Published in Hautarzt on February 01, 2011
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
Alpha-1-antitrypsin: evidence for a fifth PI M subtype and a new deficiency allele PI*Z augsburg. Hum Genet (1985) 1.11
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
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
Agarose gel isoelectrofocusing of UDP-galactose pyrophosphorylase and galactose-1-phosphate uridyltransferase. Developmental aspect of UDP-galactose pyrophosphorylase. Clin Chim Acta (1987) 0.97
Characteristics of joint involvement and relationships with systemic inflammation in systemic sclerosis: results from the EULAR Scleroderma Trial and Research Group (EUSTAR) database. J Rheumatol (2010) 0.96
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
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 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
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
Psychoendocrine and psychoneuroimmunological mechanisms in the comorbidity of atopic eczema and attention deficit/hyperactivity disorder. Psychoneuroendocrinology (2012) 0.89
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
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
DNA polymorphisms associated with a new alpha 1-antitrypsin PIQ0 variant (PIQ0riedenburg). Hum Genet (1991) 0.82
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
Two new Bf S subtypes revealed by isoelectric focusing and immunofixation. Hum Genet (1984) 0.80
Properdin factor B-polymorphism. An indication for the existence of a Bf O-allele. Z Rechtsmed (1979) 0.80
Sequence data of the rare deficient alpha 1-antitrypsin variant PI Zaugsburg. Am J Hum Genet (1990) 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
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
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
What is Pi (proteinase inhibitor) null or PiQO?: a problem highlighted by the alpha 1 antitrypsin Mheerlen mutation. J Med Genet (1992) 0.78
Orosomucoid system: 17 additional orosomucoid variants and proposal for a new nomenclature. Vox Sang (1993) 0.78
Global Allergy Forum and Second Davos Declaration 2013 Allergy: Barriers to cure--challenges and actions to be taken. Allergy (2014) 0.78
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
Characterisation of the alpha-1-antitrypsin M3 gene, a normal variant. Hum Genet (1990) 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
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
Genetic polymorphism in the Garfagnana population (Tuscany). Gene Geogr (1993) 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
[Mucocutaneous candidiasis]. Dtsch Med Wochenschr (2010) 0.75
"New" phenotypes in the human red cell isozyme system ADA. Z Rechtsmed (1986) 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
Hypothyroidism phenocopy in glycanosis CDG (carbohydrate-deficient glycoprotein syndrome) Eur J Pediatr (1994) 0.75
A1/A2 blood group variant due to fucosylation deficiency in carbohydrate deficient glycoprotein syndrome type I? Eur J Pediatr (1999) 0.75
[Early childhood oligoarthritis (antinuclear antibody positive) in alpha 1-antitrypsin deficiency of the PiIZ type]. Monatsschr Kinderheilkd (1989) 0.75
A "new" allele of esterase D in a retinoblastoma family. Hum Genet (1988) 0.75
Genetic study of orosomucoid by isoelectric focusing and immunoprinting in patients with carcinoma. Electrophoresis (1993) 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
Evidence for a new allele at the esterase D (E.C.3.1.1.1) locus. Hum Hered (1988) 0.75
High-dose intravenous melphalan in a patient with multiple myeloma and oliguric renal failure. Clin Investig (1994) 0.75
Distribution of C3 and Bf allotypes in Tuscany (Italy). Hum Hered (1986) 0.75
[Dynamic measurement of pressure distribution on the foot sole of diabetic patients and a comparison group]. Wien Klin Wochenschr (1991) 0.75
Association between atopy and cryptorchidism. J Allergy Clin Immunol (2004) 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
PGD Port Elizabeth: a new variant found in South Africa. Hum Genet (1992) 0.75
PI Scologne: a new variant in the alpha-1-antitrypsin system. Hum Genet (1988) 0.75
Transient aberrancy of alpha 1-antitrypsin glycoprotein microheterogeneity in Pseudomonas aeruginosa septicaemia. Infection (1991) 0.75
[Alcoholic ketoacidosis--3 episodes in one patient]. Wien Klin Wochenschr (1992) 0.75
[Genetics of atopic eczema. An update]. Hautarzt (2015) 0.75
[Demonstration of glyoxalase I (EC 4.4.1.5) in starch gel electrophoresis]. Med Lab (Stuttg) (1976) 0.75
[Detection of tyrosinase mRNA using reverse transcription/polymerase chain reaction with fine needle punctures of melanoma metastases]. Hautarzt (1996) 0.75
Alpha-1-antitrypsin deficiency in children: liver disease is not reflected by low serum levels of alpha-1-antitrypsin - a study on 48 pediatric patients. Eur J Med Res (2005) 0.75
[New insights into the pathogenesis of sensitive skin]. Hautarzt (2011) 0.75
Apolipoprotein J deficiency in types I and IV carbohydrate-deficient glycoprotein syndrome (glycanosis CDG) Eur J Pediatr (1997) 0.75
Extended polymorphism of the human esterase D isozyme system: description of a "new" allele EsD*11. Hum Genet (1986) 0.75
PGM1 subtypes determined by agarose gel isoelectrofocusing. Z Rechtsmed (1980) 0.75
Plasminogen (PLG): a useful genetic marker for paternity examinations. Z Rechtsmed (1985) 0.75
Pericardial effusion in glycanosis CDG type I (MIM 212 065): an inflammatory endoplasmic reticulum overload response? Eur J Pediatr (1998) 0.75
A case of junctional epidermolysis bullosa with prurigo-like lesions and reduction of collagen XVII and filaggrin. Br J Dermatol (2013) 0.75
Transferrin variants in Tuscany (Italy). Evidence for two "new" Tf alleles. Hum Genet (1985) 0.75
[Genome-associated studies in chronic inflammatory dermatoses]. Internist (Berl) (2014) 0.75
Pi subtyping by isoelectric focusing: further genetic studies and application to paternity examinations. Z Rechtsmed (1980) 0.75
Transferrin subtypes and variants in Germany; further evidence for a Tf null allele. Hum Genet (1984) 0.75
Subtyping of orosomucoid 1 (ORM1) by isoelectric focusing in agarose and polyacrylamide gels. Electrophoresis (1988) 0.75