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Results: 1-16 |
Results: 16

Authors: LARSSON NG WANG JM WILHELMSSON H OLDFORS A RUSTIN P LEWANDOSKI M BARSH GS CLAYTON DA
Citation: Ng. Larsson et al., MITOCHONDRIAL TRANSCRIPTION FACTOR-A IS NECESSARY FOR MTDNA MAINTENANCE AND EMBRYOGENESIS IN MICE, Nature genetics, 18(3), 1998, pp. 231-236

Authors: LARSSON NG OLDFORS A GARMAN JD BARSH GS CLAYTON DA
Citation: Ng. Larsson et al., DOWN-REGULATION OF MITOCHONDRIAL TRANSCRIPTION FACTOR-A DURING SPERMATOGENESIS IN HUMANS, Human molecular genetics, 6(2), 1997, pp. 185-191

Authors: LARSSON NG BARSH GS CLAYTON DA
Citation: Ng. Larsson et al., STRUCTURE AND CHROMOSOMAL LOCALIZATION OF THE MOUSE MITOCHONDRIAL-TRANSCRIPTION-FACTOR-A GENE (TFAM), Mammalian genome, 8(2), 1997, pp. 139-140

Authors: LARSSON NG GARMAN JD OLDFORS A BARSH GS CLAYTON DA
Citation: Ng. Larsson et al., A SINGLE-MOUSE GENE ENCODES THE MITOCHONDRIAL TRANSCRIPTION FACTOR-A AND A TESTIS-SPECIFIC NUCLEAR HMG-BOX PROTEIN, Nature genetics, 13(3), 1996, pp. 296-302

Authors: HOUSHMAND M LARSSON NG OLDFORS A TULINIUS M HOLME E
Citation: M. Houshmand et al., FATAL MITOCHONDRIAL MYOPATHY, LACTIC-ACIDOSIS, AND COMPLEX-I DEFICIENCY ASSOCIATED WITH A HETEROPLASMIC A-]G MUTATION AT POSITION-3251 IN THE MITOCHONDRIAL TRNALEU(UUR) GENE, Human genetics, 97(3), 1996, pp. 269-273

Authors: HOLME E TULINIUS MH LARSSON NG OLDFORS A
Citation: E. Holme et al., INHERITANCE AND EXPRESSION OF MITOCHONDRIAL-DNA POINT MUTATIONS, Biochimica et biophysica acta. Molecular basis of disease, 1271(1), 1995, pp. 249-252

Authors: TULINIUS MH HOUSHMAND M LARSSON NG HOLME E OLDFORS A HOLMBERG E WAHLSTROM J
Citation: Mh. Tulinius et al., DE-NOVO MUTATION IN THE MITOCHONDRIAL ATP SYNTHASE SUBUNIT-6 GENE (T8993G) WITH RAPID SEGREGATION RESULTING IN LEIGH-SYNDROME IN THE OFFSPRING, Human genetics, 96(3), 1995, pp. 290-294

Authors: TULINIUS MH OLDFORS A HOLME E LARSSON NG HOUSHMAND M FAHLESON P SIGSTROM L KRISTIANSSON B
Citation: Mh. Tulinius et al., ATYPICAL PRESENTATION OF MULTISYSTEM DISORDERS IN 2 GIRLS WITH MITOCHONDRIAL-DNA DELETIONS, European journal of pediatrics, 154(1), 1995, pp. 35-42

Authors: WALUM E ERIKSSON G PETERSON A HOLME E LARSSON NG ERIKSSON C ELSHAMY W
Citation: E. Walum et al., USE OF PRIMARY CULTURES AND CONTINUOUS CELL-LINES TO STUDY EFFECTS ONASTROCYTIC REGULATORY FUNCTIONS, Clinical and experimental pharmacology and physiology, 22(4), 1995, pp. 284-287

Authors: LARSSON NG TULINIUS MH HOLME E OLDFORS A
Citation: Ng. Larsson et al., PATHOGENETIC ASPECTS OF THE A8344G MUTATION OF MITOCHONDRIAL-DNA ASSOCIATED WITH MERRF SYNDROME AND MULTIPLE SYMMETRICAL LIPOMAS, Muscle & nerve, 1995, pp. 102-106

Authors: LARSSON NG CLAYTON DA
Citation: Ng. Larsson et Da. Clayton, MOLECULAR-GENETIC ASPECTS OF HUMAN MITOCHONDRIAL DISORDERS, Annual review of genetics, 29, 1995, pp. 151-178

Authors: OLDFORS A MOSLEMI AR FYHR IM HOLME E LARSSON NG LINDBERG C
Citation: A. Oldfors et al., MITOCHONDRIAL-DNA DELETIONS IN MUSCLE-FIBERS IN INCLUSION-BODY MYOSITIS, Journal of neuropathology and experimental neurology, 54(4), 1995, pp. 581-587

Authors: OLDFORS A HOLME E TULINIUS M LARSSON NG
Citation: A. Oldfors et al., TISSUE DISTRIBUTION AND DISEASE MANIFESTATIONS OF THE TRNA(LYS) A-]G((8344)) MITOCHONDRIAL-DNA MUTATION IN A CASE OF MYOCLONUS EPILEPSY ANDRAGGED-RED FIBERS, Acta Neuropathologica, 90(3), 1995, pp. 328-333

Authors: HOUSHMAND M LARSSON NG HOLME E OLDFORS A TULINIUS MH ANDERSEN O
Citation: M. Houshmand et al., AUTOMATIC SEQUENCING OF MITOCHONDRIAL TRANSFER-RNA GENES IN PATIENTS WITH MITOCHONDRIAL ENCEPHALOMYOPATHY, Biochimica et biophysica acta. Molecular basis of disease, 1226(1), 1994, pp. 49-55

Authors: LARSSON NG OLDFORS A HOLME E CLAYTON DA
Citation: Ng. Larsson et al., LOW-LEVELS OF MITOCHONDRIAL TRANSCRIPTION FACTOR-A IN MITOCHONDRIAL-DNA DEPLETION, Biochemical and biophysical research communications, 200(3), 1994, pp. 1374-1381

Authors: LARSSON NG OLDFORS A HOUSHMAND M HOLME E TULINIUS MH CLAYTON DA
Citation: Ng. Larsson et al., LOW-LEVELS OF THE MITOCHONDRIAL TRANSCRIPTION FACTOR A IN A PATIENT WITH MTDNA DEPLETION IN MUSCLE, American journal of human genetics, 53(3), 1993, pp. 159-159
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