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Authors: POUSI B HAUTALA T HYLAND JC SCHROTER J ECKES B KIVIRIKKO KI MYLLYLA R
Citation: B. Pousi et al., A COMPOUND HETEROZYGOTE PATIENT WITH EHLERS-DANLOS-SYNDROME TYPE-VI HAS A DELETION IN ONE ALLELE AND A SPLICING DEFECT IN THE OTHER ALLELE OF THE LYSYL HYDROXYLASE GENE, Human mutation, 11(1), 1998, pp. 55-61

Authors: POUSI B HAUTALA T HYLAND JC SCHROTER J ECKES B KIVIRIKKO KI MYLLYLA R
Citation: B. Pousi et al., A COMPOUND HETEROZYGOTE PATIENT WITH EHLERS-DANLOS-SYNDROME TYPE-VI HAS A DELETION IN ONE ALLELE AND A SPLICING DEFECT IN THE OTHER ALLELE OF THE LYSYL HYDROXYLASE GENE, Human mutation, 11(1), 1998, pp. 55-61

Authors: PAPPONEN H TOPPINEN T BAUMANN P MYLLYLA VV LEISTI J KUIVANIEMI H TROMP G MYLLYLA R
Citation: H. Papponen et al., MYOTONIA-CONGENITA IN NORTHERN FINLAND - FOUNDER MUTATIONS EXPLAIN THE HIGH PREVALENCE OF THE DISEASE, Molecular biology of the cell, 9, 1998, pp. 1952-1952

Authors: PAJUNEN L SUOKAS M HAUTALA T KELLOKUMPU S TEBBE B KIVIRIKKO KI MYLLYLA R
Citation: L. Pajunen et al., A SPLICE-SITE MUTATION THAT INDUCES EXON SKIPPING AND REDUCTION IN LYSYL HYDROXYLASE MESSENGER-RNA LEVELS BUT DOES NOT CREATE A NONSENSE CODON IN EHLERS-DANLOS-SYNDROME TYPE-VI, DNA and cell biology, 17(2), 1998, pp. 117-123

Authors: HEIM P RAGHUNATH M MEISS L HEISE U MYLLYLA R KOHLSCHUTTER A STEINMANN B
Citation: P. Heim et al., EHLERS-DANLOS-SYNDROME TYPE-VI (EDS-VI) - PROBLEMS OF DIAGNOSIS AND MANAGEMENT, Acta paediatrica, 87(6), 1998, pp. 708-710

Authors: HUTTUNEN P SAMPI M MYLLYLA R
Citation: P. Huttunen et al., ETHANOL-INDUCED HYPOTHERMIA AND THERMOGENESIS OF BROWN ADIPOSE-TISSUEIN THE RAT, Alcohol, 15(4), 1998, pp. 315-318

Authors: BOSCH T DANDLIKER R DONATI S HAUSLER G LESCURE M MYLLYLA R
Citation: T. Bosch et al., SPECIAL ISSUE ON OPTOELECTRONIC DISTANCE DISPLACEMENT MEASUREMENTS AND APPLICATIONS/, Journal of optics, 29(3), 1998, pp. 3-3

Authors: MYLLYLA R MARSZALEC J KOSTAMOVAARA J MANTYNIEMI A ULBRICH GJ
Citation: R. Myllyla et al., IMAGING DISTANCE MEASUREMENTS USING TOF LIDAR, Journal of optics, 29(3), 1998, pp. 188-193

Authors: ZHANG JL KILPELA A MAATTA K MYLLYLA R
Citation: Jl. Zhang et al., LOW-NOISE, WIDE-BAND RECEIVER FOR IMAGING LIDAR IN SPACE APPLICATIONS, Journal of optics, 29(3), 1998, pp. 216-219

Authors: VALTAVAARA M SZPIRER C SZPIRER J MYLLYLA R
Citation: M. Valtavaara et al., PRIMARY STRUCTURE, TISSUE DISTRIBUTION, AND CHROMOSOMAL LOCALIZATION OF A NOVEL ISOFORM OF LYSYL HYDROXYLASE (LYSYL HYDROXYLASE-3), The Journal of biological chemistry, 273(21), 1998, pp. 12881-12886

Authors: SZPIRER C SZPIRER J RIVIERE M VANVOOREN P VALTAVAARA M MYLLYLA R
Citation: C. Szpirer et al., LOCALIZATION OF THE GENE ENCODING A NOVEL ISOFORM OF HYDROXYLASE, Mammalian genome, 8(9), 1997, pp. 707-708

Authors: KELLOKUMPU S SUOKAS M RISTELI L MYLLYLA R
Citation: S. Kellokumpu et al., PROTEIN DISULFIDE-ISOMERASE AND NEWLY SYNTHESIZED PROCOLLAGEN CHAINS FORM HIGHER-ORDER STRUCTURES IN THE LUMEN OF THE ENDOPLASMIC-RETICULUM, The Journal of biological chemistry, 272(5), 1997, pp. 2770-2777

Authors: VALTAVAARA M PAPPONEN H PIRTTILA AM HILTUNEN K HELANDER H MYLLYLA R
Citation: M. Valtavaara et al., CLONING AND CHARACTERIZATION OF A NOVEL HUMAN LYSYL HYDROXYLASE ISOFORM HIGHLY EXPRESSED IN PANCREAS AND MUSCLE, The Journal of biological chemistry, 272(11), 1997, pp. 6831-6834

Authors: HEIKKINEN J TOPPINEN T YEOWELL H KRIEG T STEINMANN B KIVIRIKKO KI MYLLYLA R
Citation: J. Heikkinen et al., DUPLICATION OF 7 EXONS IN THE LYSYL HYDROXYLASE GENE IS ASSOCIATED WITH LONGER FORMS OF A REPETITIVE SEQUENCE WITHIN THE GENE AND IS A COMMON-CAUSE FOR THE TYPE-VI VARIANT OF EHLERS-DANLOS-SYNDROME, American journal of human genetics, 60(1), 1997, pp. 48-56

Authors: PIRSKANEN A KAIMIO AM MYLLYLA R KIVIRIKKO KI
Citation: A. Pirskanen et al., SITE-DIRECTED MUTAGENESIS OF HUMAN LYSYL HYDROXYLASE EXPRESSED IN INSECT CELLS, Matrix biology, 15(3), 1996, pp. 196-196

Authors: AILISTO H KOSTAMOVAARA J LAMMASNIEMI J MYLLYLA R
Citation: H. Ailisto et al., LIDAR MEASURES UP, Photonics spectra, 30(3), 1996, pp. 96-100

Authors: MAJAMAA K TOLONEN U RUSANEN H REMES AM MYLLYLA R HASSINEN IE
Citation: K. Majamaa et al., POLYNEUROPATHY IN THE MTDNA BASE-PAIR-3243 POINT MUTATION - REPLY, Neurology, 46(5), 1996, pp. 1495-1496

Authors: PIRSKANEN A KAIMIO AM MYLLYLA R KIVIRIKKO KI
Citation: A. Pirskanen et al., SITE-DIRECTED MUTAGENESIS OF HUMAN LYSYL HYDROXYLASE EXPRESSED IN INSECT CELLS - IDENTIFICATION OF HISTIDINE-RESIDUES AND AN ASPARTIC-ACID RESIDUE CRITICAL FOR CATALYTIC ACTIVITY, The Journal of biological chemistry, 271(16), 1996, pp. 9398-9402

Authors: MAKYNEN A KOSTAMOVAARA J MYLLYLA R
Citation: A. Makynen et al., POSITIONING RESOLUTION OF THE POSITION-SENSITIVE DETECTORS IN HIGH BACKGROUND ILLUMINATION, IEEE transactions on instrumentation and measurement, 45(1), 1996, pp. 324-326

Authors: KASKA DD KASKA SC NGUYEN AT PERCIVAL FW CHRISTOFFERSEN R COOPER JB MYLLYLA R
Citation: Dd. Kaska et al., ISOLATION OF CYTOCHROME-P450 CLONES FROM SCOTS PINE BY PCR, Molecular biology of the cell, 6, 1995, pp. 2573-2573

Authors: KARPPINEN A KILPELA A KARRAS M TORNBERG J MYLLYLA R
Citation: A. Karppinen et al., PAPERMAKING FURNISH PROPERTIES ESTIMATED BY TIME-RESOLVED SPECTROSCOPY, Journal of pulp and paper science, 21(5), 1995, pp. 151-154

Authors: MAKYNEN A KOSTAMOVAARA J MYLLYLA R
Citation: A. Makynen et al., LASER-RADAR-BASED 3-DIMENSIONAL SENSOR FOR TEACHING ROBOT PATHS, Optical engineering, 34(9), 1995, pp. 2596-2602

Authors: RUSANEN H MAJAMAA K TOLONEN U REMES AM MYLLYLA R HASSINEN IE
Citation: H. Rusanen et al., DEMYELINATING POLYNEUROPATHY IN A PATIENT WITH THE TRNA(LEU(UUR)), MUTATION AT BASE-PAIR-3243 OF THE MITOCHONDRIAL-DNA, Neurology, 45(6), 1995, pp. 1188-1192

Authors: VAINSHTEIN S ROSSIN VV KILPELA A KOSTAMOVAARA J MYLLYLA R MAATTA K
Citation: S. Vainshtein et al., INTERNAL Q-SWITCHING IN SEMICONDUCTOR-LASERS - HIGH-INTENSITY PULSES OF THE PICOSECOND RANGE AND THE SPECTRAL PECULIARITIES, IEEE journal of quantum electronics, 31(6), 1995, pp. 1015-1021

Authors: HEIKKINEN J HAUTALA T KIVIRIKKO KI MYLLYLA R
Citation: J. Heikkinen et al., STRUCTURE AND EXPRESSION OF THE HUMAN LYSYL HYDROXYLASE GENE (PLOD) -INTRON-9 AND INTRON-16 CONTAIN ALU SEQUENCES AT THE SITES OF RECOMBINATION IN EHLERS-DANLOS-SYNDROME TYPE-VI PATIENTS, Genomics, 24(3), 1994, pp. 464-471
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