| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2011PLoSO...621498K |
| P356 | DOI | 10.1371/JOURNAL.PONE.0021498 |
| P932 | PMC publication ID | 3123344 |
| P698 | PubMed publication ID | 21731768 |
| P5875 | ResearchGate publication ID | 51469804 |
| P50 | author | Greg Elgar | Q30519112 |
| P2093 | author name string | Heather Callaway | |
| Gayle K McEwen | |||
| Emma J Kenyon | |||
| P2860 | cites work | Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients | Q77148833 |
| Phenotypes Associated with SHOX Deficiency | Q77337722 | ||
| Minor change, major difference: divergent functions of highly conserved cis-regulatory elements subsequent to whole genome duplication events | Q34558026 | ||
| Enhancer elements upstream of the SHOX gene are active in the developing limb | Q41736356 | ||
| Ancient duplicated conserved noncoding elements in vertebrates: a genomic and functional analysis | Q42274741 | ||
| Modulation of epidermal cell shaping and extracellular matrix during caudal fin morphogenesis in the zebra fish Brachydanio rerio | Q42436329 | ||
| Homozygous deletion of SHOX in a mentally retarded male with Langer mesomelic dysplasia | Q43076209 | ||
| Evidence that mechanisms of fin development evolved in the midline of early vertebrates. | Q47193446 | ||
| Long-range conserved non-coding SHOX sequences regulate expression in developing chicken limb and are associated with short stature phenotypes in human patients | Q50702801 | ||
| Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3. | Q51985004 | ||
| Expression of the short stature homeobox gene Shox is restricted by proximal and distal signals in chick limb buds and affects the length of skeletal elements | Q52010079 | ||
| Activator effect of coinjected enhancers on the muscle-specific expression of promoters in zebrafish embryos | Q52193396 | ||
| Anterior Duplication of the Sonic hedgehog Expression Pattern in the Pectoral Fin Buds of Zebrafish Treated with Retinoic Acid | Q52207450 | ||
| Independent Hox-cluster duplications in lampreys | Q56991607 | ||
| CompleteSHOX deficiency causes Langer mesomelic dysplasia | Q57828223 | ||
| The development of the paired fins in the Zebrafish (Danio rerio) | Q60307652 | ||
| Highly conserved non-coding sequences are associated with vertebrate development | Q21092819 | ||
| SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb development | Q24314232 | ||
| PHOG, a candidate gene for involvement in the short stature of Turner syndrome | Q24323155 | ||
| The mouse Engrailed-1 gene and ventral limb patterning | Q24336735 | ||
| Stages of embryonic development of the zebrafish | Q27860947 | ||
| Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome | Q28237330 | ||
| Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis | Q28271044 | ||
| Induction of the LIM homeobox gene Lmx1 by WNT6a establishes dorsoventral pattern in the vertebrate limb | Q28291179 | ||
| Targeted mutation reveals essential functions of the homeodomain transcription factor Shox2 in sinoatrial and pacemaking development | Q28506813 | ||
| Shox2 function couples neural, muscular and skeletal development in the proximal forelimb | Q28586634 | ||
| Shared developmental mechanisms pattern the vertebrate gill arch and paired fin skeletons | Q28754770 | ||
| LAGAN and Multi-LAGAN: efficient tools for large-scale multiple alignment of genomic DNA | Q28775786 | ||
| Sonic hedgehog mediates the polarizing activity of the ZPA | Q29616565 | ||
| CONDOR: a database resource of developmentally associated conserved non-coding elements | Q33296096 | ||
| Constraints on reinitiation of translation in mammals | Q34004574 | ||
| Interference of nonsense mutations with eukaryotic messenger RNA stability | Q34037213 | ||
| A functionally conserved homolog of the Drosophila segment polarity gene hh is expressed in tissues with polarizing activity in zebrafish embryos | Q34346998 | ||
| The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome. | Q34508002 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Danio rerio | Q169444 |
| P304 | page(s) | e21498 | |
| P577 | publication date | 2011-06-24 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Functional analysis of conserved non-coding regions around the short stature hox gene (shox) in whole zebrafish embryos | |
| P478 | volume | 6 |
| Q37147401 | A Track Record on SHOX: From Basic Research to Complex Models and Therapy |
| Q47768125 | Comparative transgenic analysis of enhancers from the human SHOX and mouse Shox2 genomic regions |
| Q41718774 | In vivo loss of function study reveals the short stature homeobox-containing (shox) gene plays indispensable roles in early embryonic growth and bone formation in zebrafish |
| Q39854835 | Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions |
| Q48172096 | On the Evolution of the Cardiac Pacemaker |
| Q36774245 | Phenotypic characterization of patients with deletions in the 3’-flanking SHOXregion |
| Q36343359 | Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape |
| Q26748496 | SHOX Haploinsufficiency as a Cause of Syndromic and Nonsyndromic Short Stature |
| Q22122079 | Sequencing of the sea lamprey (Petromyzon marinus) genome provides insights into vertebrate evolution |
| Q33958594 | Spectrum of phenotypic anomalies in four families with deletion of the SHOX enhancer region. |
| Q34055731 | Structural and numerical changes of chromosome X in patients with esophageal atresia |
| Q33774631 | The Short-Stature Homeobox-Containing Gene (shox/SHOX) Is Required for the Regulation of Cell Proliferation and Bone Differentiation in Zebrafish Embryo and Human Mesenchymal Stem Cells |
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