| academic journal | Q737498 |
| scientific journal | Q5633421 |
| P495 | country of origin | United Kingdom | Q145 |
| P407 | language of work or name | English | Q1860 |
| P1476 | title | Molecular Biology & Medicine |
| Q72403207 | A DNA polymorphism adjacent to the human apolipoprotein CII gene |
| Q36599422 | A cDNA clone encoding a product of activated human T lymphocytes |
| Q28118126 | A complementary DNA sequence that predicts a human pancreatic amylase primary structure consistent with the electrophoretic mobility of the common isozyme, Amy2 A |
| Q50561165 | A cysteine for glycine substitution at position 1017 in an alpha 1(I) chain of type I collagen in a patient with mild dominantly inherited osteogenesis imperfecta. |
| Q72415696 | A frequent restriction fragment length polymorphism in the human metallothionein-II processed gene region is evolutionarily conserved |
| Q69018976 | A melanocyte-specific complementary DNA clone whose expression is inducible by melanotropin and isobutylmethyl xanthine |
| Q45887596 | A somatic mosaic for haemophilia A detected at the DNA level. |
| Q70964520 | A test of the role of two oncogenes in inherited predisposition to colon cancer |
| Q45887835 | Accuracy and limitations of pulsed field gel electrophoresis in sizing partial deletions of the factor VIII gene |
| Q36430275 | Activated (Ia+) T-cells and their subsets in Graves' disease and Hashimoto's thyroiditis using dual laser flow microfluorocytometric analysis. |
| Q43886981 | Activity of a metallothionein-transthyretin fusion gene in transgenic mice. Possible effect of plasmid sequences on tissue-specific expression |
| Q28244727 | Additional mutations in argininosuccinate synthetase causing citrullinemia |
| Q38262093 | Adenovirus region E3 proteins that prevent cytolysis by cytotoxic T cells and tumor necrosis factor. |
| Q37479179 | Alcaptonuria and ochronotic arthritis |
| Q38324128 | Allelic exclusion and lymphocyte development. Lessons from transgenic mice |
| Q48716391 | Allelic heterogeneity in adult hereditary fructose intolerance. Detection of structural mutations in the aldolase B molecule. |
| Q72415699 | Allelic variation and linkage properties of a highly polymorphic restriction fragment in humans |
| Q72403210 | An HLA-B locus probe clarifies endonuclease polymorphism of major histocompatibility complex class I genes |
| Q41591845 | An approach to the cloning of cell surface protein genes. Selection by cell sorting of mouse L-cells that express HLA or 4F2 antigens after transformation with total human DNA. |
| Q52245500 | An in situ transgenic enzyme marker to monitor migration of cells in the mid-gestation mouse embryo. Somite contribution to the early forelimb bud. |
| Q69431410 | Analysis of deletions at the human argininosuccinate synthetase locus |
| Q38781731 | Analysis of milk protein gene expression in transgenic mice |
| Q37924410 | Anatomy of the rat albumin promoter |
| Q72398712 | Antenatal diagnosis of the haemoglobin disorders by analysis of foetal DNA |
| Q72416237 | Assignment of tissue-type plasminogen activator to chromosome 8 in man and identification of a common restriction length polymorphism within the gene |
| Q46339952 | Association study between Alzheimer's disease and restriction fragment length polymorphisms at the human amyloid beta protein gene locus |
| Q64390421 | Ataxia-telangiectasia: a human mutation giving high-frequency misrepair of DNA double-stranded scissions |
| Q42467430 | Autocrine activity of interleukin 6 secreted by hepatocarcinoma cell lines |
| Q39432683 | Autoimmune thyroid disease--a perspective. |
| Q45882222 | Autologous fibroblast implantation. Feasibility and potential problems in gene replacement therapy |
| Q70961677 | Biochemical analysis of the polymorphism of three HLA-D region antigens |
| Q71222853 | Bioenergetics of intact human muscle. A 31P nuclear magnetic resonance study |
| Q72403213 | Biological effects in vitro of monoclonal antibodies to human epidermal growth factor receptors |
| Q69156325 | Biological properties of chimeric antibodies. Interaction with complement |
| Q72383346 | Cellular protein and RNA antigens in autoimmune disease |
| Q68484738 | Characterization of human centromeric regions using restriction enzyme banding, alphoid DNA and structural alterations |
| Q42466437 | Characterization of pathological dystrophin transcripts from the lymphocytes of a muscular dystrophy carrier |
| Q28287603 | Characterization of the human aldolase B gene |
| Q37876225 | Characterization of the humoral immune response to genital papillomaviruses |
| Q70775679 | Cholesterol requirement of NS-1 mouse myeloma cells for growth in serum-free medium |
| Q36592977 | Chromosomal assignments of three random RFLP loci defined by base-pair changes in MspI sites. |
| Q38242961 | Class II histocompatibility genes and insulin-dependent diabetes mellitus |
| Q68732108 | Class III alleles and high-risk MHC haplotypes in type I diabetes mellitus, Graves' disease and Hashimoto's thyroiditis |
| Q69897004 | Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene region |
| Q45807016 | Clonal selection of human T-cell leukemia virus-infected cells in vivo and in vitro |
| Q38669529 | Cloned autoantigens in the study and diagnosis of autoimmune diseases |
| Q34555163 | Cloning and characterization of a cDNA encoding human galactose-1-phosphate uridyl transferase |
| Q48364365 | Cloning of cDNA coding for human tissue-type plasminogen activator and its expression in Escherichia coli. |
| Q36587385 | Cloning of human prealbumin complementary DNA. Localization of the gene to chromosome 18 and detection of a variant prealbumin allele in a family with familial amyloid polyneuropathy |
| Q71222850 | Complement polymorphism, the major histocompatibility complex and associated diseases: a speculation |
| Q38325993 | Congenital varicella-zoster virus infection and the failure to establish virus-specific cell-mediated immunity |
| Q37027611 | Considerations affecting selection of thrombolytic agents |
| Q69431414 | CpG dinucleotides are "hotspots" for mutation in the antithrombin III gene. Twelve variants identified using the polymerase chain reaction |
| Q54331454 | Cyclic AMP inhibits the growth of human breast cancer cells in defined medium |
| Q72403196 | Cystic fibrosis is not caused by a defect in the gene coding for human complement C3 |
| Q40079143 | Cytogenetics and molecular biology combine in the investigation of chromosomal translocation and human leukaemia. |
| Q44615819 | DNA cross-linked by cisplatin: a new probe for the DNA repair defect in xeroderma pigmentosum. |
| Q68827786 | DNA fragmentation in childhood T-cell acute lymphoblastic leukaemia |
| Q71223616 | DNA methylation and X-chromosome inactivation |
| Q59783988 | DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia |
| Q58420442 | DNA rearrangements of immunoglobulin genes correlate with phenotypic markers in B-cell malignancies |
| Q37876222 | DNA replication of herpesviruses during the lytic phase of their life-cycles |
| Q45807158 | DNA sequence analysis of the EcoRI Dhet fragment of B95-8 Epstein-Barr virus containing the terminal repeat sequences |
| Q45807162 | DNA sequence and transcription of the BamHI fragment B region of B95-8 Epstein-Barr virus |
| Q45806760 | Defective human T-cell leukemia virus in adult T-cell leukemia patients |
| Q70397460 | Degradation of rat or sheep glomerular basement membrane by rabbit neutrophils in vitro. The roles of proteinases, complement and oxygen-derived radicals |
| Q38781741 | Detection of new mutation disease in man and mouse. |
| Q37983873 | Development of antigen-specific therapies for autoimmune disease |
| Q67659706 | Differential in vitro transcription from the promoter of a rat alpha 2u globulin gene in liver and spleen nuclear extracts |
| Q68161206 | Direct gene diagnosis of cystic fibrosis by allele-specific polymerase chain reactions |
| Q38669550 | Duchenne muscular dystrophy: the gene and the protein |
| Q44480489 | Effect of cholera toxin on L-[14C]glycine uptake and intestinal cell enzymes in rabbit |
| Q70507731 | Effects of monoclonal anti-lymphocyte antibodies in vivo in monkeys and humans |
| Q38324112 | Effects of polyoma virus oncogenes in transgenic mice. |
| Q69134857 | Embryonal tumors from transgenic mouse zygotes carrying human activated c-Ha-ras genes |
| Q38781714 | Embryonic stem cell culture and gene targeting in transgenic mice. |
| Q42806643 | Evidence against ras activation in human ovarian carcinomas |
| Q70246422 | Evidence for involvement of a Robertsonian translocation 13 chromosome in formation of a ring chromosome 13 |
| Q42494345 | Exonuclease activity that degrades histone mRNA is stable when DNA or protein synthesis is inhibited. |
| Q41194356 | Expression of collagen genes in the liver |
| Q57338716 | Expression of genes transferred to haemopoietic stem cells by recombinant retroviruses |
| Q44769589 | Expression of human tissue-type plasminogen activator from lytic viral vectors and in established cell lines. |
| Q41232823 | Expression of mitogenically active human recombinant platelet-derived growth factor A-chain |
| Q38376546 | Expression of the Thy-1 gene and Thy-1-derived fusion genes in transgenic mice |
| Q68096033 | Extensive loss of human DNA accompanies loss of antibody production in heteromyeloma hybridoma cells |
| Q69903609 | Fimbrial phase variation and DNA rearrangements in uropathogenic isolates of Escherichia coli |
| Q34133959 | Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop codon and lipoprotein lipase deficiency |
| Q69129912 | Functional human CD4 protein produced in milk of transgenic mice |
| Q70260212 | Further evidence of the involvement of the c-abl oncogene in chronic myelogenous leukemia and acute lymphocytic leukemia |
| Q68158754 | G to A substitution in the promoter region of the apolipoprotein AI gene is associated with elevated serum apolipoprotein AI and high density lipoprotein cholesterol concentrations |
| Q39687264 | Gene expression of carbohydrate metabolism in cellular senescence and aging |
| Q45888791 | Gene therapy for thioguanine-resistant human leukemia. |
| Q38781753 | Genetic ablation in transgenic mice |
| Q52246916 | Genetic activity of a trans-regulatory locus in hepatoma hybrid cells. |
| Q38759190 | Genetic control of human alpha-1-antitrypsin |
| Q38770464 | Genetics and molecular pathogenesis of Legionella pneumophila, an intracellular parasite of macrophages |
| Q37924408 | Genetics of alpha 1-antitrypsin deficiency in relation to neonatal liver disease |
| Q70034763 | Genetics of the spontaneous diabetic syndrome. Interaction of MHC and non-MHC-associated factors |
| Q68076901 | Genotypic analyses of Hodgkin's disease |
| Q72398710 | Globin gene mapping studies in Sardinian patients homozygous for beta zero Thalassaemia |
| Q68732111 | Goitrous Hashimoto's thyroiditis. Lack of association with HLA antigens |
| Q39510752 | Growth factor receptors and cell transformation |
| Q53559020 | Growth factors, cell proliferation and cancer: an overview. |
| Q68795877 | HLA and autoimmune endocrine disease 1985 |
| Q38669535 | HLA class II sequences infer mechanisms for major histocompatibility complex-associated disease susceptibility |
| Q52272254 | Haemopoietic progenitor cell heterogeneity revealed by a single monoclonal antibody, YW 13.1.1. |
| Q68563592 | Hepatic gene function in health and disease |
| Q39479323 | Hepatitis B virus and primary liver cell carcinoma. The application of molecular biology |
| Q28241770 | Hepatitis B virus as an insertional mutagene in a human hepatocellular carcinoma |
| Q38759192 | Hepatitis B virus gene expression in transgenic mice. |
| Q38770452 | Hepatitis B virus gene products as immunological targets in chronic infection |
| Q70281642 | Heterogeneity by cluster analysis techniques of Graves' patients typed for HLA DR and IgG heavy chain markers |
| Q68183587 | High-level expression in Escherichia coli of a soluble and fully active recombinant interleukin-1 beta |
| Q54760992 | High-level production of fully active human alpha 1-antitrypsin in Escherichia coli. |
| Q28244681 | Histidase and histidinemia. Clinical and molecular considerations |
| Q70808279 | Human DNA polymerase alpha. Compensation for heat-labile mouse DNA polymerase alpha and its gene localization on the X chromosome |
| Q54492279 | Human X human hybridoma producing monoclonal antibody against autologous cervical carcinoma |
| Q45390559 | Human and murine CD4 T cell epitopes map to the same region of the malaria circumsporozoite protein: Limited immunogenicity of sporozoites and circumsporozoite protein |
| Q34245830 | Human skeletal muscle acylphosphatase: the primary structure |
| Q34516779 | Human transthyretin (prealbumin) gene and molecular genetics of familial amyloidotic polyneuropathy |
| Q37027641 | Hybrid molecules: insights into plasminogen activator function |
| Q28305840 | Identification of a human salivary amylase gene. Partial sequence of genomic DNA suggests a mode of regulation different from that of mouse, Amy1 |
| Q64448663 | Identification of phenotypically distinct subpopulations of cytotoxic T lymphocytes |
| Q37914721 | Immunobiology of the human immunodeficiency virus envelope and its relationship to vaccine strategies |
| Q42444797 | Immunofluorescent studies of human cervical epithelia in vivo and in vitro using antibodies against specific keratin components |
| Q44309557 | Immunoglobulin gene organization of ultraviolet-illuminated human lymphoblastoid cell lines producing both IgM and IgG. |
| Q70350846 | Immunoglobulin heavy chain and T-cell receptor gamma and beta chain gene rearrangements in acute myeloid leukemias |
| Q68891203 | Immunoreactivity to a 64,000 Mr human islet cell antigen in sera from insulin-dependent diabetes mellitus patients and individuals with abnormal glucose tolerance |
| Q72751213 | Immunosuppression with monoclonal antibodies. A model to determine the rules for effective serotherapy |
| Q68226025 | In situ hybridization and the detection of biotinylated DNA probes |
| Q39590179 | Inappropriate major histocompatibility complex class II expression by thyroid follicular cells in thyroid autoimmune disease and by pancreatic beta cells in type I diabetes |
| Q38759197 | Induction of hepatic cytochrome P450 gene expression by 2,3,7,8-tetrachlorodibenzo-p-dioxin |
| Q38669523 | Inherited collagen disorders |
| Q44132858 | Insertional inactivation of the downless gene in a family of transgenic mice. |
| Q39168077 | Instability of the human immunoglobulin heavy chain constant region locus indicated by different inherited chromosomal deletions |
| Q37894884 | Integration of hepatitis B virus DNA and its implications for hepatocarcinogenesis. |
| Q41739575 | Interaction of trans-acting factors and re-expression of liver functions in hepatoma hybrid cells |
| Q37827390 | Interferon-gamma and the sexual dimorphism of autoimmunity |
| Q67673436 | Interleukin 6 is a negative regulator of the acute phase alpha 1-inhibitor III gene |
| Q67712780 | Interleukin 6 response factor binds co-operatively at two adjacent sites in the promoter upstream region of the rat alpha 2-macroglobulin gene |
| Q37924407 | Interleukin-6: a regulator of plasma protein gene expression in hepatic and non-hepatic tissues |
| Q44723832 | Is beta t a component of HLA-A,B,C in thymus derived cells? |
| Q68969363 | Islet cell antigens. Initial studies of their biology and function |
| Q70817638 | Isolation and sequencing of a cDNA clone for a human HLA-ABC antigen |
| Q36610083 | Isolation of a series of HLA class I clones from a human chromosome 6 genomic library |
| Q70507733 | Kinetic defects in the processing of the low density lipoprotein receptor in fibroblasts from WHHL rabbits and a family with familial hypercholesterolemia |
| Q68675023 | Leishmania major: a very sensitive dot-blot ELISA for detection of parasites in cutaneous lesions |
| Q59389510 | Linkage between fetal A gamma globin chain polymorphism and DNA polymorphism of the human beta gene cluster in beta thalassaemia |
| Q38244154 | Listeria monocytogenes. A model system for the molecular study of intracellular parasitism |
| Q69431413 | Liver growth factor purified from human plasma is an albumin-bilirubin complex |
| Q69431412 | Long-term correction of genetic defect of liver function in rat by transplantation of liver cells after ultraviolet irradiation |
| Q44363728 | Loss of genes on the long arm of chromosome 22 in human meningiomas |
| Q57338711 | Lymphomagenesis in Emu-myc transgenic mice does not require transgene rearrangement or mutation of myc exon 1 |
| Q28244715 | Maple syrup urine disease: domain structure, mutations and exon skipping in the dihydrolipoyl transacylase (E2) component of the branched-chain alpha-keto acid dehydrogenase complex |
| Q38766345 | Mechanism of chromosomal integration of microinjected DNA. |
| Q37914723 | Mechanisms of enveloped virus entry into cells |
| Q39643101 | Messenger RNA turnover in eukaryotic cells. |
| Q37800897 | Methods of detection of single base substitutions in clinical genetic practice |
| Q37585042 | Modes of transformation by the human T-cell leukemia viruses |
| Q37132155 | Modulation of cardiac genes by mechanical stress. The oncogene signalling hypothesis |
| Q37894885 | Molecular and cellular biology of serum amyloid A. |
| Q39464698 | Molecular basis of phenylketonuria and its clinical applications |
| Q37479130 | Molecular basis of prolidase (peptidase D) deficiency. |
| Q37027593 | Molecular biology of myogenic regulatory factors |
| Q39588238 | Molecular biology of the HLA class I and class II genes |
| Q39596041 | Molecular biology of tissue plasminogen activator and endogenous inhibitors. |
| Q45806814 | Molecular characterization of the Epstein-Barr virus DNA in three new Burkitt's lymphoma-derived cell lines |
| Q28244704 | Molecular defects in the E1 alpha subunit of the branched-chain alpha-ketoacid dehydrogenase complex that cause maple syrup urine disease |
| Q39667033 | Molecular genetic techniques for mapping the human genome |
| Q39463830 | Molecular genetics of hemophilia A in man (factor VIII deficiency). |
| Q39739677 | Molecular genetics of insulin-dependent diabetes mellitus |
| Q70397569 | Molecular mechanism for the formation of the high-affinity complex of interleukin 2 and its receptor |
| Q36530387 | Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency |
| Q37983870 | Molecular pathology of type 1 diabetes. |
| Q34144249 | Molecular regulation of 5-aminolevulinate synthase. Diseases related to heme biosynthesis |
| Q72378378 | Monoclonal antibodies that distinguish between human cellular and plasma fibronectin |
| Q47204762 | Monoclonal antibody HMFG-2 retains activity in vivo and binds to high molecular weight components expressed by metastatic breast cancers. |
| Q57198155 | Multiple consequences of human growth hormone expression in transgenic mice |
| Q72403198 | Multiple origins of the sickle mutation: evidence from beta S globin gene cluster polymorphisms |
| Q37027590 | Mutations in cardiac myosin heavy chain genes cause familial hypertrophic cardiomyopathy |
| Q44209417 | Neonatal growth delay in alpha-1-antitrypsin disease. Influence of genetic background |
| Q44321002 | Neurological disorder in transgenic mice that express the large T antigen of polyoma virus in the nervous system. |
| Q37479185 | Non-ketotic hyperglycinemia: an aim of the second generation of studies on pathogenesis. |
| Q70309960 | Non-kinetochore directed autoantibodies in scleroderma/CREST. Identification of an activity recognizing a metaphase chromosome core non-histone protein |
| Q70291044 | Non-radioactive in situ hybridization of DNA probes to chromosomes and nuclei. A comparison of techniques |
| Q44183968 | Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism |
| Q55242583 | Nucleotide sequence analysis of a provirus derived from HTLV-1-associated myelopathy (HAM). |
| Q53559018 | Nucleotide sequence of the transforming region of human cytomegalovirus. |
| Q45844141 | Oncogenic potential of hepatitis B virus |
| Q69467772 | Ordering loci on human chromosome 22 |
| Q48364461 | Organization of the T-cell receptor alpha-chain gene and rearrangement in human T-cell leukaemias |
| Q43212113 | Origin of adult T-cell leukemia virus. Implication for its zoonosis |
| Q45888584 | Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patients. |
| Q34262974 | Partial purification and characterization of the messenger RNA for human glucose-6-phosphate dehydrogenase |
| Q37914725 | Pathways for the penetration of enteroinvasive Yersinia into mammalian cells |
| Q37479170 | Phenylketonuria and the phenylalanine hydroxylase gene. |
| Q69431415 | Phenylketonuria in the Greek population. Haplotype analysis of the phenylalanine hydroxylase gene and identification of a PKU mutation |
| Q45796194 | Plasma membranes from influenza virus-infected cells induce in vitro human secondary virus-specific cytotoxic T lymphocyte responses |
| Q45841278 | Plasmid origin of replication of Epstein-Barr virus, oriP, does not limit replication in cis. |
| Q36587110 | Plasmid vectors for the rapid isolation and transcriptional analysis of human beta-globin gene alleles |
| Q36603157 | Plasmodium falciparum complementary DNA clones expressed in Escherichia coli encode many distinct antigens |
| Q43574222 | Polymorphisms in the apolipoprotein AI-CIII gene complex |
| Q44710509 | Postpartum thyroid disease |
| Q38781762 | Potential for genetic manipulation of mammals |
| Q38669540 | Prenatal diagnosis of the major haemoglobin disorders |
| Q70350842 | Production and characterization of the extracytoplasmic portion of the human interleukin-2 receptor |
| Q44678123 | Production of interleukin 6 by hepatoma cells |
| Q38669566 | Propeptide cleavage: evidence from human proalbumins |
| Q40216448 | Properties of human interleukin-2 receptors expressed on non-lymphoid cells by cDNA transfection |
| Q37966025 | Prospects for gene therapy of familial hypercholesterolemia |
| Q70390653 | Purification and inactivation of the factor X activator of Russell's viper venom with monoclonal antibodies |
| Q38180599 | RNA-mediated (?) dispersion of the L1 family of long interspersed repetitive DNA in mammalian genomes. |
| Q38669555 | Recent advances in the genetics of renal cystic disease. |
| Q37876227 | Recognition of simian virus 40 T antigen by cytotoxic T lymphocytes |
| Q70356578 | Reconstitution of high affinity IL-2 receptor expression in a human T-cell line using a retroviral cDNA expression vector |
| Q54302807 | Regulation and expression of type V (tartrate-resistant) acid phosphatase in human mononuclear phagocytes. |
| Q38185229 | Regulation of acute phase gene expression by inflammatory mediators. |
| Q36575509 | Regulation of hepatic acute phase plasma protein genes by hepatocyte stimulating factors and other mediators of inflammation |
| Q37894871 | Regulation of the human C-reactive protein gene, a major marker of inflammation and cancer |
| Q38770461 | Regulation of virulence genes in Shigella |
| Q70397463 | Removal of T cells from bone marrow for transplantation. Comparison of rat monoclonal anti-lymphocyte antibodies of different isotypes |
| Q37027647 | Retroviral vector-mediated gene transfer into endothelial cells |
| Q38759186 | Retrovirus vector-mediated gene transfer into hepatocytes. |
| Q44212978 | Retrovirus-mediated gene transfer of beta-nerve growth factor into mouse pituitary line AtT-20. |
| Q69576014 | Retrovirus-mediated transfer of the human glucocerebrosidase gene to Gaucher fibroblasts |
| Q37800894 | Role of acrocentric cen-pter satellite DNA in Robertsonian translocation and chromosomal non-disjunction |
| Q52626284 | Secondary structure prediction of human SAA1. Presumptive identification of calcium and lipid binding sites. |
| Q54760550 | Selection of mutations that increase alpha 1-antitrypsin gene expression in Escherichia coli. |
| Q70964523 | Selective expression within the human alpha globin gene complex following chromosome-dependent transfer into diploid mouse erythroleukaemia cells |
| Q71222857 | Selective isolation of murine erythropoietin-responsive progenitor cells (CFU-E) with monoclonal antibodies |
| Q45807331 | Sequence analysis of the 17,166 base-pair EcoRI fragment C of B95-8 Epstein-Barr virus. |
| Q42986938 | Sequence diversity of hepatitis C viral genomes |
| Q34254200 | Sequence of a cDNA encoding human galactose-1-phosphate uridyl transferase |
| Q58479983 | Sequence of rat alpha 1-macroglobulin, a broad-range proteinase inhibitor from the alpha-macroglobulin-complement family |
| Q48334069 | Sequence variation in S-antigen genes of Plasmodium falciparum. |
| Q28117306 | Serendipitous cloning of a mitochondrial cDNA and its polymorphism |
| Q40787555 | Serum amyloid A (SAA) gene variations in familial Mediterranean fever. |
| Q47920336 | Sorting large numbers of clones expressing Plasmodium falciparum antigens in Escherichia coli by differential antibody screening |
| Q46314902 | Specificity of proto-oncogene amplification in human malignant diseases |
| Q70246428 | Spontaneous and radiation-induced genetic instability of heteromyeloma hybridoma cells |
| Q69364668 | State of hepatitis B viral genomes in cirrhotic and hepatocellular carcinoma nodules |
| Q37027627 | Strategies for administration of tissue plasminogen activator |
| Q37027596 | Stress proteins and cardiovascular disease |
| Q48361987 | Structure and expression of the mutant prealbumin gene associated with familial amyloidotic polyneuropathy |
| Q44572571 | Structure of the FIRA gene of Plasmodium falciparum. |
| Q70151867 | Structure of the mutant prealbumin gene responsible for familial amyloidotic polyneuropathy |
| Q71222843 | Studies on differentiation of human mammary epithelial cells in culture: distinctive specificities of conditioned media |
| Q43835495 | Study of the c-Ha-ras-1 locus polymorphism in an Italian population with high incidence of gastric cancer |
| Q45882226 | Suppression of immunological response against a novel gene product delivered by implants of genetically modified fibroblasts |
| Q68802551 | Syngeneic sensitization of mouse lymphocytes on monolayers of thyroid epithelial cells. IX. Thyroid epithelial cells are antigen presenting cells |
| Q46071866 | Synthesis of alpha-fetoprotein in hepatocytes is co-ordinately regulated with cell-cell and cell-matrix interactions. |
| Q37603659 | T cell recognition of stress proteins. A link between infectious and autoimmune disease |
| Q58007128 | T lymphocyte culture established by repeated stimulation with the autologous lymphoblastoid line. MHC class II restricted interactions with B blasts |
| Q39667027 | The T cell receptor and autoimmune diseases |
| Q70309956 | The WI-L2-729-HF2 human hybridoma system. Arrangement of lambda genes in monoclonal hybrids |
| Q54492283 | The WI-L2-729-HF2 human hybridoma system. Stable hybrids at high frequency |
| Q58420454 | The breakpoint of the Philadelphia chromosome 22 in chronic myeloid leukaemia is distal to the immunoglobulin lambda light chain constant region genes |
| Q70806983 | The cellular protein p53 in human tumours |
| Q45807160 | The complete nucleotide sequence of the influenza virus neuraminidase gene of A/NJ/8/76 strain and its evolution by segmental duplication and deletion |
| Q39739681 | The genetic epidemiology of type I diabetes mellitus and autoimmune thyroid disease. Molecular interactions at the population level |
| Q70135241 | The interaction of MHC and Gm in liability to autoimmune thyroid disease |
| Q38669547 | The molecular and cell biology of apolipoprotein-B. |
| Q38669531 | The molecular pathology of the serpins |
| Q37834811 | The mucopolysaccharidoses. Diagnosis, molecular genetics and treatment. |
| Q71222847 | The quantitative expression of delta and beta human globin genes is controlled by both 5' and 3' untranslated regions |
| Q44419571 | The ring-infected erythrocyte surface antigen (RESA) polypeptide of Plasmodium falciparum contains two separate blocks of tandem repeats encoding antigenic epitopes that are naturally immunogenic in man. |
| Q68795874 | The role of HLA antigens in the manifestation and course of Graves' disease |
| Q39511498 | The simian virus 40 large T antigen. A lot packed into a little |
| Q37027637 | Thrombolytic therapy: enhancement by platelet and platelet-derived mediator antagonists |
| Q37983876 | Tolerance to self-antigens in transgenic mice |
| Q45888788 | Towards gene therapy for hemophilia B. |
| Q46595815 | Transcriptional regulation of the albumin gene in cultured rat hepatocytes. Role of basement-membrane matrix |
| Q54474200 | Transfer of human globin genes to human erythroleukemia cells |
| Q38766351 | Transgenic approach for the study of pathogenesis induced by human viruses |
| Q44969813 | Transgenic mice as a model to test the immunogenicity of proteins altered by site-specific mutagenesis |
| Q38324117 | Transgenic mouse model of familial amyloidotic polyneuropathy. |
| Q45831125 | Transmission and genetic shift of human immunodeficiency virus (HIV) in vivo. |
| Q42664246 | Two families of abl-related transcripts in human haematopoietic cells differing in their homology to v-abl. |
| Q48349885 | Two human tRNA(Ala) families are recognized by autoantibodies in polymyositis sera. |
| Q44014963 | Unusual virus produced by cultured cells from a patient with AIDS |
| Q70260215 | Variation in p126, a parasitophorous vacuole antigen of Plasmodium falciparum |
| Q38229797 | X-linked chronic granulomatous disease: more than two years later. |
| Q68970234 | X-ray scattering and diffraction by wet gels of AA amyloid fibrils |
| Q40433927 | 5-Aminolevulinate synthase and the first step of heme biosynthesis |
| Q36667141 | A Novel Hepatocytic Transcription Factor That Binds the α-Fetoprotein Promoter-Linked Coupling Element |
| Q34305060 | A molecular approach to galactosemia |
| Q40746424 | Acute Phase Protein, Serum Amyloid A, Inhibits IL-1- and TNF-Induced Fever and Hypothalamic PGE2 in Mice |
| Q35228887 | Adenovirus-Based Expression Vectors and Recombinant Vaccines |
| Q34267400 | Advances in Duchenne muscular dystrophy gene therapy |
| Q67486841 | Amyloid enhancing factor activity is associated with ubiquitin |
| Q41683573 | Analysis of abnormal expression of G-CSF gene in a novel tumor cell line (KHC 287) elaborating G-CSF, IL-1 and IL-6 with co-amplification of c-myc and c-ki-ras |
| Q41681910 | Analysis of unstable RNA transcripts of insecticidal crystal protein genes of Bacillus thuringiensis in transgenic plants and electroporated protoplasts |
| Q71843940 | Aromatic hydrocarbon receptor in cultured fetal cells from C57BL/6J and DBA/2J mice: similarity in molecular mass to receptors in adult livers |
| Q55484170 | Binding of epidermal growth factor-dextran conjugates to cultured glioma cells |
| Q34568254 | Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anonymous DNA polymorphisms and the proteolipid protein (PLP) gene cDNA |
| Q36695291 | Characterization of a linear epitope within the human pancreatic 64‐kDa glutamic acid decarboxylase and its autoimmune recognition by sera from insulin‐dependent diabetes mellitus patients |
| Q38304544 | Characterization of the distal alpha-fetoprotein enhancer, a strong, long distance, liver-specific activator |
| Q41643801 | Chemical cross-linking of the cytosolic and nuclear forms of the Ah receptor in hepatoma cell line 1c1c7 |
| Q33489324 | Chronic Myelomonocytic Leukemia Associated with Primary Amyloidosis |
| Q71972436 | Clinicopathological findings and p53 expression of thyroid cancer in children |
| Q45165092 | Comparison of the murine humoral immune response to recombinant simian virus 40 large tumor antigen: Epitope specificity and idiotype expression |
| Q33279741 | Detection of Mobile Proteins by Proton Nuclear Magnetic Resonance Spectroscopy in the Guinea Pig Brain Ex Vivo and Their Partial Purification |
| Q36536905 | Diagnostic utility of oncogenes and their products in human cancer |
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