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 184 of 10600

Crude isolation of DNA from unselected human pancreatic tissue and amplification by the polymerase chain reaction of Ki-ras oncogene to detect point mutations in pancreatic cancer.
Acta oncologica (Stockholm, Sweden) | 1992-01-01 | PMID 1632977
Masson P, Andrén-Sandberg A
Construction and characterization of a spectral probe mutant of troponin C: application to analyses of mutants with increased Ca2+ affinity.
Biochemistry | 1992-07-21 | PMID 1633166
Pearlstone J R, Borgford T, Chandra M and 7 more
Steady-state kinetics and isotope effects on the mutant catalytic trimer of aspartate transcarbamoylase containing the replacement of histidine 134 by alanine.
Biochemistry | 1992-07-21 | PMID 1633170
Waldrop G L, Turnbull J L, Parmentier L E and 3 more
Human mitochondrial complex I dysfunction.
Biochimica et biophysica acta | 1992-07-17 | PMID 1633185
Cooper J M, Mann V M, Krige D and 1 more
Hydrogen bond network of cytochrome P-450cam: a network connecting the heme group with helix K.
Biochimica et biophysica acta | 1992-07-13 | PMID 1633194
Yoshikawa K, Noguti T, Tsujimura M and 4 more
[Association between post-initial remission and HLA phenotype in Type I diabetics].
Anales de medicina interna (Madrid, Spain : 1984) | 1992-07-01 | PMID 1633235
García-Mayor R V, Andrade A, del Pozo M and 5 more
Crossed signals: oncogenic transcription factors.
Current opinion in genetics & development | 1992-02-01 | PMID 1633422
Forrest D, Curran T
Proto-oncogenes in mammalian development.
Current opinion in genetics & development | 1992-02-01 | PMID 1633424
Forrester L M, Brunkow M, Bernstein A
Genetic variation and quasi-species.
Current opinion in genetics & development | 1992-02-01 | PMID 1633428
Domingo E
The human skeletal alpha-actin gene is regulated by a muscle-specific enhancer that binds three nuclear factors.
Gene expression | 1992-01-01 | PMID 1633435
Muscat G E, Perry S, Prentice H and 1 more
Mechanism of tissue-specific transcription: interplay between positive and negative regulatory factors.
Gene expression | 1992-01-01 | PMID 1633436
Zhou M D, Wu Y, Kumar A and 1 more
The detection of minimal residual disease in acute lymphoblastic leukaemia.
Blood reviews | 1992-06-01 | PMID 1633509
Potter M N
The rapid generation of mutation data matrices from protein sequences.
Computer applications in the biosciences : CABIOS | 1992-06-01 | PMID 1633570
Jones D T, Taylor W R, Thornton J M
Genes: PAM
Gaucher patients with oculomotor abnormalities do not have a unique genotype.
Clinical genetics | 1992-01-01 | PMID 1633639
Sidransky E, Tsuji S, Stubblefield B K and 3 more
Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?
Clinical genetics | 1992-01-01 | PMID 1633641
van Maldergem L, Wetzburger C, Verloes A and 2 more
Interstitial deletion of chromosome 1 del (1) (q32 q42): case report and review of the literature.
Clinical genetics | 1992-01-01 | PMID 1633642
Sarda P, Lefort G, Taviaux S and 2 more
Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence.
Clinical genetics | 1992-01-01 | PMID 1633645
Graham D A, Jewitt M M, Fitzgerald P H
On the variable expression of the Brachmann-de Lange syndrome.
Clinical genetics | 1992-01-01 | PMID 1633646
de Die-Smulders C, Theunissen P, Schrander-Stumpel C and 1 more
Treatment for B-cell-type lymphoma in a girl associated with Bloom's syndrome.
Clinical genetics | 1992-01-01 | PMID 1633647
Oto S, Miyamoto S, Kudoh F and 3 more
Severe Silver-Russell syndrome and translocation (17;20) (q25;q13)
Clinical genetics | 1992-01-01 | PMID 1633648
Ramírez-Dueñas M L, Medina C, Ocampo-Campos R and 1 more
A unique de novo interstitial deletion del(17)(q21.3q23) in a phenotypically abnormal infant.
Clinical genetics | 1992-01-01 | PMID 1633649
Park J P, Moeschler J B, Berg S Z and 2 more
An HLA study in 74 Danish haemochromatosis patients and in 21 of their families.
Clinical genetics | 1992-01-01 | PMID 1633650
Milman N, Graudal N, Nielsen L S and 1 more
Characterisation of a haem active-site mutant of horseradish peroxidase, Phe41----Val, with altered reactivity towards hydrogen peroxide and reducing substrates.
European journal of biochemistry | 1992-07-15 | PMID 1633806
Smith A T, Sanders S A, Thorneley R N and 2 more
A mutation at Gly314 of the beta subunit of the Escherichia coli pyridine nucleotide transhydrogenase abolishes activity and affects the NADP(H)-induced conformational change.
European journal of biochemistry | 1992-07-15 | PMID 1633824
Ahmad S, Glavas N A, Bragg P D
On the functional role of the Tyr-639 residue of bacteriophage T7 RNA polymerase.
FEBS letters | 1992-07-20 | PMID 1633867
Rechinsky V O, Kostyuk D A, Tunitskaya V L and 1 more
Independence of the carotene and sterol pathways of Phycomyces.
FEBS letters | 1992-07-20 | PMID 1633878
Bejarano E R, Cerdá-Olmedo E
Assessing the underlying pattern of human germline mutations: lessons from the factor IX gene.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 1992-07-01 | PMID 1634040
Sommer S S
Dynamic changes in HIV-1 quasispecies from azidothymidine (AZT)-treated patients.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 1992-07-01 | PMID 1634047
Wahlberg J, Albert J, Lundeberg J and 3 more
Two-locus mitochondrial and nuclear gene models for mitochondrial disorders.
Genetic epidemiology | 1992-01-01 | PMID 1634105
Bu X, Yang H Y, Shohat M and 1 more
Detection of linkage under heterogeneity: comparison of the two-locus vs. admixture models.
Genetic epidemiology | 1992-01-01 | PMID 1634107
Goldin L R
Sensitivity of transmission probabilities to paternity exclusion in segregation analysis.
Genetic epidemiology | 1992-01-01 | PMID 1634108
Bonaïti-Pellié C, Poisson N, Bechtel Y and 1 more
Functional analysis of two long terminal repeats from the HTLV-I retrovirus.
Gene | 1992-07-15 | PMID 1634112
Gonzalez-Dunia D, Chirinian-Syan S, Brahic M and 1 more
Gibbon and marmoset c-myc nucleotide sequences.
Gene | 1992-07-15 | PMID 1634119
Eladari M E, Mohammad-Ali K, Argaut C and 1 more
Sex determination and sex reversal: genotype, phenotype, dogma and semantics.
Human genetics | 1992-07-01 | PMID 1634224
Mittwoch U
Genes: SRY
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen gene.
Human genetics | 1992-07-01 | PMID 1634225
Mottes M, Sangalli A, Valli M and 5 more
Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7).
Human genetics | 1992-07-01 | PMID 1634227
Marchetti G, Patracchini P, Gemmati D and 6 more
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene.
Human genetics | 1992-07-01 | PMID 1634228
Munier F, Spence M A, Pescia G and 5 more
Characterization of a new mutation (R292G) and a deletion at the human uroporphyrinogen decarboxylase locus in two patients with hepatoerythropoietic porphyria.
Human genetics | 1992-07-01 | PMID 1634232
de Verneuil H, Bourgeois F, de Rooij F and 4 more
Genes: UROD
Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p.
Human genetics | 1992-07-01 | PMID 1634233
Izquierdo L, Porteous M, Paramo P G and 1 more
Absence of mutations in the promoter region of the low density lipoprotein receptor gene in a large number of familial hypercholesterolaemia patients as revealed by denaturing gradient gel electrophoresis.
Human genetics | 1992-07-01 | PMID 1634234
Top B, Uitterlinden A G, van der Zee A and 4 more
Genes: LDLR
Novel promoter and splice junction defects add to the genetic, clinical or geographic heterogeneity of beta-thalassaemia in the Portuguese population.
Human genetics | 1992-07-01 | PMID 1634236
Faustino P, Osório-Almeida L, Barbot J and 6 more
A novel mutation in the beta-protein coding region of the amyloid beta-protein precursor (APP) gene.
Human genetics | 1992-07-01 | PMID 1634237
Balbín M, Abrahamson M, Gustafson L and 3 more
Genes: APP
A single nucleotide substitution in the phosphoglycerate kinase (PGK)-1 gene occurred after the separation of PGK-1 and PGK-2.
Human genetics | 1992-07-01 | PMID 1634238
Fujii H, Kanno H, Hirono A and 1 more
A new alpha chain variant, Hb Turriff [alpha 99(G6)Lys----Glu]: the interference of abnormal hemoglobins in Hb A1c determination.
Hemoglobin | 1992-01-01 | PMID 1634357
Langdown J V, Davidson R J, Williamson D
The unstable Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser observed in an Indian child; identification by HPLC and by sequence analysis of amplified DNA.
Hemoglobin | 1992-01-01 | PMID 1634359
Cunningham T A, Baker F, Kobrinsky N L and 4 more
The nondeletional types of Hb H disease in Guangxi.
Hemoglobin | 1992-01-01 | PMID 1634361
Wen X J, Liang S, Jin Q and 1 more
Types of thalassemia among patients attending a large university clinic in Kuala Lumpur, Malaysia.
Hemoglobin | 1992-01-01 | PMID 1634362
George E, Li H J, Fei Y J and 7 more
Genes: SEA
The effect of body condition, live weight, breed, age, calf performance, and calving date on reproductive performance of spring-calving beef cows.
Journal of animal science | 1992-06-01 | PMID 1634389
Osoro K, Wright I A
Genotype and treatment biases in estimation of carcass lean of swine.
Journal of animal science | 1992-06-01 | PMID 1634395
Gu Y, Schinckel A P, Martin T G and 3 more
Growth, development, and carcass composition in five genotypes of swine.
Journal of animal science | 1992-06-01 | PMID 1634396
Gu Y, Schinckel A P, Martin T G
A bioeconomic simulation model for a hierarchical swine breeding structure.
Journal of animal science | 1992-06-01 | PMID 1634400
Faust M A, Tess M W, Robison O W
Performance of Bos indicus-influenced bulls in serving capacity tests and multiple-sire breeding groups.
Journal of animal science | 1992-06-01 | PMID 1634403
Carpenter B B, Forrest D W, Sprott L R and 5 more
Development and characterization of breast carcinoma cell lines as in vitro and in vivo models for breast cancer diagnosis and therapy.
In vitro cellular & developmental biology : journal of the Tissue Culture Association | 1992-06-01 | PMID 1634439
Ceriani R L, Peterson J A, Blank E W and 2 more
Transforming growth factor-beta: its effect on phenotype reexpression by dedifferentiated chondrocytes in the presence and absence of osteogenin.
In vitro cellular & developmental biology : journal of the Tissue Culture Association | 1992-06-01 | PMID 1634443
Harrison E T, Luyten F P, Reddi A H
Thymidine kinase-deficient mutants of Aedes albopictus mosquito cells.
In vitro cellular & developmental biology : journal of the Tissue Culture Association | 1992-06-01 | PMID 1634444
Mazzacano C A, Fallon A M
Relation between the insulin receptor number in cells, autophosphorylation and insulin-stimulated Ras.GTP formation.
The Journal of biological chemistry | 1992-07-25 | PMID 1634512
Osterop A P, Medema R H, Bos J L and 5 more
Minimal essential domains specifying toxicity of the light chains of tetanus toxin and botulinum neurotoxin type A.
The Journal of biological chemistry | 1992-07-25 | PMID 1634516
Kurazono H, Mochida S, Binz T and 7 more
Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient.
The Journal of clinical investigation | 1992-07-01 | PMID 1634606
Ritter J K, Yeatman M T, Ferreira P and 1 more
Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia.
The Journal of clinical investigation | 1992-07-01 | PMID 1634607
Kure S, Takayanagi M, Narisawa K and 2 more
The familial hypercholesterolemia (FH)-North Karelia mutation of the low density lipoprotein receptor gene deletes seven nucleotides of exon 6 and is a common cause of FH in Finland.
The Journal of clinical investigation | 1992-07-01 | PMID 1634609
Koivisto U M, Turtola H, Aalto-Setälä K and 5 more
Molecular basis of fibrinogen Naples associated with defective thrombin binding and thrombophilia. Homozygous substitution of B beta 68 Ala----Thr.
The Journal of clinical investigation | 1992-07-01 | PMID 1634610
Koopman J, Haverkate F, Lord S T and 2 more
Expression of a missense mutation in the messenger RNA for beta-myosin heavy chain in myocardial tissue in hypertrophic cardiomyopathy.
The Journal of clinical investigation | 1992-07-01 | PMID 1634614
Perryman M B, Yu Q T, Marian A J and 5 more
MHC class II deletion mutant expresses normal levels of transgene encoded class II molecules that have abnormal conformation and impaired antigen presentation ability.
Journal of immunology (Baltimore, Md. : 1950) | 1992-08-01 | PMID 1634767
Ceman S, Rudersdorf R, Long E O and 1 more
Genes: TAP1
Comparison of the major outer membrane protein variant sequence regions of B/Ba isolates: a molecular epidemiologic approach to Chlamydia trachomatis infections.
The Journal of infectious diseases | 1992-08-01 | PMID 1634810
Dean D, Schachter J, Dawson C R and 1 more
The analysis of new short-period circadian rhythm mutants suggests features of D. melanogaster period gene function.
Journal of neurogenetics | 1992-05-01 | PMID 1634995
Rutila J E, Edery I, Hall J C and 1 more
Additive gene actions on the fiber number in the anterior optic tract of Drosophila melanogaster.
Journal of neurogenetics | 1992-05-01 | PMID 1634996
Houbé B, Fischbach K F
Genetic and age related models of neurodegeneration in mice: dystrophic axons.
Journal of neurogenetics | 1992-05-01 | PMID 1634998
Bronson R T, Sweet H O, Spencer C A and 1 more
Mutations on the second chromosome affecting the Drosophila eye.
Journal of neurogenetics | 1992-05-01 | PMID 1634999
Baker N E, Moses K, Nakahara D and 3 more
Parasites as probes for biodiversity.
The Journal of parasitology | 1992-08-01 | PMID 1635018
Gardner S L, Campbell M L
Allozyme analysis of Trichinella isolates from various host species and geographical regions.
The Journal of parasitology | 1992-08-01 | PMID 1635022
La Rosa G, Pozio E, Rossi P and 1 more
Serologic response of the opossum Didelphis virginiana to a temperature-sensitive mutant (ts-4) of Toxoplasma gondii.
The Journal of parasitology | 1992-08-01 | PMID 1635036
Patton S, Funk R S
High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.
Japanese journal of ophthalmology | 1992-01-01 | PMID 1635296
Nakamura M, Ara F, Yamada M and 7 more
A case of testicular feminization syndrome with bulimia nervosa.
The Japanese journal of psychiatry and neurology | 1992-03-01 | PMID 1635303
Hashiramoto K, Yoshida T, Sakane N and 3 more
Use of batch and fed-batch fermentation for studies on the variation of glutathione content and its influence on the genotoxicity of methyl-nitro-nitrosoguanidine in yeast.
Mutagenesis | 1992-01-01 | PMID 1635452
Berthe-Corti L, Hulsch R, Nevries U and 1 more
A shuttle vector system for the investigation of immunoglobulin gene hypermutation: absence of enhanced mutability in intermediate B cell lines.
Molecular immunology | 2000-01-01 | PMID 1635557
Johnston J M, Yu M T, Carroll W L
Deficient corpus callosum in hybrids between ddN and three other abnormal mouse strains.
Neuroscience letters | 1992-02-17 | PMID 1635672
Wahlsten D, Ozaki H S, Livy D
[Genetic traits in the area of Bodrogköz].
Orvosi hetilap | 1992-07-26 | PMID 1635773
Béres J, Tauszik T, Horányi M and 4 more
Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome.
Pediatric research | 1992-06-01 | PMID 1635816
Fischel-Ghodsian N, Bohlman M C, Prezant T R and 3 more
The frequency of revertants in mdx mouse genetic models for Duchenne muscular dystrophy.
Pediatric research | 1992-07-01 | PMID 1635838
Danko I, Chapman V, Wolff J A
[Detection of mutated ras-oncogene in pancreatic cancers: improved diagnostic possibilities using molecular biology techniques?].
Zeitschrift fur Gastroenterologie | 1992-06-01 | PMID 1636278
Herzig K H, Schäffer M, Rosewicz S and 1 more
Immunophenotypic analysis of infiltrating leukocytes and microglia in an experimental rat glioma.
Acta neuropathologica | 1992-01-01 | PMID 1636377
Morioka T, Baba T, Black K L and 1 more
Use of rosy mutant strains of Drosophila melanogaster to probe the structure and function of xanthine dehydrogenase.
The Biochemical journal | 1992-07-15 | PMID 1637342
Hughes R K, Doyle W A, Chovnick A and 3 more
The signal for Golgi retention of bovine beta 1,4-galactosyltransferase is in the transmembrane domain.
The Journal of biological chemistry | 1992-02-25 | PMID 1637374
Teasdale R D, D'Agostaro G, Gleeson P A
[DNA polymorphism in a Brazilian population: relationship to allele frequencies in France].
Revue francaise de transfusion et d'hemobiologie : bulletin de la Societe nationale de transfusion sanguine | 1992-03-01 | PMID 1637421
Soares J A, Van Huffel V, Salmon D and 2 more
[Etiologies of atopic dermatitis].
Allergie et immunologie | 1992-05-01 | PMID 1637487
Le Sellin J
Molecular modeling to predict the structural and biological effects of mutations in a highly conserved histone mRNA loop sequence.
Journal of biomolecular structure & dynamics | 1992-06-01 | PMID 1637506
Gabb H A, Harris M E, Pandey N B and 2 more
The assessment of in vivo somatic mutations in survivors of childhood malignancy.
British journal of cancer | 1992-07-01 | PMID 1637665
Hewitt M, Mott M G
Patterns of risk of hereditary retinoblastoma and applications to genetic counselling.
British journal of cancer | 1992-07-01 | PMID 1637670
Draper G J, Sanders B M, Brownbill P A and 1 more
Relationship of myc protein expression to the phenotype and to the growth potential of HOC-7 ovarian cancer cells.
British journal of cancer | 1992-07-01 | PMID 1637683
Somay C, Grunt T W, Mannhalter C and 1 more
Transcriptional expression of a testis-specific variant of the mouse pyruvate dehydrogenase E1 alpha subunit.
Biology of reproduction | 1992-07-01 | PMID 1637947
Iannello R C, Dahl H H
Performing the exact test of Hardy-Weinberg proportion for multiple alleles.
Biometrics | 1992-06-01 | PMID 1637966
Guo S W, Thompson E A
Absence of immunoglobulin variable region hypermutation in a large cell lymphoma after in vivo and in vitro propagation.
Blood | 1992-08-01 | PMID 1638025
Stiernholm N, Kuzniar B, Berinstein N L
Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site.
Blood | 1992-08-01 | PMID 1638030
Alloisio N, Wilmotte R, Morlé L and 7 more
Genes: GAA
Confirmation of the influence of a chromosome 7 locus on susceptibility to audiogenic seizures.
Mammalian genome : official journal of the International Mammalian Genome Society | 1992-01-01 | PMID 1638084
Neumann P E, Collins R L
Evidence for a pseudoautosomal locus for schizophrenia. I: A replication study using phenotype analysis.
The British journal of psychiatry : the journal of mental science | 1992-07-01 | PMID 1638329
Gorwood P, Leboyer M, d'Amato T and 5 more
Evidence for a pseudoautosomal locus for schizophrenia. II: Replication of a non-random segregation of alleles at the DXYS14 locus.
The British journal of psychiatry : the journal of mental science | 1992-07-01 | PMID 1638330
d'Amato T, Campion D, Gorwood P and 7 more
No evidence for a pseudoautosomal locus for schizophrenia. Linkage analysis of multiply affected families.
The British journal of psychiatry : the journal of mental science | 1992-07-01 | PMID 1638331
Asherson P, Parfitt E, Sargeant M and 7 more
Postnatal development of the locus coeruleus in trisomy 19 mice: morphological and morphometric study.
Brain research bulletin | 1992-06-01 | PMID 1638419
Lorke D E, Klimaschewski L P
Abnormal structure and expression of the p53 gene in human ovarian carcinoma cell lines.
Cancer research | 1992-08-01 | PMID 1638534
Yaginuma Y, Westphal H
Expression of platelet-derived growth factor-independent phenotypes in BALB/c 3T3 cell variant with high susceptibility to chemically or physically induced neoplastic cell transformation: dissociation from activation of protein kinase C.
Cancer research | 1992-08-01 | PMID 1638537
Tatsuka M, Owada M K, Mitsui H