scholarly article | Q13442814 |
P50 | author | Aziz A. Aboobaker | Q54206627 |
P2093 | author name string | Daniel A Felix | |
Belen Tejada-Romero | |||
Robert A Blassberg | |||
P2860 | cites work | The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH | Q24605482 |
Combining classical and molecular approaches elaborates on the complexity of mechanisms underpinning anterior regeneration | Q27312105 | ||
SMG-1 and mTORC1 act antagonistically to regulate response to injury and growth in planarians | Q27334311 | ||
dlx and sp6-9 Control optic cup regeneration in a prototypic eye | Q27338145 | ||
The TALE class homeobox gene Smed-prep defines the anterior compartment for head regeneration | Q27347706 | ||
Planarian Hh signaling regulates regeneration polarity and links Hh pathway evolution to cilia | Q30494271 | ||
Smed-Evi/Wntless is required for beta-catenin-dependent and -independent processes during planarian regeneration. | Q51826212 | ||
Silencing of Smed-betacatenin1 generates radial-like hypercephalized planarians. | Q51963787 | ||
Planarian homologs of netrin and netrin receptor are required for proper regeneration of the central nervous system and the maintenance of nervous system architecture. | Q52043748 | ||
An in situ hybridization protocol for planarian embryos: monitoring myosin heavy chain gene expression. | Q52044695 | ||
Regeneration and pattern formation in planarians. I. The pattern of mitosis in anterior and posterior regeneration in Dugesia (G) tigrina, and a new proposal for blastema formation | Q70677689 | ||
Smed-betacatenin-1 is required for anteroposterior blastema polarity in planarian regeneration | Q80156777 | ||
The maintenance and regeneration of the planarian excretory system are regulated by EGFR signaling | Q30503349 | ||
Planarian Hedgehog/Patched establishes anterior-posterior polarity by regulating Wnt signaling | Q33564284 | ||
Segment-specific neuronal subtype specification by the integration of anteroposterior and temporal cues | Q33582048 | ||
A dual platform approach to transcript discovery for the planarian Schmidtea mediterranea to establish RNAseq for stem cell and regeneration biology | Q33778543 | ||
Expression of secreted Wnt pathway components reveals unexpected complexity of the planarian amputation response | Q34131150 | ||
Planarian stem cells: a simple paradigm for regeneration. | Q34167037 | ||
Clonogenic neoblasts are pluripotent adult stem cells that underlie planarian regeneration | Q34184695 | ||
The Meis homeoprotein regulates the axolotl Prod 1 promoter during limb regeneration | Q34193660 | ||
Telomere maintenance and telomerase activity are differentially regulated in asexual and sexual worms | Q34257327 | ||
The Drosophila Extradenticle and Homothorax selector proteins control branchless/FGF expression in mesodermal bridge-cells | Q34360433 | ||
Gene expression of pluripotency determinants is conserved between mammalian and planarian stem cells. | Q36049563 | ||
Double-stranded RNA specifically disrupts gene expression during planarian regeneration | Q36336691 | ||
Stem cell-based growth, regeneration, and remodeling of the planarian intestine | Q36375720 | ||
Hox and Pbx factors control retinoic acid synthesis during hindbrain segmentation. | Q36916855 | ||
A wound-induced Wnt expression program controls planarian regeneration polarity. | Q37346221 | ||
Pbx homeodomain proteins: TALEnted regulators of limb patterning and outgrowth | Q37854540 | ||
Proximodistal identity during vertebrate limb regeneration is regulated by Meis homeodomain proteins | Q38322021 | ||
A regulatory program for excretory system regeneration in planarians | Q38536413 | ||
Organizing the DV axis during planarian regeneration. | Q38577542 | ||
Competition for cofactor-dependent DNA binding underlies Hox phenotypic suppression | Q39332108 | ||
The Mi-2-like Smed-CHD4 gene is required for stem cell differentiation in the planarian Schmidtea mediterranea | Q39849555 | ||
Spoltud-1 is a chromatoid body component required for planarian long-term stem cell self-renewal | Q41780026 | ||
A comparative transcriptomic analysis reveals conserved features of stem cell pluripotency in planarians and mammals | Q41829171 | ||
Genetic regulators of a pluripotent adult stem cell system in planarians identified by RNAi and clonal analysis | Q41896125 | ||
Molecular analysis of stem cells and their descendants during cell turnover and regeneration in the planarian Schmidtea mediterranea | Q41922401 | ||
Molecular patterning mechanism underlying metamorphosis of the thoracic leg in Manduca sexta | Q42033816 | ||
Defining the molecular profile of planarian pluripotent stem cells using a combinatorial RNAseq, RNA interference and irradiation approach. | Q42113314 | ||
Regeneration and maintenance of the planarian midline is regulated by a slit orthologue. | Q42123378 | ||
Beta-catenin defines head versus tail identity during planarian regeneration and homeostasis | Q42142686 | ||
A Bmp/Admp regulatory circuit controls maintenance and regeneration of dorsal-ventral polarity in planarians | Q42239465 | ||
Planarian regeneration involves distinct stem cell responses to wounds and tissue absence | Q42413468 | ||
Polarized notum activation at wounds inhibits Wnt function to promote planarian head regeneration | Q42555211 | ||
Expression of homothorax and extradenticle mRNA in the legs of the crustacean Parhyale hawaiensis: evidence for a reversal of gene expression regulation in the pancrustacean lineage | Q42559998 | ||
Morphogenesis defects are associated with abnormal nervous system regeneration following roboA RNAi in planarians | Q42610077 | ||
Conserved regulation of proximodistal limb axis development by Meis1/Hth | Q42807847 | ||
Mutations in the Drosophila gene extradenticle affect the way specific homeo domain proteins regulate segmental identity | Q44066543 | ||
Diverse miRNA spatial expression patterns suggest important roles in homeostasis and regeneration in planarians. | Q44656131 | ||
The roles of two C. elegans HOX co-factor orthologs in cell migration and vulva development | Q46497333 | ||
Roles of the Homothorax/Meis/Prep homolog UNC-62 and the Exd/Pbx homologs CEH-20 and CEH-40 in C. elegans embryogenesis. | Q47069472 | ||
Antagonism between extradenticle function and Hedgehog signalling in the developing limb | Q47814820 | ||
A Bruno-like gene is required for stem cell maintenance in planarians | Q48085602 | ||
FGFR-related gene nou-darake restricts brain tissues to the head region of planarians | Q48278854 | ||
A planarian orthopedia homolog is specifically expressed in the branch region of both the mature and regenerating brain | Q48516867 | ||
Early planarian brain regeneration is independent of blastema polarity mediated by the Wnt/β-catenin pathway. | Q48972335 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P1104 | number of pages | 10 | |
P304 | page(s) | 730-739 | |
P577 | publication date | 2013-01-14 | |
P1433 | published in | Development | Q3025404 |
P1476 | title | PBX/extradenticle is required to re-establish axial structures and polarity during planarian regeneration | |
P478 | volume | 140 |
Q92060135 | 'Building a perfect body': control of vertebrate organogenesis by PBX-dependent regulatory networks |
Q27318464 | A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration |
Q35945586 | Comparative analysis of Wnt expression identifies a highly conserved developmental transition in flatworms. |
Q30946349 | Digital gene expression approach over multiple RNA-Seq data sets to detect neoblast transcriptional changes in Schmidtea mediterranea |
Q37144523 | Forkhead containing transcription factor Albino controls tetrapyrrole-based body pigmentation in planarian |
Q59137018 | Genome-wide transcriptome profiling and spatial expression analyses identify signals and switches of development in tapeworms |
Q28073913 | Go ahead, grow a head! A planarian's guide to anterior regeneration |
Q48306920 | Integrin suppresses neurogenesis and regulates brain tissue assembly in planarian regeneration. |
Q40848483 | JNK signalling is necessary for a Wnt- and stem cell-dependent regeneration programme. |
Q88107247 | Neoblast-enriched zinc finger protein FIR1 triggers local proliferation during planarian regeneration |
Q64283461 | Nuclear receptor NR4A is required for patterning at the ends of the planarian anterior-posterior axis |
Q38810344 | PHRED-1 is a divergent neurexin-1 homolog that organizes muscle fibers and patterns organs during regeneration |
Q36974686 | Physiological controls of large-scale patterning in planarian regeneration: a molecular and computational perspective on growth and form |
Q43500590 | Reactivating head regrowth in a regeneration-deficient planarian species |
Q35769230 | Reactive Oxygen Species in Planarian Regeneration: An Upstream Necessity for Correct Patterning and Brain Formation. |
Q43929265 | Stem cell-dependent formation of a functional anterior regeneration pole in planarians requires Zic and Forkhead transcription factors. |
Q57025286 | The Cellular and Molecular Basis for Planarian Regeneration |
Q41949115 | The miR-124 family of microRNAs is crucial for regeneration of the brain and visual system in the planarian Schmidtea mediterranea |
Q36236909 | Types or States? Cellular Dynamics and Regenerative Potential |
Q41483639 | Wnt, Ptk7, and FGFRL expression gradients control trunk positional identity in planarian regeneration |
Q35178918 | teashirt is required for head-versus-tail regeneration polarity in planarians. |
Q27315030 | zic-1 Expression in Planarian neoblasts after injury controls anterior pole regeneration |