Molecular basis of alpha-1-antitrypsin deficiency.
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[1] R. Crystal,et al. Evaluation of the S-type of alpha-1-antitrypsin as an in vivo and in vitro inhibitor of neutrophil elastase. , 1988, The American review of respiratory disease.
[2] H. E. Khadem. 6 – Structure of Oligosaccharides , 1988 .
[3] R. Crystal,et al. Emphysema associated with complete absence of alpha 1- antitrypsin in serum and the homozygous inheritance [corrected] of a stop codon in an alpha 1-antitrypsin-coding exon. , 1988, American journal of human genetics.
[4] R. Crystal,et al. Comparison of alpha-1-antitrypsin levels and antineutrophil elastase capacity of blood and lung in a patient with the alpha-1-antitrypsin phenotype null-null before and during alpha-1-antitrypsin augmentation therapy. , 2015, The American review of respiratory disease.
[5] C. Mittman,et al. Pulmonary Emphysema and Proteolysis 1986 , 1987 .
[6] R. Crystal,et al. Z-type alpha 1-antitrypsin is less competent than M1-type alpha 1-antitrypsin as an inhibitor of neutrophil elastase. , 1987, The Journal of clinical investigation.
[7] R. Crystal,et al. alpha 1-Antitrypsin nullGranite Falls, a nonexpressing alpha 1-antitrypsin gene associated with a frameshift to stop mutation in a coding exon. , 1987, The Journal of biological chemistry.
[8] R. Cortese,et al. Cis‐ and trans‐acting elements responsible for the cell‐specific expression of the human alpha 1‐antitrypsin gene. , 1987, The EMBO journal.
[9] R. Cortese,et al. The human alpha 1‐antitrypsin gene is transcribed from two different promoters in macrophages and hepatocytes. , 1987, The EMBO journal.
[10] R. Crystal,et al. Characterization of the M1(Ala213) type of alpha 1-antitrypsin, a newly recognized, common "normal" alpha 1-antitrypsin haplotype. , 1987, Biochemistry.
[11] C. Caskey. Disease diagnosis by recombinant DNA methods. , 1987, Science.
[12] R. Foreman. Disruption of the Lys‐290‐Glu‐342 salt bridge in human α1‐antitrypsin does not prevent its synthesis and secretion , 1987, FEBS letters.
[13] R. Crystal,et al. Replacement therapy for alpha 1-antitrypsin deficiency associated with emphysema. , 1987, The New England journal of medicine.
[14] R. Lovell-Badge,et al. Species- and tissue-specific expression of human alpha 1-antitrypsin in transgenic mice. , 1987, Genes & development.
[15] F. DeMayo,et al. Tissue specific expression of the human alpha-1-antitrypsin gene in transgenic mice. , 1987, Nucleic acids research.
[16] L. Nelles,et al. Primary structure of human alpha 2-antiplasmin, a serine protease inhibitor (serpin). , 1987, The Journal of biological chemistry.
[17] K. Kurachi,et al. Characterization of a cDNA for human protein C inhibitor. A new member of the plasma serine protease inhibitor superfamily. , 1987, The Journal of biological chemistry.
[18] D. Cox,et al. Prenatal diagnosis of alpha 1 antitrypsin deficiency and estimates of fetal risk for disease. , 1987, Journal of medical genetics.
[19] A. Elbein,et al. Inhibitors of the biosynthesis and processing of N-linked oligosaccharide chains. , 1987, Annual review of biochemistry.
[20] J. Rothman,et al. Biosynthetic protein transport and sorting by the endoplasmic reticulum and Golgi. , 1987, Annual review of biochemistry.
[21] M D Snider,et al. Topography of glycosylation in the rough endoplasmic reticulum and Golgi apparatus. , 1987, Annual review of biochemistry.
[22] R. Crystal,et al. Identification of a second mutation in the protein-coding sequence of the Z type alpha 1-antitrypsin gene. , 1986, The Journal of biological chemistry.
[23] P. Ward,et al. PRENATAL DIAGNOSIS OF α1-ANTITRYPSIN DEFICIENCY BY RESTRICTION FRAGMENT LENGTH POLYMORPHISMS, AND COMPARISON WITH OLIGONUCLEOTIDE PROBE ANALYSIS , 1986, The Lancet.
[24] R. Huber,et al. X‐ray crystal structure of the complex of human leukocyte elastase (PMN elastase) and the third domain of the turkey ovomucoid inhibitor. , 1986, The EMBO journal.
[25] D. Cox,et al. Aggregation of plasma Z type α1‐antitrypsin suggests basic defect for the deficiency , 1986 .
[26] R. Carrell,et al. alpha 1-Antitrypsin Christchurch, 363 Glu----Lys: mutation at the P'5 position does not affect inhibitory activity. , 1986, Biochimica et biophysica acta.
[27] J. Millán,et al. Cloning and sequence of a cDNA coding for the human beta-migrating endothelial-cell-type plasminogen activator inhibitor. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[28] R. Crystal,et al. Expression of the alpha-1-antitrypsin gene in mononuclear phagocytes of normal and alpha-1-antitrypsin-deficient individuals. , 1986, The Journal of clinical investigation.
[29] V. Kidd,et al. Complete absence of serum alpha-1-antitrypsin in conjunction with an apparently normal gene structure. , 1986, American journal of human genetics.
[30] R. Mecham. Regulation of matrix Accumulation , 1986 .
[31] R. Crystal,et al. Alpha 1-antitrypsin deficiency and emphysema caused by homozygous inheritance of non-expressing alpha 1-antitrypsin genes. , 1986, The New England journal of medicine.
[32] J. Carlson,et al. Risk of cirrhosis and primary liver cancer in alpha 1-antitrypsin deficiency. , 1986, The New England journal of medicine.
[33] F. Ruddle,et al. Regional location of α1-antichymotrypsin and α1-antitrypsin genes on human chromosome 14 , 1986 .
[34] J H Lewis,et al. Alpha-1-antitrypsin-Pittsburgh. A potent inhibitor of human plasma factor XIa, kallikrein, and factor XIIf. , 1986, The Journal of clinical investigation.
[35] R. Crystal,et al. Evaluation of "at risk" alpha 1-antitrypsin genotype SZ with synthetic oligonucleotide gene probes. , 1986, The Journal of clinical investigation.
[36] Peilin Xu,et al. Primate η-globin DNA sequences and man's place among the great apes , 1986, Nature.
[37] J. Bieth. Elastases: Catalytic and Biological Properties , 1986 .
[38] R. Carrell,et al. Kinetic studies on the interaction of alpha 1-proteinase inhibitor (Pittsburgh) with trypsin-like serine proteinases. , 1986, Biological chemistry Hoppe-Seyler.
[39] H. Colten,et al. The cellular defect in alpha 1-proteinase inhibitor (alpha 1-PI) deficiency is expressed in human monocytes and in Xenopus oocytes injected with human liver mRNA. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[40] A. Görg,et al. Improved resolution of PI (alpha 1-antitrypsin) phenotypes by a large-scale immobilized pH gradient. , 1985, American journal of human genetics.
[41] A Janoff,et al. Elastases and emphysema. Current assessment of the protease-antiprotease hypothesis. , 1985, The American review of respiratory disease.
[42] D. Cox,et al. DNA restriction fragments associated with α1-antitrypsin indicate a single origin for deficiency allele PI Z , 1985, Nature.
[43] J. Jeppsson,et al. Isolation and characterization of two minor fractions of alpha 1-antitrypsin by high-performance liquid chromatographic chromatofocusing. , 1985, Journal of chromatography.
[44] R. Cortese,et al. Cell-specific expression of a transfected human α1 -antitrypsin gene , 1985, Cell.
[45] A. Hercz. Proteolytic cleavages in α1-antitrypsin and microheterogeneity , 1985 .
[46] R. Carrell,et al. Isolation and properties of recombinant DNA produced variants of human alpha 1-proteinase inhibitor. , 1985, The Journal of biological chemistry.
[47] M. Griffith,et al. Reactive site peptide structural similarity between heparin cofactor II and antithrombin III. , 1985, The Journal of biological chemistry.
[48] J. Catanese,et al. Primary structure of the reactive site of human C1-inhibitor. , 1985, The Journal of biological chemistry.
[49] P. Kilbridge,et al. Expression of the alpha 1-proteinase inhibitor gene in human monocytes and macrophages. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[50] S. Rasmussen,et al. Sequence homology between barley endosperm protein Z and protease inhibitors of the α1‐antitrypsin family , 1985 .
[51] R. Carrell,et al. SMOKING, LUNG FUNCTION, AND α1-ANTITRYPSIN DEFICIENCY , 1985, The Lancet.
[52] R. Crystal,et al. Synthesis in E. coli of α1-antitrypsin variants of therapeutic potential for emphysema and thrombosis , 1985, Nature.
[53] S. Humphries,et al. Possible Applications of Recombinant DNA Technology to the Diagnosis and Study of Variants of α1-Antitrypsin , 1985, Annals of clinical biochemistry.
[54] R. Crystal,et al. Oxidants, antioxidants and the pathogenesis of emphysema. , 1985, European journal of respiratory diseases. Supplement.
[55] B. Cohen,et al. Collaborative study to assess risk of lung disease in Pi MZ phenotype subjects. , 2015, The American review of respiratory disease.
[56] J. Bieth,et al. In vivo significance of kinetic constants of protein proteinase inhibitors. , 1984, Biochemical medicine.
[57] P. M. George,et al. Structural and functional characterization of the abnormal Z α1‐antitrypsin isolated from human liver , 1984, FEBS letters.
[58] K. Kurachi,et al. Complete sequence of the cDNA for human alpha 1-antitrypsin and the gene for the S variant. , 1984, Biochemistry.
[59] H. Baumann,et al. Plasma protease inhibitors in mouse and man: divergence within the reactive centre regions , 1984, Nature.
[60] S. Eriksson,et al. Monoclonal antibody specific for the mutant PiZ alpha 1-antitrypsin and its application in an ELISA procedure for identification of PiZ gene carriers. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[61] R. Huber,et al. Human alpha 1-proteinase inhibitor. Crystal structure analysis of two crystal modifications, molecular model and preliminary analysis of the implications for function. , 1984, Journal of molecular biology.
[62] R. Kageyama,et al. Primary structure of human preangiotensinogen deduced from the cloned cDNA sequence. , 1984, Biochemistry.
[63] H. Lodish,et al. Glucose removal from N-linked oligosaccharides is required for efficient maturation of certain secretory glycoproteins from the rough endoplasmic reticulum to the Golgi complex , 1984, The Journal of cell biology.
[64] A. Colman,et al. Xenopus oocytes can synthesise but do not secrete the Z variant of human α1‐antitrypsin , 1984 .
[65] K. Itakura,et al. Prenatal diagnosis of alpha 1-antitrypsin deficiency by direct analysis of the mutation site in the gene. , 1984, The New England journal of medicine.
[66] Shirley A. Miller,et al. Distribution of α1-Antitrypsin Variants in a US White Population , 1984 .
[67] J. Travis,et al. Kinetic and chemical evidence for the inability of oxidized alpha 1-proteinase inhibitor to protect lung elastin from elastolytic degradation. , 1984, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.
[68] S. Orkin,et al. The mutation and polymorphism of the human beta-globin gene and its surrounding DNA. , 1984, Annual review of genetics.
[69] R. Sesboüé,et al. Human alpha 1-antitrypsin genetic polymorphism: PI N subtypes. , 1984, Human heredity.
[70] Hunninghake Gw,et al. Cigarette smoking and lung destruction: accumulation of neutrophils in the lungs of cigarette smokers , 1983 .
[71] J. Rogers,et al. The isolation of a clone for human α 1-antitrypsin and the detection of α 1-antitrypsin in mRNA from liver and leukocytes , 1983 .
[72] K. Robson,et al. Sequence homology between human alpha 1-antichymotrypsin, alpha 1-antitrypsin, and antithrombin III. , 1983, Biochemistry.
[73] J H Lewis,et al. Mutation of antitrypsin to antithrombin. alpha 1-antitrypsin Pittsburgh (358 Met leads to Arg), a fatal bleeding disorder. , 1983, The New England journal of medicine.
[74] K. Itakura,et al. α1-Antitrypsin deficiency detection by direct analysis of the mutation in the gene , 1983, Nature.
[75] D. Comings. Metabolic basis of inherited disease , 1983 .
[76] S. Eriksson. The effect of tamoxifen in intermediate alpha 1-antitrypsin deficiency associated with the phenotype PiSZ. , 1983, Annals of clinical research.
[77] R. Carrell,et al. Translation and processing of normal (PiMM) and abnormal (PiZZ) human α1‐antitrypsin , 1983 .
[78] M. Tobin,et al. Alpha 1 antitrypsin deficiency: the clinical and physiological features of pulmonary emphysema in subjects homozygous for Pi type Z. A survey by the British Thoracic Association. , 1983, British journal of diseases of the chest.
[79] G. Salvesen,et al. Human plasma proteinase inhibitors. , 1983, Annual review of biochemistry.
[80] M. Tobin,et al. Alpha 1 antitrypsin deficiency: clinical and physiological features in heterozygotes of Pi type SZ. A survey by the British Thoracic Association. , 1983, British journal of diseases of the chest.
[81] D. Cockcroft,et al. A new anodal alpha 1-antitrypsin variant associated with emphysema: Pi Bsaskatoon. , 2015, The American review of respiratory disease.
[82] R. Carrell,et al. In vitro synthesis of M and Z forms of human α1‐antitrypsin , 1982, FEBS Letters.
[83] H. Sharp. Alpha-1-Antitrypsin: An Ignored Protein in Understanding Liver Disease , 1982, Seminars in liver disease.
[84] R. Heilig,et al. The ovalbumin gene family: complete sequence and structure of the Y gene. , 1982, Nucleic acids research.
[85] R. Carrell,et al. Structure and variation of human α1–antitrypsin , 1982, Nature.
[86] W. Walker,et al. TRANSPORT OF PROTEASES ACROSS NEONATAL INTESTINE AND DEVELOPMENT OF LIVER DISEASE IN INFANTS WITH α1-ANTITRYPSIN DEFICIENCY , 1982, The Lancet.
[87] K. Kurachi,et al. Sequence homology and structural comparison between the chromosomal human α1-antitrypsin and chicken ovalbumin genes , 1982, Nature.
[88] R. Carrell,et al. alpha 1-Antitrypsin microheterogeneity. Isolation and physiological significance of isoforms. , 1982, Biochimica et biophysica acta.
[89] R. Carrell,et al. Human α1‐antitrypsin: carbohydrate attachment and sequence homology , 1981 .
[90] R. Crystal,et al. Antielastases of the human alveolar structures. Implications for the protease-antiprotease theory of emphysema. , 1981, The Journal of clinical investigation.
[91] D. Cox. New variants of alpha 1-antitrypsin: comparison of Pi typing techniques. , 1981, American journal of human genetics.
[92] M. Fagerhol,et al. PiPclifton: a new α1-antitrypsin allele in an American Negro family* , 1981 .
[93] J. Travis,et al. [55] Human α1-proteinase inhibitor , 1981 .
[94] Fagerhol Mk,et al. The Pi polymorphism: genetic, biochemical, and clinical aspects of human alpha 1-antitrypsin. , 1981 .
[95] J. Pierce,et al. MPsaintlouis: a new antitrypsin phenotype. , 1981, Human heredity.
[96] R. Sesboüé,et al. Genetic variations of serum alpha-1-antitrypsin (Pi types) in Normans. Common Pi M subtypes and new phenotypes. , 1981, Human heredity.
[97] K. Nakajima,et al. Studies on reactivity of human leukocyte elastase, cathepsin G, and porcine pancreatic elastase toward peptides including sequences related to the reactive site of alpha 1-protease inhibitor (alpha 1-antitrypsin). , 1980, Biochemistry.
[98] N. Harpaz,et al. Characterization of the oligosaccharides of liver Z variant alpha 1-antitrypsin. , 1980, Canadian journal of biochemistry.
[99] M. O. Dayhoff,et al. A surprising new protein superfamily containing ovalbumin, antithrombin-III, and alpha 1-proteinase inhibitor. , 1980, Biochemical and biophysical research communications.
[100] R. Crystal,et al. Danazol-induced augmentation of serum alpha 1-antitrypsin levels in individuals with marked deficiency of this antiprotease. , 1980, The Journal of clinical investigation.
[101] A. Yoshida,et al. Studies on the oligosaccharide chains of human alpha 1-protease inhibitor. II. Structure of oligosaccharides. , 1980, The Journal of biological chemistry.
[102] A. Yoshida,et al. Studies on the oligosaccharide chains of human alpha 1-protease inhibitor. I. Isolation of glycopeptides. , 1980, Journal of Biological Chemistry.
[103] J. Travis,et al. Kinetics of association of serine proteinases with native and oxidized alpha-1-proteinase inhibitor and alpha-1-antichymotrypsin. , 1980, The Journal of biological chemistry.
[104] G. Misson,et al. Familial alpha-1-antitrypsin dificiency with Pi-Z and a new Pi-Gcler variant. , 1980, Biomedicine / [publiee pour l'A.A.I.C.I.G.].
[105] A. Johnson,et al. Report of Nomenclature Meeting for alpha 1-antitrypsin, INSERM, Rouen/Bois-Guillaume-1978. , 1980, Human genetics.
[106] R. Peters,et al. Liver transplantation for advanced liver disease with alpha-1-antitrypsin deficiency. , 1980, The New England journal of medicine.
[107] R. Frants,et al. A New Unstable PI M Variant of a1-Antitrypsin in a Finnish Isolate , 1980 .
[108] R. Crystal,et al. Cigarette smoking induces functional antiprotease deficiency in the lower respiratory tract of humans. , 1979, Science.
[109] J. C. Taylor,et al. An alpha 1-antitrypsin variant, Pi B Alhambra (Lys to Asp, Glu to Asp), with rapid anodal electrophoretic mobility. , 1979, American journal of human genetics.
[110] S. Harada,et al. Distribution of α1-antitrypsin phenotypes in Japanese: Description of Pi M subtypes by isoelectric focusing , 1979, Japanese Journal of Human Genetics.
[111] D. Johnson,et al. The oxidative inactivation of human alpha-1-proteinase inhibitor. Further evidence for methionine at the reactive center. , 1979, The Journal of biological chemistry.
[112] S. D. Litwin. Genetic determinants of pulmonary disease , 1978 .
[113] C. Larsson. Natural history and life expectancy in severe alpha1-antitrypsin deficiency, Pi Z. , 2009, Acta medica Scandinavica.
[114] C. Larsson. Intermediate alpha1-antitrypsin deficiency, Pi M-. , 2009, Acta medica Scandinavica.
[115] J. O. Morse. Alpha1-antitrypsin deficiency (second of two parts). , 1978, The New England journal of medicine.
[116] J. O. Morse,et al. alpha1-antitrypsin deficiency (first of two parts). , 1978 .
[117] R. Allen,et al. A new allele of human alpha1-antitrypsin: PiNhampton. , 1978, American journal of human genetics.
[118] D. Johnson,et al. Structural evidence for methionine at the reactive site of human alpha-1-proteinase inhibitor. , 1978, The Journal of biological chemistry.
[119] J. Wilson,et al. alpha1-Antitrypsin: the presence of excess mannose in the Z variant isolated from liver. , 1978, Science.
[120] H. Fudenberg,et al. Genetic polymorphism of serum alpha-1-protease inhibitor (alpha-1-antitrypsin): Pi i, a deficient allele of the Pi system. , 1978, The Journal of laboratory and clinical medicine.
[121] C. Steer,et al. Metabolism of Intact and Desialylated α1-Antitrypsin , 1978 .
[122] F. Kueppers,et al. Alpha1-antitrypsin: further genetic heterogeneity revealed by isoelectric focusing. , 1978, American journal of human genetics.
[123] T. Sveger. alpha 1-antitrypsin deficiency in early childhood. , 1978, Pediatrics.
[124] D. Cox,et al. Catabolic rate of alpha1-antitrypsin of of Pi types S, and MMalton and of asialylated M-protein in man. , 1978, Clinical science and molecular medicine.
[125] α‐1‐Antitrypsin: Structural relationships of the substitutions of the S and Z variants , 1978 .
[126] J. Jeppsson,et al. Properties of isolated human alpha1-antitrypsins of Pi types M, S and Z. , 1978, European journal of biochemistry.
[127] 秀紀 中井,et al. 家族性α1-antitrypsin欠損症(“Pi null” type)の一家系 , 1978 .
[128] G. Utz,et al. Alpha1-antitrypsin deficiency with M-like phenotype. , 1977, Journal of medical genetics.
[129] H. Evans,et al. Prevalence of of alpha 1-antitrypsin Pi types among newborn infants of different ethnic backgrounds. , 1977, The Journal of pediatrics.
[130] T. Starzl,et al. Liver replacement for alpha1-antitrypsin deficiency. , 1977, Surgery.
[131] J. Lieberman,et al. Intermediate alpha1-antitrypsin deficiency resulting from a null gene (M-phenotype). , 1976, Chest.
[132] D. Johnson,et al. Human alpha-1-proteinase inhibitor mechanism of action: evidence for activation by limited proteolysis. , 1976, Biochemical and biophysical research communications.
[133] R. Charlionet,et al. Genetic variants of serum alpha1-antitrypsin (Pi types) in Portuguese. , 1976, Human heredity.
[134] F. Kueppers. Alpha 1 antitrypsin M1: a new common genetically determined variant. , 1976, American Journal of Human Genetics.
[135] T Sveger,et al. Liver disease in alpha1-antitrypsin deficiency detected by screening of 200,000 infants. , 1976, The New England journal of medicine.
[136] J. Jeppsson. Amino acid substitution Glu→Lys in α1‐antitrypsin PiZ , 1976 .
[137] A. Yoshida,et al. Molecular abnormality of human alpha1-antitrypsin variant (Pi-ZZ) associated with plasma activity deficiency. , 1976, Proceedings of the National Academy of Sciences of the United States of America.
[138] Johnson Am. Genetic typing of alpha1-antitrypsin by immunofixation electrophoresis, identification of subtypes of Pi M. , 1976 .
[139] R. Frants,et al. alpha1-antitrypsin: common subtypes of Pi M. , 1976, Human heredity.
[140] J. Lieberman,et al. A new deficient variant of alpha1-antitrypsin (MDUARTE). Inability to detect the heterozygous state by antitrypsin phenotyping. , 1976, The American review of respiratory disease.
[141] C. Larsson,et al. Lung function studies in asymptomatic individuals with moderately (Pi SZ) and severely (Pi Z) reduced levels of alpha1-antitrypsin. , 1976, Scandinavian journal of respiratory diseases.
[142] G. Feldmann,et al. The ultrastructure of hepatocytes in alpha-1-antitrypsin deficiency with the genotype Pi--. , 1975, Gut.
[143] Martin Jp. Further examples confirming the existence of Pi null (Pi , 1975 .
[144] D. Rees,et al. Molecular basis for the α1-protease inhibitor deficiency , 1975, Nature.
[145] J. Pierce,et al. Antitrypsin phenotypes in St. Louis. , 1975, JAMA.
[146] P. Cook. The genetics of α1‐antitrypsin: a family study in England and Scotland , 1975, Annals of human genetics.
[147] H. E. Jones,et al. Letter: Splenectomy in acute lymphatic leukaemia. , 1975, Lancet.
[148] R. George,et al. Comparison of commercially available radial immunodiffusion kits for the determination of serum alpha 1-antitrypsin concentrations. , 1975, The American review of respiratory disease.
[149] J. Travis,et al. Isolation and properties of human plasma α-1-proteinase inhibitor , 1974 .
[150] G. Ljunggren,et al. α1,‐ANTITRYPSIN DEFICIENCY Pi Genotype ZO, SO und MO , 1974 .
[151] R. Allen,et al. A new method for determination of alpha-1-antitrypsin phenotypes using isoelectric focusing on polyacrylamide gel slabs. , 1974, American journal of clinical pathology.
[152] L. F. Black,et al. Alpha1-antitrypsin and its deficiency. , 1974, The American review of respiratory disease.
[153] D. Cox,et al. Inherited variants of alpha1-antitrypsin: a new allele PiN. , 1974, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.
[154] C. Ropartz,et al. α1− Polymorphism of a Bantu population: Description of a mew allele PiL , 1974, Humangenetik.
[155] C. Ropartz,et al. PiB, a new allele of alpha1 antitrypsin genetic variants. , 1973, Biomedicine / [publiee pour l'A.A.I.C.I.G.].
[156] R. Talamo,et al. α1-Antitrypsin Deficiency: A Variant with No Detectable α1-Antitrypsin , 1973, Science.
[157] T. Kawai. Synthesis of the Plasma Proteins , 1973 .
[158] H. Goedde,et al. Population genetic studies of serum protein polymorphisms in four Spanish populations. II. , 1973, Human heredity.
[159] M. Robinet-lévy,et al. Techniques d'identification des groupes Pi: Premières statistiques languedociennes , 1972 .
[160] C. Kindmark,et al. Sequential changes of plasma proteins after surgical trauma. , 1972, Scandinavian journal of clinical and laboratory investigation. Supplementum.
[161] J. Rivera. Protides of Biological Fluids , 1971 .
[162] W. Krivit,et al. Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder. , 1969, The Journal of laboratory and clinical medicine.
[163] M. Fagerhol,et al. SERU Pi TYPES IN PATIENTS WITH PULMONARY DISEASES , 1969, Acta allergologica.
[164] M. Fagerhol. Quantitative Studies on the Inherited Variants of Serum α1-antitrypsin , 1969 .
[165] T. Waldmann,et al. Metabolism of immunoglobulins. , 1969, Progress in allergy.
[166] M. Fagerhol,et al. Serum Pi types in some European, American, Asian and African populations. , 2009, Acta pathologica et microbiologica Scandinavica.
[167] M. Fagerhol,et al. The Pi Phenotype MP , 1968 .
[168] W. F. Miller,et al. Pulmonary emphysema and alpha 1-antitrypsin deficiency. , 1968, The American journal of medicine.
[169] J. Thorell,et al. Effect of administration of a combined estrogen-progestin contraceptive on the level of individual plasma proteins. , 1968, Scandinavian journal of clinical and laboratory investigation.
[170] C. Laurell,et al. The polymorphism of “prealbumins” and α1-antitrypsin in human sera , 1967 .
[171] P. Gross,et al. EXPERIMENTAL EMPHYSEMA: ITS PRODUCTION WITH PAPAIN IN NORMAL AND SILICOTIC RATS. , 1965, Archives of environmental health.
[172] C. Laurell. Electrophoretic Microheterogeneity of Serum α1-Antitrypsin , 1965 .
[173] S. Eriksson,et al. PULMONARY EMPHYSEMA AND ALPHA1-ANTITRYPSIN DEFICIENCY. , 2009, Acta medica Scandinavica.
[174] C. Laurell,et al. The Electrophoretic α;1-Globulin Pattern of Serum in α;1-Antitrypsin Deficiency , 1963 .