Tissue-specific and allelic expression of the complement regulator CD46 is controlled by alternative splicing.
European journal of immunology | 1992-06-01 | PMID 1601037
Russell S M, Sparrow R L, McKenzie I F and 1 more
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 178 of 10600
Modifiers of bx1 alter the distribution of Ubx proteins in haltere imaginal discs of Drosophila.
Developmental biology | 1992-06-01 | PMID 1601188
Manoukian A S, Krause H M, Larsen E W
DNA typing of forensic material with mixed genotypes using allele-specific enzymatic amplification (polymerase chain reaction).
Forensic science international | 1992-01-01 | PMID 1601347
Gyllensten U B, Josefsson A, Schemschat K and 2 more
Point mutations and polymorphisms in the human dystrophin gene identified in genomic DNA sequences amplified by multiplex PCR.
Human genetics | 1992-05-01 | PMID 1601417
Kilimann M W, Pizzuti A, Grompe M and 1 more
Genes: DMD
Missense mutations and the magnitude of functional deficit: the example of factor IX.
Human genetics | 1992-05-01 | PMID 1601420
Sommer S S, Bowie E J, Ketterling R P and 1 more
Direct estimate of the haemophilia B (factor IX deficiency) mutation rate and of the ratio of the sex-specific mutation rates in Sweden.
Human genetics | 1992-05-01 | PMID 1601423
Montandon A J, Green P M, Bentley D R and 4 more
Protease inhibitor (Pi) locus, fertility and twinning.
Human genetics | 1992-05-01 | PMID 1601424
Boomsma D I, Frants R R, Bank R A and 1 more
Mutation analysis of phenylketonuria in Spain: prevalence of two Mediterranean mutations.
Human genetics | 1992-05-01 | PMID 1601425
Pérez B, Desviat L R, Die M and 1 more
Gene frequencies of alcohol dehydrogenase2 and aldehyde dehydrogenase2 in Northwest Coast Amerindians.
Human genetics | 1992-05-01 | PMID 1601427
Chen S H, Zhang M, Scott C R
Highly informative dinucleotide repeat polymorphism at the D11S29 locus on chromosome 11q23.
Human genetics | 1992-05-01 | PMID 1601428
Warnich L, Groenewald I, Theart L and 1 more
Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor gene.
Human genetics | 1992-05-01 | PMID 1601429
Warnich L, Kotze M J, Langenhoven E and 1 more
Genes: AGA
The growth rate of two transplantable murine tumors, 3LL lung carcinoma and B16F10 melanoma, is influenced by Hyal-1, a locus determining hyaluronidase levels and polymorphism.
International journal of cancer | 1992-06-19 | PMID 1601526
De Maeyer E, De Maeyer-Guignard J
Heritability of growth curve parameters and heritability of final size: a simulation study.
Growth, development, and aging : GDA | 1992-01-01 | PMID 1601573
Gebhardt-Henrich S G
The high affinity calcium-binding site involved in protein C activation is outside the first epidermal growth factor homology domain.
The Journal of biological chemistry | 1992-06-15 | PMID 1601845
Rezaie A R, Esmon N L, Esmon C T
Genes: EGF
Cell surface and intracellular functions for ricin galactose binding.
The Journal of biological chemistry | 1992-06-15 | PMID 1601861
Newton D L, Wales R, Richardson P T and 6 more
Prostaglandin endoperoxide synthase. The aspirin acetylation region.
The Journal of biological chemistry | 1992-06-15 | PMID 1601897
Shimokawa T, Smith W L
Polymorphism in the human apolipoprotein A-I gene promoter region. Association of the minor allele with decreased production rate in vivo and promoter activity in vitro.
The Journal of clinical investigation | 1992-06-01 | PMID 1601989
Smith J D, Brinton E A, Breslow J L
A novel point mutation in the human insulin gene giving rise to hyperproinsulinemia (proinsulin Kyoto).
The Journal of clinical investigation | 1992-06-01 | PMID 1601997
Yano H, Kitano N, Morimoto M and 3 more
A new variant of Glanzmann's thrombasthenia (Strasbourg I). Platelets with functionally defective glycoprotein IIb-IIIa complexes and a glycoprotein IIIa 214Arg----214Trp mutation.
The Journal of clinical investigation | 1992-06-01 | PMID 1602006
Lanza F, Stierlé A, Fournier D and 4 more
Genes: SDS
Homozygosity for the HLA-DRB1 allele selects for extraarticular manifestations in rheumatoid arthritis.
The Journal of clinical investigation | 1992-06-01 | PMID 1602009
Weyand C M, Xie C, Goronzy J J
[Leber's optic neuropathy: new diagnostic prospects].
Journal francais d'ophtalmologie | 1992-01-01 | PMID 1602101
Pagot V, Malecaze F, Rötig A and 4 more
HLA-J, a second inactivated class I HLA gene related to HLA-G and HLA-A. Implications for the evolution of the HLA-A-related genes.
Journal of immunology (Baltimore, Md. : 1950) | 1992-06-15 | PMID 1602142
Messer G, Zemmour J, Orr H T and 3 more
Recognition of Histoplasma capsulatum yeast-cell antigens by human lymphocytes and human T-cell clones.
Journal of leukocyte biology | 1992-05-01 | PMID 1602236
Henderson H M, Deepe G S
Ontogenetic development, differentiation, and phenotypic expression of macrophages in fetal rat lungs.
Journal of leukocyte biology | 1992-05-01 | PMID 1602238
Higashi K, Naito M, Takeya M and 3 more
Intracellular processing of the paramyxovirus F protein: critical role of the predicted amphipathic alpha helix adjacent to the fusion domain.
Journal of virology | 1992-07-01 | PMID 1602539
Wang C, Raghu G, Morrison T and 1 more
Role of cell-associated enveloped vaccinia virus in cell-to-cell spread.
Journal of virology | 1992-07-01 | PMID 1602540
Blasco R, Moss B
Mutational analysis of the promoter required for influenza virus virion RNA synthesis.
Journal of virology | 1992-07-01 | PMID 1602547
Li X, Palese P
Genes: CAT
Generation and analysis of defective genomes of Autographa californica nuclear polyhedrosis virus.
Journal of virology | 1992-07-01 | PMID 1602548
Lee H Y, Krell P J
Vaccinia virus B1 kinase: phenotypic analysis of temperature-sensitive mutants and enzymatic characterization of recombinant proteins.
Journal of virology | 1992-07-01 | PMID 1602551
Rempel R E, Traktman P
Changes in both gp120 and gp41 can account for increased growth potential and expanded host range of human immunodeficiency virus type 1.
Journal of virology | 1992-07-01 | PMID 1602552
Fujita K, Silver J, Peden K
Role of the fusogenic peptide sequence in syncytium induction and infectivity of human immunodeficiency virus type 2.
Journal of virology | 1992-07-01 | PMID 1602558
Steffy K R, Kraus G, Looney D J and 1 more
Dominant-negative mutants are clustered in a domain of the human T-cell leukemia virus type I Rex protein: implications for trans dominance.
Journal of virology | 1992-07-01 | PMID 1602559
Weichselbraun I, Berger J, Dobrovnik M and 5 more
In vivo genetic variability of the human immunodeficiency virus type 2 V3 region.
Journal of virology | 1992-07-01 | PMID 1602560
Boeri E, Giri A, Lillo F and 6 more
Application of a PCR-mismatch technique to the BCL-2 gene: detection of point mutations in BCL-2 genes of malignancies with A t(14,18).
Leukemia | 1992-01-01 | PMID 1602814
Tanaka S, Louie D, Kant J and 1 more
Murine leukemia virus induced central nervous system diseases.
Leukemia | 1992-01-01 | PMID 1602815
Wong P K, Shikova E, Lin Y C and 5 more
The oncogenicity of Jun.
Leukemia | 1992-01-01 | PMID 1602820
Vogt P K, Morgan I M, Håvarstein L and 3 more
Generation of nucleoside-resistant variants of HIV-1 by in vitro selection in the presence of AZT or DDI but no by combinations.
Leukemia | 1992-01-01 | PMID 1602823
Gao Q, Parniak M A, Gu Z and 1 more
Transfection of chronic lymphocytic leukemic cells with myc and ras.
Leukemia | 1992-01-01 | PMID 1602824
Zheng C Y, Skinnider L F, Xian J and 1 more
Virulence in lymphomagenesis is modulated by alterations in proteins binding to CORE and GRE-LVa elements of the MoMuLV enhancer.
Leukemia | 1992-01-01 | PMID 1602832
Yuen P H, Khang Y H, Matherne C
Role of the p53 tumor suppressor gene in the pathogenesis and in the suppression of acute lymphoblastic T-cell leukemia.
Leukemia | 1992-01-01 | PMID 1602834
Yeargin J, Cheng J, Haas M
Phosphorylation of IcsA by cAMP-dependent protein kinase and its effect on intracellular spread of Shigella flexneri.
Molecular microbiology | 1992-04-01 | PMID 1602963
d'Hauteville H, Sansonetti P J
Rhizobium leguminosarum has two glucosamine synthases, GlmS and NodM, required for nodulation and development of nitrogen-fixing nodules.
Molecular microbiology | 1992-04-01 | PMID 1602964
Marie C, Barny M A, Downie J A
Analysis of an Escherichia coli mutant strain resistant to the cell-killing function encoded by the gef gene family.
Molecular microbiology | 1992-04-01 | PMID 1602968
Poulsen L K, Larsen N W, Molin S and 1 more
The D1 protein of the photosystem II reaction-centre complex accumulates in the absence of D2: analysis of a mutant of the cyanobacterium Synechocystis sp. PCC 6803 lacking cytochrome b559.
Molecular microbiology | 1992-04-01 | PMID 1602969
Shukla V K, Stanbekova G E, Shestakov S V and 1 more
Cloning and whole nucleotide sequence of the gene for the light chain component of botulinum type E toxin from Clostridium butyricum strain BL6340 and Clostridium botulinum type E strain Mashike.
Microbiology and immunology | 1992-01-01 | PMID 1602997
Fujii N, Kimura K, Yashiki T and 5 more
Studies on osmotic stability of liposomes prepared with bacterial membrane lipids by carboxyfluorescein release.
Microbiology and immunology | 1992-01-01 | PMID 1602998
Nagamachi E, Hirai Y, Tomochika K and 1 more
Heterogeneity of S-layer proteins of Lactobacillus acidophilus strains.
Microbiology and immunology | 1992-01-01 | PMID 1602999
Masuda K
The identification of the Bs breakpoint and of two possible Bar genes.
Molecular & general genetics : MGG | 1992-05-01 | PMID 1603054
Norris E, Sanders M, Crumety V and 1 more
Selection and analysis of non-interactive mutants in the Escherichia coli tryptophan synthase alpha subunit.
Molecular & general genetics : MGG | 1992-05-01 | PMID 1603055
Swift S, Kuhn J, Stewart G S
Genes: AGA
Functional analysis of the expression of the 3'-phosphoglycerate kinase pgk gene in Aspergillus nidulans.
Molecular & general genetics : MGG | 1992-05-01 | PMID 1603065
Streatfield S J, Toews S, Roberts C F
Genetic and molecular analysis of the dpy-14 region in Caenorhabditis elegans.
Molecular & general genetics : MGG | 1992-05-01 | PMID 1603066
McKim K S, Starr T, Rose A M
Different mechanisms generating sequence variability are revealed in distinct regions of the hydroxyproline-rich glycoprotein gene from maize and related species.
Molecular & general genetics : MGG | 1992-05-01 | PMID 1603067
Raz R, José M, Moya A and 2 more
Identification of a nodD-like gene in Frankia by direct complementation of a Rhizobium nodD-mutant.
Molecular & general genetics : MGG | 1992-05-01 | PMID 1603071
Chen L M, Cui Y H, Qin M and 3 more
The yeast RNA1 protein, necessary for RNA processing, is homologous to the human ribonuclease/angiogenin inhibitor (RAI).
Molecular & general genetics : MGG | 1992-05-01 | PMID 1603072
Schneider R, Schweiger M
Mutations in the DnaA binding sites of the replication origin of Escherichia coli.
Molecular & general genetics : MGG | 1992-05-01 | PMID 1603077
Holz A, Schaefer C, Gille H and 2 more
Glucose transport in the yeast Kluyveromyces lactis. I. Properties of an inducible low-affinity glucose transporter gene.
Molecular & general genetics : MGG | 1992-05-01 | PMID 1603078
Wésolowski-Louvel M, Goffrini P, Ferrero I and 1 more
Genes: RAG1
Glucose transport in the yeast Kluyveromyces lactis. II. Transcriptional regulation of the glucose transporter gene RAG1.
Molecular & general genetics : MGG | 1992-05-01 | PMID 1603079
Chen X J, Wésolowski-Louvel M, Fukuhara H
Genes: RAG1
Characterization of estrogen receptor variant mRNAs from human breast cancers.
Molecular endocrinology (Baltimore, Md.) | 1992-05-01 | PMID 1603086
Dotzlaw H, Alkhalaf M, Murphy L C
Inactivation of wild-type and rad mutant Caenorhabditis elegans by 8-methoxypsoralen and near ultraviolet radiation.
Photochemistry and photobiology | 1992-01-01 | PMID 1603841
Hartman P S, Marshall A
[Genetic counseling in neurology].
Revue neurologique | 1992-01-01 | PMID 1604129
Landrieu P
[Alpha-1-antitrypsin deficiency in chronic inflammatory rheumatism and mechanical arthropathies. Preliminary results].
Revue du rhumatisme et des maladies osteo-articulaires | 1992-02-01 | PMID 1604223
Eulry F, Kremer P, Faudon R and 3 more
Complete amino acid sequence of the variable regions of two highly related heavy and light chains of human IgG (SFL) and IgM (RIV) rheumatoid factors.
Scandinavian journal of immunology | 1992-06-01 | PMID 1604239
Newkirk M M
Sexually antagonistic genes: experimental evidence.
Science (New York, N.Y.) | 1992-06-05 | PMID 1604317
Rice W R
LTR sequence and phylogenetic analyses of a newly discovered variant of HTLV-I isolated from the Hagahai of Papua New Guinea.
Virology | 1992-07-01 | PMID 1604804
Saksena N K, Sherman M P, Yanagihara R and 2 more
Pathways of viral gene expression during acute neuronal infection with HSV-1.
Virology | 1992-07-01 | PMID 1604806
Margolis T P, Sedarati F, Dobson A T and 2 more
Functional analysis of biologically distinct genetic variants of simian immunodeficiency virus isolated from a mandrill.
Virology | 1992-07-01 | PMID 1604807
Sakai H, Sakuragi J, Sakuragi S and 2 more
Retained in vitro infectivity and cytopathogenicity of HIV-1 despite truncation of the C-terminal tail of the env gene product.
Virology | 1992-07-01 | PMID 1604808
Wilk T, Pfeiffer T, Bosch V
Nucleotide sequence analysis of the HA1 coding portion of the haemagglutinin gene of swine H1N1 influenza viruses.
Virus research | 1992-04-01 | PMID 1604929
Neumeier E, Meier-Ewert H
Cell culture propagation modifies the African swine fever virus replication phenotype in macrophages and generates viral subpopulations differing in protein p54.
Virus research | 1992-04-01 | PMID 1604931
Alcaraz C, Brun A, Ruiz-Gonzalvo F and 1 more
Biology of cancer invasion and metastasis.
Acta oto-rhino-laryngologica Belgica | 1992-01-01 | PMID 1605015
Mareel M M, Crombez R
Chronic inflammatory arthritis after treatment with high-dose interleukin-2 for malignancy.
The American journal of medicine | 1992-06-01 | PMID 1605152
Massarotti E M, Liu N Y, Mier J and 1 more
Premutation for the Martin-Bell syndrome analyzed in a large Sardinian family: II. Neuropsychological and behavioral data.
American journal of medical genetics | 2000-01-01 | PMID 1605176
Cianchetti C, Filippi G, Sannio-Fancello G and 4 more
Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development.
American journal of medical genetics | 2000-01-01 | PMID 1605193
Devys D, Biancalana V, Rousseau F and 3 more
Molecular studies of the fragile X syndrome.
American journal of medical genetics | 2000-01-01 | PMID 1605194
Knight S J, Hirst M C, Roche A and 7 more
Genes: NTM
Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic association.
American journal of medical genetics | 2000-01-01 | PMID 1605195
Oberlé I, Boué J, Croquette M F and 3 more
Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotype.
American journal of medical genetics | 2000-01-01 | PMID 1605196
Dennis N R, Curtis G, Macpherson J N and 1 more
Methylation and mutation patterns in the fragile X syndrome.
American journal of medical genetics | 2000-01-01 | PMID 1605200
Malmgren H, Steén-Bondeson M L, Gustavson K H and 6 more
Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?
American journal of medical genetics | 2000-01-01 | PMID 1605202
Fisch G S, Shapiro L R, Simensen R and 7 more
Notes on the population genetics of fragile X syndrome.
American journal of medical genetics | 2000-01-01 | PMID 1605208
Vianna-Morgante A M, Otto P A
High prevalence of the fra(X) syndrome cannot be explained by a high mutation rate.
American journal of medical genetics | 2000-01-01 | PMID 1605209
Smits A, Smeets D, Hamel B and 2 more
Genes: NTM
Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children.
American journal of medical genetics | 2000-01-01 | PMID 1605210
Reiss A L, Freund L
Collaborative prospective study of the fragile X syndrome: one-year progress report.
American journal of medical genetics | 2000-01-01 | PMID 1605212
Sherman S L, Barbi G, Brøndum-Nielsen K and 7 more
Penetrance estimate of the fra(X) gene using Pointer versus direct estimate.
American journal of medical genetics | 2000-01-01 | PMID 1605213
de Haan A F, Smits A P, Smeets D F and 1 more
Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting male.
American journal of medical genetics | 2000-01-01 | PMID 1605214
Smits A P, van Oost B A, de Haan A F and 3 more
Genes: NTM
XLMR genes: update 1992.
American journal of medical genetics | 2000-01-01 | PMID 1605215
Neri G, Chiurazzi P, Arena F and 2 more
Localization of non-specific X-linked mental retardation genes.
American journal of medical genetics | 2000-01-01 | PMID 1605217
Kerr B, Gedeon A, Mulley J and 1 more
Aarskog syndrome: the changing phenotype with age.
American journal of medical genetics | 2000-01-01 | PMID 1605221
Fryns J P
MRX8: an X-linked mental retardation condition with linkage to Xq21.
American journal of medical genetics | 2000-01-01 | PMID 1605227
Schwartz C E, May M, Huang T and 6 more
X-linked mental retardation and characteristic physical features in two brothers with duplication Xp22-Xpter.
American journal of medical genetics | 2000-01-01 | PMID 1605229
Cianchetti C, Muntoni F, Falchi A M and 4 more
Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second family.
American journal of medical genetics | 2000-01-01 | PMID 1605231
Bialer M G, Lawrence L, Stevenson R E and 5 more
New X-linked syndrome with apraxia, ataxia, and mental deficiency: clinical, cytogenetic and neuropsychological studies in two Danish families.
American journal of medical genetics | 2000-01-01 | PMID 1605232
Tranebjaerg L, Lou H, Andresen J
Recognizable behavioral and somatic phenotype in patients with proximal interstitial 18q deletion: report on a new affected child and follow-up on the original reported familial cases.
American journal of medical genetics | 1992-06-01 | PMID 1605245
Chudley A E, Kovnats S, Ray M
Autosomal dominant polycystic kidney disease: new information for genetic counselling.
American journal of medical genetics | 1992-06-01 | PMID 1605247
Bear J C, Parfrey P S, Morgan J M and 2 more
Genes: PKD1
Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype.
American journal of medical genetics | 1992-06-01 | PMID 1605248
Krasikov N, Takaesu N, Hassold T and 3 more
Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons.
American journal of medical genetics | 1992-06-01 | PMID 1605253
Kirkilionis A J, Chudley A E, Greenberg C R and 3 more
Completeness of catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes.
American journal of medical genetics | 1992-06-01 | PMID 1605257
ten Kate L P
[Cytogenetic study of a family with 15p+ chromosomal plymorphism].
Anales espanoles de pediatria | 1992-04-01 | PMID 1605408
Manzanal Martínez A I, Robledo Batanero M, Ramos Corrales C and 2 more
[Importance of molecular diagnosis in the detection of healthy male transmitters of the fragile X syndrome].
Anales espanoles de pediatria | 1992-04-01 | PMID 1605409
Tizzano Ferrari E, Gallano Petit P, Baiget Bastus M
Acetylator genotype-dependent N-acetylation of arylamines in vivo and in vitro by hepatic and extrahepatic organ cytosols of Syrian hamsters congenic at the polymorphic acetyltransferase locus.
Archives of toxicology | 1992-01-01 | PMID 1605725
Hein D W, Rustan T D, Martin W J and 3 more
Epithelial polarity and cell separation in the neoplastic l(1)dlg-1 mutant of Drosophila.
Mechanisms of development | 1992-03-01 | PMID 1606019
Abbott L A, Natzle J E