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gl13 gene





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 1  +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  -1 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  +2 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 .
 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  +1 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  +95 wikipedia.org
GLI3 - Wikipedia, the free encyclopediaThis gene encodes a protein that belongs to the C2H2-type zinc finger proteins subclass of the Gli family. They are characterized as DNA-binding transcription  ...
 7  +7 ghc.org
Pallister Hall Syndrome - Group Health CooperativePallister-Hall syndrome (PHS) is an extremely rare genetic disorder that may be .... To date, all affected families have unique mutations in the GL13 gene so  ...
 8  +92 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;  ...
 9  +91 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  -6 researchgate.net
Point mutations throughout the GL13 gene cause Greig Publication » Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome.
 11  -3 eurekamag.com
Greig Syndrome Analysis of the GL13 gene - EurekaMag.comGrzeschik, K. H.; Gessler, M.; Heid, C.; Vortkamp, A., 1994: Greig Syndrome Analysis of the GL13 gene . American Journal Of Human Genetics. 55(3 Suppl.)  ...
 12  +88 iastate.edu
The Maize glossy13 Gene , Cloned via BSR-Seq and ... - Schnable Labthe hypothesis that gene GRMZM2G118243 is gl13. Consistent with ... As a first step in cloning the gl13 gene a collection of EMS- induced [20]  ...
 13  -1 confex.com
PDF file - ConfexWalking Approach to Facilitate Gene Cloning. Sanzhen Liu ... Application to gene cloning. 2 .... SeqWalking on the UNCLONED gene – gl13 .
 14  +3 zfin.org
Genotype: mtl^ gl13 - ZfinGenotype: mtl gl13 . Background: Unspecified. Affected Gene : mtl. Current Source: No data available. GENOTYPE COMPOSITION. Genomic Feature, Construct  ...
 15  +85 readcube.com
The Maize glossy13 Gene , Cloned via BSR-Seq and Seq-Walking (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   ...
 16  ~ agsa-geneticsupport.org.au8 PALLISTER-HALL SYNDROME FACTS - Association of Genetic Further 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.
 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  -8 epilepsyfoundation.org
Hypothalamic Hamartoma - Epilepsy FoundationThere 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   ...
 19  ~ 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  ...
 20  ~ 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.
 21  +18 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  ...
 22  -11 cshl.edu
GR:0200716 - Genewiki - BivouacGene Name. glossy13. Gene Symbol. gl13 . Gene Type. Not classified. Genus species. Zea mays subsp. mays (Maize). Description. Necrotic  ...
 23  +5 medschat.com
Gl 13 - Topics - MedsChat - The People's Medicine CommunityResults 1 - 20 of 68 ... Learn about and discuss gl 13 at The People's Medicine Community. ... ChEMBL: 5736 GeneCards: GCG Gene Gene Ontology Molecular  ...
 24  +14 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.
 25  +75 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  ...
 26  +14 gramene.org
23. Effects of a glabrousness gene , gl-1, on agronomic traitsAn F\1\ plant from a cross between a glabrous line ( gl-13 ) and a normal cultivar ... These data suggest that the glabrous gene has some pleiotropic effect on the  ...
 27  -7 oxfordjournals.org
( GL-13 ) in Guinea Pigs 1,2 - Journal of the National Cancer Instituteunique transplantable granulocytic leukemia ( GL-13 ) of strain 13 guinea pigs. .... when, in the future, gene loci are mapped for the terminal ends of the long arm  ...
 28  +7 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).
 29  +2 ingenuity.com
Mst98Ca/Mst98Cb gene interaction network - Target ExplorerCategory: gene , Type: other, Synonyms: anon-WO0140519.46, CG11719, CG18396, Dmel CG11719, Dmel CG18396, Mst, mst(3)gl-12, mst(3) gl-13 , mst336,  ...
 30  +18 eur.nl
gene mapping of complex disorders - RePub - Erasmus Universiteit No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes ..... Vortkamp A, Gessler M, Grzeschik KI-I. GL13 zinc-finger gene interrupt by.
 31  -6 prezi.com
Greig Syndrome by Willie McKenzie on PreziBy Willie McKenzie Greig Syndrome is caused by mutations in the GL13 gene , located in the 7th chromosome. Greig Syndrome is a autosomal  ...
 32  +2 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  ...
 33  -11 maizegdb.org
MaizeGDB: Interesting and/or Newly Reported GenesThe genes are sorted by the last time the gene has been updated. .... 62 days ago, gl13 , glossy13: necrotic glossy leaf; plants that survive to maturity are sterile   ...
 34  +66 app.com
Help make a misacle | 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  ...
 35  -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  ...
 36  ~ 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.
 37  ~ aacrjournals.org
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) show wild-type bands and additional aberrant bands when compared  ...
 38  -9 udel.edu
eGIFT - Extracting Gene Information From TextSelected documents for gene BPI - Bactericidal/permeability-increasing protein · see iTerms | see all documents. These documents contain iTerm(s) host.
 39  +6 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].
 40  +60 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>.
 41  +60 cbsnews.com
Rare Disease Day: Handprints across America - Photo 1 - Pictures p>For Rare Disease Day, Feb. 28, organizations around the world are gearing up to raise awareness for the public and policy-makers to research debilitating  ...
 42  ~ asas.roGENE POLYMORPHISM OF PRION PROTEIN (PrP) AND ... - ASASAll mammalian genomes analyzed provide a copy of the PrP gene . Genes coding for PrP or PrP-like .... χ2= 5,7623; G.L.=13 ; p>0,05. Genotypic structure at the  ...
 43  +58 wiley.com
Pallister–Hall syndrome: Unreported skeletal features of a GLI3 DNA was only available for sequencing analysis in patient 2 and the mutation, c.3386_3387delTT was detected in exon 14 of the GL13 gene .
 44  -31 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  ...
 46  +1 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.
 47  +2 mit.edu
Certified by - DSpace@MITwhich only one of a set of two or more exons in a gene is included in the
 48  -22 knoji.com
Greig Cephalopolysyndactyly Syndrome - Genetic Disorders - KnojiGreig Cephalopolysyndactyly Syndrome is caused by a mutated GL13 gene . The GL13 gene sends instructions on how to pattern or shape the  ...
 49  +52 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.
 50  ~ actaorthopaedica.beCURRENT CONCEPTS REVIEW GENES AND ORTHOPEDICS Mutations in these genes are often responsible for the congenital skeletal