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CECR5 Recombinant Protein (P01)-Abnova Corporation
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author: Abnova
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http://www.clontech.com/clontech/atlas/genelists/excel/huplastic12k.xls
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article ID:
updated: 24/05/2005
matching:
cat ey syndrom chromosom region candid 5
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PT3699-3E (PR27547) Hu Plas 12K
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author: emmachleder
updated: 22/08/2002
matching:
cat ey syndrom chromosom region candid 5
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PT3699-3E (PR27547) Hu Plas 12K page 8
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author: emmachleder
updated: 22/08/2002
matching:
cat ey syndrom chromosom region candid 5
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http://www.clontech.com/clontech/atlas/genelists/7931-1_HuPlastic12K.txt
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article ID:
updated: 22/08/2002
matching:
cat ey syndrom chromosom region candid 5
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TJL BSS Panel: Chr 6 refs
Dok1 encoding p62dok maps to mouse Chromosome 6 in a region of translocation in chronic lymphocytic leukemia.
The gene for death agonist BID maps to the region of human 22q11.2 duplicated in cat eye syndrome chromosomes and to mouse chromosome 6.
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Microsoft Word - 851-pcl
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author: dkohli
updated: 10/02/2006
matching:
cat ey syndrom chromosom region candid 5
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PT3699-3E (PR27547) Hu Plas 12K page 404
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author: emmachleder
updated: 22/08/2002
matching:
cat ey syndrom chromosom region candid 5
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PT3699-3E (PR27547) Hu Plas 12K page 362
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author: emmachleder
updated: 22/08/2002
matching:
cat ey syndrom chromosom region candid 5
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http://www.clontech.com/clontech/atlas/genelists/7907-1_MoGlass38I.txt
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article ID:
updated: 09/11/2001
matching:
cat ey syndrom chromosom region candid 5
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Atlas Primer Database
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author: Kristi Dohner
updated: 16/05/2001
matching:
cat ey syndrom chromosom region candid 5
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http://www.clontech.com/clontech/atlas/genelists/7903-1_7904-1_HuGlass38.txt
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article ID:
updated: 16/05/2001
matching:
cat ey syndrom chromosom region candid 5
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PT3699-3E (PR27547) Hu Plas 12K page 310
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author: emmachleder
updated: 22/08/2002
matching:
cat ey syndrom chromosom region candid
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http://www.clontech.com/clontech/atlas/genelists/7905-1_HuPlastic8K.pdf page 230
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updated: 16/05/2001
matching:
cat ey syndrom chromosom region candid
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TJL BSS Panel: Chr X refs
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region.
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region.
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TJL BSS Panel: Chr 19 refs
Mart1 is located on mouse Chromosome 19 and is excluded as a candidate for ep and ru.
Mart1 is located on mouse Chromosome 19 and is excluded as a candidate for ep and ru.
Mart1 is located on mouse Chromosome 19 and is excluded as a candidate for ep and ru.
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TJL BSS Panel: Chr 16 refs
New nomen Dgcr2, DiGeorge syndrome critical region gene 2 assigned May 2002.
The probe hybridizes to DNA from a somatic cell hybrid line containing the following human chromosomes: 2, 3, 5, 6, 9, 10, 22.
Down's Syndrome candidate gene for mental retardation and heart defect.
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TJL BSS Panel: Chr 14 refs
Defects in the cappuccino (cno) gene on mouse cgromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism.
Assignment of the transcription factor GATA4 gene to human chromosome 8 and mouse Chromosome 14: Gata4 is a candidate gene for Ds (Disorganization).
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TJL BSS Panel: Chr 7 refs
Tjp1 Reference: Mohandas, Chen, Rowe, Birkenmeier, Fanning, Anderson, and Korenberg 1995 Localization of the tight junction protein gene Tjp1 to human chromosome 15q13, distal to the Prader-Willi/Angelman region and to mouse Chromosome 7 Genomics 30: 594-597.
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TJL BSS Panel: Chr 2 refs
Genetic linkage analysis of the Ak1, Col5a1, Epb7.2, Fpgs, Grp78, Pbx3, and Notch genes in the region of mouse Chromosome 2 homologous to human Chromosome 9q.
Genetic linkage analysis of the Ak1, Col5a1, Epb7.2, Fpgs, Grp78, Pbx3, and Notch genes in the region of mouse Chromosome 2 homologous to human Chromosome 9q.
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Alstrom Syndrome Conference Report
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author: J rgen Naggert
subject: Alstrom Syndrome Conference Report
updated: 22/03/2006
matching:
ey syndrom chromosom region candid 5
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master_table - The Jackson Laboratory
KO - tm semicircular canal defects [253] Ntf3 neurotrophin 3 6 61 KO - tm hair cell innervation [86, 92, 99] Ntn1 netrin 1 U - KO - tm semicircular canal formation; homozygous lethal [270] Ntrk2 neurotrophic tyrosine kinase, receptor, type 2 13 36 KO - tm hair cell innervation [98, 276] - homozygous lethal Ntrk3 neurotrophic tyrosine kinase, receptor, type 3 7 39 KO - tm hair cell...
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Microsoft Word - Bibliography, 2004.doc
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author: mariak
updated: 16/08/2006
matching:
cat syndrom chromosom region candid 5
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Lab Vision Corporation
The gene encoding human p57Kip2 is located on chromosome 11p15.5, a region implicated in both sporadic cancers, Wilm's tumor, and Beckwith-Wiedemann syndrome (BWS), a cancer syndrome, making it a tumor suppressor candidate.
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Lab Vision Corporation
The gene encoding human p57Kip2 is located on chromosome 11p15.5, a region implicated in both sporadic cancers, Wilm's tumor, and Beckwith-Wiedemann syndrome (BWS), a cancer syndrome, making it a tumor suppressor candidate.
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