| P50 | author | Laura Anne Lowery | Q57321295 |
| P2093 | author name string | Erin L. Rutherford | |
| P2860 | cites work | Comparative analysis of a novel gene from the Wolf-Hirschhorn/Pitt-Rogers-Danks syndrome critical region | Q22010268 |
| | Development and evolution of the neural crest: an overview | Q22337309 |
| | TACC1-chTOG-Aurora A protein complex in breast cancer | Q24299319 |
| | Cellular signaling by fibroblast growth factor receptors | Q24301087 |
| | WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma | Q24322575 |
| | Fibroblast growth factor receptor 3 is a negative regulator of bone growth | Q24322706 |
| | Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2. | Q24531948 |
| | The centrosomal protein TACC3 is essential for hematopoietic stem cell function and genetically interfaces with p53-regulated apoptosis | Q24534711 |
| | Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells | Q24550947 |
| | Autosomal Recessive Primary Microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum | Q24570114 |
| | The TACC domain identifies a family of centrosomal proteins that can interact with microtubules | Q24672611 |
| | The ch-TOG/XMAP215 protein is essential for spindle pole organization in human somatic cells | Q24672810 |
| | The LETM1/YOL027 gene family encodes a factor of the mitochondrial K+ homeostasis with a potential role in the Wolf-Hirschhorn syndrome. | Q27932161 |
| | LETM1, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, flanks the Wolf-Hirschhorn syndrome (WHS) critical region and is deleted in most WHS patients | Q28116065 |
| | Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis | Q28131703 |
| | First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation | Q28205042 |
| | The etiology of Wolf-Hirschhorn syndrome | Q28236976 |
| | IQGAP1: a key regulator of adhesion and migration | Q28250427 |
| | FGF receptors: cancer biology and therapeutics | Q28291186 |
| | A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region | Q28305534 |
| | Fibroblast growth factor receptors cooperate to regulate neural progenitor properties in the developing midbrain and hindbrain | Q28506314 |
| | Interaction between FOG-1 and the corepressor C-terminal binding protein is dispensable for normal erythropoiesis in vivo | Q28510968 |
| | Disruption of fibroblast growth factor receptor 3 signaling results in defects in cellular differentiation, neuronal patterning, and hearing impairment | Q28511525 |
| | Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development | Q28513519 |
| | Isolation and characterization of AINT: a novel ARNT interacting protein expressed during murine embryonic development | Q28585602 |
| | Wnt signaling mediates regional specification in the vertebrate face | Q28588683 |
| | A histone H3 lysine 36 trimethyltransferase links Nkx2-5 to Wolf-Hirschhorn syndrome | Q28593584 |
| | TACC3-ch-TOG track the growing tips of microtubules independently of clathrin and Aurora-A phosphorylation | Q29347519 |
| | Mitochondrial reactive oxygen species trigger hypoxia-induced transcription | Q29614203 |
| | Reactive oxygen species generated at mitochondrial complex III stabilize hypoxia-inducible factor-1alpha during hypoxia: a mechanism of O2 sensing | Q29617570 |
| | The Xenopus embryo as a model system for studies of cell migration | Q30435289 |
| | FGF8 signaling is chemotactic for cardiac neural crest cells | Q30500159 |
| | Xenopus TACC2 is a microtubule plus end-tracking protein that can promote microtubule polymerization during embryonic development. | Q30822145 |
| | Cyclin D1 is not an immediate target of beta-catenin following Apc loss in the intestine | Q33216786 |
| | Xenopus skip modulates Wnt/beta-catenin signaling and functions in neural crest induction. | Q33526741 |
| | The target of the NSD family of histone lysine methyltransferases depends on the nature of the substrate | Q33553524 |
| | Primary microcephaly: do all roads lead to Rome? | Q33629131 |
| | TACC2 is an androgen-responsive cell cycle regulator promoting androgen-mediated and castration-resistant growth of prostate cancer | Q33636574 |
| | LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein | Q33974957 |
| | Dissection of Xenopus laevis neural crest for in vitro explant culture or in vivo transplantation | Q34009403 |
| | WHSC1L1, on human chromosome 8p11.2, closely resembles WHSC1 and maps to a duplicated region shared with 4p16.3. | Q34090593 |
| | Deficiency on the short arms of a chromosome No. 4 | Q34241073 |
| | Deletion of short arms of chromosome 4?5 in a child with defects of midline fusion | Q34241369 |
| | The transforming acidic coiled coil proteins interact with nuclear histone acetyltransferases | Q34295310 |
| | Wolf-Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions | Q34325417 |
| | LETM1-dependent mitochondrial Ca2+ flux modulates cellular bioenergetics and proliferation. | Q34356130 |
| | TACC3 is a microtubule plus end-tracking protein that promotes axon elongation and also regulates microtubule plus end dynamics in multiple embryonic cell types | Q34428668 |
| | Wolf-Hirschhorn syndrome: A review and update | Q34488100 |
| | Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay. | Q51854794 |
| | TWIST activation by hypoxia inducible factor-1 (HIF-1): implications in metastasis and development. | Q51952297 |
| | Essential role of non-canonical Wnt signalling in neural crest migration. | Q52051294 |
| | TACC3 promotes epithelial-mesenchymal transition (EMT) through the activation of PI3K/Akt and ERK signaling pathways. | Q53123068 |
| | A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features. | Q53228045 |
| | [Aurora kinases and cancer] | Q64132609 |
| | TACC3 is required for the proper mitosis of sclerotome mesenchymal cells during formation of the axial skeleton | Q79947120 |
| | The transforming acidic coiled coil 3 protein is essential for spindle-dependent chromosome alignment and mitotic survival | Q34659420 |
| | Epigenetic regulation in neural crest development | Q34663839 |
| | Neural crest specification and migration independently require NSD3-related lysine methyltransferase activity. | Q34680417 |
| | Coiled-coil coactivators play a structural role mediating interactions in hypoxia-inducible factor heterodimerization | Q35199417 |
| | Histone lysine methyltransferase Wolf-Hirschhorn syndrome candidate 1 is involved in human carcinogenesis through regulation of the Wnt pathway | Q35444274 |
| | Xenopus TACC1 is a microtubule plus-end tracking protein that can regulate microtubule dynamics during embryonic development | Q35903431 |
| | Cdk5rap2 exposes the centrosomal root of microcephaly syndromes | Q36021561 |
| | FGFR3-TACC3: A novel gene fusion in cervical cancer | Q36039883 |
| | Neural Explant Cultures from Xenopus laevis | Q36375166 |
| | The multiple myeloma associated MMSET gene contributes to cellular adhesion, clonogenic growth, and tumorigenicity. | Q36384699 |
| | The histone methyltransferase MMSET/WHSC1 activates TWIST1 to promote an epithelial-mesenchymal transition and invasive properties of prostate cancer | Q36390674 |
| | The control of histone lysine methylation in epigenetic regulation | Q36571342 |
| | WNT/β-catenin signaling mediates human neural crest induction via a pre-neural border intermediate. | Q36597429 |
| | Letm1, the mitochondrial Ca2+/H+ antiporter, is essential for normal glucose metabolism and alters brain function in Wolf-Hirschhorn syndrome. | Q36932269 |
| | Set2 mediated H3 lysine 36 methylation: regulation of transcription elongation and implications in organismal development | Q37158054 |
| | The TACC proteins: TACC-ling microtubule dynamics and centrosome function | Q37227249 |
| | Mouse models of Wolf-Hirschhorn syndrome | Q37302911 |
| | IQGAP1 protein regulates nuclear localization of β-catenin via importin-β5 protein in Wnt signaling | Q37404988 |
| | Oxidative stress, neurodegeneration, and the balance of protein degradation and protein synthesis | Q38045663 |
| | The role of the non-canonical Wnt-planar cell polarity pathway in neural crest migration | Q38170173 |
| | Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder. | Q38307737 |
| | MMSET deregulation affects cell cycle progression and adhesion regulons in t(4;14) myeloma plasma cells. | Q39908262 |
| | The MMSET protein is a histone methyltransferase with characteristics of a transcriptional corepressor | Q40031496 |
| | Transforming acidic coiled-coil protein 3 (TACC3) controls friend of GATA-1 (FOG-1) subcellular localization and regulates the association between GATA-1 and FOG-1 during hematopoiesis | Q40575090 |
| | Direct evidence for a role of beta-catenin/LEF-1 signaling pathway in induction of EMT. | Q40721147 |
| | CPEB, maskin, and cyclin B1 mRNA at the mitotic apparatus: implications for local translational control of cell division | Q40841882 |
| | Meier-Gorlin syndrome and Wolf-Hirschhorn syndrome: two developmental disorders highlighting the importance of efficient DNA replication for normal development and neurogenesis | Q41932004 |
| | Functional characterization of the zebrafish WHSC1-related gene, a homolog of human NSD2 | Q42858891 |
| | Directional cell migration in vivo: Wnt at the crest | Q43190503 |
| | Quantitative analysis of orofacial development and median clefts in Xenopus laevis | Q44992991 |
| | Ectodermal Wnt function as a neural crest inducer. | Q46043546 |
| | Molecular interactions coordinating the development of the forebrain and face. | Q46567732 |
| | Lung tumor-associated dendritic cell-derived resistin promoted cancer progression by increasing Wolf-Hirschhorn syndrome candidate 1/Twist pathway | Q47753819 |
| | Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3. | Q49042849 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Wolf-Hirschhorn syndrome | Q610075 |
| | cell motility | Q14873676 |
| | embryonic structure | Q30062554 |
| | physiological phenomenon | Q66615932 |
| P1104 | number of pages | 10 | |
| P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
| P304 | page(s) | 1-10 | |
| P577 | publication date | 2016-12-01 | |
| P1433 | published in | Developmental Biology | Q3025402 |
| P1476 | title | Exploring the developmental mechanisms underlying Wolf-Hirschhorn Syndrome: Evidence for defects in neural crest cell migration | |
| P478 | volume | 420 | |