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Mouse Embryonic Stem Cell and
Transgenesis Core
Laboratories
The Medical College of Georgia Mouse ES Cell and Transgenesis
Core Facility requires investigators, as a condition of service, to
acknowledge the Core and the services provided by the Core in any ‘primary’
publication (i.e. the first peer-reviewed publication in which cells or mice
generated, at least in part, through the services of the Core are described
or employed) and/or in all other forms of public or private dissemination of
information (seminars, abstracts, advertisements, etc.). An appropriate
form of words might be, for example: xxx targeted mice were generated with
the services of the Medical College of Georgia Mouse ES Cell and
Transgenesis Core Facility. This information is important to future
planning of the Core, which is heavily reliant on Institutional subsidies.
If you have any new information about ‘primary’ publications, please let the
Core know by sending an email to the
Director.
A
partial list of ‘primary’ publications arising from services provided by the
Medical College of Georgia Mouse ES Cell and Transgenesis Core Facility is
presented below.
1. Min
JN, Zhang Y, Moskophidis D, Mivechi NF: Unique contribution of heat shock
transcription factor 4 in ocuar lens development and fiber cell
differentiation. Genesis 40(4):205, 2004
2. Wang
G, Zhang J, Moskophidis D, Mivechi NF: Targeted disruption of the heat shock
transcription factor (hsf)-2 gene results in increased embryonic lethality,
neuronal defects, and reduced spermatogenesis. Genesis 36(1):48, 2003.
3. Su DM,
Navarre S, Oh WJ, Condie BG, Manley NR: A domain of Foxn1 required for
crosstalk-dependent thymic epithelial cell differentiation. Nat Immunol
4(11):1128, 2003.
4. Mellor
AL, Baban B, Chandler P, Marshall B, Jhaver K, Hansen A, Koni PA, Iwashima
M, Munn DH: Cutting edge: induced indoleamine 2,3 dioxygenase expression in
dendritic cell subsets suppresses T cell clonal expansion. J Immunol
171(4):1652, 2003.
5.
Sullivan BA, Kraj P, Weber DA, Ignatowicz L, Jensen PE: Positive selection
of a Qa-1-restricted T cell receptor with specificity for insulin. Immunity
17(1):95, 2002.
6. Zhang
Y, Huang L, Zhang J, Moskophidis D, Mivechi NF: Targeted disruption of hsf1
leads to lack of thermotolerance and defines tissue-specific regulation for
stress-inducible Hsp molecular chaperones. J Cell Biochem 86(2):376, 2002.
7.
Hashimoto K, Joshi SK, Koni PA: A conditional null allele of the major histocompatibility
IA-beta chain gene. Genesis 32(2):152, 2002.
8.
Koushik SV, Chen H, Wang J, Conway SJ: Generation of a conditional loxP
allele of the Pax3 transcription factor that enables selective deletion of
the homeodomain. Genesis 32(2):114, 2002.
9. Westmoreland
JJ, Hancock CR, Condie BG: Neuronal development of embryonic stem cells: a
model of GABAergic neuron differentiation. Biochem Biophys Res Commun
284(3):674, 2001.
10. Kraj
P, Pacholczyk R, Ignatowicz H, Kisielow P, Jensen P, Ignatowicz L: Positive
selection of CD4(+) T cells is induced in vivo by agonist and inhibited by
antagonist peptides. J Exp Med 194(4):407, 2001.
11.
Pacholczyk R, Kraj P, Ignatowicz L: An incremental increase in the
complexity of peptides bound to class II MHC changes the diversity of
positively selected alpha beta TCRs. J Immunol 166(4):2357, 2001.
12.
Koushik SV, Wang J, Rogers R, Moskophidis D, Lambert NA, Creazzo TL, Conway
SJ: Targeted inactivation of the sodium-calcium exchanger (Ncx1) results in
the lack of a heartbeat and abnormal myofibrillar organization. Faseb J
15(7):1209, 2001.
13. Huang L, Mivechi NF, Moskophidis
D: Insights into regulation and function of the major stress-induced hsp70
molecular chaperone in vivo: analysis of mice with targeted gene disruption
of the hsp70.1 or hsp70.3 gene. Mol Cell Biol 21(24):8575, 2001.
14. Kraj P, Pacholczyk R, Ignatowicz
L: Alpha beta TCRs differ in the degree of their specificity for the
positively selecting MHC/peptide ligand. J Immunol 166(4):2251, 2001.
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