1
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Protein sequence requirements for function of the human T-cell leukemia virus type 1 Rex nuclear export signal delineated by a novel in vivo randomization-selection assay.
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Mol Cell Biol
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1996
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4.10
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2
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Identification of a novel cellular cofactor for the Rev/Rex class of retroviral regulatory proteins.
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Cell
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1995
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3.55
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3
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Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.
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Science
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1998
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3.39
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4
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Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.
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Science
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1998
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3.00
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5
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HIV-1-induced cell fusion is mediated by multiple regions within both the viral envelope and the CCR-5 co-receptor.
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EMBO J
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1997
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2.86
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6
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Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2.
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Genomics
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1999
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1.97
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7
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Structure and transcription of the Drosophila melanogaster vermilion gene and several mutant alleles.
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Mol Cell Biol
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1990
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1.66
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8
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Genetic evidence that the Tat proteins of human immunodeficiency virus types 1 and 2 can multimerize in the eukaryotic cell nucleus.
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J Virol
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1993
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1.62
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9
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Identification and functional characterization of a novel nuclear localization signal present in the yeast Nab2 poly(A)+ RNA binding protein.
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Mol Cell Biol
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1998
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1.35
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10
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The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells.
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Hum Mol Genet
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2000
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1.29
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11
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Synergistic enhancement of both initiation and elongation by acidic transcription activation domains.
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EMBO J
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1996
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1.03
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12
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Murine CXCR-4 is a functional coreceptor for T-cell-tropic and dual-tropic strains of human immunodeficiency virus type 1.
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J Virol
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1997
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0.93
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13
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Nucleocytoplasmic shuttling by protein nuclear import factors.
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Eur J Cell Biol
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1998
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0.88
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14
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Trypanosoma kansasensis sp. n. from Neotoma floridana in Kansas.
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J Wildl Dis
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1989
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0.86
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15
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DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.
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Adv Otorhinolaryngol
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2000
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0.81
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16
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Myosin XVA expression in the pituitary and in other neuroendocrine tissues and tumors.
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Am J Pathol
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2001
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0.79
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17
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A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.
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Clin Genet
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2008
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0.77
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18
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Absence of in-vitro fluoride-binding by the organic matrix of developing bovine enamel.
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Arch Oral Biol
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1988
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0.75
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