review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Taneli Raivio | Q30347924 |
P2093 | author name string | Parinya Noisa | |
P2860 | cites work | Early acquisition of neural crest competence during hESCs neuralization | Q21136066 |
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules | Q24311797 | ||
Alternative neural crest cell fates are instructively promoted by TGFbeta superfamily members | Q24336262 | ||
CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome | Q24595634 | ||
Dynamic transcriptomes during neural differentiation of human embryonic stem cells revealed by short, long, and paired-end sequencing | Q24620865 | ||
CHD7 cooperates with PBAF to control multipotent neural crest formation | Q24630725 | ||
Generation of human induced pluripotent stem cells by direct delivery of reprogramming proteins | Q24653753 | ||
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome | Q24657612 | ||
Genetic correction of human induced pluripotent stem cells from patients with spinal muscular atrophy | Q27328843 | ||
Rapid and efficient conversion of integration-free human induced pluripotent stem cells to GMP-grade culture conditions | Q27342678 | ||
Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors | Q27860937 | ||
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules | Q28118633 | ||
SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism | Q28218691 | ||
Specification of the neural crest occurs during gastrulation and requires Pax7 | Q28239511 | ||
Extracellular matrix protein anosmin promotes neural crest formation and regulates FGF, BMP, and WNT activities | Q28273253 | ||
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion | Q28275699 | ||
Brg1 governs distinct pathways to direct multiple aspects of mammalian neural crest cell development | Q28592308 | ||
Pluripotent stem cells induced from mouse somatic cells by small-molecule compounds | Q29616608 | ||
Generation of induced pluripotent stem cells using recombinant proteins | Q29619162 | ||
Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos | Q30538511 | ||
A Pax3/Dmrt2/Myf5 regulatory cascade functions at the onset of myogenesis | Q33549660 | ||
Clinical, molecular, and cell biological aspects of Chediak-Higashi syndrome | Q33755016 | ||
Fgf8a induces neural crest indirectly through the activation of Wnt8 in the paraxial mesoderm | Q33922679 | ||
Cloning and characterization of three Xenopus slug promoters reveal direct regulation by Lef/beta-catenin signaling. | Q33950969 | ||
DNA methyltransferase3A as a molecular switch mediating the neural tube-to-neural crest fate transition | Q41468449 | ||
Olfactory ensheathing glia are required for embryonic olfactory axon targeting and the migration of gonadotropin-releasing hormone neurons | Q41768904 | ||
FGF signaling transforms non-neural ectoderm into neural crest. | Q41998199 | ||
Modeling neural crest induction, melanocyte specification, and disease-related pigmentation defects in hESCs and patient-specific iPSCs | Q42153574 | ||
Collective chemotaxis requires contact-dependent cell polarity. | Q42158276 | ||
Unexpected functional redundancy between Twist and Slug (Snail2) and their feedback regulation of NF-kappaB via Nodal and Cerberus | Q42288548 | ||
Factors controlling the time of onset of the migration of neural crest cells in the fowl embryo | Q42468466 | ||
Snail2 controls mesodermal BMP/Wnt induction of neural crest | Q42794736 | ||
Pax3/Pax7 mark a novel population of primitive myogenic cells during development | Q42863008 | ||
The BMP signaling gradient patterns dorsoventral tissues in a temporally progressive manner along the anteroposterior axis | Q43074864 | ||
Large-scale screening using familial dysautonomia induced pluripotent stem cells identifies compounds that rescue IKBKAP expression | Q43092271 | ||
Stem cells cruise to clinic | Q44105782 | ||
Histone deacetylase inhibitor Trichostatin A induces neural tube defects and promotes neural crest specification in the chicken neural tube | Q45849709 | ||
Generation of peripheral sensory and sympathetic neurons and neural crest cells from human embryonic stem cells. | Q46481470 | ||
Efficient differentiation of hepatocytes from human embryonic stem cells exhibiting markers recapitulating liver development in vivo. | Q46779930 | ||
Zebrafish foxd3 is selectively required for neural crest specification, migration and survival | Q47073317 | ||
Long-range upstream and downstream enhancers control distinct subsets of the complex spatiotemporal Sox9 expression pattern | Q47225412 | ||
Neural crest development is regulated by the transcription factor Sox9. | Q47590677 | ||
Induced pluripotent stem cells from friedreich ataxia patients fail to upregulate frataxin during in vitro differentiation to peripheral sensory neurons | Q47953046 | ||
Anosmin-1, defective in the X-linked form of Kallmann syndrome, promotes axonal branch formation from olfactory bulb output neurons. | Q48607771 | ||
Notch signaling regulates the differentiation of neural crest from human pluripotent stem cells. | Q50685368 | ||
Isolation and directed differentiation of neural crest stem cells derived from human embryonic stem cells. | Q50856695 | ||
Wnt-regulated temporal control of BMP exposure directs the choice between neural plate border and epidermal fate. | Q51945248 | ||
Notch signaling is required for the maintenance of enteric neural crest progenitors. | Q51948386 | ||
Stage-dependent effects of ethanol on cranial neural crest cell development: partial basis for the phenotypic variations observed in fetal alcohol syndrome. | Q52011908 | ||
Snail precedes slug in the genetic cascade required for the specification and migration of the Xenopus neural crest. | Q52111064 | ||
Disruption of segmental neural crest migration and ephrin expression in delta-1 null mice. | Q52115125 | ||
Overexpression of the transcriptional repressor FoxD3 prevents neural crest formation in Xenopus embryos. | Q52135855 | ||
Wnt signalling required for expansion of neural crest and CNS progenitors. | Q52192233 | ||
Loss of occludin and functional tight junctions, but not ZO-1, during neural tube closure--remodeling of the neuroepithelium prior to neurogenesis. | Q52198071 | ||
Congenital and infantile neoplasia of the kidney. | Q53596783 | ||
Cranial neural crest migration: new rules for an old road | Q34037222 | ||
Reversal and relapse of hypogonadotropic hypogonadism: resilience and fragility of the reproductive neuroendocrine system. | Q34397759 | ||
Reiterative AP2a activity controls sequential steps in the neural crest gene regulatory network | Q34471732 | ||
Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function | Q34485728 | ||
An essential role for Notch in neural crest during cardiovascular development and smooth muscle differentiation. | Q34608845 | ||
Pax3 is essential for normal cardiac neural crest morphogenesis but is not required during migration nor outflow tract septation | Q35127152 | ||
FGF and retinoic acid activity gradients control the timing of neural crest cell emigration in the trunk | Q35156970 | ||
Multipotentiality of the neural crest | Q35555998 | ||
Wnt signaling and a Smad pathway blockade direct the differentiation of human pluripotent stem cells to multipotent neural crest cells | Q35585822 | ||
FGF/MAPK signaling is required in the gastrula epiblast for avian neural crest induction | Q35624839 | ||
Notch pathway regulation of neural crest cell development in vivo. | Q35698022 | ||
Multiple endocrine neoplasias type 2B and RET proto-oncogene. | Q36012582 | ||
Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4 | Q36512067 | ||
Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes | Q36817235 | ||
Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness | Q36817329 | ||
Mammalian DNA methyltransferases: a structural perspective | Q37002199 | ||
Teratoma formation assays with human embryonic stem cells: a rationale for one type of human-animal chimera | Q37121016 | ||
The stem cells of the neural crest | Q37138973 | ||
A gene regulatory network orchestrates neural crest formation | Q37181700 | ||
Human iPSC-derived neural crest stem cells promote tendon repair in a rat patellar tendon window defect model | Q37253750 | ||
Self-renewal capacity is a widespread property of various types of neural crest precursor cells | Q37357957 | ||
Genetic correction of tauopathy phenotypes in neurons derived from human induced pluripotent stem cells | Q37360904 | ||
Modelling pathogenesis and treatment of familial dysautonomia using patient-specific iPSCs. | Q37444336 | ||
HDAC1 and HDAC2 control the specification of neural crest cells into peripheral glia. | Q37717676 | ||
Understanding the molecular mechanisms of Friedreich's ataxia to develop therapeutic approaches. | Q37736127 | ||
Neural crest delamination and migration: from epithelium-to-mesenchyme transition to collective cell migration | Q37977230 | ||
Cell transplantation therapies for spinal cord injury focusing on induced pluripotent stem cells | Q38066391 | ||
Self-regulation of Stat3 activity coordinates cell-cycle progression and neural crest specification | Q38349452 | ||
Sox10 is required for the early development of the prospective neural crest in Xenopus embryos. | Q38352189 | ||
Pax3 and Zic1 trigger the early neural crest gene regulatory network by the direct activation of multiple key neural crest specifiers | Q38392710 | ||
Human induced pluripotent stem cell-derived neural crest stem cells integrate into the injured spinal cord in the fetal lamb model of myelomeningocele. | Q39208345 | ||
Generation of induced pluripotent stem cell lines from Friedreich ataxia patients. | Q39616684 | ||
The enlarged lysosomes in beige j cells result from decreased lysosome fission and not increased lysosome fusion | Q39787150 | ||
Transcription impairment and cell migration defects in elongator-depleted cells: implication for familial dysautonomia | Q40277489 | ||
The transcription factor Sox10 is a key regulator of peripheral glial development. | Q40423560 | ||
Origins and developmental potential of the neural crest | Q40553981 | ||
P433 | issue | 3 | |
P921 | main subject | developmental biology | Q213713 |
P304 | page(s) | 263-274 | |
P577 | publication date | 2014-09-16 | |
P1433 | published in | Birth Defects Research Part C: Embryo Today Reviews | Q15757886 |
P1476 | title | Neural crest cells: from developmental biology to clinical interventions | |
P478 | volume | 102 |
Q41556263 | A reporter mouse model for in vivo tracing and in vitro molecular studies of melanocytic lineage cells and their diseases. |
Q38442822 | Are allergic multimorbidities and IgE polysensitization associated with the persistence or re-occurrence of foetal type 2 signalling? The MeDALL hypothesis |
Q48249330 | EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome |
Q50426412 | From proliferation to target innervation: signaling molecules that direct sympathetic nervous system development |
Q56978269 | Hand Factors in Cardiac Development |
Q90355640 | Identification of a Robust Methylation Classifier for Cutaneous Melanoma Diagnosis |
Q47155637 | Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome |
Q27306225 | Meis3 is required for neural crest invasion of the gut during zebrafish enteric nervous system development |
Q28080750 | Origin and differentiation of vascular smooth muscle cells |
Q59791108 | Physiological effects of KDM5C on neural crest migration and eye formation during vertebrate development |
Q48214312 | Prevalence of Intracranial Aneurysms in Patients with Aortic Aneurysms. |
Q39208675 | The MYCN Protein in Health and Disease |
Q53377643 | Thinking from the Heart: Neurocristopathy, Aortic Abnormalities, and Intracranial Aneurysms. |
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