| scholarly article | Q13442814 |
| P50 | author | Robert D. Riddle | Q107437194 |
| P2093 | author name string | Daniel S Kessler | |
| Lily L Wong | |||
| F Patrick O'Hara | |||
| Ernestine Beck | |||
| Lauren K Barr | |||
| P2860 | cites work | Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors | Q27737008 |
| Stages of embryonic development of the zebrafish | Q27860947 | ||
| Identification of a Human LMX1 (LMX1.1)-Related Gene, LMX1.2: Tissue-Specific Expression and Linkage Mapping on Chromosome 9 | Q28259819 | ||
| Induction of the LIM homeobox gene Lmx1 by WNT6a establishes dorsoventral pattern in the vertebrate limb | Q28291179 | ||
| Localization of the Genes Encoding Two Transcription Factors, LMX1 and CDX3, Regulating Insulin Gene Expression to Human Chromosomes 1 and 13 | Q28298918 | ||
| The caudal limit of Otx2 gene expression as a marker of the midbrain/hindbrain boundary: a study using in situ hybridisation and chick/quail homotopic grafts | Q28302345 | ||
| The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo | Q28302373 | ||
| Pax2 contributes to inner ear patterning and optic nerve trajectory | Q28511597 | ||
| The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain | Q28586297 | ||
| Effects of Wnt1 signaling on proliferation in the developing mid-/hindbrain region | Q28592616 | ||
| Induction of ectopic engrailed expression and fate change in avian rhombomeres: intersegmental boundaries as barriers. | Q52208236 | ||
| Large-scale mutagenesis in the zebrafish: in search of genes controlling development in a vertebrate | Q52218193 | ||
| Expression of the proto-oncogene int-1 is restricted to specific neural cells in the developing mouse embryo | Q63487544 | ||
| Pluripotentiality of the 2-day-old avian germinative neuroepithelium | Q68759905 | ||
| Evidence for a mitogenic effect of Wnt-1 in the developing mammalian central nervous system | Q72106566 | ||
| A mitogen gradient of dorsal midline Wnts organizes growth in the CNS | Q77960718 | ||
| Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development | Q28593581 | ||
| An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination | Q29615355 | ||
| fork head domain genes in zebrafish | Q32048619 | ||
| Synergistic activation of the insulin gene by a LIM-homeo domain protein and a basic helix-loop-helix protein: building a functional insulin minienhancer complex | Q34244863 | ||
| Fgf-8 expression in the post-gastrulation mouse suggests roles in the development of the face, limbs and central nervous system. | Q34319673 | ||
| Multiple developmental defects in Engrailed-1 mutant mice: an early mid-hindbrain deletion and patterning defects in forelimbs and sternum | Q34323246 | ||
| Early anterior/posterior patterning of the midbrain and cerebellum | Q34345487 | ||
| Specification of the anterior hindbrain and establishment of a normal mid/hindbrain organizer is dependent on Gbx2 gene function | Q34434576 | ||
| The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney | Q35934032 | ||
| A second independent pathway for development of mesencephalic dopaminergic neurons requires Lmx1b. | Q38314171 | ||
| Wnt1 and wnt10b function redundantly at the zebrafish midbrain-hindbrain boundary | Q38521067 | ||
| Involvement of Wnt1 and Pax2 in the formation of the midbrain‐hindbrain boundary in the zebrafish gastrula | Q38532050 | ||
| Visualization of cranial motor neurons in live transgenic zebrafish expressing green fluorescent protein under the control of the islet-1 promoter/enhancer. | Q40783129 | ||
| Engrailed, Wnt and Pax genes regulate midbrain--hindbrain development | Q41064646 | ||
| The cellular environment controls the expression of engrailed-like protein in the cranial neuroepithelium of quail-chick chimeric embryos | Q41136089 | ||
| Early mesencephalon/metencephalon patterning and development of the cerebellum | Q41724283 | ||
| Otx2andGbx2are required for refinement and not induction of mid-hindbrain gene expression | Q43826745 | ||
| Lmx1b, Pet-1, andNkx2.2Coordinately Specify Serotonergic Neurotransmitter Phenotype | Q44645621 | ||
| Combinatorial Wnt control of zebrafish midbrain-hindbrain boundary formation | Q44899280 | ||
| The isthmic organizer signal FGF8 is required for cell survival in the prospective midbrain and cerebellum. | Q45944197 | ||
| Midbrain development induced by FGF8 in the chick embryo. | Q46013905 | ||
| Dorsal cell fate specified by chick Lmx1 during vertebrate limb development | Q46565708 | ||
| Characterization of three novel members of the zebrafish Pax2/5/8 family: dependency of Pax5 and Pax8 expression on the Pax2.1 (noi) function | Q47073232 | ||
| Fgf8 is mutated in zebrafish acerebellar (ace) mutants and is required for maintenance of midbrain-hindbrain boundary development and somitogenesis | Q47073664 | ||
| A series of no isthmus (noi) alleles of the zebrafish pax2.1 gene reveals multiple signaling events in development of the midbrain-hindbrain boundary | Q47073721 | ||
| Mutations in zebrafish genes affecting the formation of the boundary between midbrain and hindbrain | Q47073829 | ||
| Role of Pax-5 in the regulation of a mid-hindbrain organizer's activity | Q47938578 | ||
| Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome. | Q48038093 | ||
| Topographic organization of embryonic motor neurons defined by expression of LIM homeobox genes | Q48077000 | ||
| Patterning of the embryonic avian midbrain after experimental inversions: a polarizing activity from the isthmus | Q48127024 | ||
| Abnormal embryonic cerebellar development and patterning of postnatal foliation in two mouse Engrailed-2 mutants. | Q48169771 | ||
| Requirement for the zebrafish mid-hindbrain boundary in midbrain polarisation, mapping and confinement of the retinotectal projection | Q48193012 | ||
| Comparative analysis of Otx2, Gbx2, Pax2, Fgf8 and Wnt1 gene expressions during the formation of the chick midbrain/hindbrain domain. | Q48208878 | ||
| FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression. | Q48282491 | ||
| Plasticity and rigidity of differentiation of brain vesicles studied in quail-chick chimeras | Q48290171 | ||
| Sequential roles for Fgf4, En1 and Fgf8 in specification and regionalisation of the midbrain. | Q48295357 | ||
| Expression of Gbx-2 during early development of the chick embryo | Q48378620 | ||
| Expression of the homeobox gene GBX2 during chicken development | Q48378641 | ||
| Nested expression domains of four homeobox genes in developing rostral brain | Q48444447 | ||
| Relationship between Wnt-1 and En-2 expression domains during early development of normal and ectopic met-mesencephalon | Q48451883 | ||
| Role of Lmx1b and Wnt1 in mesencephalon and metencephalon development. | Q48460099 | ||
| Establishment of rostrocaudal polarity in tectal primordium: engrailed expression and subsequent tectal polarity | Q48615069 | ||
| Induction of a mesencephalic phenotype in the 2-day-old chick prosencephalon is preceded by the early expression of the homeobox gene en. | Q48717668 | ||
| Evidence that FGF8 signalling from the midbrain-hindbrain junction regulates growth and polarity in the developing midbrain | Q48791624 | ||
| Cell death in the CNS of the Wnt-1 mutant mouse | Q48881359 | ||
| The transcription factor Lmx1b maintains Wnt1 expression within the isthmic organizer. | Q52169436 | ||
| P433 | issue | 14 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Danio rerio | Q169444 |
| P1104 | number of pages | 11 | |
| P304 | page(s) | 3163-3173 | |
| P577 | publication date | 2005-06-08 | |
| P1433 | published in | Development | Q3025404 |
| P1476 | title | Zebrafish Lmx1b.1 and Lmx1b.2 are required for maintenance of the isthmic organizer | |
| P478 | volume | 132 |
| Q92283506 | A long noncoding RNA cluster-based genomic locus maintains proper development and visual function |
| Q42283424 | A novel role for FOXA2 and SHH in organizing midbrain signaling centers |
| Q46542678 | A role for receptor protein tyrosine phosphatase lambda in midbrain development |
| Q38324172 | Analysis of transcriptional codes for zebrafish dopaminergic neurons reveals essential functions of Arx and Isl1 in prethalamic dopaminergic neuron development. |
| Q38622890 | Cell fate determination, neuronal maintenance and disease state: The emerging role of transcription factors Lmx1a and Lmx1b |
| Q37106378 | Current perspectives in zebrafish reverse genetics: moving forward |
| Q37076257 | Desire, disease, and the origins of the dopaminergic system |
| Q33308346 | Expression and function of nr4a2, lmx1b, and pitx3 in zebrafish dopaminergic and noradrenergic neuronal development |
| Q46791394 | Genoarchitecture of the rostral hindbrain of a shark: basis for understanding the emergence of the cerebellum at the agnathan-gnathostome transition |
| Q37267384 | Integration of genomic and functional approaches reveals enhancers at LMX1A and LMX1B |
| Q30555221 | LMX1B is essential for the maintenance of differentiated podocytes in adult kidneys |
| Q37064644 | Ldb1 Is Essential for the Development of Isthmic Organizer and Midbrain Dopaminergic Neurons |
| Q37124994 | Lmx1a is required for segregation of sensory epithelia and normal ear histogenesis and morphogenesis |
| Q42017546 | Lmx1b and FoxC combinatorially regulate podocin expression in podocytes |
| Q24644226 | Lmx1b is essential for survival of periocular mesenchymal cells and influences Fgf-mediated retinal patterning in zebrafish |
| Q39462130 | Lmx1b is required for the glutamatergic fates of a subset of spinal cord neurons. |
| Q42723802 | Lrrn1 is required for formation of the midbrain-hindbrain boundary and organiser through regulation of affinity differences between midbrain and hindbrain cells in chick. |
| Q42040465 | Making a mes: A transcription factor-microRNA pair governs the size of the midbrain and the dopaminergic progenitor pool |
| Q38073140 | Novel mechanisms that pattern and shape the midbrain-hindbrain boundary |
| Q37735795 | Ontogeny of substantia nigra dopamine neurons. |
| Q24649943 | Overlapping function of Lmx1a and Lmx1b in anterior hindbrain roof plate formation and cerebellar growth |
| Q35745756 | Pbx proteins cooperate with Engrailed to pattern the midbrain-hindbrain and diencephalic-mesencephalic boundaries |
| Q48229313 | Sustained interactive Wnt and FGF signaling is required to maintain isthmic identity |
| Q37635066 | The PAX258 gene subfamily: a comparative perspective |
| Q38050536 | The signaling pathways of LMX1B and its role in glomerulosclerosis |
| Q47907935 | Transcription of fgf8 is regulated by activating and repressive cis-elements at the midbrain-hindbrain boundary in zebrafish embryos |
| Q95478208 | Wnt/β-Catenin Signaling in Vertebrate Posterior Neural Development |
| Q41866526 | Zic1 and Zic4 regulate zebrafish roof plate specification and hindbrain ventricle morphogenesis |
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