2012 Summer Newsletter - UC Davis Health System
2012 Summer Newsletter - UC Davis Health System
2012 Summer Newsletter - UC Davis Health System
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Department of Pediatrics <strong>Newsletter</strong><br />
Page 4<br />
Please send your<br />
papers pending<br />
publication to Phyllis<br />
Brown so she can write<br />
a news release. E-mail:<br />
phyllis.brown@ucdmc.<br />
ucdavis.edu<br />
916-734-9023<br />
Recent Funding (Continued)<br />
Robin Hansen - Wayne State:<br />
"Early Pharmacotherapy Guided by<br />
Biomarkers in Autism"<br />
$122,455.00<br />
Jacob Henderson - CTSC:<br />
"Identification of Metabolically<br />
Quiescent Cancer Stem Cells in<br />
Neuroblastoma Cell Lines using<br />
Fluorescent-Tagged Metabolites"<br />
Recent Publications<br />
Chassaing N, Sorrentino S, David<br />
EE, Martin-Coignard D, Iacovelli A,<br />
Paznekas W, Webb BD, Faye-<br />
Petersen O, Encha Razavi, F, Lequeux<br />
L, Vigouroux A, Yesilyurt A,<br />
Boyadjiev SA, Kayserili H, Loget<br />
P, Carles D, Sergi C, Puvabanditsin<br />
S, C CP, Etchevers HC, Katsanis N,<br />
Mercer CL, Calvas P, and Jabs EW.<br />
OTX2 mutations contribute to the<br />
otocephaly-dysgnathia complex. J<br />
Med Genet 49:373-379, <strong>2012</strong><br />
Chu H, Pazgier M, Jung G, Nuccio<br />
SP, Castillo PA, de Jong MF, Winter<br />
MG, Winter SE, Wehkamp J, Shen<br />
B, Salzman NH, Underwood MA,<br />
Tsolis RM, Young GM, Lu W, Lehrer<br />
RI, Bäumler AJ, and Bevins CL.<br />
Human α-Defensin 6 Promotes Mucosal<br />
Innate Immunity Through<br />
Self-Assembled Peptide Nanonets.<br />
Science. <strong>2012</strong> Jun 21. [Epub ahead<br />
of print]<br />
Godler DE, Slater HY, Bui QM, Ono<br />
M, Gehling F, Francis D, Amor DJ,<br />
Hopper J, Hennerich D, Taylor AK,<br />
$5,000. Mentor, Noriko Satake.<br />
Funded in collaboration with the Children's<br />
Miracle Network.<br />
Julie Chinn - CTSC: "Improving<br />
Asthma Management in Pediatric<br />
Resident Continuity Clinic" $5,000.<br />
Mentor, Robert Byrd. Funded in<br />
collaboration with the Children's Miracle<br />
Network.<br />
Hagerman R and Loesch DZ.<br />
Fragile x mental retardation 1<br />
(FMR1) intron 1 methylation in<br />
blood predicts verbal cognitive impairment<br />
in female carriers of expanded<br />
FMR1 alleles: evidence<br />
from a pilot study. Clin Chem<br />
58:590-598, <strong>2012</strong><br />
Hoeffer CA, Sanchez E, Hagerman<br />
RJ, Mu Y, Nguyen DV, Wong H,<br />
Whelan AM, Zukin RS, Klann E and<br />
Tassone F. Altered mTOR signaling<br />
and enhanced CYFIP2 expression<br />
levels in subjects with fragile X<br />
syndrome. Genes Brain Behav<br />
11:253-374, <strong>2012</strong><br />
Jenkins EC, Tassone F, Ye L,<br />
Hoogeveen AT, Brown WT, Hagerman<br />
RJ, and Hagerman PJ. Reduced<br />
Telomere Length in Individuals<br />
with FMR1 Premutations and<br />
Full Mutations. Am J Med Genet A<br />
158A:1060-1065, <strong>2012</strong><br />
Kim SD, Liu JL, Roscioli T, Buckley<br />
MF, Yagnik G, Boyadjiev SA, and
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