Allelic exclusion of Ly49-family genes encoding class I MHC-specific receptors on NK cells.
Nature | 1995-07-27 | PMID 7630404
Held W, Roland J, Raulet D H
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 432 of 10600
Runaway telomere elongation caused by telomerase RNA gene mutations.
Nature | 1995-08-03 | PMID 7630414
McEachern M J, Blackburn E H
Hox genes and the diversification of insect and crustacean body plans.
Nature | 1995-08-03 | PMID 7630416
Averof M, Akam M
Distinguishable functions for engrailed and invected in anterior-posterior patterning in the Drosophila wing.
Nature | 1995-08-03 | PMID 7630417
Simmonds A J, Brook W J, Cohen S M and 1 more
Specification of neuroblast identity in the Drosophila embryonic central nervous system by gooseberry-distal.
Nature | 1995-08-03 | PMID 7630418
Skeath J B, Zhang Y, Holmgren R and 2 more
Ethanol sensitivity of heteromeric NMDA receptors: effects of subunit assembly, glycine and NMDAR1 Mg(2+)-insensitive mutants.
Neuropharmacology | 1995-03-01 | PMID 7630488
Mirshahi T, Woodward J J
Motif-primed polymerase chain reaction-based allelotype of sarcomas induced by 3-methylcholanthrene in interspecific hybrid mice.
Oncogene | 1995-08-03 | PMID 7630636
Dudley M E, Sundberg J P, Roopenian D C
Frequent loss of heterozygosity on chromosome 9, and low incidence of mutations of cyclin-dependent kinase inhibitors p15 (MTS2) and p16 (MTS1) genes in gliomas.
Oncogene | 1995-08-03 | PMID 7630644
Li Y J, Hoang-Xuan K, Delattre J Y and 3 more
Pattern of ras and gsp oncogene mutations in radiation-associated human thyroid tumors.
Oncogene | 1995-08-03 | PMID 7630645
Challeton C, Bounacer A, Du Villard J A and 5 more
Familial hypercholesterolemia: molecular, biochemical, and clinical characterization of a French-Canadian pediatric population.
Pediatrics | 1995-08-01 | PMID 7630677
Assouline L, Levy E, Feoli-Fonseca J C and 2 more
Cooperative assembly of proteins in the ribosomal GTPase centre demonstrated by their interactions with mutant 23S rRNAs.
Nucleic acids research | 1995-07-11 | PMID 7630717
Rosendahl G, Douthwaite S
Electrophoresis for genotyping: temporal thermal gradient gel electrophoresis for profiling of oligonucleotide dissociation.
Nucleic acids research | 1995-07-11 | PMID 7630718
Day I N, O'Dell S D, Cash I D and 2 more
Dual regulation of the Drosophila hsp26 promoter in vitro.
Nucleic acids research | 1995-07-11 | PMID 7630725
Sandaltzopoulos R, Mitchelmore C, Bonte E and 2 more
Characterization of three new snRNAs from Saccharomyces cerevisiae: snR34, snR35 and snR36.
Nucleic acids research | 1995-07-11 | PMID 7630735
Samarsky D A, Balakin A G, Fournier M J
Allergic drug reactions. How to minimize the risks.
Postgraduate medicine | 1995-08-01 | PMID 7630844
Bernstein J A
Insertional re-activation of a chloramphenicol acetyltransferase misfolding mutant protein.
Protein engineering | 1995-02-01 | PMID 7630887
Robben J, Van der Schueren J, Verhasselt P and 2 more
Genes: CAT
Explaining local species diversity.
Proceedings. Biological sciences | 1995-06-22 | PMID 7630897
Shorrocks B, Sevenster J G
Macroevolutionary inferences from primate phylogeny.
Proceedings. Biological sciences | 1995-06-22 | PMID 7630899
Purvis A, Nee S, Harvey P H
Effects of light and chloroplast functional state on expression of nuclear genes encoding chloroplast glyceraldehyde-3-phosphate dehydrogenase in long hypocotyl (hy) mutants and wild-type Arabidopsis thaliana.
Plant physiology | 1995-07-01 | PMID 7630933
Conley T R, Shih M C
Abnormality of smooth pursuit eye movement initiation: specificity to the schizophrenia spectrum?
Psychophysiology | 1995-03-01 | PMID 7630977
Clementz B A, Reid S A, McDowell J E and 1 more
Cancer predisposition, radiosensitivity and the risk of radiation-induced cancers. I. Background.
Radiation research | 1995-08-01 | PMID 7631005
Sankaranarayanan K, Chakraborty R
The effect of defective DNA double-strand break repair on mutations and chromosome aberrations in the Chinese hamster cell mutant XR-V15B.
Radiation research | 1995-08-01 | PMID 7631007
Helbig R, Zdzienicka M Z, Speit G
The somatic hypermutation activity of a follicular lymphoma links to large insertions and deletions of immunoglobulin genes.
Scandinavian journal of immunology | 1995-07-01 | PMID 7631145
Wu H Y, Kaartinen M
Relationship between the reactivity to hepatitis B virus vaccination and the frequency of MHC class I, II and III alleles in haemodialysis patients.
Scandinavian journal of immunology | 1995-07-01 | PMID 7631146
Stachowski J, Kramer J, Füst G and 3 more
Structural analysis of VH4-21 encoded human IgM allo- and autoantibodies against red blood cells.
Scandinavian journal of immunology | 1995-07-01 | PMID 7631150
Børretzen M, Chapman C, Stevenson F K and 2 more
Mechanisms by which the I-ABM12 mutation influences susceptibility to experimental myasthenia gravis: a study in homozygous and heterozygous mice.
Scandinavian journal of immunology | 1995-08-01 | PMID 7631155
Karachunski P I, Ostlie N, Bellone M and 2 more
Genes: APC
Studies on phospholipid antibodies, APC-resistance and associated mutation in the coagulation factor V gene.
Thrombosis research | 1995-05-01 | PMID 7631299
Bokarewa M I, Bremme K, Falk G and 3 more
Genes: APC
Angiotensin-converting enzyme gene deletion polymorphism. A new risk factor for lacunar stroke but not carotid atheroma.
Stroke | 1995-08-01 | PMID 7631331
Markus H S, Barley J, Lunt R and 4 more
Isoimmune neonatal neutropenia caused by Fc gamma RIIIb antibodies in a Spanish child.
Transfusion | 1995-08-01 | PMID 7631410
Puig N, de Haas M, Kleijer M and 5 more
[Clinico-genealogical and genetic-mathematical research on cancer of the cervix uteri].
TSitologiia i genetika | 2000-01-01 | PMID 7631425
Isakova L M, Hanina K P, Osins'ka O V and 1 more
[An analysis of the genetic structure of a hybrid population of green frogs, Rana esculenta complex, from the flats of the Danube].
TSitologiia i genetika | 2000-01-01 | PMID 7631428
Morozov-Leonov S Iu, Mezhzheron S V
[A taxonomic interpretation of the morphological variability exemplified by common voles (Microtus s. lato, Rodentia)].
Zhurnal obshchei biologii | 2000-01-01 | PMID 7631522
Pozdniakov A A
Fine needle aspiration cytology of extramedullary chronic myelogenous leukemia.
Acta cytologica | 2000-01-01 | PMID 7631544
Mourad W A, Sneige N, Huh Y O and 4 more
Phenotypes of alpha-1-antitrypsin in intrinsic asthma and ASA-triad patients.
Allergologia et immunopathologia | 2000-01-01 | PMID 7631591
Prados M, Monteseirín F J, Carranco M I and 3 more
Developmental regulation of membrane protein sorting in Drosophila embryos.
The American journal of physiology | 1995-07-01 | PMID 7631747
Shiel M J, Caplan M J
Marked resistance of RAR gamma-deficient mice to the toxic effects of retinoic acid.
The American journal of physiology | 1995-07-01 | PMID 7631783
Look J, Landwehr J, Bauer F and 3 more
Mismatch repair deficiency in phenotypically normal human cells.
Science (New York, N.Y.) | 1995-05-05 | PMID 7632227
Parsons R, Li G M, Longley M and 6 more
Genetic variation and geographic distribution on the mitochondrial DNA in local populations of the musk shrew, Suncus murinus.
Idengaku zasshi | 1995-06-01 | PMID 7632440
Yamagata T, Ohishi K, Faruque M O and 6 more
Nucleotide substitution type dependence of generation time effect of molecular evolution.
Idengaku zasshi | 1995-06-01 | PMID 7632442
Kisakibaru Y, Matsuda H
Distinct changes in HIV type 1 RNA versus p24 antigen levels in serum during short-term zidovudine therapy in asymptomatic individuals with and without progression to AIDS.
AIDS research and human retroviruses | 1995-04-01 | PMID 7632462
Jurriaans S, Weverling G J, Goudsmit J and 6 more
Sex determination and DNA competition in the analysis of forensic mixed stains by PCR.
International journal of legal medicine | 1995-01-01 | PMID 7632599
Kreike J, Lehner A
Population study of 3 STR loci in the Basque Country (northern Spain).
International journal of legal medicine | 1995-01-01 | PMID 7632600
Alonso S, Castro A, Fernandez I and 4 more
Swiss population data and forensic efficiency values on 3 tetrameric short tandem repeat loci-HUMTH01, TPOX, and CSF1PO-derived using a STR multiplex system.
International journal of legal medicine | 1995-01-01 | PMID 7632601
Hochmeister M N, Budowle B, Schumm J W and 3 more
Genes: GYPA, LDLR
AMPFLP analysis of the VNTR loci D1S80 and ApoB in Hungary.
International journal of legal medicine | 1995-01-01 | PMID 7632607
Woller J, Furedi S, Padar Z
X-ray structure of two complexes of the Y143F flavocytochrome b2 mutant crystallized in the presence of lactate or phenyl lactate.
Biochemistry | 1995-08-08 | PMID 7632684
Tegoni M, Begotti S, Cambillau C
Insertion of an uncharged polypeptide into the mitochondrial inner membrane does not require a trans-bilayer electrochemical potential: effects of positive charges.
Biochimica et biophysica acta | 1995-07-26 | PMID 7632709
McBride H M, Silvius J R, Shore G C
Contribution of immunophenotypic and genotypic analyses to the diagnosis of acute leukemia.
Annals of hematology | 1995-07-01 | PMID 7632814
Stasi R, Taylor C G, Venditti A and 7 more
N-terminal cysteines essential for Golgi sorting of B-50 (GAP-43) in PC12 cells.
Neuroreport | 1995-05-09 | PMID 7632901
Aarts L H, van der Linden J A, Hage W J and 4 more
Genes: NGF
The largest variant of platelet glycoprotein Ib alpha has four tandem repeats of 13 amino acids in the macroglycopeptide region and a genetic linkage with methionine145.
Blood | 1995-08-15 | PMID 7632942
Ishida F, Furihata K, Ishida K and 4 more
Characterization of B-cell lines established from two X-linked severe combined immunodeficiency patients: interleukin-15 binds to the B cells but is not internalized efficiently.
Blood | 1995-08-15 | PMID 7632950
Kumaki S, Ochs H D, Timour M and 7 more
Molecular basis and expression of the LWa/LWb blood group polymorphism.
Blood | 1995-08-15 | PMID 7632968
Hermand P, Gane P, Mattei M G and 3 more
TTR exon scanning in peripheral neuropathies.
Neuromuscular disorders : NMD | 1995-05-01 | PMID 7633183
Torres M de F, Almeida M do R, Saraiva M J
Genes: TTR, FAP
Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic.
Neuromuscular disorders : NMD | 1995-05-01 | PMID 7633187
Ranta S, Pihko H, Santavuori P and 2 more
Roles of p53 mutation in cell line establishment and identification of the minimum transactivation and transform suppression domains.
European journal of cancer. Part B, Oral oncology | 1995-03-01 | PMID 7633285
Hirano Y, Tsutsumi-Ishii Y, Tsuchida N
Presence of human papillomavirus sequences in tumour-derived human oral keratinocytes expressing mutant p53.
European journal of cancer. Part B, Oral oncology | 1995-03-01 | PMID 7633286
Yeudall W A, Paterson I C, Patel V and 1 more
The D5 dopamine receptor gene in schizophrenia: identification of a nonsense change and multiple missense changes but lack of association with disease.
Human molecular genetics | 1995-04-01 | PMID 7633397
Sobell J L, Lind T J, Sigurdson D C and 5 more
Genes: DRD5
Splicing mutations of the polycystic kidney disease 1 (PKD1) gene induced by intronic deletion.
Human molecular genetics | 1995-04-01 | PMID 7633405
Peral B, Gamble V, San Millán J L and 4 more
Genes: PKD1
Recurrent mis-splicing of fibrillin exon 32 in two patients with neonatal Marfan syndrome.
Human molecular genetics | 1995-04-01 | PMID 7633409
Wang M, Price C, Han J and 5 more
Genes: FBN1, EGF
Hyperhomocysteinemia in premature arterial disease: examination of cystathionine beta-synthase alleles at the molecular level.
Human molecular genetics | 1995-04-01 | PMID 7633411
Kozich V, Kraus E, de Franchis R and 4 more
Genes: CBS
Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy.
Human molecular genetics | 1995-04-01 | PMID 7633412
Rodrigues N R, Owen N, Talbot K and 3 more
Four novel mutations in mucopolysaccharidosis type VII including a unique base substitution in exon 10 of the beta-glucuronidase gene that creates a novel 5'-splice site.
Human molecular genetics | 1995-04-01 | PMID 7633414
Yamada S, Tomatsu S, Sly W S and 5 more
Localization of craniosynostosis Adelaide type to 4p16.
Human molecular genetics | 1995-04-01 | PMID 7633418
Hollway G E, Phillips H A, Adès L C and 2 more
Genes: FGFR3, MSX1
Identification of Btk mutations in 20 unrelated patients with X-linked agammaglobulinaemia (XLA).
Human molecular genetics | 1995-04-01 | PMID 7633420
Jin H, Webster A D, Vihinen M and 7 more
Sequence variability of a prolonged tetranucleotide repeat.
Human molecular genetics | 1995-04-01 | PMID 7633423
Liu Y, Rasool O, Grandér D and 2 more
Reverse replication timing for the XIST gene in human fibroblasts.
Human molecular genetics | 1995-05-01 | PMID 7633440
Hansen R S, Canfield T K, Gartler S M
Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.
Human molecular genetics | 1995-05-01 | PMID 7633441
Angrist M, Bolk S, Thiel B and 5 more
Genes: RET
No evidence that common allelic variation in the Amyloid Precursor Protein (APP) gene confers susceptibility to Alzheimer's disease.
Human molecular genetics | 1995-05-01 | PMID 7633445
Liddell M B, Bayer A J, Owen M J
Genes: APP
Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.
Human molecular genetics | 1995-05-01 | PMID 7633448
Glaser B, Chiu K C, Liu L and 7 more
The distribution of linkage disequilibrium over anonymous genome regions.
Human molecular genetics | 1995-05-01 | PMID 7633449
Peterson A C, Di Rienzo A, Lehesjoki A E and 3 more
Human cell mutants with very low mitochondrial DNA copy number (rho d).
Human molecular genetics | 1995-05-01 | PMID 7633451
Vaillant F, Nagley P
Mitochondrial DNA diversity in the Kuna Amerinds of Panamá.
Human molecular genetics | 1995-05-01 | PMID 7633453
Batista O, Kolman C J, Bermingham E
Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region.
Human molecular genetics | 1995-05-01 | PMID 7633454
Bergen A A, ten Brink J B, Riemslag F and 2 more
Nucleotide sequence analysis of the apolipoprotein B 3' VNTR.
Human molecular genetics | 1995-05-01 | PMID 7633455
Ellsworth D L, Shriver M D, Boerwinkle E
Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)
Human molecular genetics | 1995-05-01 | PMID 7633457
Lunt P W, Jardine P E, Koch M C and 5 more
A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa.
Human molecular genetics | 1995-05-01 | PMID 7633458
Kivirikko S, McGrath J A, Baudoin C and 7 more
Genes: LAMA3, LAMB3, LAMC2
Definition of the blepharophimosis, ptosis, epicanthus inversus syndrome critical region at chromosome 3q23 based on the analysis of chromosomal anomalies.
Human molecular genetics | 1995-05-01 | PMID 7633459
Lawson C T, Toomes C, Fryer A and 4 more
Molecular analysis of a Drosophila melanogaster sn-glycerol-3-phosphate dehydrogenase allozyme variant that has cold labile activity.
Insect biochemistry and molecular biology | 1995-07-01 | PMID 7633467
Symonds J E, Gibson J B, Wilks A V and 1 more
Remarks on the mechanism of demographic behaviour.
Studies in human ecology | 1994-01-01 | PMID 7633486
Rószkiewicz M
Assortative mating in somatic traits and its consequences.
Studies in human ecology | 1994-01-01 | PMID 7633493
Wolański N
Purification and characterization of insulin-like growth factor II (IGF II) and an IGF II variant from human placenta.
Journal of chromatography. B, Biomedical applications | 1995-04-21 | PMID 7633596
De Ceuninck F, Willeput J, Corvol M
Genes: SDS
Frequent loss of heterozygosity at the deleted in colorectal carcinoma gene locus and its association with histologic phenotypes in breast carcinoma.
Virchows Archiv : an international journal of pathology | 1995-01-01 | PMID 7633654
Kashiwaba M, Tamura G, Ishida M
Genes: DCC
"The sarcoidosis map": a joint survey of clinical and immunogenetic findings in two European countries.
American journal of respiratory and critical care medicine | 1995-08-01 | PMID 7633707
Martinetti M, Tinelli C, Kolek V and 7 more
Prognostic factors in rheumatoid arthritis. Comparative study of two subsets of patients according to severity of articular damage.
British journal of rheumatology | 1995-06-01 | PMID 7633794
Combe B, Eliaou J F, Daurès J P and 3 more
Genes: CRP
Immunoprinting: various genes are associated with increased risk to develop rheumatoid arthritis in different groups of adult patients.
Journal of molecular medicine (Berlin, Germany) | 1995-01-01 | PMID 7633938
Gomolka M, Menninger H, Saal J E and 5 more
Apolipoprotein(a) phenotypes and lipoprotein(a) concentrations in patients with hyperthyroidism.
Journal of molecular medicine (Berlin, Germany) | 1995-01-01 | PMID 7633941
Klausen I C, Hegedüs L, Hansen P S and 3 more
Development of the osteoblast phenotype: molecular mechanisms mediating osteoblast growth and differentiation.
The Iowa orthopaedic journal | 1995-01-01 | PMID 7634023
Lian J B, Stein G S
Critical elements in proteasome assembly.
Nature structural biology | 1994-11-01 | PMID 7634086
Zwickl P, Kleinz J, Baumeister W
The S. pombe cdc15 gene is a key element in the reorganization of F-actin at mitosis.
Cell | 1995-08-11 | PMID 7634333
Fankhauser C, Reymond A, Cerutti L and 3 more
Identification of a novel cellular cofactor for the Rev/Rex class of retroviral regulatory proteins.
Cell | 1995-08-11 | PMID 7634337
Bogerd H P, Fridell R A, Madore S and 1 more
Identification of a novel nuclear pore-associated protein as a functional target of the HIV-1 Rev protein in yeast.
Cell | 1995-08-11 | PMID 7634338
Stutz F, Neville M, Rosbash M
Mutations in the Ada O6-alkylguanine-DNA alkyltransferase conferring sensitivity to inactivation by O6-benzylguanine and 2,4-diamino-6-benzyloxy-5-nitrosopyrimidine.
Carcinogenesis | 1995-08-01 | PMID 7634390
Crone T M, Kanugula S, Pegg A E
Genes: AGT
H-ras oncogene mutation spectra in B6C3F1 and C57BL/6 mouse liver tumors provide evidence for TCDD promotion of spontaneous and vinyl carbamate-initiated liver cells.
Carcinogenesis | 1995-08-01 | PMID 7634393
Watson M A, Devereux T R, Malarkey D E and 2 more
DNA mismatch repair mutants do not increase N-methyl-N'-nitro-N-nitrosoguanidine tolerance in O6-methylguanine DNA methyltransferase-deficient yeast cells.
Carcinogenesis | 1995-08-01 | PMID 7634424
Xiao W, Rathgeber L, Fontanie T and 1 more
The Hcr (hepatocarcinogen resistance) loci of DBA/2J mice partially suppress phenotypic expression of the Hcs (hepatocarcinogen sensitivity) loci of C3H/HeJ mice.
Carcinogenesis | 1995-08-01 | PMID 7634431
Lee G H, Drinkwater N R
Glutathione S-transferase GSTM1 null genotype is not overrepresented in Australian patients with nevoid basal cell carcinoma syndrome or sporadic melanoma.
Carcinogenesis | 1995-08-01 | PMID 7634433
Shanley S M, Chenevix-Trench G, Palmer J and 1 more
Genes: GSTM1
Genetic basis of the silent phenotype of serum butyrylcholinesterase in three compound heterozygotes.
Clinica chimica acta; international journal of clinical chemistry | 1995-02-28 | PMID 7634491
Maekawa M, Sudo K, Kanno T and 5 more
Genes: AGA, CGA, GCA
Association of HincII RFLP of low density lipoprotein receptor gene with obesity in essential hypertensives.
Clinical genetics | 1995-03-01 | PMID 7634533
Zee R Y, Schrader A P, Robinson B G and 2 more
Genes: LDLR
Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan.
Clinical genetics | 1995-03-01 | PMID 7634534
Leutelt J, Oehlmann R, Younus F and 5 more
Exclusion mapping of the benign hereditary chorea gene from the Huntington's disease locus: report of a family.
Clinical genetics | 1995-03-01 | PMID 7634535
Yapijakis C, Kapaki E, Zournas C and 3 more
Clinical and molecular genetic findings in five patients with Miller-Dieker syndrome.
Clinical genetics | 1995-03-01 | PMID 7634541
Köhler A, Hain J, Müller U