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Kallmann syndrome 3 (autosomal dominant) Results From BioPortfolio's Antibody Search
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GeneTex Inc. - Your source for monoclonal, polyclonal, primary ...
Mutations in this gene have been associated with Pfeiffer syndrome, Jackson- Weiss ... osteoglophonic dysplasia, and autosomal dominant Kallmann syndrome 2.
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http://www.genetex.com/WebPage/Product/ProductDetail.aspx?Ca...
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www.hypromatrix.com Hypromatrix, Inc.
3. Fioretos, T., Panagopoulos, I., Lassen, C., Swedin, A., ... cause autosomal dominant Kallmann syndrome. Nat. Genet. 33, 463-465. DATA. Immunofluorescence
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http://www.hypromatrix.com/Products/Primary_Antibody/FGFR1.p...
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FGFR1 antibody, FGFR1 Antibody, Rabbit Polyclonal Antibody
Specificity: No reaction with FGFR-2 and FGFR-3 is detected. .... Disease: Defects in FGFR1 are the cause of Kallmann syndrome type 2 (KAL2) [MIM:147950];
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http://www.genwaybio.com/product_info.php?products_id=195175...
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Kinase-Disease Associations
A splice-altering mutation seen in cases of Seckel syndrome [OMIM:210600], ..... and other skeletal errors) and dominant Kallmann syndrome 2 [OMIM:147950]. .....
MASTL, AGC, Hematopoiesis, Mut, One mutation found in autosomal dominant ....
Inhibitors: LY333531 (ruboxistaurin; Phase 3 for diabetic neuropathy and ...
http://www.cellsignal.com/reference/kinase_disease.html...
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FGFR1 antibody, FGF Receptor 1 alpha Antibody, Mouse Monoclonal ...
Disease: Defects in FGFR1 are the cause of Kallmann syndrome type 2 (KAL2) .... FGF Receptor 1 alpha interacts with Catenin beta,(exon 3), IgG (GenWay ...
http://www.genwaybio.com/product_info.php?products_id=240492...
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FGFR1 protein, FGFR1 Human recombinant protein
Multiple forms of FGFR-1 to -3 are generated by alternative splicing of the mRNAs. ... Disease: Defects in FGFR1 are the cause of Kallmann syndrome type 2
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http://www.genwaybio.com/product_info.php?products_id=46021...
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