Different PrlA proteins increase the efficiency of periplasmic production of human interleukin-6 in Escherichia coli.
Journal of biotechnology | 1996-08-20 | PMID 8879175
Pérez-Pérez J, Barbero J L, Márquez G 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 769 of 10600
Human SP-A locus: allele frequencies and linkage disequilibrium between the two surfactant protein A genes.
American journal of respiratory cell and molecular biology | 1996-10-01 | PMID 8879183
Floros J, DiAngelo S, Koptides M and 6 more
Reversal of lung lesions in transgenic transforming growth factor alpha mice by expression of mutant epidermal growth factor receptor.
American journal of respiratory cell and molecular biology | 1996-10-01 | PMID 8879184
Hardie W D, Kerlakian C B, Bruno M D and 5 more
Genes: EGF
Conservation of the lipooligosaccharide synthesis locus lgt among strains of Neisseria gonorrhoeae: requirement for lgtE in synthesis of the 2C7 epitope and of the beta chain of strain 15253.
The Journal of experimental medicine | 1996-10-01 | PMID 8879194
Erwin A L, Haynes P A, Rice P A and 1 more
Disturbed interaction of p21-rac with mutated p67-phox causes chronic granulomatous disease.
The Journal of experimental medicine | 1996-10-01 | PMID 8879195
Leusen J H, de Klein A, Hilarius P M and 7 more
TCR binding differs for a bacterial superantigen (SEE) and a viral superantigen (Mtv-9).
The Journal of experimental medicine | 1996-10-01 | PMID 8879218
Liao L, Marinescu A, Molano A and 5 more
Genes: SAG
Inactivation of the IL-6 gene prevents development of multicentric Castleman's disease in C/EBP beta-deficient mice.
The Journal of experimental medicine | 1996-10-01 | PMID 8879230
Screpanti I, Musiani P, Bellavia D and 7 more
Genes: EBP
Mild RIP-an alternative method for in vivo mutagenesis of the albino-3 gene in Neurospora crassa.
Molecular & general genetics : MGG | 1996-09-25 | PMID 8879235
Barbato C, Calissano M, Pickford A and 3 more
Altered expression of nuclear genes encoding chloroplast polypeptides in non-photosynthetic mutants of Chlamydomonas reinhardtii: evidence for post-transcriptional regulation.
Molecular & general genetics : MGG | 1996-09-25 | PMID 8879236
Hahn D, Bennoun P, Kück U
Development of gene transfer methods for Rubrivivax gelatinosus S1: construction, characterization and complementation of a puf operon deletion strain.
Molecular & general genetics : MGG | 1996-09-25 | PMID 8879238
Ouchane S, Picaud M, Reiss-Husson F and 2 more
Molecular and functional characterization of Slide, an Ac-like autonomous transposable element from tobacco.
Molecular & general genetics : MGG | 1996-09-25 | PMID 8879239
Grappin P, Audeon C, Chupeau M C and 1 more
Transcription-induced deletions in plasmid vectors: M13 DNA replication as a source of instability.
Molecular & general genetics : MGG | 1996-09-25 | PMID 8879240
Vilette D, Ehrlich S D, Michel B
SOM 1, a small new gene required for mitochondrial inner membrane peptidase function in Saccharomyces cerevisiae.
Molecular & general genetics : MGG | 1996-09-25 | PMID 8879245
Esser K, Pratje E, Michaelis G
Mutants that show increased sensitivity to hydrogen peroxide reveal an important role for the pentose phosphate pathway in protection of yeast against oxidative stress.
Molecular & general genetics : MGG | 1996-09-25 | PMID 8879247
Juhnke H, Krems B, Kötter P and 1 more
Enhanced cell permeability increases the sensitivity of a yeast test for mutagens.
Mutation research | 1996-09-13 | PMID 8879265
Staleva L, Waltscheva L, Golovinsky E and 1 more
Simultaneous immunoselection in vitro for H-Y or H-2D antigen-loss variants of a mouse-derived B cell line.
Mutation research | 1996-09-13 | PMID 8879266
King T R
The defect in the AT-like hamster cell mutants is complemented by mouse chromosome 9 but not by any of the human chromosomes.
Mutation research | 1996-10-18 | PMID 8879275
Jongmans W, Verhaegh G W, Jaspers N G and 10 more
Genes: ATM
Thiamine deficiency as predisposition to, and consequence of, increased alcohol consumption.
Alcohol and alcoholism (Oxford, Oxfordshire) | 1996-07-01 | PMID 8879292
Zimatkin S M, Zimatkina T I
Quantitative effects of the apolipoprotein E polymorphism in a biracial sample of 9-10-year-old girls.
Atherosclerosis | 1996-09-27 | PMID 8879432
Sanghera D K, Ferrell R E, Aston C E and 3 more
Genes: APOE, CAD
Heterozygous familial hypercholesterolemia in children: low-density lipoprotein receptor mutational analysis and variation in the expression of plasma lipoprotein-lipid concentrations.
Atherosclerosis | 1996-09-27 | PMID 8879444
Torres A L, Moorjani S, Vohl M C and 5 more
Genes: LDLR
X chromosome and infantile autism.
Biological psychiatry | 1996-09-15 | PMID 8879465
Petit E, Hérault J, Raynaud M and 5 more
Refinement of the differentiated phenotype of the spermatogenic cell line GC-2spd(ts)
Biology of reproduction | 1996-10-01 | PMID 8879510
Wolkowicz M J, Coonrod S A, Reddi P P and 4 more
Molecular diagnosis, detection of drug resistance and epidemiology of tuberculosis.
British journal of hospital medicine | 2000-01-01 | PMID 8879698
Drobniewski F A, Pozniak A L
alpha-Glutathione S-transferase levels in chronic hepatitis C infection and the effect of alpha-interferon therapy.
Clinica chimica acta; international journal of clinical chemistry | 1996-09-30 | PMID 8879847
Thorburn D, Bird G L, Spence E and 2 more
Effective administration methods and dosages of interferon therapy for chronic hepatitis C.
Clinical therapeutics | 2000-01-01 | PMID 8879895
Nomura H, Kimura Y, Tada H and 6 more
Absence of the Gly40-ser mutation in the glucagon receptor gene in Japanese subjects with NIDDM.
Diabetes research and clinical practice | 1996-07-01 | PMID 8879960
Ogata M, Iwasaki N, Ohgawara H and 2 more
Role of Pit-1 in the gene expression of growth hormone, prolactin, and thyrotropin.
Endocrinology and metabolism clinics of North America | 1996-09-01 | PMID 8879985
Cohen L E, Wondisford F E, Radovick S
Molecular genetic basis of the human chondrodysplasias.
Endocrinology and metabolism clinics of North America | 1996-09-01 | PMID 8879993
Horton W A
Use of polymorphic short and clustered coding-region microsatellites to distinguish strains of Candida albicans.
FEMS immunology and medical microbiology | 1996-09-01 | PMID 8880131
Field D, Eggert L, Metzgar D and 2 more
Genes: CCN1
A novel mutation in the MITF gene causes Waardenburg syndrome type 2.
Genetic analysis : biomolecular engineering | 1996-07-01 | PMID 8880147
Lautenschlager N T, Milunsky A, DeStefano A and 2 more
Genes: MITF
Phenotypic patterns of distortion product otoacoustic emission in inbred and F1 hybrid hearing mouse strains.
Hearing research | 1996-09-01 | PMID 8880177
Huang J M, Money M K, Berlin C I and 1 more
Epidemiologic typing systems.
Infection control and hospital epidemiology | 1996-09-01 | PMID 8880233
Maslow J, Mulligan M E
Pathways of Listeria monocytogenes contamination in the meat processing industry.
International journal of food microbiology | 1996-08-01 | PMID 8880305
Nesbakken T, Kapperud G, Caugant D A
Multilocus enzyme electrophoretic (MEE) analysis of Australian isolates of Salmonella enteritidis.
International journal of food microbiology | 1996-08-01 | PMID 8880314
Cox J M, Story L, Bowles R and 1 more
The sub-typing of Listeria monocytogenes isolates from food, environments surrounding food manufacturing sites, and clinical samples in New Zealand using multilocus enzyme electrophoresis.
International journal of food microbiology | 1996-08-01 | PMID 8880322
Flint S H, Kells N J
Effects of selection for scrotal circumference in Limousin bulls on reproductive and growth traits of progeny.
Journal of animal science | 1996-09-01 | PMID 8880405
Moser D W, Bertrand J K, Benyshek L L and 2 more
Genetic parameters for growth and carcass traits in Japanese brown cattle estimated from field records.
Journal of animal science | 1996-09-01 | PMID 8880413
Hirooka H, Groen A F, Matsumoto M
Follicular growth and maturation in hyperprolific and large white sows.
Journal of animal science | 1996-09-01 | PMID 8880427
Driancourt M A, Terqui M
Genotyping hepatitis C virus isolates from Spain, Brazil, China, and Macau by a simplified PCR method.
Journal of clinical microbiology | 1996-10-01 | PMID 8880482
Holland P V, Barrera J M, Ercilla M G and 6 more
Genotypic characterization of sequential Aspergillus fumigatus isolates from patients with cystic fibrosis.
Journal of clinical microbiology | 1996-10-01 | PMID 8880528
Verweij P E, Meis J F, Sarfati J and 3 more
Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome.
Journal of medical genetics | 1996-09-01 | PMID 8880570
Froggatt N J, Brassett C, Koch D J and 4 more
Genes: MSH2, MLH1, PMS1, PMS2
Clinical and genetic heterogeneity of hypochondroplasia.
Journal of medical genetics | 1996-09-01 | PMID 8880574
Rousseau F, Bonaventure J, Legeai-Mallet L and 5 more
Genes: FGFR3
Genetic heterogeneity of Usher syndrome type II in a Dutch population.
Journal of medical genetics | 1996-09-01 | PMID 8880575
Pieke-Dahl S, van Aarem A, Dobin A and 2 more
A clinical severity grading scale for Marfan syndrome.
Journal of medical genetics | 1996-09-01 | PMID 8880576
Gray J R, Davies S J
Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome.
Journal of medical genetics | 1996-09-01 | PMID 8880577
Wang M, Kishnani P, Decker-Phillips M and 3 more
Genes: FBN1
Rett syndrome, classical and atypical: genealogical support for common origin.
Journal of medical genetics | 1996-09-01 | PMID 8880578
Akesson H O, Hagberg B, Wahlström J
A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalities.
Journal of medical genetics | 1996-09-01 | PMID 8880579
Telvi L, Ion A, Carel J C and 7 more
Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.
Journal of medical genetics | 1996-09-01 | PMID 8880580
Pivnick E K, Velagaleti G V, Wilroy R S and 4 more
Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome).
Journal of medical genetics | 1996-09-01 | PMID 8880581
Morrison P J, Nevin N C
Genes: RET
Chromosome 3p23 break with ring formation and translocation of displaced 3p23-->pter segment to 6pter.
Journal of medical genetics | 1996-09-01 | PMID 8880584
Yip M Y, MacKenzie H, Kovacic A and 1 more
Non-expression of a common mutation in the 21-hydroxylase gene: implications for prenatal diagnosis and carrier testing.
Journal of medical genetics | 1996-09-01 | PMID 8880587
Rumsby G, Massoud A F, Avey C and 1 more
Evidence to exclude SOX9 as a candidate gene for XY sex reversal without skeletal malformation.
Journal of medical genetics | 1996-09-01 | PMID 8880588
Kwok C, Goodfellow P N, Hawkins J R
Genes: SOX9
The GTP-cyclohydrolase I gene in atypical parkinsonian patients: a clinico-genetic study.
Journal of the neurological sciences | 1996-09-15 | PMID 8880688
Bandmann O, Daniel S, Marsden C D and 2 more
Effect of cerebrospinal fluid from normal and Alzheimer's patients with different apolipoprotein E phenotypes on in vitro aggregation of amyloid beta-protein.
Journal of the neurological sciences | 1996-09-15 | PMID 8880693
Chauhan A, Pirttilä T, Mehta P and 2 more
A dynamic bundle of four adjacent hydrophobic segments in the denatured state of staphylococcal nuclease.
Protein science : a publication of the Protein Society | 1996-09-01 | PMID 8880914
Wang Y, Shortle D
Coupling between trans/cis proline isomerization and protein stability in staphylococcal nuclease.
Protein science : a publication of the Protein Society | 1996-09-01 | PMID 8880915
Truckses D M, Somoza J R, Prehoda K E and 2 more
Crystallization and preliminary X-ray diffraction studies of the Lb proteinase from foot-and-mouth disease virus.
Protein science : a publication of the Protein Society | 1996-09-01 | PMID 8880919
Guarné A, Kirchweger R, Verdaguer N and 4 more
Refined structures of bobwhite quail lysozyme uncomplexed and complexed with the HyHEL-5 Fab fragment.
Proteins | 1996-09-01 | PMID 8880929
Chacko S, Silverton E W, Smith-Gill S J and 8 more
Structural stability of disulfide mutants of basic pancreatic trypsin inhibitor: a molecular dynamics study.
Proteins | 1996-09-01 | PMID 8880930
Schiffer C A, van Gunsteren W F
A database of mutants and effects of site-directed mutagenesis experiments on G protein-coupled receptors.
Proteins | 1996-09-01 | PMID 8880932
Kristiansen K, Dahl S G, Edvardsen O
Genes: GRAP
Requirements for perpendicular helix pairing.
Proteins | 1996-09-01 | PMID 8880933
Beasley J R, Pielak G J
Cloning and chromosomal mapping of the mouse DNA-dependent protein kinase gene.
Immunogenetics | 1996-01-01 | PMID 8881030
Hamatani K, Matsuda Y, Araki R and 2 more
A roadmap for HLA-A, HLA-B, and HLA-C peptide binding specificities.
Immunogenetics | 1996-01-01 | PMID 8881033
Chelvanayagam G
Recognition by human Vgamma9/Vdelta2 T cells of melanoma cells upon fusion with Daudi cells.
Immunogenetics | 1996-01-01 | PMID 8881034
Viale O, van der Bruggen P, Meuer E and 5 more
Genes: TNF
Enhancers of hypermutation.
Immunogenetics | 1996-01-01 | PMID 8881038
Bachl J, Wabl M
[Pituitary adenoma: mechanisms of endocrine oncogenesis].
La Revue du praticien | 1996-06-15 | PMID 8881160
Bertherat J, Bertagna X
Genes: GHRH
Is there a human [psi]?
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie | 1996-06-01 | PMID 8881282
Jean-Jean O, Le Goff X, Philippe M
[Mutations of ACTH receptor gene and familial syndrome of glucocorticoid deficiency].
Annales d'endocrinologie | 1996-01-01 | PMID 8881288
Naville D, Barjhoux L, Jaillard C and 6 more
[Contribution of cytology and lymphocyte phenotyping in the biological diagnosis in infectious mononucleosis due to Epstein-Barr virus].
Annales de biologie clinique | 1996-01-01 | PMID 8881359
Pierard I, Dupret P, François P
[Genetics of Alzheimer's disease].
La Revue de medecine interne | 1996-01-01 | PMID 8881379
Hannequin D, Campion D, Brice A and 4 more
Genes: APP
Molecular pathogenesis of peripheral neuropathy.
Revue neurologique | 1996-05-01 | PMID 8881422
Trapp B D, Haney C, Yin X
Anastomosis between both hypoglossal nerves in a 30 mm human embryo.
Anatomy and embryology | 1996-03-01 | PMID 8881470
Gonzalez-Compta X, Domenech-Mateu J M
[Genetics of hypertrophic cardiomyopathies: what are the clinical perspectives?].
Archives des maladies du coeur et des vaisseaux | 1996-07-01 | PMID 8881500
Komajda M
COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular rupture.
The British journal of dermatology | 1996-08-01 | PMID 8881656
Pope F M, Narcisi P, Nicholls A C and 3 more
Analysis of peptide-binding motifs for two disease associated HLA-DR13 alleles using an M13 phage display library.
Immunology | 1996-08-01 | PMID 8881746
Davenport M P, Quinn C L, Valsasnini P and 3 more
Structural mutations in the constant region of the T-cell antigen receptor (TCR)beta chain and their effect on TCR alpha and beta chain interaction.
Immunology | 1996-08-01 | PMID 8881752
Li Z G, Wu W P, Manolios N
Sequence analysis of rearranged IgVH genes from microdissected human Peyer's patch marginal zone B cells.
Immunology | 1996-08-01 | PMID 8881766
Dunn-Walters D K, Isaacson P G, Spencer J
Association of HLA class II genes with susceptibility to Crohn's disease.
Gut | 1996-07-01 | PMID 8881812
Danzé P M, Colombel J F, Jacquot S and 8 more
Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood.
Journal of child neurology | 1996-03-01 | PMID 8881991
Ouvrier R
Genes: PMP22
Genetics of osteoarthritis.
Annals of the rheumatic diseases | 1996-09-01 | PMID 8882145
Cicuttini F M, Spector T D
Retroviral vaccines: challenges for the developing world.
AIDS research and human retroviruses | 1996-03-20 | PMID 8882311
Essex M
Anti-HBe titre in patients infected with wild-type and e-minus variant of hepatitis B virus.
Research in virology | 2000-01-01 | PMID 8882339
Tu H, Li P Y, Wen Y M
Mild phenotype associated with inv dup 8 (q21.2-q22.3) of maternal origin.
American journal of medical genetics | 1996-03-15 | PMID 8882396
Tupler R, Pagliano E, Barbierato L and 3 more
Definition of an HLA-A3-like supermotif demonstrates the overlapping peptide-binding repertoires of common HLA molecules.
Human immunology | 1996-02-01 | PMID 8882405
Sidney J, Grey H M, Southwood S and 6 more
Genetic polymorphisms of the major histocompatibility complex-encoded antigen-processing genes TAP and LMP in sarcoidosis.
Human immunology | 1996-02-01 | PMID 8882407
Ishihara M, Ohno S, Mizuki N and 5 more
Genes: TAP1, TAP2
Discrimination of HLA-B27 alleles by group-specific amplification followed by solid-phase sequencing.
Human immunology | 1996-02-01 | PMID 8882409
Blasczyk R, Weber M, van Lessen A and 3 more
Description of a novel HLA-B35 (B*3514) allele found in a Mexican family of Nahua Aztec descent.
Human immunology | 1996-02-01 | PMID 8882414
Vargas-Alarcon G, Martinez-Laso J, Granados J and 5 more
T-cell receptor BV6S1 null alleles and HLA-DR1 haplotypes in polyarticular outcome juvenile rheumatoid arthritis.
Human immunology | 1996-02-01 | PMID 8882415
Grom A A, von Knorre C, Murray K J and 3 more
Bioactive steroidal alkaloids from Solanum umbelliferum.
Journal of natural products | 1996-03-01 | PMID 8882430
Kim Y C, Che Q M, Gunatilaka A A and 1 more
Autoregulation of mariner transposase activity by overproduction and dominant-negative complementation.
Molecular biology and evolution | 1996-04-01 | PMID 8882498
Lohe A R, Hartl D L
Epilepsy etiology with special emphasis on immune dysfunction and neurovirology.
Brain & development | 1995-01-01 | PMID 8882574
Eeg-Olofsson O, Bergström T, Osterland C K and 2 more
Molecular neurobiological approach to the pathogenesis of epilepsy: a preliminary study.
Brain & development | 1995-01-01 | PMID 8882576
Xi-Ru W, Zhao-Hui W, Wai-Song S and 4 more
Genes: CCK
The role of MCM/P1 proteins in the licensing of DNA replication.
Trends in biochemical sciences | 1996-03-01 | PMID 8882583
Chong J P, Thömmes P, Blow J J
Genes: RLF
Ecdysone and insect immunity: the maturation of the inducibility of the diptericin gene in Drosophila larvae.
Insect biochemistry and molecular biology | 1996-02-01 | PMID 8882658
Meister M, Richards G
Seasonal variation in the concentration of vitamins A and E in the blood plasma of fat-tailed sheep.
Acta veterinaria Hungarica | 1995-01-01 | PMID 8882743
Asadian A, Mirhadi S A, Mézes M
Variations in the yield, composition and somatic cell count of ewe's milk during lactation.
Acta veterinaria Hungarica | 1995-01-01 | PMID 8882744
Bedö S, Nikodémusz E, Gundel K
Delineation of the Marfan phenotype associated with mutations in exons 23-32 of the FBN1 gene.
American journal of medical genetics | 1996-03-29 | PMID 8882780
Putnam E A, Cho M, Zinn A B and 3 more
Genes: FBN1
Stage-specific and cell type-specific aspects of genomic imprinting effects in mammals.
Differentiation; research in biological diversity | 1995-12-01 | PMID 8882812
Latham K E
N-type inactivation and the S4-S5 region of the Shaker K+ channel.
The Journal of general physiology | 1996-09-01 | PMID 8882863
Holmgren M, Jurman M E, Yellen G
Sequence variations in the Fanconi anaemia gene, FAC: pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant.
Human genetics | 1996-11-01 | PMID 8882868
Lo ten Foe J R, Barel M T, Thuss P and 3 more