Restriction fragment length polymorphisms at the GLUT4 and GLUT1 gene loci in type 2 diabetes.
Diabetic medicine : a journal of the British Diabetic Association | 2000-01-01 | PMID 1348023
Alcolado J C, Baroni M G
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 124 of 10600
Molecular analysis of a new cytoplasmic male sterile genotype in sunflower.
FEBS letters | 1992-02-03 | PMID 1348035
Spassova M, Christov M, Bohorova N and 5 more
Mode of origin and sources of genotypic diversity in triploid gynogenetic fish clones (Poeciliopsis: Poeciliidae).
Genetics | 1992-03-01 | PMID 1348041
Quattro J M, Avise J C, Vrijenhoek R C
Evolution of the mouse H-2K region: a hot spot of mutation associated with genes transcribed in embryos and/or germ cells.
Genetics | 1992-03-01 | PMID 1348042
Yeom Y I, Abe K, Artzt K
Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians.
Human genetics | 1992-03-01 | PMID 1348044
Bétard C, Kessling A M, Roy M and 3 more
Polymorphisms at the GLUT1 (HepG2) and GLUT4 (muscle/adipocyte) glucose transporter genes and non-insulin-dependent diabetes mellitus (NIDDM).
Human genetics | 1992-03-01 | PMID 1348045
Baroni M G, Oelbaum R S, Pozzilli P and 4 more
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C gene.
Human genetics | 1992-03-01 | PMID 1348046
Grundy C B, Schulman S, Krawczak M and 3 more
Genes: CGA
Lung involvement, the delta F508 mutation and DNA haplotype analysis in cystic fibrosis.
Human genetics | 1992-03-01 | PMID 1348048
Santamaria F, Salvatore D, Castiglione O and 3 more
Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?
Journal of medical genetics | 1992-03-01 | PMID 1348094
Stern H J, Saal H M, Lee J S and 4 more
Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.
Journal of medical genetics | 1992-03-01 | PMID 1348095
Sharland M, Taylor R, Patton M A and 1 more
P pili in uropathogenic E. coli are composite fibres with distinct fibrillar adhesive tips.
Nature | 1992-03-19 | PMID 1348107
Kuehn M J, Heuser J, Normark S and 1 more
Synergistic effect of Adh alleles in Drosophila melanogaster.
Proceedings. Biological sciences | 1992-01-22 | PMID 1348124
Li X M
Familial association of autoimmune thrombocytopenia and hyperthyroidism.
American journal of hematology | 1992-04-01 | PMID 1348160
Bizzaro N
Structure of a ricin mutant showing rescue of activity by a noncatalytic residue.
Biochemistry | 1992-03-31 | PMID 1348187
Kim Y, Mlsna D, Monzingo A F and 3 more
Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9.
Cell | 1992-04-03 | PMID 1348213
Gailani M R, Bale S J, Leffell D J and 7 more
Peptide transport by the multidrug resistance pump.
The Journal of biological chemistry | 1992-03-25 | PMID 1348245
Sharma R C, Inoue S, Roitelman J and 2 more
Does lineage determine the dopamine phenotype in the tadpole hypothalamus?: A quantitative analysis.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1992-04-01 | PMID 1348272
Huang S, Moody S A
Genetic diagnosis of Gaucher's disease.
Lancet (London, England) | 1992-04-11 | PMID 1348297
Mistry P K, Smith S J, Ali M and 3 more
Restriction fragment length polymorphisms associated with alpha-hemolysin determinants are correlating with the expression of alpha-hemolysin in strains of Escherichia coli.
Zentralblatt fur Bakteriologie : international journal of medical microbiology | 1992-01-01 | PMID 1348436
Prada J, Zimmermann S, Stephan R and 1 more
Restriction fragment length polymorphism and virulence pattern of the veterinary pathogen Escherichia coli O139:K82:H1.
Zentralblatt fur Bakteriologie : international journal of medical microbiology | 1992-01-01 | PMID 1348438
Tschäpe H, Bender L, Ott M and 2 more
Determination of S fimbriae among Escherichia coli strains from extraintestinal infections by colony hybridization and dot enzyme immunoassay.
Zentralblatt fur Bakteriologie : international journal of medical microbiology | 1992-01-01 | PMID 1348439
Schönian G, Sokolowska-Köhler W, Bollmann R and 3 more
Origin of mutation in sporadic cases of haemophilia-B.
European journal of haematology | 1992-03-01 | PMID 1348478
Kling S, Ljung R, Sjörin E and 4 more
The combination of dissimilar alleles of the A alpha and A beta gene complexes, whose proteins contain homeo domain motifs, determines sexual development in the mushroom Coprinus cinereus.
Genes & development | 1992-04-01 | PMID 1348484
Kües U, Richardson W V, Tymon A M and 5 more
Linkage mapping of human chromosome 10 microsatellite polymorphisms.
Genomics | 1992-03-01 | PMID 1348490
Decker R A, Moore J, Ponder B and 1 more
Alleles of the rat T-cell receptor beta chain gene complex.
Immunogenetics | 1992-01-01 | PMID 1348495
Blankenhorn E P, Smith P D, Williams C B and 1 more
ts1, a temperature-sensitive mutant of Moloney murine leukemia virus TB, can infect both CD4+ and CD8+ T cells but requires CD4+ T cells in order to cause paralysis and immunodeficiency.
Journal of virology | 1992-05-01 | PMID 1348544
Saha K, Wong P K
Ovine lentivirus is macrophagetropic and does not replicate productively in T lymphocytes.
Journal of virology | 1992-05-01 | PMID 1348546
Gorrell M D, Brandon M R, Sheffer D and 2 more
Homeodomain-independent activity of the fushi tarazu polypeptide in Drosophila embryos.
Nature | 1992-04-16 | PMID 1348571
Fitzpatrick V D, Percival-Smith A, Ingles C J and 1 more
Non-phenotypic selection of N-methyl-N-nitrosourea-induced mutations in human cells.
Nucleic acids research | 1992-03-25 | PMID 1348577
Palombo F, Bignami M, Dogliotti E
Genes: GPT
Histiocytes in familial and infection-induced/idiopathic hemophagocytic syndromes may exhibit phenotypic differences.
Pediatric pathology | 2000-01-01 | PMID 1348582
Buckley P J, O'Laughlin S, Komp D M
Genomic analysis of Theileria sergenti stocks in Japan with DNA probes.
Veterinary parasitology | 1992-02-01 | PMID 1348593
Matsuba T, Kawakami Y, Iwai H and 1 more
Colocalization of vasoactive intestinal polypeptide and GABA immunoreactivities in a population of wide-field amacrine cells in the rabbit retina.
Visual neuroscience | 1992-04-01 | PMID 1348629
Casini G, Brecha N C
Genes: VIP
Molecular determination of cell tropism of human immunodeficiency virus.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America | 1992-03-01 | PMID 1348647
Johnson M A, Cann A J
The alcohol dehydrogenase polymorphism in natural populations of Drosophila melanogaster: ADH activity variation restriction site polymorphism and the Adh cline.
Heredity | 1992-04-01 | PMID 1348740
Jiang J C, Gibson J B
HLA-DP distribution in Shanghai Chinese--a study by polymerase chain reaction--restriction fragment length polymorphism.
Human immunology | 1992-02-01 | PMID 1348742
Wang F Q, al-Daccak R, Ju L Y and 4 more
Polymerase chain reaction--single-strand conformation polymorphism analysis of polymorphism in DPA1 and DPB1 genes: a simple, economical, and rapid method for histocompatibility testing.
Human immunology | 1992-02-01 | PMID 1348744
Hoshino S, Kimura A, Fukuda Y and 2 more
Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies.
Journal of neurology, neurosurgery, and psychiatry | 1992-03-01 | PMID 1348783
Tranchant C, Doh-ura K, Warter J M and 5 more
Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome.
Neurology | 1992-04-01 | PMID 1348851
Kretzschmar H A, Kufer P, Riethmüller G and 3 more
Genes: GSS
Neisseria gonorrhoeae PilC expression provides a selective mechanism for structural diversity of pili.
Proceedings of the National Academy of Sciences of the United States of America | 1992-04-15 | PMID 1348857
Jonsson A B, Pfeifer J, Normark S
Genetic transfer of non-P-glycoprotein-mediated multidrug resistance (MDR) in somatic cell fusion: dissection of a compound MDR phenotype.
Proceedings of the National Academy of Sciences of the United States of America | 1992-04-15 | PMID 1348862
Eijdems E W, Borst P, Jongsma A P and 6 more
Balancing selection at allozyme loci in oysters: implications from nuclear RFLPs.
Science (New York, N.Y.) | 1992-04-03 | PMID 1348870
Karl S A, Avise J C
Functional complementation of yeast ste6 by a mammalian multidrug resistance mdr gene.
Science (New York, N.Y.) | 1992-04-10 | PMID 1348873
Raymond M, Gros P, Whiteway M and 1 more
Mutations in the P53 tumour suppressor gene in primary lung cancer in Japan.
Biochemical and biophysical research communications | 1992-03-31 | PMID 1348931
Kondo K, Umemoto A, Akimoto S and 4 more
Genomic differences between O6-methylguanine-DNA methyltransferase proficient (Mex+) and deficient (Mex-) cell lines: possible role of genetic and epigenetic changes in conversion of Mex+ into Mex-.
Biochemical and biophysical research communications | 1992-03-31 | PMID 1348932
Fritz G, Kaina B
Genes: MGMT
Homeosis in the mouse induced by a null mutation in the Hox-3.1 gene.
Cell | 1992-04-17 | PMID 1348969
Le Mouellic H, Lallemand Y, Brûlet P
Linkage analysis of insulin-receptor gene in familial NIDDM.
Diabetes | 1992-05-01 | PMID 1348997
Elbein S C, Sorensen L K, Taylor M
Genetic divergence between the Wistar-Kyoto rat and the spontaneously hypertensive rat.
Hypertension (Dallas, Tex. : 1979) | 1992-05-01 | PMID 1349001
Johnson M L, Ely D L, Turner M E
Increased oncogenic potential of ErbB is associated with the loss of a COOH-terminal domain serine phosphorylation site.
The Journal of biological chemistry | 1992-04-25 | PMID 1349014
Theroux S J, Taglienti-Sian C, Nair N and 3 more
Genes: EGF
Heterodimerization of c-erbB2 with different epidermal growth factor receptor mutants elicits stimulatory or inhibitory responses.
The Journal of biological chemistry | 1992-04-25 | PMID 1349015
Spivak-Kroizman T, Rotin D, Pinchasi D and 3 more
Genes: EGFR, EGF
Mutant debrisoquine hydroxylation genes in Parkinson's disease.
Lancet (London, England) | 1992-04-25 | PMID 1349052
Armstrong M, Daly A K, Cholerton S and 2 more
Identical genetic locus for Baltic and Mediterranean myoclonus.
Lancet (London, England) | 1992-05-02 | PMID 1349105
Malafosse A, Lehesjoki A E, Genton P and 6 more
De-novo mutation in hereditary motor and sensory neuropathy type I.
Lancet (London, England) | 1992-05-02 | PMID 1349106
Hoogendijk J E, Hensels G W, Gabreëls-Festen A A and 7 more
Identification of separate determinants on the thyrotropin receptor reactive with Graves' thyroid-stimulating antibodies and with thyroid-stimulating blocking antibodies in idiopathic myxedema: these determinants have no homologous sequence on gonadotropin receptors.
Molecular endocrinology (Baltimore, Md.) | 1992-02-01 | PMID 1349156
Kosugi S, Ban T, Akamizu T and 1 more
p53 mutations in spontaneously immortalized 3T12 but not 3T3 mouse embryo cells.
Oncogene | 1992-05-01 | PMID 1349164
Rittling S R, Denhardt D T
Germ-line and somatic p53 gene mutations in multifocal osteogenic sarcoma.
Proceedings of the National Academy of Sciences of the United States of America | 1992-05-01 | PMID 1349175
Iavarone A, Matthay K K, Steinkirchner T M and 1 more
Sperm size and sperm competition in birds.
Proceedings. Biological sciences | 1992-02-22 | PMID 1349186
Briskie J V, Montgomerie R
Genes: SST
Investigation of the mode of inheritance of insulin-dependent diabetes mellitus in Japanese subjects.
American journal of human genetics | 1992-05-01 | PMID 1349195
Jenkins D, Penny M A, Uchigata Y and 7 more
DNA mutations associated with the human butyrylcholinesterase J-variant.
American journal of human genetics | 1992-05-01 | PMID 1349196
Bartels C F, James K, La Du B N
Genes: BCHE, GAA, GCA
Nonsynonymous polymorphic sites in the apolipoprotein (apo) A-IV gene are associated with changes in the concentration of apo B- and apo A-I-containing lipoproteins in a normal population.
American journal of human genetics | 1992-05-01 | PMID 1349197
von Eckardstein A, Funke H, Schulte M and 3 more
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.
American journal of human genetics | 1992-05-01 | PMID 1349198
Farrer L A, Grundfast K M, Amos J and 7 more
Genes: ALPP, SAG
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2.
American journal of human genetics | 1992-05-01 | PMID 1349200
Biancalana V, Briard M L, David A and 7 more
Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11-q21.
Genomics | 1992-04-01 | PMID 1349298
Troelstra C, Landsvater R M, Wiegant J and 4 more
Genes: ERCC6
Unstable DNA sequence in myotonic dystrophy.
Lancet (London, England) | 1992-05-09 | PMID 1349364
Harley H G, Rundle S A, Reardon W and 5 more
A key role for type 1 pili in enterobacterial communicability.
Molecular microbiology | 1992-03-01 | PMID 1349417
Bloch C A, Stocker B A, Orndorff P E
Trisomy and chromosome size changes in hybrid trypanosomes from a genetic cross between Trypanosoma brucei rhodesiense and T. b. brucei.
Molecular and biochemical parasitology | 1992-04-01 | PMID 1349422
Gibson W, Garside L, Bailey M
Ablation of stimulation of a cAMP-responsive promoter in CHO cell lines defective in their cAMP-dependent protein kinase system.
Somatic cell and molecular genetics | 1992-03-01 | PMID 1349445
Fleischmann R D, Jeng C, Gottesman M M
Genes: TAT
Genetic association and linkage analysis of the apolipoprotein CII locus and familial Alzheimer's disease.
Annals of neurology | 1992-02-01 | PMID 1349467
Schellenberg G D, Boehnke M, Wijsman E M and 3 more
Homozygosity of the short arm of chromosome 17 in cervical carcinoma.
Cancer letters | 1992-04-30 | PMID 1349505
Russell S E, Lowry W S, Atkinson R J and 1 more
Organogenesis in Drosophila melanogaster: embryonic salivary gland determination is controlled by homeotic and dorsoventral patterning genes.
Development (Cambridge, England) | 1992-01-01 | PMID 1349523
Panzer S, Weigel D, Beckendorf S K
Clonal differences within M-types of the group A Streptococcus revealed by pulsed field gel electrophoresis.
FEMS microbiology letters | 1992-02-01 | PMID 1349544
Single L A, Martin D R
apterous, a gene required for imaginal disc development in Drosophila encodes a member of the LIM family of developmental regulatory proteins.
Genes & development | 1992-05-01 | PMID 1349545
Cohen B, McGuffin M E, Pfeifle C and 2 more
Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia using the polymerase chain reaction.
Human genetics | 1992-04-01 | PMID 1349559
Owerbach D, Draznin M B, Carpenter R J and 1 more
Glucose-6-phosphate dehydrogenase (G6PD) electrophoretic variants and the PvuII polymorphism in southern African populations.
Human genetics | 1992-04-01 | PMID 1349560
Coetzee M J, Bartleet S C, Ramsay M and 1 more
Genotype mosaicism in fragile X fetal tissues.
Human genetics | 1992-04-01 | PMID 1349561
Wöhrle D, Hirst M C, Kennerknecht I and 2 more
Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis.
Human genetics | 1992-04-01 | PMID 1349563
Boretto J, Jouanolle A M, Yaouanq J and 7 more
Alpha alpha alpha alpha anti-3.7 type II: a new alpha-globin gene rearrangement suggesting that the alpha-globin gene duplication could be caused by intrachromosomal recombination.
Human genetics | 1992-04-01 | PMID 1349564
De Angioletti M, Lacerra G, Castaldo C and 4 more
Allotype distribution of human T cell receptor beta and gamma chain genes in Caucasians, Asians and Australian aborigines: relevance to chronic hepatitis B.
Human genetics | 1992-04-01 | PMID 1349565
Soeharso P, Summers K M, Cooksley W G
Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in Portugal.
Human genetics | 1992-04-01 | PMID 1349566
Caillaud C, Vilarinho L, Vilarinho A and 7 more
Screening for nonsense mutations in patients with severe hemophilia A can provide rapid, direct carrier detection.
Human genetics | 1992-04-01 | PMID 1349567
Reiner A P, Thompson A R
Genes: CGA
Polymerase chain reaction-based genotyping for allotypic markers of immunoglobulin kappa shows allelic association of Km with kappa variable segment.
Genomics | 1992-05-01 | PMID 1349568
Moxley G, Gibbs R S
Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1.
Genomics | 1992-05-01 | PMID 1349573
Brown K A, Sutcliffe M J, Steel K P and 1 more
A glycine-to-glutamate substitution abolishes alanine:glyoxylate aminotransferase catalytic activity in a subset of patients with primary hyperoxaluria type 1.
Genomics | 1992-05-01 | PMID 1349575
Purdue P E, Lumb M J, Allsop J and 2 more
Genes: AGT, AGXT
Identification of three novel PKU mutations among Chinese: evidence for recombination or recurrent mutation at the PAH locus.
Genomics | 1992-05-01 | PMID 1349576
Wang T, Okano Y, Eisensmith R C and 6 more
Genes: PAH
Wobbler, a mutation affecting motoneuron survival and gonadal functions in the mouse, maps to proximal chromosome 11.
Genomics | 1992-05-01 | PMID 1349581
Kaupmann K, Simon-Chazottes D, Guénet J L and 1 more
An approach to the localization of the susceptibility genes for generalized myasthenia gravis by mapping recombinant ancestral haplotypes.
Immunogenetics | 1992-01-01 | PMID 1349584
Degli-Esposti M A, Andreas A, Christiansen F T and 3 more
Genes: TNF
Coexpression of UmuD' with UmuC suppresses the UV mutagenesis deficiency of groE mutants.
Journal of bacteriology | 1992-05-01 | PMID 1349601
Donnelly C E, Walker G C
Electrostatic interactions stabilizing ferredoxin electron transfer complexes. Disruption by "conservative" mutations.
The Journal of biological chemistry | 1992-05-05 | PMID 1349603
Coghlan V M, Vickery L E
Direct comparison of biological effectiveness of protons and alpha-particles of the same LET. II. Mutation induction at the HPRT locus in V79 cells.
International journal of radiation biology | 1992-05-01 | PMID 1349626
Belli M, Goodhead D T, Ianzini F and 2 more
[Genotyping for drug metabolism capacity can give valuable clinical information].
Lakartidningen | 1992-05-06 | PMID 1349665
Ingelman-Sundberg M, Johansson I, Dahl M L and 3 more
A dementing illness associated with a novel insertion in the prion protein gene.
Brain research. Molecular brain research | 1992-03-01 | PMID 1349721
Owen F, Poulter M, Collinge J and 4 more
Detection of beta and delta globin gene mutations by PCR and direct DNA sequencing in an individual with normal HbA2 beta thalassemia.
Pathology | 1992-01-01 | PMID 1349739
Trent R J, Thein S L
Unraveling the knots in plant development.
Trends in genetics : TIG | 1992-03-01 | PMID 1349773
Hake S
Detection of a single base substitution of the gene for prothrombin Tokushima. The application of PCR-SSCP for the genetic and molecular analysis of dysprothrombinemia.
International journal of hematology | 1992-02-01 | PMID 1349838
Iwahana H, Yoshimoto K, Shigekiyo T and 3 more
Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3.
Mammalian genome : official journal of the International Mammalian Genome Society | 1992-01-01 | PMID 1349842
Ramesh V, Cheng S V, Kozak C A and 4 more
Genes: OAT
p53 mutations are associated with 17p allelic loss in grade II and grade III astrocytoma.
Cancer research | 1992-05-15 | PMID 1349850
von Deimling A, Eibl R H, Ohgaki H and 7 more
Molecular genetics of the Drosophila melanogaster ovo locus, a gene required for sex determination of germline cells.
Genetics | 1992-04-01 | PMID 1349870
Garfinkel M D, Lohe A R, Mahowald A P
Genetic analysis of the additional sex combs locus of Drosophila melanogaster.
Genetics | 1992-04-01 | PMID 1349871
Sinclair D A, Campbell R B, Nicholls F and 2 more
Independence of VNTR alleles defined as fixed bins.
Genetics | 1992-04-01 | PMID 1349872
Weir B S
GM and KM allotypes and GM RFLP allogenotypes in Micronesians from Nauru.
Human biology | 1992-02-01 | PMID 1349875
Propert D N, Nandan R, Jazwinska E C
Extensive allelic variation in Cryptococcus neoformans.
Journal of clinical microbiology | 1992-05-01 | PMID 1349897
Casadevall A, Freundlich L F, Marsh L and 1 more