Proliferation studies

KT Katelynn A. Toomer
MY Mengyao Yu
DF Diana Fulmer
LG Lilong Guo
KM Kelsey S. Moore
RM Reece Moore
KD Ka’la D. Drayton
JG Janiece Glover
NP Neal Peterson
SR Sandra Ramos-Ortiz
AD Alex Drohan
BC Breiona J. Catching
RS Rebecca Stairley
AW Andy Wessels
JL Joshua H. Lipschutz
FD Francesca N. Delling
XJ Xavier Jeunemaitre
CD Christian Dina
RC Ryan L. Collins
HB Harrison Brand
MT Michael E. Talkowski
FM Federica del Monte
RM Rupak Mukherjee
AA Alexander Awgulewitsch
SB Simon Body
GH Gary Hardiman
EH E. Starr Hazard
WS Willian A. da Silveira
BW Baolin Wang
ML Maire Leyne
RD Ronen Durst
RM Roger R. Markwald
SS Solena Le Scouarnec
AH Albert Hagege
TT Thierry Le Tourneau
PK Peter Kohl
ER Eva A. Rog-Zielinska
PE Patrick T. Ellinor
RL Robert A. Levine
DM David J. Milan
JS Jean-Jacques Schott
NB Nabila Bouatia-Naji
SS Susan A. Slaugenhaupt
RN Russell A. Norris
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Ki67-positive cells and total cell numbers were counted throughout eight sections, with each section separated by 20 mm (to ensure counts were not duplicated) per heart. For NfatC1Cre(+);Ift88+/+ (control), a total of five individual anterior and posterior leaflets were analyzed. For NfatC1Cre(+);Ift88f/+ (conditional heterozygote), a total of eight individual anterior and posterior leaflets were analyzed. For NfatC1Cre(+);Ift88f/f (conditional knockout), a total of seven individual anterior and posterior leaflets were analyzed. The average number of Ki67-positive cells and total number of cells counted throughout the eight sections were averaged among the five leaflets analyzed per genotype. Measurements were compared to control data to obtain fold change values. To detect statistically significant differences between test groups with two-sided α = 0.05, Student’s t test was used. Error bars represent SD.

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