about
P26
Removal of a cryptic intron and subcellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightlyStandards for plant synthetic biology: a common syntax for exchange of DNA parts.Optimization of trans-splicing ribozyme efficiency and specificity by in vivo genetic selection.Marking cell lineages in living tissues.Positional information in root epidermis is defined during embryogenesis and acts in domains with strict boundaries.Arabidopsis thaliana outer ovule integument morphogenesis: ectopic expression of KNAT1 reveals a compensation mechanism.A map of KNAT gene expression in the Arabidopsis root.Diarch symmetry of the vascular bundle in Arabidopsis root encompasses the pericycle and is reflected in distich lateral root initiation.A simple way to identify non-viable cells within living plant tissue using confocal microscopy.Gibberellin signaling in the endodermis controls Arabidopsis root meristem size.A Role for KNAT Class II Genes in Root DevelopmentA molecular framework for the inhibition of Arabidopsis root growth in response to boron toxicity.Coordination of plant cell division and expansion in a simple morphogenetic system.High-resolution live imaging of plant growth in near physiological bright conditions using light sheet fluorescence microscopy.Armadillo-related proteins promote lateral root development in Arabidopsis.Root gravitropism requires lateral root cap and epidermal cells for transport and response to a mobile auxin signal.Miranda mediates asymmetric protein and RNA localization in the developing nervous systemEctopic divisions in vascular and ground tissues of Arabidopsis thaliana result in distinct leaf venation defects.Striking similarities in amino acid sequence among nonstructural proteins encoded by RNA viruses that have dissimilar genomic organization.The uses of green fluorescent protein in plants.Design of highly specific cytotoxins by using trans-splicing ribozymes.Synthetic Biology: opportunities for Chilean bioindustry and education.GAL4-GFP enhancer trap lines for genetic manipulation of lateral root development in Arabidopsis thaliana.Orthogonal intercellular signaling for programmed spatial behavior.Chrysanthemum stunt viroid: primary sequence and secondary structure.Evolution and replication of tobacco ringspot virus satellite RNA mutants.Following cell fate in the living mouse embryo.A system for modelling cell-cell interactions during plant morphogenesis.Characterization of Intrinsic Properties of Promoters.GAL4 GFP enhancer trap lines for analysis of stomatal guard cell development and gene expression.Synthetic biology: history, challenges and prospectsSimple RNA enzymes with new and highly specific endoribonuclease activities. 1988.cg12 expression is specifically linked to infection of root hairs and cortical cells during Casuarina glauca and Allocasuarina verticillata actinorhizal nodule development.A computational method for automated characterization of genetic components.Structure, self-cleavage, and replication of two viroid-like satellite RNAs (virusoids) of subterranean clover mottle virus.Promiscuous and specific phospholipid binding by domains in ZAC, a membrane-associated Arabidopsis protein with an ARF GAP zinc finger and a C2 domain.Cell polarity-driven instability generates self-organized, fractal patterning of cell layers.Programmed hierarchical patterning of bacterial populations.Time of day modulates low-temperature Ca signals in Arabidopsis.Spatial control of transgene expression in rice (Oryza sativa L.) using the GAL4 enhancer trapping system.
P50
Q24564800-C64F7FED-25BF-4E8E-8D40-44FF84F5F4A2Q30316378-EB707C6E-A408-455B-BAB0-24C04434731BQ31121964-756DC066-4C35-42EE-A5CC-2E7648D767A2Q31161594-E6651F07-869D-4813-AFED-6F54FD010B00Q32067129-155B4EAC-1238-478A-8E7E-E79C91867910Q33328123-4ACAC615-D53B-4749-8200-424955EE44DCQ33342093-AEB3C6DB-A36D-44DC-832F-D81F750D3F94Q33344822-D84F7818-7BBA-4ECC-B3E3-DAA35C1C43B3Q33345901-2521981B-D4A8-4EF4-A37C-35017049DEBCQ33347380-E6545239-1E5F-4411-87E7-42A6A9FE2069Q33347746-AD599237-7157-432D-995C-4BA47D85B84CQ33352321-FEE203B2-3368-431E-B499-EA10316AD658Q33664332-9DC9D7B6-12DA-4E36-BE2D-20035A3551D3Q34196113-64BA533E-D9D4-4E63-B990-BAC7157D88F3Q34334851-1378E285-9741-42B8-B895-C496FC7E31CCQ34462224-3140639A-2B94-4827-8FAF-888FF02D60C3Q35202358-3274DE77-580B-46DF-B3B2-851F8EB99BF3Q36199709-F83ACB4F-712D-4A77-AA17-AA301041B152Q36272140-D6460104-4609-400B-A50D-0261488C35D0Q36334570-100BC10A-977B-495F-B15C-2A6237356AB9Q36441726-BEB7EF8E-D045-40A6-87F2-B98E34B401C9Q38186594-FFA20450-3FDF-40CA-B5D0-10FA07AA8171Q38323221-A44011E7-E6AA-4B93-A56C-5FE430D2F4F2Q40058077-066B414F-B865-4709-90C1-12F207768307Q40496642-5407780D-DC0B-4B61-B750-BAAEFDEF8694Q40873511-C5078970-247A-4E87-B20A-79523DF64526Q41123242-E833FCC6-790C-4A72-95F3-E63F6F6CC71CQ42152907-D13D808B-EFA3-4EB3-8B07-F750640121B0Q42197915-D7B6B915-8621-4619-BFD0-BB4C473EC817Q42711554-820DE0A5-A521-495A-9925-521CD3B914F2Q42860873-8FB99F1B-DF4E-4F43-AF14-327347F53737Q44426582-3C9B8809-CE00-4FD2-98A5-CCE84E70D6D1Q45177002-8B834649-8B54-4867-A16E-F98224B22DEEQ45394739-81A901AF-5564-4DBC-A8E4-83E3B92805A0Q45860242-1F995BA1-A605-4F89-BB67-FDDFD9EA5C38Q48379864-C4405DD0-3605-4B6C-970F-D960D17A4968Q48722866-C8272194-C7EE-4D5E-8C27-707A75A87694Q50300046-C329C8DD-C9BC-44A1-8838-CEE7E797A6A5Q50701221-2F3A86F4-BB30-4CF0-B3B7-D28A237150F1Q50778285-B371E589-5EAC-48D8-9E51-CA3759E72A16
P50
description
Synthetic biologist at the University of Cambridge
@en
onderzoeker
@nl
name
Jim Haseloff
@ast
Jim Haseloff
@en
Jim Haseloff
@es
Jim Haseloff
@nl
Jim Haseloff
@sl
type
label
Jim Haseloff
@ast
Jim Haseloff
@en
Jim Haseloff
@es
Jim Haseloff
@nl
Jim Haseloff
@sl
altLabel
James Phillip Haseloff
@en
prefLabel
Jim Haseloff
@ast
Jim Haseloff
@en
Jim Haseloff
@es
Jim Haseloff
@nl
Jim Haseloff
@sl
P214
P244
P106
P1153
7004035181
P1960
UNi_SX4AAAAJ
P2002
jimhaseloff
P2038
Jim_Haseloff
P21
P214
P244
no2010061709
P2456
P26
P31
P496
0000-0003-4793-8058
P734
P735
P7859
lccn-no2010061709