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Results: 1-9 |
Results: 9
FUNCTIONAL OVERLAP BETWEEN MURINE INPP5B AND OCRL1 MAY EXPLAIN WHY DEFICIENCY OF THE MURINE ORTHOLOG FOR OCRL1 DOES NOT CAUSE LOWE-SYNDROMEIN MICE
Authors: JANNE PA SUCHY SF BERNARD D MACDONALD M CRAWLEY J GRINBERG A WYNSHAWBORIS A WESTPHAL H NUSSBAUM RL
Citation: Pa. Janne et al., FUNCTIONAL OVERLAP BETWEEN MURINE INPP5B AND OCRL1 MAY EXPLAIN WHY DEFICIENCY OF THE MURINE ORTHOLOG FOR OCRL1 DOES NOT CAUSE LOWE-SYNDROMEIN MICE, The Journal of clinical investigation, 101(10), 1998, pp. 2042-2053
SCREENING FOR HOMOLOGOUS RECOMBINATION IN ES CELLS USING RT-PCR
Authors: DANOFF TM CHIANG M JANNE PA NEILSON EG
Citation: Tm. Danoff et al., SCREENING FOR HOMOLOGOUS RECOMBINATION IN ES CELLS USING RT-PCR, BioTechniques, 22(1), 1997, pp. 22
PHYSICAL MAPPING AND GENOMIC STRUCTURE OF THE LOWE SYNDROME GENE OCRL1
Authors: NUSSBAUM RL ORRISON BM JANNE PA CHARNAS L CHINAULT AC
Citation: Rl. Nussbaum et al., PHYSICAL MAPPING AND GENOMIC STRUCTURE OF THE LOWE SYNDROME GENE OCRL1, Human genetics, 99(2), 1997, pp. 145-150
MICE DEFICIENT IN INPP5B, AN AUTOSOMAL PHOSPHATIDYLINOSITOL BISPHOSPHATE 5-PHOSPHATASE HOMOLOGOUS TO THE LOWE-SYNDROME PROTEIN
Authors: HELLSTEN EO JANNE PA BERNARD DJ ECKHAUS M OWENS J SUCHY SF PEARLINE RV NUSSBAUM RL
Citation: Eo. Hellsten et al., MICE DEFICIENT IN INPP5B, AN AUTOSOMAL PHOSPHATIDYLINOSITOL BISPHOSPHATE 5-PHOSPHATASE HOMOLOGOUS TO THE LOWE-SYNDROME PROTEIN, American journal of human genetics, 61(4), 1997, pp. 140-140
MAPPING OF THE 75-KDA INOSITOL POLYPHOSPHATE-5-PHOSPHATASE (INPP5B) TO DISTAL MOUSE CHROMOSOME-4 AND ITS EXCLUSION AS A CANDIDATE GENE FOR DYSGENETIC LENS
Authors: JANNE PA ROCHELLE JM MARTINDELEON PA STAMBOLIAN D SELDIN MF NUSSBAUM RL
Citation: Pa. Janne et al., MAPPING OF THE 75-KDA INOSITOL POLYPHOSPHATE-5-PHOSPHATASE (INPP5B) TO DISTAL MOUSE CHROMOSOME-4 AND ITS EXCLUSION AS A CANDIDATE GENE FOR DYSGENETIC LENS, Genomics, 28(2), 1995, pp. 280-285
PRODUCTION OF MICE DEFICIENT IN THE LOWE SYNDROME GENE (OCRL-1) AND ITS HIGHLY RELATED HOMOLOG, INOSITOL POLYPHOSPHATE 5-PHOSPHATASE (INPP5B)
Authors: JANNE PA BERNARD D CANNA C WYNSHAWBORIS A GRIMES P MCDONALD M CRAWLEY J OLIVOSGLANDER IM SUCHY SF NUSSBAUM RL
Citation: Pa. Janne et al., PRODUCTION OF MICE DEFICIENT IN THE LOWE SYNDROME GENE (OCRL-1) AND ITS HIGHLY RELATED HOMOLOG, INOSITOL POLYPHOSPHATE 5-PHOSPHATASE (INPP5B), American journal of human genetics, 57(4), 1995, pp. 57-57
THE LOWE SYNDROME GENE-PRODUCT HAS A DISTINCT DISSOCIATION PATTERN FROM GOLGI IN RESPONSE TO BREFELDIN-A
Authors: OLIVOSGLANDER IM JANNE PA NUSSBAUM RL
Citation: Im. Olivosglander et al., THE LOWE SYNDROME GENE-PRODUCT HAS A DISTINCT DISSOCIATION PATTERN FROM GOLGI IN RESPONSE TO BREFELDIN-A, American journal of human genetics, 57(4), 1995, pp. 846-846
THE OCULOCEREBRORENAL SYNDROME GENE-PRODUCT IS A 105-KD PROTEIN LOCALIZED TO THE GOLGI-COMPLEX
Authors: OLIVOSGLANDER IM JANNE PA NUSSBAUM RL
Citation: Im. Olivosglander et al., THE OCULOCEREBRORENAL SYNDROME GENE-PRODUCT IS A 105-KD PROTEIN LOCALIZED TO THE GOLGI-COMPLEX, American journal of human genetics, 57(4), 1995, pp. 817-823
LOCALIZATION OF THE 75-KDA INOSITOL POLYPHOSPHATE-5-PHOSPHATASE (INPP5B) TO HUMAN-CHROMOSOME BAND-1P34
Authors: JANNE PA DUTRA AS DRACOPOLI NC CHARNAS LR PUCK JM NUSSBAUM RL
Citation: Pa. Janne et al., LOCALIZATION OF THE 75-KDA INOSITOL POLYPHOSPHATE-5-PHOSPHATASE (INPP5B) TO HUMAN-CHROMOSOME BAND-1P34, Cytogenetics and cell genetics, 66(3), 1994, pp. 164-166
Risultati: 1-9 |