Mitchell C and 2 more
Velocardiofacial manifestations and microdeletions in schizophrenic inpatients.
American journal of medical genetics | 1997-11-12 | PMID 9375731
Gothelf D, Frisch A, Munitz H and 6 more
Amyloidosis: a review of recent diagnostic and therapeutic developments.
British journal of haematology | 1997-11-01 | PMID 9375734
Gillmore J D, Hawkins P N, Pepys M B
Phenotypic homozygous activated protein C resistance associated with compound heterozygosity for Arg506Gln (factor V Leiden) and His1299Arg substitutions in factor V.
British journal of haematology | 1997-11-01 | PMID 9375735
Castaman G, Lunghi B, Missiaglia E and 2 more
Genes: APC
A hitherto unknown splice site defect in the protein S gene (PROS1): the mutation results in allelic exclusion and causes type I and type III protein S deficiency.
British journal of haematology | 1997-11-01 | PMID 9375743
Mustafa S, Pabinger I, Vàradi K and 5 more
Genes: PROS1
Ala601-Thr type dysplasminogenaemia genetically diagnosed in patients with retinochoroidal vascular disorders.
British journal of haematology | 1997-11-01 | PMID 9375744
Murata M, Ooe A, Izumi T and 5 more
Deletion of a consensus oestrogen response element half-site in the glucocorticoid receptor of human multiple myeloma.
British journal of haematology | 1997-11-01 | PMID 9375757
Karkera J D, Taymans S E, Turner G and 3 more
Poor prognosis in non-villous splenic marginal zone cell lymphoma is associated with p53 mutations.
British journal of haematology | 1997-11-01 | PMID 9375758
Baldini L, Guffanti A, Cro L and 5 more
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome.
British journal of haematology | 1997-11-01 | PMID 9375768
Galanello R, Perseu L, Melis M A and 6 more
A rapid non-invasive method for the detection of the haemochromatosis C282Y mutation.
British journal of haematology | 1997-11-01 | PMID 9375773
Merryweather-Clarke A T, Liu Y T, Shearman J D and 2 more
MspI restriction fragment length polymorphism at the glycoprotein hormone alpha-subunit locus. Association of certain genotypes with neoplasia.
Biochimica et biophysica acta | 1997-10-09 | PMID 9375796
Cox G S, Cosgrove D E, Haas M J and 2 more
Two new mutations in the human E1 beta subunit of branched chain alpha-ketoacid dehydrogenase associated with maple syrup urine disease.
Biochimica et biophysica acta | 1997-10-24 | PMID 9375800
McConnell B B, Burkholder B, Danner D J
Molecular evidence for nosocomial spread of two different hepatitis C virus strains in one hemodialysis unit.
Nephron | 1997-01-01 | PMID 9375819
Seme K, Poljak M, Zuzec-Resek S and 3 more
Detailed analysis of phenotypes of macrophages infiltrating glomeruli in rat anti-Thy1 nephritis.
Nephron | 1997-01-01 | PMID 9375829
Kobayashi H, Orikasa M, Naito M and 7 more
Imprinting mutations on human chromosome 15.
Human mutation | 1997-01-01 | PMID 9375847
Horsthemke B, Dittrich B, Buiting K
Molecular basis of dystrophic epidermolysis bullosa: mutations in the type VII collagen gene (COL7A1).
Human mutation | 1997-01-01 | PMID 9375848
Järvikallio A, Pulkkinen L, Uitto J
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic value.
Human mutation | 1997-01-01 | PMID 9375849
Boot R G, Hollak C E, Verhoek M and 8 more
Hunter disease in a girl caused by R468Q mutation in the iduronate-2-sulfatase gene and skewed inactivation of the X chromosome carrying the normal allele.
Human mutation | 1997-01-01 | PMID 9375851
Sukegawa K, Song X Q, Masuno M and 9 more
Fourteen novel mucopolysaccharidosis IVA producing mutations in GALNS gene.
Human mutation | 1997-01-01 | PMID 9375852
Tomatsu S, Fukuda S, Cooper A and 15 more
Genes: GALNS
APC mutations in familial adenomatous polyposis families in the Northwest of England.
Human mutation | 1997-01-01 | PMID 9375853
Armstrong J G, Davies D R, Guy S P and 2 more
Genes: APC, FAP
Missense mutation R1066C in the second transmembrane domain of CFTR causes a severe cystic fibrosis phenotype: study of 19 heterozygous and 2 homozygous patients.
Human mutation | 1997-01-01 | PMID 9375855
Casals T, Pacheco P, Barreto C and 17 more
Genes: CFTR
SSCP analysis of long DNA fragments in low pH gel.
Human mutation | 1997-01-01 | PMID 9375857
Kukita Y, Tahira T, Sommer S S and 1 more
Strategy for identification of sequence variants in COL7A1 and a novel 2-bp deletion mutation in recessive dystrophic epidermolysis bullosa.
Human mutation | 1997-01-01 | PMID 9375858
Christiano A M, Hoffman G G, Zhang X and 4 more
Association of factor V Leiden with Behçet's disease.
The Journal of rheumatology | 1997-11-01 | PMID 9375883
Mammo L, Al-Dalaan A, Bahabri S S and 1 more
Two new polymorphisms in the arylsulfatase A gene and their haplotype associations with normal, metachromatic leukodystrophy and pseudodeficiency alleles.
American journal of medical genetics | 1997-11-28 | PMID 9375919
Coulter-Mackie M, Gagnier L
Hand and foot postaxial polydactyly: two different traits.
American journal of medical genetics | 1997-11-28 | PMID 9375922
Castilla E E, da Graca Dutra M, Lugarinho da Fonseca R and 1 more
Do NF1 gene deletions result in a characteristic phenotype?
American journal of medical genetics | 1997-11-28 | PMID 9375928
Tonsgard J H, Yelavarthi K K, Cushner S and 2 more
HLA markers in a community-based rheumatoid arthritis series.
Annals of medicine | 1997-08-01 | PMID 9375985
Hakala M, Silvennoinen-Kassinen S, Ikäheimo I and 2 more
Genes: ACR
A case of fatal hemolytic disease of the newborn associated with-D-/-D-phenotype.
American journal of perinatology | 1997-09-01 | PMID 9376014
Han K S, Kim H C, Han K S and 1 more
Idiotypic analysis of anti-nucleosome monoclonal antibodies derived from lupus mice.
Journal of autoimmunity | 1997-10-01 | PMID 9376069
Brard F, Gilbert D, Jovelin F and 1 more
TP53 mutations in stage I gallbladder carcinoma with special attention to growth patterns.
European journal of cancer (Oxford, England : 1990) | 1997-06-01 | PMID 9376195
Hanada K, Itoh M, Fujii K and 7 more
Beta-adrenergic receptor kinase-1 acutely regulates PTH/PTHrP receptor signalling in human osteoblastlike cells.
Cellular signalling | 1997-09-01 | PMID 9376230
Fukayama S, Kong G, Benovic J L and 2 more
Genes: PTH
Limited specificity and large overlap of the functions of the mouse RAR gamma 1 and RAR gamma 2 isoforms.
Mechanisms of development | 1997-08-01 | PMID 9376317
Subbarayan V, Kastner P, Mark M and 3 more
Organogenesis of the liver, thymus and spleen is affected in jumonji mutant mice.
Mechanisms of development | 1997-08-01 | PMID 9376320
Motoyama J, Kitajima K, Kojima M and 2 more
The expression pattern of nodal and lefty in the mouse mutant Ft suggests a function in the establishment of handedness.
Mechanisms of development | 1997-08-01 | PMID 9376323
Heymer J, Kuehn M, Rüther U
Characterization of DnudC, the Drosophila homolog of an Aspergillus gene that functions in nuclear motility.
Mechanisms of development | 1997-08-01 | PMID 9376324
Cunniff J, Chiu Y H, Morris N R and 1 more
Leucine is the most stabilizing aliphatic amino acid in the d position of a dimeric leucine zipper coiled coil.
Biochemistry | 1997-10-14 | PMID 9376362
Moitra J, Szilák L, Krylov D and 1 more
Probing the proximity of the core domain of an HIV-1 Tat fragment in a Tat-TAR complex by affinity cleaving.
Biochemistry | 1997-10-14 | PMID 9376365
Huq I, Rana T M
Major increase in endopeptidase activity of human cathepsin B upon removal of occluding loop contacts.
Biochemistry | 1997-10-14 | PMID 9376367
Nägler D K, Storer A C, Portaro F C and 3 more
[Prenatal molecular diagnosis of cystic fibrosis. Report of 3 cases].
Investigacion clinica | 1997-09-01 | PMID 9376420
Morales-Machín A, Borjas-Fajardo L, Pineda-Del Villar L and 6 more
Genes: CFTR
Multilineage long-term engraftment potential of drug-resistant hematopoietic progenitors.
Blood | 1997-10-15 | PMID 9376583
Bertolini F, Battaglia M, Lanza A and 5 more
Mice lacking both granulocyte colony-stimulating factor (CSF) and granulocyte-macrophage CSF have impaired reproductive capacity, perturbed neonatal granulopoiesis, lung disease, amyloidosis, and reduced long-term survival.
Blood | 1997-10-15 | PMID 9376584
Seymour J F, Lieschke G J, Grail D and 3 more
An in vitro analysis of the combination of hemophilia A and factor V(LEIDEN).
Blood | 1997-10-15 | PMID 9376587
van 't Veer C, Golden N J, Kalafatis M and 3 more
Fibronectins are essential for heart and blood vessel morphogenesis but are dispensable for initial specification of precursor cells.
Blood | 1997-10-15 | PMID 9376588
George E L, Baldwin H S, Hynes R O
A Leu117-->Trp mutation within the RGD-peptide cross-linking region of beta3 results in Glanzmann thrombasthenia by preventing alphaIIb beta3 export to the platelet surface.
Blood | 1997-10-15 | PMID 9376589
Basani R B, Brown D L, Vilaire G and 2 more
Defective actin reorganization and polymerization of Wiskott-Aldrich T cells in response to CD3-mediated stimulation.
Blood | 1997-10-15 | PMID 9376590
Gallego M D, Santamaría M, Peña J and 1 more
Natural killer (NK) cells are functionally abnormal and NK cell progenitors are diminished in granulocyte colony-stimulating factor-mobilized peripheral blood progenitor cell collections.
Blood | 1997-10-15 | PMID 9376591
Miller J S, Prosper F, McCullar V
Epidemiology of cagA/vacA genes in H. pylori isolated from children and adults in Poland.
Journal of physiology and pharmacology : an official journal of the Polish Physiological Society | 1997-09-01 | PMID 9376616
Gzyl A, Berg D E, Dzierzanowska D
Metabolic rate changes proportionally to circadian frequency in tau mutant Syrian hamsters.
Journal of biological rhythms | 1997-10-01 | PMID 9376640
Oklejewicz M, Hut R A, Daan S and 2 more
Stress, developmental stability and sexual selection.
EXS | 1997-01-01 | PMID 9376690
Møller A P
[Chorionic gonadotropin concentration dependence on the phenotype of the Rhesus system].
Vestnik Rossiiskoi akademii meditsinskikh nauk | 1997-01-01 | PMID 9376723
Chivilev E V, Zolotukhina T V, Spitsyn V A and 1 more
Apal polymorphism in insulin-like growth factor II (IGF2) gene and weight in middle-aged males.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity | 1997-09-01 | PMID 9376897
O'Dell S D, Miller G J, Cooper J A and 5 more
Genes: IGF2, INS
Trp64Arg substitution in the beta 3-adrenergic receptor does not relate to body weight in healthy, premenopausal women.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity | 1997-09-01 | PMID 9376898
Moriarty M, Wing R R, Kuller L H and 1 more
HLA-DRB1*04 subtypes are associated with increased inflammatory activity in early rheumatoid arthritis.
British journal of rheumatology | 1997-09-01 | PMID 9376988
Seidl C, Koch U, Buhleier T and 6 more
Atypical late infantile and juvenile forms of neuronal ceroid lipofuscinosis and their diagnostic difficulties.
Folia neuropathologica | 1997-01-01 | PMID 9377079
Wiśniewski K E, Zhong N, Kida E and 5 more
Genes: CLN3
HIV-infected individuals with the CCR delta32/CCR5 genotype have lower HIV RNA levels and higher CD4 cell counts in the early years of the infection than do patients with the wild type. Copenhagen AIDS Cohort Study Group.
Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association | 1997-09-01 | PMID 9377119
Katzenstein T L, Eugen-Olsen J, Hofmann B and 8 more
Genes: CCR5
HIV-2 genetic variation and DNA load in asymptomatic carriers and AIDS cases in Guinea-Bissau.
Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association | 1997-09-01 | PMID 9377122
Norrgren H, Marquina S, Leitner T and 9 more
Taxon composition and genetic variation of water frogs in the Mid-Rhône floodplain.
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie | 1997-09-01 | PMID 9377180
Pagano A, Joly P, Hotz H
Down syndrome: a review of the literature.
Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics | 1997-09-01 | PMID 9377191
Desai S S
Podocytes in metanephric organ culture express characteristic in vivo phenotypes.
Histochemistry and cell biology | 1997-07-01 | PMID 9377221
Nagata M, Watanabe T
Multiplex DNA typing of short-tandem-repeat loci on the Y chromosome.
Biological chemistry | 1997-08-01 | PMID 9377490
Redd A J, Clifford S L, Stoneking M
Induction of antitumor cytotoxic T lymphocytes with a MAGE-3-encoded synthetic peptide presented by human leukocytes antigen-A24.
Cancer research | 1997-10-15 | PMID 9377553
Tanaka F, Fujie T, Tahara K and 5 more
Inactivation of H19, an imprinted and putative tumor repressor gene, is a preneoplastic event during Wilms' tumorigenesis.
Cancer research | 1997-10-15 | PMID 9377554
Cui H, Hedborg F, He L and 4 more
Genes: IGF2
Mutations in beta-catenin are uncommon in colorectal cancer occurring in occasional replication error-positive tumors.
Cancer research | 1997-10-15 | PMID 9377556
Kitaeva M N, Grogan L, Williams J P and 6 more
Aclacinomycin A stabilizes topoisomerase I covalent complexes.
Cancer research | 1997-10-15 | PMID 9377570
Nitiss J L, Pourquier P, Pommier Y
A DNA double-strand break defective fibroblast cell line (180BR) derived from a radiosensitive patient represents a new mutant phenotype.
Cancer research | 1997-10-15 | PMID 9377575
Badie C, Goodhardt M, Waugh A and 9 more
Genomic imprinting and Igf2 influence liver tumorigenesis and loss of heterozygosity in SV40 T antigen transgenic mice.
Cancer research | 1997-10-15 | PMID 9377577
Haddad R, Held W A
Loss of beta-catenin regulation by the APC tumor suppressor protein correlates with loss of structure due to common somatic mutations of the gene.
Cancer research | 1997-10-15 | PMID 9377578
Rubinfeld B, Albert I, Porfiri E and 2 more
Genes: APC
Thiazolidinediones inhibit alkaline phosphatase activity while increasing expression of uncoupling protein, deiodinase, and increasing mitochondrial mass in C3H10T1/2 cells.
Cell and tissue research | 1997-10-01 | PMID 9377645
Paulik M A, Lenhard J M
Phenotype expression of human bone cells cultured on implant substrates.
Cell biochemistry and function | 1997-09-01 | PMID 9377794
Locci P, Becchetti E, Pugliese M and 5 more
Expand Long PCR for fragile X mutation detection.
Clinical genetics | 1997-09-01 | PMID 9377803
Hećimović S, Barisić I, Müller A and 4 more
Genes: FMR1
Differences in the prevalence of a TaqI RFLP in the 3' flanking region of the alpha 1-proteinase inhibitor gene between asthmatic and non-asthmatic black and white South Africans.
Clinical genetics | 1997-09-01 | PMID 9377805
Green S L, Gaillard M C, Dewar J B and 3 more
Influence of APOH protein polymorphism on apoH levels in normal and diabetic subjects.
Clinical genetics | 1997-09-01 | PMID 9377806
Ruiu G, Gambino R, Veglia F and 2 more
Genes: APOH
Familial inv(X) (p22q22): ovarian dysgenesis in two sisters with del Xq and fertility in one male carrier.
Clinical genetics | 1997-09-01 | PMID 9377809
Madariaga M L, Rivera H
Polymorphism in apolipoprotein(a) kringle IV 37(Met/Thr): frequency in a London population and its association with coronary artery disease.
Clinical cardiology | 1997-10-01 | PMID 9377824
Syrris P, Schwartzman R, Jeffery S and 2 more
Genes: CAD
Lack of association between the insertion/deletion polymorphism of the angiotensin-converting enzyme gene and vasospastic angina.
Clinical cardiology | 1997-10-01 | PMID 9377825
Kuroki S, Ikeda U, Maeda Y and 2 more
Genes: ACE
Undectable expression of hMLH1 protein in sporadic colorectal cancer with replication error phenotype.
Diseases of the colon and rectum | 1997-10-01 | PMID 9378008
Koike J, Yamada K, Takano S and 7 more
Hereditary nonpolyposis colorectal cancer: an update.
Diseases of the colon and rectum | 1997-10-01 | PMID 9378019
Baba S
Conventional molecular diagnosis of steroid 21-hydroxylase deficiency using mismatched primers and polymerase chain reaction.
Endocrine research | 1997-08-01 | PMID 9378109
Tajima T, Mikami A, Fukushi M and 3 more
Spontaneous and induced minisatellite instability.
Electrophoresis | 1997-08-01 | PMID 9378111
Jeffreys A J, Bois P, Buard J and 10 more
Amplification of anonymous DNA fragments using pairs of long primers generates reproducible DNA fingerprints that are sensitive to genetic variation.
Electrophoresis | 1997-08-01 | PMID 9378113
Gillings M, Holley M
Ancient and modern mitochondrial DNA sequences and the colonization of the Pacific.
Electrophoresis | 1997-08-01 | PMID 9378116
Hagelberg E
Mitochondrial D-loop diversity in Australian riverine and Australian desert Aborigines.
Electrophoresis | 1997-08-01 | PMID 9378118
van Holst Pellekaan S, Frommer M, Sved J and 1 more
A study of the genetic diversity of Mycobacterium tuberculosis isolated from patients in the eastern province of South Africa using random amplified polymorphic DNA profiling.
Electrophoresis | 1997-08-01 | PMID 9378124
Richner S M, Meiring J, Kirby R
On simple repetitive DNA sequences and complex diseases.
Electrophoresis | 1997-08-01 | PMID 9378125
Epplen C, Santos E J, Mäueler W and 2 more
Genes: GAA, LTA, TNF
Genetic diversity at six short tandem repeat loci within the state of Victoria, Australia.
Electrophoresis | 1997-08-01 | PMID 9378127
Wilson-Wilde L M, van Oorschot R A, Mitchell R J
Applications of microsatellite-based Y chromosome haplotyping.
Electrophoresis | 1997-08-01 | PMID 9378129
Kayser M, de Knijff P, Dieltjes P and 6 more
High microvariation sequence polymorphism at short tandem repeat loci: human beta-actin related pseudogene as an example.
Electrophoresis | 1997-08-01 | PMID 9378131
Miścicka-Sliwka D, Grzybowski T
Variation at three short tandem repeat (STR) loci in Australians: forensic and ethnic considerations.
Electrophoresis | 1997-08-01 | PMID 9378132
Kaska D E, van Oorschot R A, Mitchell R J
Tetra- and pentanucleotide short tandem repeat instability in gastric cancer.
Electrophoresis | 1997-08-01 | PMID 9378135
Silva F, Gusmão L, Alves C and 3 more
Genes: FES
United Arab Emirates population data on three DNA tetrameric short tandem repeat loci: HUMTHO1, TPOX and CSF1PO--derived using multiplex polymerase chain reaction and manual typing.
Electrophoresis | 1997-08-01 | PMID 9378136
Bayoumi R A, al-Gazali L I, Jaffer U and 5 more
Linkage analysis of bronchial hyperreactivity and atopy with chromosome 11q13.
Electrophoresis | 1997-08-01 | PMID 9378137
Wong Z Y, Tsonis D, van Herwerden L and 5 more
Angiotensinogen gene variation in a population case-control study of preeclampsia/eclampsia in Australians and Chinese.
Electrophoresis | 1997-08-01 | PMID 9378138
Guo G, Wilton A N, Fu Y and 3 more
Genes: AGT