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Wainwright Brandon J.
Wainwright Brandon
Wainwright B.J.
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http://hub.abes.fr/oup/periodical/nar/1986/volume_14/issue_7/101093nar1473149/authorship/1
http://hub.abes.fr/oup/periodical/nar/1986/volume_14/issue_5/101093nar1451951/authorship/2
http://hub.abes.fr/oup/periodical/hmg/1995/volume_4/issue_3/101093hmg43351/authorship/6
http://hub.abes.fr/bmj/periodical/jmedgenet/1986/volume_23/issue_5/B3591CB963AC14CDE053120B220A6689/authorship/1
http://hub.abes.fr/oup/periodical/hmg/1994/volume_3/issue_1/101093hmg31211/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2002/volume_11/issue_9/101093hmg1191059/authorship/8
http://hub.abes.fr/oup/periodical/nar/1985/volume_13/issue_12/101093nar13124610/authorship/1
http://hub.abes.fr/oup/periodical/nar/1986/volume_14/issue_21/101093nar14218681/authorship/10
http://hub.abes.fr/oup/periodical/hmg/1993/volume_2/issue_7/101093hmg271007/authorship/4
http://hub.abes.fr/oup/periodical/hmg/1999/volume_8/issue_2/101093hmg82291/authorship/9
http://hub.abes.fr/bmj/periodical/jmedgenet/1986/volume_23/issue_4/B3591CB9638014CDE053120B220A6689/authorship/7
http://hub.abes.fr/springer/periodical/11248/1992/volume_1/issue_2/B93CCAD707F84220E053120B220A671F/authorship/8
http://hub.abes.fr/springer/periodical/439/1987/volume_77/issue_2/B9280FB2F1FE5EE6E053120B220A60AA/authorship/4
http://hub.abes.fr/springer/periodical/11188/1989/volume_15/issue_6/B8F3FC40BB820E61E053120B220A409A/authorship/6
http://hub.abes.fr/springer/periodical/439/1986/volume_74/issue_3/B927DD9E89D15D90E053120B220A1EA8/authorship/4
http://hub.abes.fr/springer/periodical/439/1990/volume_84/issue_3/B927DD9E8C575D90E053120B220A1EA8/authorship/2
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Molecular cloning and localization to chromosome 6 of mouseINT1L1 gene
Analysis of the transgenome of MET transfectant cell lines reveals that MET activation is accompanied by an interstitial insertion
Genetic homogeneity of cystic fibrosis
RELP identified by the anonymous DNA segment pBAM34 at 19q13.3-qter [HGM8 assignment D19S6]
RFLP for a human cytochrome P-450 gene at 19ql3.1 - qter (HGM8 provisional designation CYPI)
Isolation of a further anonymous informative DNA sequence from chromosome seven closely linked to cystic flbrosis
DNA binding capacity of the WT1 protein is abolished by Denys—Drash syndrome WT1 point mutations
Haplotype analysis to determine the position of a mutation among closely linked DNA markers
Gene complementation of airway epithelium in the cystic fibrosis mouse is necessary and sufficient to correct the pathogen clearance and inflammatory abnormalities
Simple repeat polymorphism at the D9S151 locus
Isolation and Characterization of Human Patched 2 (PTCH2), a Putative Tumour Suppressor Gene in Basal Cell Carcinoma and Medulloblastoma on Chromosome 1p32
Successful targeting of the mouse cystic fibrosis transmembrane conductance regulator gene in embryonal stem cells
Chromosome assignment and restriction fragment length polymorphism analysis of the anonymous DNA probe B79a at 7q22 (HMG8 assignment D7S13)
Isolation of a polymorphic genomic clone from chromosome 7
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