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PT3547-3E (PR27493) Hu Can 1.2 page 41
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author: emmachleder
updated: 22/08/2002
matching:
jag 1 alagille syndrom
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PT3699-3E (PR27547) Hu Plas 12K page 423
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author: emmachleder
updated: 22/08/2002
matching:
jag 1 alagille syndrom
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http://www.clontech.com/clontech/atlas/genelists/7903-1_HuGlass38I.pdf page 11
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updated: 13/03/2002
matching:
jag 1 alagille syndrom
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http://www.clontech.com/clontech/atlas/genelists/7910-1_HuGlass38II.pdf page 83
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updated: 04/12/2001
matching:
jag 1 alagille syndrom
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http://www.clontech.com/clontech/atlas/genelists/7905-1_HuPlastic8K.pdf page 312
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updated: 16/05/2001
matching:
jag 1 alagille syndrom
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http://www.genexbioscience.com/products.cfm?productID=341
2489 Technology Drive, Hayward CA 94545 Tel: 510-266-3777 Fax: 510-266-0777 - -Search Our Company Products Product Name Catalog Number - Click on the letter below to see the list of products that begins on that letter A - B - C - D - E - F - G - H - I - J - K - L - M - N - O - P - Q - R - S - T - U - V - W - X - Y - Z - -Product Name:- Anti-Jagged 1 picture goes here...
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Signaling Pathways: Notch Signaling
In addition, loss-of-function Notch receptor and ligand mutati ons are implicated in several disorders, including Alagille syndrome and an autosomal dominant form of cerebral arteriopathy (CADASIL), which have collectively spurred the interest for pharmacological pathway intervention in human disease.
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Jagged1 (28H8) Rabbit mAb #2620
-|- contact -|- browsers & accessibility -|- careers Jagged1 (28H8) Rabbit mAb #2620 Jagged1 (28H8) Rabbit mAb #2620 AGS ALAGILLE SYNDROME CD CD 339 CD-339 CD339 CD339 ANTIGEN HJ HJ 1 HJ-1 HJ1 JAG JAG 1 JAG-1 JAG1 JAGGED JAGGED 1 JAGGED-1 JAGGED1 JAGGED1 28H8 RABBIT MAB JAGL JAGL 1 JAGL-1...
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Jagged1 (1C4) Rabbit mAb #2155
-|- contact -|- browsers & accessibility -|- careers Jagged1 (1C4) Rabbit mAb #2155 Jagged1 (1C4) Rabbit mAb #2155 AGS ALAGILLE SYNDROME CD CD 339 CD-339 CD339 CD339 ANTIGEN HJ HJ 1 HJ-1 HJ1 JAG JAG 1 JAG-1 JAG1 JAGGED JAGGED 1 JAGGED-1 JAGGED1 JAGGED1 1C4 RABBIT MAB JAGL JAGL 1 JAGL-1...
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Notch2 (8A1) Rabbit mAb #2420
Lane 1 contains lysate input and lane 2 was immunoprecipitated with Notch2 (8A1) Rabbit mAb.
Background Notch1 is a transmembrane protein functioning in development and the determination of cell fate (1).
Notch2 is a member of Notch family and mutation in Notch2 is associated with Alagille syndrome (5).
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Purified Anti-mouse Notch 2 Antibody - BioLegend
- - Notch 1 and Notch 2 exhibit the highest structural similarity among the four mammalian Notch receptors.
Mutation of Notch2 can cause a rare genetic disorder, Alagille syndrome, with multiple defects in liver, heart and other systems.
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PE Anti-mouse Notch 2 Antibody - BioLegend
- - Notch 1 and Notch 2 exhibit the highest structural similarity among the four mammalian Notch receptors.
Mutation of Notch2 can cause a rare genetic disorder, Alagille syndrome, with multiple defects in liver, heart and other systems.
Ligand Receptor: Jag1,2; Delta 1,2 Antigen References: 1.
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LEAF Purified Anti-mouse Notch 2 Antibody - BioLegend
- - Notch 1 and Notch 2 exhibit the highest structural similarity among the four mammalian Notch receptors.
Mutation of Notch2 can cause a rare genetic disorder, Alagille syndrome, with multiple defects in liver, heart and other systems.
Ligand Receptor: Jag1,2; Delta 1,2 Antigen References: 1.
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New Gene Mutations - The Jackson Laboratory
Mutation Symbol Mutation Name Gene Symbol Phenotype Chr bdd bulging disc disease skeletal 2 Trl Trembler-like neurological 11 trls-2J tremor and reduced lifespan 2 Jackson neurological 10 agil-2J agitans-like 2 Jackson neurological 14 twi-5J twitcher 5 Jackson Galc neurological 12 Mfs mutant fur is striped skin and hair 13 fsq flying squirrel neurological 10 dkd darkened dorsal skin...
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Mutations Causing Inner Ear Dysfunction - The Jackson Laboratory
Jag1 jagged 1 2 77 Htu, slalom, KO headturner, slalom, targeted inactivation ch, ch, tm inner ear development; homozgous lethal Xue et al.
Jag2 jagged 2 12 58 KO -targeted inactivation tm hair cell development; homozygous lethal Lanford et al.
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Map positions of mouse mutations - The Jackson Laboratory
(see Mouse Models ) Chr 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , X Chromosome cM Position Genes and mutations 1 10.4 Eya1 , eyes absent 1 homolog (Drosophila) [spontaneous and targeted mutations] S 1 15.0 Col9a1 , procollagen, type IX, alpha 1 [targeted mutation] 1 16.5 Dst , dystonin [dystonia...
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Bibliography for R-415
PubMed · R-415 "Soluble Jagged 1 represses the function of its transmembrane form to induce the formation of the Src-dependent chord-like phenotype." Small D, Kovalenko D, Kacer D, Liaw L, Landriscina M, Di Serio C, Prudovsky I, Maciag T.
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Microsoft Word - Bibliography, 2004.doc page 27
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author: mariak
updated: 16/08/2006
matching:
jag 1 syndrom
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http://www.rndsystems.com/DAM_public/5313.pdf
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updated: 18/05/2005
matching:
jag 1 syndrom
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http://www.clontech.com/clontech/atlas/genelists/7746-1_HuCellInt.pdf page 8
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updated: 16/05/2001
matching:
jag 1 syndrom
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