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http://www.clontech.com/clontech/atlas/genelists/7905-1_HuPlastic8K.txt
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article ID:
updated: 13/03/2002
matching:
waardenburg syndrom type 2b
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Development of Somitic Lineages Poster References, May 2006 - R&D Systems
"Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome." Hum Mol Genet9(13): 1907-17.
"A new long form of Sox5 (L-Sox5), Sox6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen gene." Embo J17(19): 5718-33.
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PAX3 Antibody PAX3
Additional Names PAX3, WS1, CDHS, HUP2, paired box gene 3 (Waardenburg syndrome 1), paired domain gene 3, paired box homeotic gene 3 (Waardenburg syndrome 1) Description Left: Western blot analysis of PAX3 in paraffin embedded Human Oesophagus using PAX3 antibody (3μg/ml).
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Microphthalmia (Transcription Factor) (MiTF).
Lab Vision IHC System Solutions - Rabbit Monoclonal Antibodies View Immunostains View references Read more NEWS New Antibodies launched Oct 2008 Read more....
The mutation of Mi causes Waardenburg Syndrome type II in humans.
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Microphthalmia (Transcription Factor) (MiTF) Ab-2
Lab Vision IHC System Solutions - Rabbit Monoclonal Antibodies View Immunostains View references Read more NEWS New Antibodies launched Oct 2008 Read more....
The mutation of Mi causes Waardenburg Syndrome type II in humans.
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Microphthalmia (Transcription Factor) (MiTF) Ab-1
Lab Vision IHC System Solutions - Rabbit Monoclonal Antibodies View Immunostains View references Read more NEWS New Antibodies launched Oct 2008 Read more....
The mutation of Mi causes Waardenburg Syndrome type II in humans.
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Mouse Models of Human Hearing Disorders - The Jackson Laboratory
(1996) Development 122:3381 PAX3 WS1, Waardenburg syndrome type I; WS3, Klein-Waardenburg syndrome Tassabehji et al.
(2001) Hum Mol Genet 10:153 SNAI2 - WS2, Waardenburg- syndrome, type-II- Sanchez-Martin et al.
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Boston Biochem: UPP-Related Publications
(2005) -The Papain-Like Protease of Severe Acute Respiratory Syndrome Coronavirus Has Deubiquitinating Activity.- J.
(2004) -Biochemical Analysis of Angelman Syndrome-associated Mutations in the E3 Ubiquitin Ligase E6-associated Protein.- J.
van Waardenburg, R.
van Waardenburg, R.
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Catalog Master (Exalpha) page 1
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author: Scott Sanville
updated: 17/11/2008
matching:
waardenburg syndrom type
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Catalog Master (Exalpha)
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author: Scott Sanville
updated: 17/11/2008
matching:
waardenburg syndrom type
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Microsoft Word - 10264.doc
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author: c00mje
updated: 23/09/2008
matching:
waardenburg syndrom type
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Microsoft Word - 772
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author: c00mje
updated: 23/09/2008
matching:
waardenburg syndrom type
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Are You suprised ?
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author: LSK
subject: Birthday
updated: 23/09/2008
matching:
waardenburg syndrom type
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Microsoft Word - 10264-PCL
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author: c00mje
updated: 01/06/2007
matching:
waardenburg syndrom type
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PT3699-3E (PR27547) Hu Plas 12K page 82
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author: emmachleder
updated: 22/08/2002
matching:
waardenburg syndrom type
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- The Jackson Laboratory
The Jackson Laboratory Skip to content About us News Support us Careers Contact us Search Entire site About us Advances in human health Courses and education JAX ® Mice and Services Research and resource initiatives Advances in human health Diseases we research Our contributions Our researchers care Meet our supporters Giving makes a difference Support us Courses and education...
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- The Jackson Laboratory
Waardenburg syndrome in man and splotch mutants in the mouse: a paradigm of the usefulness of linkage and synteny homologies in mouse and man for the genetic analysis of human congenital malformations.
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Microsoft Word - 46-138.doc
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updated: 09/12/2008
matching:
waardenburg syndrom
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Slug (C19G7) Rabbit mAb #9585
Deletion mutations in the corresponding Slug gene are associated with the pigmentation disorders Waardenburg Syndrome and Piebaldism, while a genetic duplication resulting in Slug overexpression is associated with a collection of congenital heart defects termed tetralogy of Fallot (7).
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http://www.clontech.com/clontech/atlas/genelists/7903-1_HuGlass38I.pdf page 112
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updated: 13/03/2002
matching:
waardenburg syndrom
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http://www.clontech.com/clontech/atlas/genelists/7905-1_HuPlastic8K.pdf page 62
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updated: 16/05/2001
matching:
waardenburg syndrom
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Citations Search
(2003) Expression and activity of cytochromes P450 2E1, 2A, and 2B in the mouse ovary: The effect of 4-vinylcyclohexene and its diepoxide metabolite.
Total mouse ovary RNA was reverse transcribed using the Reverse Transcription System and random primers, followed by quantitative PCR using primers specific for CYP2E1, 2A and 2B.
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Citations Search
The researchers-used a luciferase construct that contained the cyclin D1 promoter to test the effects of erlotinib on cyclin d1 regulation.-This construct, along with the pRL-TK vector, were co-transfected into BEAS-2B cells.-Groups of cells were then treated with or without EGF and erlotinib and assayed for luciferase activity-using the Dual-Luciferase A® Reporter Assay...
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Citations Search
(2003) Expression and activity of cytochromes P450 2E1, 2A, and 2B in the mouse ovary: The effect of 4-vinylcyclohexene and its diepoxide metabolite.
Total mouse ovary RNA was reverse transcribed using the Reverse Transcription System and random primers, followed by quantitative PCR using primers specific for CYP2E1, 2A and 2B.
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Citations Search
(1998) A dominant negative isoform of the long QT syndrome 1 gene product J.
The pCI Mammalian Expression Vector was used to express the proteins Purα (321 amino acids) and Purβ (324 amino acids) in mouse embryo-derived AKR-2B fibroblasts.
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