Published in Hum Genet on January 01, 1985
Why has it been so difficult to prove the efficacy of alpha-1-antitrypsin replacement therapy? Insights from the study of disease pathogenesis. Drug Des Devel Ther (2011) 0.92
The deficient alpha-I-antitrypsin phenotype PI P is associated with an A-to-T transversion in exon III of the gene. Am J Hum Genet (1989) 0.89
Rare deficiency types of alpha 1-antitrypsin: electrophoretic variation and DNA haplotypes. Am J Hum Genet (1989) 0.87
Does the PI polymorphism alone control alpha-1-antitrypsin expression? Am J Hum Genet (1987) 0.82
Sequence data of the rare deficient alpha 1-antitrypsin variant PI Zaugsburg. Am J Hum Genet (1990) 0.80
Characterization of the normal alpha 1-antitrypsin allele Vmunich: a variant associated with a unique protein isoelectric focusing pattern. Am J Hum Genet (1990) 0.76
Three-dimensional atomic model of F-actin decorated with Dictyostelium myosin S1. Nature (1993) 2.44
Common variants in FCER1A influence total serum IgE levels from cord blood up to six years of life. Allergy (2009) 1.54
Microheterogeneity of serum glycoproteins and their liver precursors in patients with carbohydrate-deficient glycoprotein syndrome type I: apparent deficiencies in clusterin and serum amyloid P. J Lab Clin Med (1997) 1.42
Invasion of human keratinocytes by Staphylococcus aureus and intracellular bacterial persistence represent haemolysin-independent virulence mechanisms that are followed by features of necrotic and apoptotic keratinocyte cell death. Br J Dermatol (2002) 1.42
Putative association of a TLR9 promoter polymorphism with atopic eczema. Allergy (2007) 1.39
Stratum corneum lipids, skin barrier function and filaggrin mutations in patients with atopic eczema. Allergy (2010) 1.19
A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease. Genomics (1993) 1.15
Argiotoxin detects molecular differences in AMPA receptor channels. Neuron (1993) 1.15
[On the thio ether and S-oxide derivatives of adenosine]. Chem Ber (1965) 1.06
Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiency. Acta Paediatr (2002) 1.01
Analysis of the high affinity IgE receptor genes reveals epistatic effects of FCER1A variants on eczema risk. Allergy (2009) 1.01
Methods of preparing well-orientated sols of f-actin containing filaments suitable for X-ray diffraction. J Mol Biol (1987) 1.01
Role of Staphylococcus aureus surface-associated proteins in the attachment to cultured HaCaT keratinocytes in a new adhesion assay. J Invest Dermatol (1998) 1.00
Evaluating atomic models of F-actin with an undecagold-tagged phalloidin derivative. J Mol Biol (1998) 0.99
Agarose gel isoelectrofocusing of UDP-galactose pyrophosphorylase and galactose-1-phosphate uridyltransferase. Developmental aspect of UDP-galactose pyrophosphorylase. Clin Chim Acta (1987) 0.97
Network formation of lipid membranes: triggering structural transitions by chain melting. Proc Natl Acad Sci U S A (1999) 0.96
[Synthesis of 5'-substituted adenosine derivatives]. Chem Ber (1965) 0.95
Allotypes of alpha 1-antitrypsin in patients with cystic fibrosis, homozygous and heterozygous for deltaF508. Pediatr Pulmonol (1994) 0.95
Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung disease. Lancet (1992) 0.95
Silybin inhibition of amatoxin uptake in the perfused rat liver. Arzneimittelforschung (1980) 0.94
Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activities. Allergy (2011) 0.92
Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M allele. Am J Hum Genet (1994) 0.91
The course of eczema in children aged 5-7 years and its relation to atopy: differences between boys and girls. Br J Dermatol (2006) 0.89
The deficient alpha-I-antitrypsin phenotype PI P is associated with an A-to-T transversion in exon III of the gene. Am J Hum Genet (1989) 0.89
Integrative genetic and metabolite profiling analysis suggests altered phosphatidylcholine metabolism in asthma. Allergy (2013) 0.89
Psychoendocrine and psychoneuroimmunological mechanisms in the comorbidity of atopic eczema and attention deficit/hyperactivity disorder. Psychoneuroendocrinology (2012) 0.89
Subunit-specific block of cloned NMDA receptors by argiotoxin636. FEBS Lett (1993) 0.88
Monocyte-derived dendritic cells from highly atopic individuals are not impaired in their pro-inflammatory response to toll-like receptor ligands. Clin Exp Allergy (2007) 0.83
Disposition and metabolism of cetrorelix, a potent luteinizing hormone-releasing hormone antagonist, in rats and dogs. Drug Metab Dispos (2000) 0.83
Molecular characterisation of the defective alpha 1-antitrypsin alleles PI Mwurzburg (Pro369Ser), Mheerlen (Pro369Leu), and Q0lisbon (Thr68Ile). Eur J Hum Genet (1999) 0.83
Alpha1-antitrypsin: evidence for a fourth PiM allele. Distribution of the PiM subtypes in Southern Germany. Z Rechtsmed (1982) 0.83
Similarity between the effect of experimental congestion of the isolated perfused rat liver and the action of cytochalasin B. Naunyn Schmiedebergs Arch Pharmacol (1973) 0.83
[Determination of body height from fragments of the femur]. Gegenbaurs Morphol Jahrb (1980) 0.83
Esterase D polymorphism: description of the "new" allele EsD4. Hum Genet (1976) 0.83
[The effects on circulation of 5'-substituted adenosine derivatives]. Naunyn Schmiedebergs Arch Exp Pathol Pharmakol (1965) 0.82
DNA polymorphisms associated with a new alpha 1-antitrypsin PIQ0 variant (PIQ0riedenburg). Hum Genet (1991) 0.82
Interaction between rabbit muscle actin and several chaetoglobosins or cytochalasins. Anal Biochem (1979) 0.82
Endocytosis in the isolated perfused rat liver, induced by cytochalasin B. Naturwissenschaften (1975) 0.81
Novel procedures for derivatization of ribosomes for crystallographic studies. J Biol Chem (1989) 0.81
[Uptake of water and substances of high molecular weight by the isolated perfused liver during phalloidin poisoning and during increased posthepatic pressure]. Naunyn Schmiedebergs Arch Pharmacol (1972) 0.81
Epidemiology of urticaria in infants and young children in Germany--results from the German LISAplus and GINIplus Birth Cohort Studies. Pediatr Allergy Immunol (2013) 0.81
Sequence data of the rare deficient alpha 1-antitrypsin variant PI Zaugsburg. Am J Hum Genet (1990) 0.80
Visualization of a filamentous network in cryo sections of liver tissue. Eur J Cell Biol (1980) 0.80
Increased efficacy of omalizumab in atopic dermatitis patients with wild-type filaggrin status and higher serum levels of phosphatidylcholines. Allergy (2013) 0.80
Properdin factor B-polymorphism. An indication for the existence of a Bf O-allele. Z Rechtsmed (1979) 0.80
Two new Bf S subtypes revealed by isoelectric focusing and immunofixation. Hum Genet (1984) 0.80
Cytochalasin D is able to mimic the effects of phalloidin on the rat liver. Experientia (1979) 0.80
Metal compounds as tools for the construction and the interpretation of medium-resolution maps of ribosomal particles. J Struct Biol (1999) 0.80
Three new orosomucoid (ORM) variants revealed by isoelectric focusing and print immunofixation. Hum Genet (1987) 0.80
Identification and molecular characterization of the new alpha-1-antitrypsin deficient allele PI Y barcelona (Asp256-->Val and Pro391-->His). Mutations in brief no. 174. Online. Hum Mutat (1998) 0.79
Histopathology of chemically induced testicular atrophy in rats. Exp Toxicol Pathol (1995) 0.79
[Studies on antamanide. XIV. Mode of action]. Hoppe Seylers Z Physiol Chem (1972) 0.79
Itches and scratches – is there a link between eczema, ADHD, sleep disruption and food hypersensitivity? Allergy (2011) 0.79
[Diagnosis and nosology of glycanosis CDG ("carbohydrate deficient glycoprotein syndrome")]. Monatsschr Kinderheilkd (1992) 0.78
Population genetics of glyoxalase I (E.C.4.4.1.5) in human erythrocytes. Z Rechtsmed (1977) 0.78
DR2-positive monozygotic twins discordant for narcolepsy. Sleep (1990) 0.78
What is Pi (proteinase inhibitor) null or PiQO?: a problem highlighted by the alpha 1 antitrypsin Mheerlen mutation. J Med Genet (1992) 0.78
Polyamine spider toxins and mammalian N-methyl-D-aspartate receptors. Structural basis for channel blocking and binding of argiotoxin636. Eur J Biochem (1996) 0.78
Orosomucoid system: 17 additional orosomucoid variants and proposal for a new nomenclature. Vox Sang (1993) 0.78
Purification and characterization of subtilisin cleaved actin lacking the segment of residues 43-47 in the DNase I binding loop. Biochemistry (1995) 0.77
Development of a new aerosol delivery system for systemic pulmonary delivery in anaesthetized and orotracheal intubated rats. Lab Anim (2001) 0.77
Characterisation of the alpha-1-antitrypsin M3 gene, a normal variant. Hum Genet (1990) 0.77
[Coincidence of pulmonary fibrosis and bronchial carcinoma (author's transl)]. MMW Munch Med Wochenschr (1981) 0.77
[N6-(naphthyl-(1))-methyladenosine, an adenosine derivative with prolonged coronary effect]. Arzneimittelforschung (1969) 0.77
Isoelectric focusing with immobilized pH gradients for the analysis of transferrin (Tf) subtypes and variants. Hum Genet (1983) 0.77
GSTM1, GSTT1 and GSTP1 gene polymorphism in polymorphous light eruption. J Eur Acad Dermatol Venereol (2012) 0.77
The cytoskeleton of rat liver parenchymal cells. Naturwissenschaften (1980) 0.77
AIDS: no association with the genetic systems GC (D-binding protein), ORM (orosomucoid = alpha-1-acid glycoprotein), and A2HS (alpha-2-HS-glycoprotein). Infection (1988) 0.77
Surgical thrombectomy in horses with aortoiliac thrombosis: 17 cases. Equine Vet J (2009) 0.77
Argiotoxin636 inhibits NMDA-activated ion channels expressed in Xenopus oocytes. Neurosci Lett (1991) 0.76
Genetic polymorphism in the Garfagnana population (Tuscany). Gene Geogr (1993) 0.76
Visualization of a ternary complex of the Escherichia coli Phe-tRNA(Phe) and Tu.GTP from Thermus thermophilus by scanning transmission electron microscopy. J Struct Biol (1993) 0.76
A common atopy-associated variant in the Th2 cytokine locus control region impacts transcriptional regulation and alters SMAD3 and SP1 binding. Allergy (2014) 0.76
Characterization of the normal alpha 1-antitrypsin allele Vmunich: a variant associated with a unique protein isoelectric focusing pattern. Am J Hum Genet (1990) 0.76
Pyruvate kinase isozyme patterns of human neoplastic, fetal and adult tissues. Humangenetik (1975) 0.76
Compartment syndrome and shin splints of the lower leg. J Manipulative Physiol Ther (1993) 0.76
Plasminogen (PLG): a useful genetic marker for paternity examinations. Z Rechtsmed (1985) 0.75
[Demonstration of glyoxalase I (EC 4.4.1.5) in starch gel electrophoresis]. Med Lab (Stuttg) (1976) 0.75
"New" phenotypes in the human red cell isozyme system ADA. Z Rechtsmed (1986) 0.75
Subtyping of orosomucoid 1 (ORM1) by isoelectric focusing in agarose and polyacrylamide gels. Electrophoresis (1988) 0.75
A "new" allele of esterase D in a retinoblastoma family. Hum Genet (1988) 0.75
Description of a new variant in the glutamate-oxaloacetate transaminase system by thin-layer agarose gel isoelectric focusing. Electrophoresis (1991) 0.75
Variation of alpha 1-antitrypsin glycoprotein microheterogeneity in hepatic postresuscitation disease. Eur J Pediatr (1990) 0.75
Pi subtyping by isoelectric focusing: further genetic studies and application to paternity examinations. Z Rechtsmed (1980) 0.75
Transferrin variants in Tuscany (Italy). Evidence for two "new" Tf alleles. Hum Genet (1985) 0.75
[Dynamic measurement of pressure distribution on the foot sole of diabetic patients and a comparison group]. Wien Klin Wochenschr (1991) 0.75
New mutation versus exclusion at the alpha-1-antitrypsin locus: a multifaceted approach in a problematical paternity case. Hum Hered (1991) 0.75
[Early childhood oligoarthritis (antinuclear antibody positive) in alpha 1-antitrypsin deficiency of the PiIZ type]. Monatsschr Kinderheilkd (1989) 0.75
Transferrin subtypes and variants in Germany; further evidence for a Tf null allele. Hum Genet (1984) 0.75
Evidence for a new allele at the esterase D (E.C.3.1.1.1) locus. Hum Hered (1988) 0.75
Distribution of C3 and Bf allotypes in Tuscany (Italy). Hum Hered (1986) 0.75
Genetic polymorphism of alpha-2-HS-glycoprotein in a Spanish population. Hum Hered (1991) 0.75
Classification of transferrin (Tf) subtypes by isoelectric focusing. Z Rechtsmed (1980) 0.75
Transient aberrancy of alpha 1-antitrypsin glycoprotein microheterogeneity in Pseudomonas aeruginosa septicaemia. Infection (1991) 0.75
Extended polymorphism of the human esterase D isozyme system: description of a "new" allele EsD*11. Hum Genet (1986) 0.75
PI Scologne: a new variant in the alpha-1-antitrypsin system. Hum Genet (1988) 0.75
PGM1 subtypes determined by agarose gel isoelectrofocusing. Z Rechtsmed (1980) 0.75