48 research outputs found
Von Recklinghausen neurofibromatosis and genetic linkage studies: clinical considerations.
No full textSUBSTANTIAL AMOUNTS OF IMMUNOREACTIVE BAM-12P AND BAM-22P ARE PRESENT IN BOVINE ADRENAL MEDULLA BUT NOT IN THE BRAIN
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Peptide based P21RAS farnesyl transferase inhibitors: systematic modification of the tetrapeptide CA1A2X motif
Full text linkFurther exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markers.
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The gene for Lap18, leukemia-associated phosphoprotein p18 (metablastin), maps to distal mouse Chromosome 4
No full textStatistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma.
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Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17
No full textThe mutant gene causing von Recklinghausen neurofibromatosis (NF1) was recently shown to map to chromosome 17. We have used additional markers for chromosome 17 to narrow further the location of the gene defect. A preliminary multipoint linkage analysis suggests that the NF1 gene is located on the long arm of chromosome 17, flanked by D17Z1 and NGFR. Linkage analysis with the human oncogene homolog erbA1, which maps to this region, suggests that this cancer-related gene is not the primary cause of NF1
