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1.
Hum Mutat ; 15(3): 254-60, 2000.
Article in English | MEDLINE | ID: mdl-10679941

ABSTRACT

Phenylketonuria (PKU) is an important error of amino acid metabolism which results in most patients from phenylalanine hydroxylase (PAH) deficiency. PKU displays a marked genotypic heterogeneity both within and between different populations. The aim of this study was to establish the genotypic spectrum of PKU in eastern Germany, and to compare this to the distribution of mutations in western Germany. The study population included 302 patients in 290 families who were followed at treatment centers in Berlin, Leipzig and Jena. The study showed marked genotypic variability with a total of 75 mutations, including 15 that have so far not been described (eleven missense mutations, one splicing mutation, and three small deletions). One of these novel mutations, E183Q, occurred in cis to a R408W mutation. In the non-immigrant eastern German population, the frequency of R408W accounted for 40.1% of the PKU alleles. In the immigrant Turkish population of the former West Berlin, the most prevalent mutation was IVS10-11G>A (57%). There was a marked difference of the genotypic spectrum between the population studied here and the data reported from the western part of the country.


Subject(s)
Phenylalanine/blood , Phenylketonurias/genetics , Amino Acid Substitution , DNA/chemistry , DNA/genetics , DNA Mutational Analysis , Family Health , Female , Germany , Humans , Male , Mutation , Phenylketonurias/blood , Point Mutation , Sequence Deletion
2.
Clin Cancer Res ; 3(11): 1923-30, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9815581

ABSTRACT

The purpose of this study was to investigate the prognostic value of the expression of intercellular adhesion molecule 1 (ICAM-1), leukocyte function antigen 3 (LFA-3), human leukocyte differentiation antigen (HLA)-ABC, HLA-DR, and 5T4 with regard to disease-free survival in Dukes' B and C colorectal carcinoma patients. Forty-one patients (28 Dukes' B and 13 Dukes' C) were entered into this study. Immunocytochemistry was performed on cytospin preparations of enzymatically digested colorectal carcinoma cell suspensions. The frequency of metastases and the duration of disease-free survival were compared between the 25% lowest expressers and the 75% remaining patients for ICAM-1, LFA-3, HLA-ABC, and HLA-DR, and between the 25% highest expressers and the 75% remaining patients for 5T4. Low numbers of ICAM-1-expressing tumor cells were associated with a shorter disease-free survival (P < 0. 001), independent of Dukes' stage. High numbers of 5T4-expressing tumor cells were associated with shorter disease-free survival in Dukes' B patients (P = 0.04). Cox proportional hazard analysis indicated that low numbers of ICAM-1(+) and high numbers of 5T4(+) cells were independent prognostic factors with relative risks of 13. 0 (P = 0.0002) and 4.7 (P = 0.02), respectively. The combination of 5T4 and ICAM-1 marker information identified subgroups of patients with a good (high ICAM-1) or poor (low ICAM-1/high 5T4) prognosis. Neither a lack of HLA-ABC and LFA-3 expression nor the presence of HLA-DR on the tumor cells gave additional prognostic information. These findings demonstrate that low ICAM-1 and high 5T4 expression on tumor cells are prognostic markers, additional to Dukes' stage, for reduced disease-free survival in Dukes' B and C colorectal carcinoma patients.


Subject(s)
Colorectal Neoplasms/pathology , Intercellular Adhesion Molecule-1/analysis , Membrane Glycoproteins/analysis , Aged , Antigens, Neoplasm/analysis , Blood Transfusion , CD58 Antigens/analysis , Colorectal Neoplasms/immunology , Colorectal Neoplasms/mortality , Colorectal Neoplasms/surgery , Disease-Free Survival , Female , Follow-Up Studies , HLA-DR Antigens/analysis , Histocompatibility Antigens Class I/analysis , Humans , Male , Neoplasm Staging , Proportional Hazards Models , Survival Rate , Time Factors
3.
Am J Physiol ; 271(4 Pt 2): R1025-32, 1996 Oct.
Article in English | MEDLINE | ID: mdl-8897996

ABSTRACT

Postnatal adaptation should be associated with changes in cardiac rhythmic behavior. To examine the development of heart rate variability, instantaneous heart rate (IHR) and the corresponding breathing signals of 16 healthy infants were analyzed. This was pursued by use of fast Fourier transformation beginning with the 1st day until the 6th mo of life. Power in the low-frequency range (LF, 0.02-0.2 Hz) and high-frequency range (HF, 0.2-1.5 Hz), total power (TP), the quotient LF/HF, and the frequency of the peak in LF and HF (LFF and HFF, respectively) were derived from the IHR spectrum. The peak frequency in HF (RF) was detected in the respiratory spectrum. Power and frequency of IHR rhythms undergo a marked development. TP, LF, and HF are lowest from the end of the 1st mo until the 2nd mo. LF predominates over HF, with LF/HF reaching its peak during 1- to 2-mo period. HF, recording respiratory related rhythms is negatively correlated with the breathing rate (BR). HFF and RF both show an increasing tendency during the 1st mo followed by a decrease down to the 6th mo. However, HFF is lower than RF if BR is high, mainly during the first 2 mo. The distinct changes in BR and its important influence on the IHR spectrum underscore the importance of monitoring respiration as a further measure in the diagnosis of infants. LFF is on average between 0.075 and 0.095 Hz, exhibiting an irregular course with minimum at the 10th, 21st-28th, and 90th day being apparent. The developmental pattern of LFF may by interpreted in terms of the maturation of the nervous system involved in the generation of circulatory rhythms.


Subject(s)
Heart Rate , Heart/physiology , Infant, Newborn/physiology , Respiration/physiology , Aging/physiology , Female , Fourier Analysis , Humans , Infant , Male
4.
Cancer Immunol Immunother ; 42(6): 351-6, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8830738

ABSTRACT

Mucins (MUC) are highly glycosylated molecules widely expressed on epithelia of different origins, including colonic mucosa. Altered glycosylation processes in tumour cells result in the exposure of normally cryptic peptide epitopes, which may then be recognized as tumour-specific antigens. Recently, MUC1-specific antibodies were detected in the serum of a broad range of cancer patients, and from different tumours tumour-specific cytotoxic T lymphocytes (CTL) were isolated that recognized MUC1. Absence of HLA restriction in the recognition has been ascribed to the highly repetitive sequence of the polypeptide core, allowing simultaneous recognition of multiple identical epitopes and cross-linking and aggregation of T cell receptor on mucin-specific T cells. We investigated the expression of MUC1 epitopes in 56 cell suspensions from Dukes' B to D colorectal carcinomas using antibodies that recognize distinct peptide sequences on the glycosylated or deglycosylated MUC1 protein backbone. No relation was observed between MUC1 expression, or the extent of its glycosylation, and Dukes' stage, tumour location and tumour differentiation, but a positive correlation was detected between the percentages of tumour cells expressing mucin-1 and the numbers of CD3+ infiltrating cells. These tumour-infiltrating lymphocytes contained, however, only a few MUC1-specific T lymphocytes, as CTL showing preferential killing of MUC1-expressing target cells were only obtained from one tumour. Since, in addition, the majority of colorectal carcinomas were found to express the fully glycosylated MUC1 glycoprotein, its potential role as a target antigen for T-lymphocyte-mediated immunotherapy in this tumour type is probably limited.


Subject(s)
Colorectal Neoplasms/immunology , Colorectal Neoplasms/pathology , Lymphocytes, Tumor-Infiltrating/immunology , Mucin-1/analysis , T-Lymphocytes, Cytotoxic/immunology , Antibodies, Monoclonal , CD3 Complex/immunology , Epitopes/analysis , Glycosylation , Humans , Mucin-1/immunology , Mucin-1/metabolism , Neoplasm Staging
5.
Fetal Diagn Ther ; 9(4): 256-60, 1994.
Article in English | MEDLINE | ID: mdl-7945907

ABSTRACT

Beckwith-Wiedemann syndrome (BWS), though a well-delineated clinical and morphological entity, can be difficult to diagnose by prenatal ultrasound examination when incomplete forms occur. We present a case with sonographic results including hydronephrosis, cardiomegalia, hepatomegalia, macroglossia, and prominent forehead. No abdominal wall defect was detected. Karyotype was normal. In spite of intensive prenatal diagnostics, BWS could not be diagnosed definitely until birth.


Subject(s)
Beckwith-Wiedemann Syndrome/diagnostic imaging , Ultrasonography, Prenatal , Adult , Amniocentesis , Beckwith-Wiedemann Syndrome/diagnosis , Cordocentesis , Cryptorchidism , Diagnosis, Differential , Female , Hernia, Umbilical/diagnostic imaging , Humans , Hypertelorism , Karyotyping , Macroglossia , Male , Pregnancy , Prenatal Diagnosis
6.
Eur J Clin Microbiol Infect Dis ; 8(2): 127-30, 1989 Feb.
Article in English | MEDLINE | ID: mdl-2498093

ABSTRACT

The prevalence of Chlamydia trachomatis infection in a population of women with no symptoms of sexually transmitted disease was investigated. These women, aged 35-55 years, participated in a screening program for cervical cancer. With the use of a direct immunofluorescence method, 109 out of 2,470 smears tested were positive for Chlamydia trachomatis, indicating an overall prevalence of 4.4%. No changes in prevalence were found when five-year cohorts of this group were analyzed, indicating that age-dependent changes or epidemiological factors do not result in a different (decreased) prevalence over the ages 35 to 55 years. The prevalence of Trichomonas vaginalis and fungi, as detected by cytological screening, was lower than that observed for Chlamydia trachomatis: 3.1 and 2.1%, respectively. Of the 109 smears positive for Chlamydia trachomatis, 90 showed cervical cells with reactive changes (out of 1,490 smears with PAP II), whereas no cytological changes were found in 15 cases (out of 884 smears with PAP I). Changes suggestive of mild or moderate dysplasia were found in only four cases (out of 93 smears with PAP III). The results indicate that Chlamydia trachomatis is associated with reactive changes of endocervical cells and raise serious questions about whether prevention of possible secondary effects such as infertility and pelvic inflammatory disease can be achieved by a combined screening program for cervical cancer and Chlamydia trachomatis.


Subject(s)
Chlamydia Infections/epidemiology , Uterine Cervical Neoplasms/diagnosis , Adult , Chlamydia Infections/diagnosis , Chlamydia trachomatis , Cross-Sectional Studies , Female , Fluorescent Antibody Technique , Humans , Middle Aged , Netherlands , Uterine Cervical Dysplasia/diagnosis , Vaginal Smears
7.
Zentralbl Gynakol ; 111(10): 669-77, 1989.
Article in German | MEDLINE | ID: mdl-2665390

ABSTRACT

Early detection of fetal malformations has become possible owing to the availability of highly advanced ultrasound systems. Majority of malformations, 30 per cent, has been recordable from urinary system. This system is early of access for the examiner, so that even sophisticated diagnosis of malformation is possible. High accuracy diagnosis has been increasingly helpful in forecasting pregnancy prognosis. Hence, with adequate perinatological management, it will be possible to influence on perinatal morbidity and mortality positively. 70 fetuses with malformations of kidneys and to urinary system have been observed in the context of this study. An assessment was made of diagnostic efficiency, postpartum development and long-range prognosis. Recommendations are derived from the above mentioned findings for perinatological approach in cases of diagnosed malformations of kidneys and the other urinary system.


Subject(s)
Abnormalities, Multiple/diagnosis , Kidney/abnormalities , Prenatal Diagnosis/methods , Ultrasonography/methods , Urinary Tract/abnormalities , Abortion, Induced , Adult , Female , Humans , Hydronephrosis/diagnosis , Infant, Newborn , Kidney Diseases, Cystic/diagnosis , Pregnancy , Prune Belly Syndrome/diagnosis , Risk Factors
8.
Article in German | MEDLINE | ID: mdl-2658030

ABSTRACT

The contribution deals with the following topics: --A possible utilization of the biological soil remediation techniques. --Laboratory investigations for remediation projects. --Development of pilot treatments projects. --Technical treatments, monitoring, and the enhancement of microbial activities on a full scale.


Subject(s)
Bacteria/metabolism , Hydrocarbons, Halogenated/metabolism , Soil Pollutants , Water Pollution , Biodegradation, Environmental , Soil Microbiology , Water Microbiology
9.
Z Gesamte Inn Med ; 42(16): 450-3, 1987 Aug 15.
Article in German | MEDLINE | ID: mdl-3687136

ABSTRACT

The article describes a method for the quantification of plasma fibronectin (FN) by means of electroimmunodiffusion after Laurell. By this means the fibronectin concentrations of healthy, mature newborns as well as of their mothers were determined. The average FN-level of the newborns lies at 33% related to the value for adults and at 48%, respectively, related to the maternal FN-content. There is no difference between male and female newborns. The FN-concentrations of the adults stated by us with 330 and 314 mg/l, respectively, for males and females correspond to the data in literature. Furthermore, the FN-content in plasma preparations was determined, with an average value of 2,356 mg/l this was highest in the factor-VIII-concentrate. The expediency and the prerequisites for a possible fibronectin substitution are discussed.


Subject(s)
Blood Transfusion , Fibronectins/blood , Infant, Newborn/blood , Maternal-Fetal Exchange , Female , Humans , Pregnancy , Reference Values
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