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Results: 1-9 |
Results: 9
AUTOSOMAL-DOMINANT CHARCOT-MARIE-TOOTH DISEASE TYPE 1A AND HEREDITARYNEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - DETECTION OF THE RECOMBINATION HOTSPOT IN SLOVENE PATIENTS AND EXCLUSION OF THE POTENTIALLYRECESSIVE THR118MET PMP22 POINT MUTATION
Authors: LEONARDIS L ZIDAR J EKICI A PETERLLIN B RAUTENSTRAUSS B
Citation: L. Leonardis et al., AUTOSOMAL-DOMINANT CHARCOT-MARIE-TOOTH DISEASE TYPE 1A AND HEREDITARYNEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - DETECTION OF THE RECOMBINATION HOTSPOT IN SLOVENE PATIENTS AND EXCLUSION OF THE POTENTIALLYRECESSIVE THR118MET PMP22 POINT MUTATION, INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 1(2), 1998, pp. 495-501
ASSAY OF TRANSFECTION RATE IN INSECT CELLS ON A SINGLE-CELL LEVEL
Authors: RAUTENSTRAUSS B FUCHS C EKICI A NELIS E VANBROECKHOVEN C LIEHR T
Citation: B. Rautenstrauss et al., ASSAY OF TRANSFECTION RATE IN INSECT CELLS ON A SINGLE-CELL LEVEL, GENET A-BIO, 14(3), 1998, pp. 103-104
FATTY-ACID ELONGATION IN YEAST - BIOCHEMICAL CHARACTERISTICS OF THE ENZYME-SYSTEM AND ISOLATION OF ELONGATION-DEFECTIVE MUTANTS
Authors: DITTRICH F ZAJONC D HUHNE K HOJA U EKICI A GREINER E KLEIN H HOFMANN J BESSOULE JJ SPERLING P SCHWEIZER E
Citation: F. Dittrich et al., FATTY-ACID ELONGATION IN YEAST - BIOCHEMICAL CHARACTERISTICS OF THE ENZYME-SYSTEM AND ISOLATION OF ELONGATION-DEFECTIVE MUTANTS, European journal of biochemistry, 252(3), 1998, pp. 477-485
CLINICAL AND MORPHOLOGICAL PHENOTYPE OF HMSN 1A MOSAICISM
Authors: GREHL H RAUTENSTRAUSS B LIEHR T BICKEL A EKICI A BATHKE K NEUNDORFER B
Citation: H. Grehl et al., CLINICAL AND MORPHOLOGICAL PHENOTYPE OF HMSN 1A MOSAICISM, Neuromuscular disorders, 7(1), 1997, pp. 27-31
MOSAICISM FOR THE CHARCOT-MARIE-TOOTH DISEASE TYPE 1A DUPLICATION SUGGESTS SOMATIC REVERSION
Authors: LIEHR T RAUTENSTRAUSS B GREHL H BATHKE KD EKICI A RAUCH A ROTT HD
Citation: T. Liehr et al., MOSAICISM FOR THE CHARCOT-MARIE-TOOTH DISEASE TYPE 1A DUPLICATION SUGGESTS SOMATIC REVERSION, Human genetics, 98(1), 1996, pp. 22-28
REGIONAL LOCALIZATION OF RAT MYELIN PROTEIN ZERO MPZ GENE TO CHROMOSOME 13Q24-25 BY MEANS OF FISH
Authors: LIEHR T EKICI A HILLENBRAND R RAUTENSTRAUSS B
Citation: T. Liehr et al., REGIONAL LOCALIZATION OF RAT MYELIN PROTEIN ZERO MPZ GENE TO CHROMOSOME 13Q24-25 BY MEANS OF FISH, Mammalian genome, 6(11), 1995, pp. 824-825
EVIDENCE FOR A MODIFIED RECOMBINATION EVENT IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP)
Authors: BATHKE KD LIEHR T EKICI A TIMMERMAN V VANBROECKHOVEN C GREHL H NEUNDORFER B RAUTENSTRAUSS B
Citation: Kd. Bathke et al., EVIDENCE FOR A MODIFIED RECOMBINATION EVENT IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP), American journal of human genetics, 57(4), 1995, pp. 1195-1195
ASSIGNMENT OF PMP22 AND PO, CANDIDATE GENES FOR CHARCOT-MARIE-TOOTH (CMT) DISEASE TYPE 1A AND 1B TO RAT CHR 10Q22 AND 13Q24-26 BY FISH
Authors: LIEHR T EKICI A HILLENBRAND R SCHACHNER M RAUTENSTRAUSS B
Citation: T. Liehr et al., ASSIGNMENT OF PMP22 AND PO, CANDIDATE GENES FOR CHARCOT-MARIE-TOOTH (CMT) DISEASE TYPE 1A AND 1B TO RAT CHR 10Q22 AND 13Q24-26 BY FISH, American journal of human genetics, 57(4), 1995, pp. 1888-1888
MYELIN-ASSOCIATED GLYCOPROTEIN IMMUNOREACTIVITY AND CHARCOT-MARIE-TOOTH (CMT) DISEASE TYPE 1A - ASSOCIATION OF CMT AND MULTIPLE-SCLEROSIS
Authors: RAUTENSTRAUSS B GOTZ A LIEHR T GREHL H SOSTARKO M BATHKE KD EKICI A PARK O DUMSER T HAUSMANN R HILLENBRAND R SCHACHNER M PFEIFFER RA NEUNDORFER B
Citation: B. Rautenstrauss et al., MYELIN-ASSOCIATED GLYCOPROTEIN IMMUNOREACTIVITY AND CHARCOT-MARIE-TOOTH (CMT) DISEASE TYPE 1A - ASSOCIATION OF CMT AND MULTIPLE-SCLEROSIS, American journal of human genetics, 57(4), 1995, pp. 1975-1975
Risultati: 1-9 |