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Current Search: turner: 593, syndrom: 3641, 1: 321133

RPS4X Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
It has been suggested that haploinsufficiency of the ribosomal protein S4 genes plays a role in Turner syndrome; however, this hypothesis is controversial.
-- -Applications ------ELISA, WB, Antibody Production, Assay Development, Protein Array Related Monoclonal Antibody 　-1 - 　match - H00006191-M01 RPS4X monoclonal antibody (M01), clone 3E10 -...
author: Abnova

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SHOX2 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
SHOX is a pseudoautosomal homeo box gene that is thought to be responsible for idiopathic short stature and implicated to play a role in the short stature phenotype of Turner syndrome patients.
This gene is considered to be a candidate gene for Cornelia de Lange syndrome.
author: Abnova

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Microsoft Word - Bibliography, 2004.doc
...

author: mariak updated: 16/08/2006 matching: turner syndrom 1

TJL BSB Panel: Chr X refs
DXBir9 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSB Panel: Chr 17 refs
D17Bir5 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
D17Bir9 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSB Panel: Chr 13 refs
D13Bir12 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
D13Bir18 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSB Panel: Chr 8 refs
D8Bir11 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
D8Bir12 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSS Panel: Chr X refs
Il13ra1 Reference: Donaldson DD, Whitters MJ, Fitz LJ, Neben TY, Finnerty H, Henderson SL, O'Hara RM Jr, Beier DR, Turner KJ, Wood CR, Collins M.
Il13ra2 Reference: Donaldson DD, Whitters MJ, Fitz LJ, Neben TY, Finnerty H, Henderson SL, O'Hara RM Jr, Beier DR, Turner KJ, Wood CR, Collins M, 1998.

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TJL BSS Panel: Chr 19 refs
Anxa1 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
Pltr4 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSS Panel: Chr 18 refs
Ttr Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
Mltr7 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSS Panel: Chr 17 refs
D17Wsu1e Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog Syndrome) gene homologues.

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TJL BSS Panel: Chr 16 refs
New nomen Dgcr2, DiGeorge syndrome critical region gene 2 assigned May 2002.
D16Mit145 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
Down's Syndrome candidate gene for mental retardation and heart defect.

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TJL BSS Panel: Chr 15 refs
Trps1, trichorhinophalangeal syndrome I (human).
New nomen Trps1, trichorhinophalangeal syndrome I (human), assigned March 2002.
Xltr5 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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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.
Plau Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSS Panel: Chr 13 refs
Plf Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
Tpbpa Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSS Panel: Chr 8 refs
D8Bir17 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
Mltr2 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSS Panel: Chr 7 refs
D7Wsu1e Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
Pltr3 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSS Panel: Chr 6 refs
Tcrb Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
D6Wsu1e Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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TJL BSS Panel: Chr 5 refs
Zp3 Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.
Actb Reference: Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH, 1994.

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master_table - The Jackson Laboratory
Gene Symbol - Gene Name Chr cM Mutation Mutation Name Type a Ear Pathology References- b - - - - - - - - - - - - - - - - - - - Agc1 aggrecan 1 7 39 cmd cartilage matrix deficiency sp cartilage abnormality [335] Alms1 Alstrom syndrome 1 homolog 6 36 KO gene trap gt intracellular trafficking [39] Ap3d1 adaptor-related protein complex 3, delta 1 subunit 10 43 mh...

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Pietro -0ttawa for internet.ppt
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author: Jan D. Marshall updated: 21/03/2006 matching: turner syndrom 1

Bibliography - The Jackson Laboratory
"Experimental parameters affecting the Morris water maze performance of a mouse model of Down syndrome." Behav Brain Res 154(1): 1-17.
PMID: 11771737-- Turner, C.A., Presti, M.F., Newman, H.A., Bugnehagen, P., Crnic, L., and Lewis, M.H.

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