The Norway spruce genome sequence and conifer genome evolutionThe significance of developmental robustness for species diversityLoss of deeply conserved C-class floral homeotic gene function and C- and E-class protein interaction in a double-flowered ranunculid mutantStructural basis for the oligomerization of the MADS domain transcription factor SEPALLATA3 in Arabidopsis.The ABCs of flower development: mutational analysis of AP1/FUL-like genes in rice provides evidence for a homeotic (A)-function in grasses.MADS goes genomic in conifers: towards determining the ancestral set of MADS-box genes in seed plants.Live and let die - the B(sister) MADS-box gene OsMADS29 controls the degeneration of cells in maternal tissues during seed development of rice (Oryza sativa).Molecular mechanisms involved in convergent crop domestication.DEF- and GLO-like proteins may have lost most of their interaction partners during angiosperm evolution.Molecular genetic basis of pod corn (Tunicate maize)Selaginella Genome Analysis - Entering the "Homoplasy Heaven" of the MADS World.Phylogenomics of MADS-Box Genes in Plants - Two Opposing Life Styles in One Gene Family.Did Convergent Protein Evolution Enable Phytoplasmas to Generate 'Zombie Plants'?Phylogenomics reveals surprising sets of essential and dispensable clades of MIKC(c)-group MADS-box genes in flowering plants.Arabidopsis SEPALLATA proteins differ in cooperative DNA-binding during the formation of floral quartet-like complexes.The seirena B class floral homeotic mutant of California Poppy (Eschscholzia californica) reveals a function of the enigmatic PI motif in the formation of specific multimeric MADS domain protein complexes.Horizontal gene transfer and functional diversification of plant cell wall degrading polygalacturonases: Key events in the evolution of herbivory in beetles.Evidence that an evolutionary transition from dehiscent to indehiscent fruits in Lepidium (Brassicaceae) was caused by a change in the control of valve margin identity genes.Functional conservation of MIKC*-Type MADS box genes in Arabidopsis and rice pollen maturation.Conservation of fruit dehiscence pathways between Lepidium campestre and Arabidopsis thaliana sheds light on the regulation of INDEHISCENT.Robust views on plasticity and biodiversity.Non-canonical structure, function and phylogeny of the Bsister MADS-box gene OsMADS30 of rice (Oryza sativa).FLOWERING LOCUS C in monocots and the tandem origin of angiosperm-specific MADS-box genes.When the BRANCHED network bears fruit: How carpic dominance causes fruit dimorphism in Aethionema.The pleiotropic SEPALLATA-like gene OsMADS34 reveals that the 'empty glumes' of rice (Oryza sativa) spikelets are in fact rudimentary lemmas.Array of MADS-Box Genes: Facilitator for Rapid Adaptation?Missing Links: DNA‐Binding and Target Gene Specificity of Floral Homeotic ProteinsBeneficial and Pathogenic Arabidopsis Root-Interacting Fungi Differently Affect Auxin Levels and Responsive Genes During Early InfectionA conserved leucine zipper-like motif accounts for strong tetramerization capabilities of SEPALLATA-like MADS-domain transcription factors.
P50
Q22122154-695D8270-7A39-4F89-B2A5-B76ED137A1A2Q31060822-2A6EF7A7-D2C3-4415-8CEB-00798D88EF6FQ33354049-E58B58A0-A7EE-49C1-BC81-169E8232212BQ33359110-4F009793-9B81-414E-9244-DA30F33840B6Q33363980-2CE47F99-61A5-45A9-A3A9-66D46F3E9E57Q34379092-8BA5DF98-87DC-466A-8168-339530062F4CQ34516635-88A85ADA-340B-4208-A9A1-10D4EC54C7E9Q34987098-A85AB929-3332-45DA-B88E-2E6C0DD6068AQ35182443-E167C10C-A581-495E-8304-06FBC8217E38Q35935606-D8D81E25-AAF4-4BAA-A3C0-F667BAE8E797Q36233772-E8260C89-0A2D-4C9A-BAF8-4D195EEAD2D8Q37651431-3782E318-C67C-4352-B995-F5BD234FD505Q38606301-74BDB7E3-2DBF-4099-8677-E5D3187E74ABQ41440985-68D29A61-514D-4BC1-A50A-93255C63D59FQ42153664-454FBF8D-7BBC-471E-A648-9026AF695EB8Q42434856-E940BEAD-F42F-4EA8-B5C6-695BA2031D8AQ42669236-B9A839FF-5792-4423-AAA6-126D97D426DCQ43492713-4425392C-E14E-43B4-9502-05835BEA17E6Q43738562-73EA4620-BD52-4E6B-A039-DB6625BE6974Q44625480-35FA2D5A-E76B-4ABE-8D20-001C1E9F5663Q45805020-05BBAC28-DD3C-4471-9358-97BE37B5F7DCQ46653187-F61674BD-9C94-49D3-9EE0-0E11B967387EQ47754243-D9F10C14-073D-4C27-BD5C-49609B705569Q50054163-10EA6F6B-6AAA-40AD-B32C-B23C86F97BA8Q51128197-0119C392-92FA-4768-83B5-213D3D66799FQ56395892-6ACD04A3-CBBD-4D5B-8BF0-DAF5C7F273FBQ58834927-A75C5DD2-048E-448B-979C-88CF61ACF963Q64102426-0689D65D-ADED-4824-8485-02E287DD5A38Q64944341-227D242F-8939-447B-A505-F6226B1273CB
P50
description
Duits klinische genetica
@nl
German geneticist
@en
German geneticist
@en-ca
German geneticist
@en-gb
deutscher Genetiker
@de
genetista alemán
@es
genetista tedesco
@it
géineolaí Gearmánach
@ga
professor académico alemão
@pt
tysk professor
@da
name
Günter Theißen
@ast
Günter Theißen
@ca
Günter Theißen
@da
Günter Theißen
@de
Günter Theißen
@en
Günter Theißen
@es
Günter Theißen
@fr
Günter Theißen
@it
Günter Theißen
@nb
Günter Theißen
@nds
type
label
Günter Theißen
@ast
Günter Theißen
@ca
Günter Theißen
@da
Günter Theißen
@de
Günter Theißen
@en
Günter Theißen
@es
Günter Theißen
@fr
Günter Theißen
@it
Günter Theißen
@nb
Günter Theißen
@nds
prefLabel
Günter Theißen
@ast
Günter Theißen
@ca
Günter Theißen
@da
Günter Theißen
@de
Günter Theißen
@en
Günter Theißen
@es
Günter Theißen
@fr
Günter Theißen
@it
Günter Theißen
@nb
Günter Theißen
@nds
P214
P227
P1412
P1559
Günter Theißen
@de
P21
P214
P227
1027426107
P2798
P31
P569
1962-01-16T00:00:00Z
P735
P7859
viaf-278647125