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gl13 gene





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 1  ~ nih.gov
GLI3 - GLI family zinc finger 3 - Genetics Home ReferenceThe GLI3 gene belongs to a family of genes that are involved in the normal shaping (patterning) of many tissues and organs during embryonic development. ‎Name - ‎Normal function - ‎Genetic changes - ‎Gene location
 2  ~ hinsdale86.org
Postaxial PolydactylyThe GL13 gene is involved in the normal shaping of many tissues and organs during embryonic development. Proteins made by the GL13 gene attach to the ...
 3  +3 wikipedia.org
GLI3 - Wikipedia, the free encyclopediaThe protein encoded by this gene localizes in the cytoplasm and activates patched Drosophila homolog (PTCH1) gene expression. It is also thought to play a ...
 4  ~ hopeforhh.orgUnderstanding Hypothalamic Hamartomas | hopeforhh.orgThere are studies that suggest that somatic mutations in the GL13 gene may be responsible. Regardless of the cause, the resulting challenges can be difficult to  ...
 5  ~ google.com
Catalog of Teratogenic Agents - Google Books ResultThomas H. Shepard, Ronald J. Lemire - ‎2004 - 510 pages1375 Glioma-associated Oncogene GL13 gene Greig Syndrome Pallister-Hall Syndrome Post-axial polydactyl type A Syndrome Grey Cephalopolysyndactaly ...
 6  -3 yahoo.com
Pallister-Hall Syndrome: What You Need to Know - Yahoo Voices These are believed to by the result of new genetic mutations and they ... to find the cause, but they do know that it occurs on the GL13 gene .
 7  +1 figshare.com
The gl13 gene encodes a putative ABC transporter G family protein.Li, Li; Li, Delin; Liu, Sanzhen; Ma, Xiaoli; Dietrich, Charles R.; Hu, Heng-Cheng; Zhang, Gaisheng; Liu, Zhiyong; Zheng, Jun; Wang, Guoying; ...
 8  +2 researchgate.net
Point mutations throughout the GLI3 gene cause Greig ABSTRACT Greig cephalopolysyndactyly syndrome, characterized by craniofacial and limb anomalies (GCPS; MIM 175700), previously has been demonstrated ...
 9  ~ plosone.org
Table S3. Domain analysis for gl13 gene . - PLoS ONETable S3. Domain analysis for gl13 gene . *Hmm: Profile hidden Markov models for protein domain analysis. Protein ID. Alignment start. Alignment end. Hmm.
 10  +4 zfin.org
Genotype: mtl^ gl13 - ZfinGenotype: mtl gl13 . Background: Unspecified. Affected Gene : mtl. Current Source: No data available. GENOTYPE COMPOSITION. Genomic Feature, Construct ...
 11  +2 confex.com
PDF file - ConfexWalking Approach to Facilitate Gene Cloning. Sanzhen Liu ... Application to gene cloning. 2 .... SeqWalking on the UNCLONED gene – gl13 .
 12  +89 osti.gov
SciTech Connect: Greig syndrome: Analysis of the GL13 gene - OSTIDisruption of the zinc finger gene GL13 by translocation events has been implicated as the cause for cephalopolysyndactyly syndrome (GCPS) in several ...
 13  +2 readcube.com
The Maize glossy13 Gene , Cloned via BSR-Seq and ... - ReadCube(A) Figure 3 : Sequence analysis of 11 gl13 alleles.The positions of detected lesions are Figure 4 : The gl13 gene encodes a putative ABC transporter G family  ...
 14  +86 k-state.edu
The maize glossy13 gene , cloned via BSR-Seq and Seq ... - K-RExThe maize glossy13 gene , cloned via BSR-Seq and Seq-Walking encodes a ... allele of gl13 , validates the hypothesis that gene GRMZM2G118243 is gl13 .
 15  +8 medschat.com
Gl 13 - Topics - MedsChat - The People's Medicine CommunityResults 1 - 20 of 75 ... Learn about and discuss gl 13 at The People's Medicine Community. ... HomoloGene:1553 ChEMBL: 5736 GeneCards: GCG Gene Gene  ...
 16  +5 nig.ac.jp
23. Effects of a glabrousness gene , gl-1, on agronomic traits - SHIGENAn F1 plant from a cross between a glabrous line ( gl-13 ) and a normal cultivar of ... These data suggest that the glabrous gene has some pleiotropic effect on the ...
 17  ~ maday-fdr--pages.wikispaces.comMaday FDR Pages - P7- Robert Walker PolydactylyThere is also a specific gene that can cause Polydactyly; this gene is known as GL13 . GL13 is only one of the many different number genes that is responsible ...
 18  +1 ed.ac.uk
Investigating the role of GL13 in Development of the Telencephalon Investigating the role of GL13 in Development of the Telencephalon using Nested CRE-LOXP Gene Targeting. Project: Funded Project › Research. Mason, John ...
 19  ~ ibcbettas.orgGL-13 : Betta Genetics Part XIIIJan/Feb 1972. GL-13 . BETTA GENETICS. PART XIII. Gene A. Lucas, Ph.D. Department of Biology. THE “OPAQUE” FACTOR. PASTEL BETTAS. Drake University.
 20  +7 oxfordjournals.org
NF2 gene in neurofibromatosis type 2 patients - Human Molecular encoded by the NF2 gene shows a close relationship to the family of .... probe (B) . Statement GL13 demonstrated a rearranged band with probe 5. (arrow).
 21  +80 genetics.edu.au
8 pallister-hall syndrome facts - Centre for Genetics EducationFurther information and details of your local genetic counselling service can be found at ... PHS is caused by a faulty copy of the GL13 gene , located on the.
 22  +79 medind.nic.in
Polydactyly and Genes - medINDgene or genes involved in a common pathway. The. Polydactyly and .... polydactyly.21, 22, 23 The phrase “ GL13 morphopathies” was coined to ...
 23  +6 ingenuity.com
Mst98Ca/Mst98Cb gene pathways - Target ExplorerCategory: gene , Type: other, Synonyms: anon-WO0140519.46, CG11719, ... Mst, mst(3)gl-12, mst(3) gl-13 , mst336, Mst98C, Mst98Ca, Mst98Ca/Mst98Cb, ...
 24  ~ utcom2010.wikispaces.comutcom2010 - Developmental and Reproductive GeneticsReview the genetic mechanisms that control how a cell differentiates from an ... GL13 gene - Greig cephalopholysyndactyly and Pallister-Hall syndrome
 25  +9 app.com
Your News | The Asbury Park Press NJ | app.comNicholas's incredibly rare syndrome is Pallister-Hall Syndrome caused by a change in the gl13 gene . This change caused among other things ...
 26  +74 cshlp.org
Abstract - Genes & DevelopmentdHAND, in turn, excludes anterior genes such asGli3 and Alx4 from posterior mesenchyme. Furthermore, genetic interaction of GLI3 and dHAND directs ...
 27  -3 nature.com
Localization of the gene for Cowden disease to chromosome 10q22 7CRC Genetic Epidemiology Research Group, Inst of Public Health, .... K.-H. GL13 zinc-finger gene interrupted by translocations in Greig syndrome families.
 29  -4 gofundme.com
Help a Miracle by Z Eileen Hudnut - GoFundMeNicholas's incredibly rare syndrome is Pallister-Hall Syndrome caused by a change in the gl13 gene . This change caused among other things ...
 30  +1 prezi.com
Polydactyly by Erika Brandon on PreziPolydactyly is caused by the GL13 gene . If an individual has one copy of polydactyly gene, then he/she would have extra digits. While the other ...
 32  -4 missouri.edu
gl13 recovered from Maize COOP stocks --Philip Stinard gl13 , once The mutant is referred to by Anderson in MNL 29:5-6 (1955; the reference to gl13 in the 1993 and 1994 MNL gene lists is a mistaken reference to a gl3 allele).
 33  +4 aacrjournals.org
Point Mutations and Deletions of the Bcl10 Gene in Solid Tumors Point Mutations and Deletions of the Bcl10 Gene in Solid Tumors ... A and B, SSCPs of DNA from tumors (T) of case GL 13 (A) and GT 53 (B) ...
 34  +14 knoji.com
Greig Cephalopolysyndactyly Syndrome - Genetic Disorders - Knoji Greig Cephalopolysyndactyly Syndrome is caused by a mutated GL13 gene . The GL13 gene sends instructions on how to pattern or shape the ...
 35  -2 maizegdb.org
MaizeGDB: Interesting and/or Newly Reported GenesThe genes are sorted by the last time the gene has been updated.
 36  +10 straininfo.net
Can J Microbiol 56(10), 864-873, 2010 Publication Passport ... 2010/11/22, 338. HM991722, Hypocrea virens strain Gl-13 translation elongation factor EF-1 alpha (Tef1) gene , partial sequence, 2010/11/22, 336.
 37  -2 uic.edu
Genetic Control of Embryonic Development - University of Illinois at Genetic Control During Embryonic Development ... Forkhead‑like 15 Thyroid agenesis, cleft palate; Gl13 Grieg syndrome; HOXA‑13 Hand‑foot‑genital syndrome ...
 38  +11 ankara.edu.tr
A Greig Syndrome Case Diagnosed In One Of The Singleton Of Mutations in the GLI3 gene located on chromosome 7p3 are ... cations that interrupt the gene , micro- deletions, and ... GL13 gen mutation. GL13 mutation.
 40  +1 cbsnews.com
Rare Disease Day: Handprints across America - Photo 10 - Pictures Brayden, 4 months old, from Ohio has ABCA-3 Surfactant Deficiency. <p></p> The severe, rare respiratory disease is caused by a genetic mutation in the <a ...
 41  ~ fisherbiotec.com.auVarious Genetic Disorders - Fisher BiotecP450 oxireductase gene (POR). Congenital long QT ... FCGR Genes 1q23.3 basic research. FCGR Genes 1q23.3 .... GL13 7p13, HOXD13 2q31, ROR2 9q22.
 42  -10 wordswithfriends.net
GL-13 - Words With Friends | Manage My TournamentGL-13 . Start Date: 2011-08-01. Tourney Status: Complete | Round 31. Player Status: ... Trueheartd says: Gene just couldn't get a break with the letters. I definitely ...
 43  +8 bmj.com
The acrocallosal syndrome and Greig syndrome are not allelic fragment from the 3' end of the GLI3 gene , which has been found to
 44  +9 uniprot.org
Polyhydroxyalkanoate synthase 1 - Pseudomonas sp. gl13 - UniProtGene names. Name: phaC1 EMBL ACJ02400.1. Organism, Pseudomonas sp. gl13 EMBL ACJ02400.1. Taxonomic identifier, 530577 [NCBI]. Taxonomic lineage ...
 45  -2 wiley.com
Pallister–Hall syndrome: Unreported skeletal features of a GLI3 ... Nosology and classification of genetic skeletal disorders: 2010 revision ... c. 3386_3387delTT was detected in exon 14 of the GL13 gene .
 46  -6 ebscohost.com
The Maize <i>glossy13</i> Gene , Cloned via BSR-Seq and ... - ebscoTitle: The Maize <i>glossy13</i> Gene , Cloned via BSR-Seq and ... allele of <i> gl13 </i>, validates the hypothesis that gene GRMZM2G118243 is <i> gl13 </i>.
 47  ~ actaorthopaedica.beCURRENT CONCEPTS REVIEW GENES AND ORTHOPEDICS Mutations in these genes are often responsible for the congenital skeletal
 48  +52 cesco.com
Midwest GL-13 1 Ground Locknut - Crescent Electric Supply CompanyGL-13 MIDWEST 1 GRND LOCKNUT. ... Vendor: Midwest. Price: Cat #: GL-13 . $4.18. SKU: 614407. UPC: 784564200136. each ...
 49  -5 wetpaint.com
Grey's Anatomy Doc Speak: What is an HH Tumor ... - WetpaintThe cause of these tumors is unknown, though some scientists suggest it may be a mutation in the GL13 gene . However, there are real-life ...
 50  -11 wikigenes.org
WikiGenes - POU3F4 - POU class 3 homeobox 4Highlights are the chromosomal localization of at least five genes for ... been implicated for four of the genes discussed: POU3F4, SOX9, PAX6, and GL13 [6].
 51  -4 mit.edu
Certified by - DSpace@MITwhich only one of a set of two or more exons in a gene is included in the
 52  ~ nbrp.jpOLA06- Gl13 < DNA < OLA06 < メダカ @ BioResource World(BRW)Gene Ontology · Taxonomy · Disease Ontology · Reference. Resource count: 6,370,160. Resource Information OLA06- Gl13 ... Resource name, OLA06- Gl13 .