Activin A Efficiently Specifies Definitive Endoderm from Human Embryonic Stem Cells Only When Phosphatidylinositol 3‐Kinase Signaling Is Suppressed von McLean, Amanda B., D'Amour, Kevin A., Jones, Karen L., Krishnamoorthy, Malini, Kulik, Michael J., Reynolds, David M., Sheppard, Alan M., Liu, Huiqing, Xu, Ying, Baetge, Emmanuel E., Dalton, Stephen

Volltext

Human Pluripotent Stem Cell-Derived Multipotent Vascular Progenitors of the Mesothelium Lineage Have Utility in Tissue Engineering and Repair von Colunga, Thomas, Hayworth, Miranda, Kreß, Sebastian, Reynolds, David M., Chen, Luoman, Nazor, Kristopher L., Baur, Johannes, Singh, Amar M., Loring, Jeanne F., Metzger, Marco, Dalton, Stephen

Volltext

Whole-Genome Sequencing and iPLEX MassARRAY Genotyping Map an EMS-Induced Mutation Affecting Cell Competition in Drosophila melanogaster von Lee, Chang-Hyun, Rimesso, Gerard, Reynolds, David M, Cai, Jinlu, Baker, Nicholas E

Volltext

Somatic Inactivation of Pkd2 Results in Polycystic Kidney Disease von Wu, Guanqing, D'Agati, Vivette, Cai, Yiqiang, Markowitz, Glen, Park, Jong Hoon, Reynolds, David M, Maeda, Yoshiko, Le, Thanh C, Hou, Harry, Kucherlapati, Raju, Edelmann, Winfried, Somlo, Stefan

Volltext

Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder von Berko, Esther R, Suzuki, Masako, Beren, Faygel, Lemetre, Christophe, Alaimo, Christine M, Calder, R Brent, Ballaban-Gil, Karen, Gounder, Batya, Kampf, Kaylee, Kirschen, Jill, Maqbool, Shahina B, Momin, Zeineen, Reynolds, David M, Russo, Natalie, Shulman, Lisa, Stasiek, Edyta, Tozour, Jessica, Valicenti-McDermott, Maria, Wang, Shenglong, Abrahams, Brett S, Hargitai, Joseph, Inbar, Dov, Zhang, Zhengdong, Buxbaum, Joseph D, Molholm, Sophie, Foxe, John J, Marion, Robert W, Auton, Adam, Greally, John M

Volltext

Comparative Diagnostic Performance of Estimated Fetal Weight and Isolated Abdominal Circumference for the Detection of Fetal Growth Restriction von Whitham, Megan D., Reynolds, David M., Urban, Amanda R., Ennen, Christopher S., Dudley, Donald J.

Volltext

Identification of a Locus for Autosomal Dominant Polycystic Liver Disease, on Chromosome 19p13.2-13.1 von Reynolds, David M., Falk, Cathy T., Li, Airong, King, Bernard F., Kamath, Patrick S., Huston, John, Shub, Clarence, Iglesias, Diana M., Martin, Rodolfo S., Pirson, Yves, Torres, Vicente E., Somlo, Stefan

Volltext

PKD2, a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein von Mochizuki, Toshio, Wu, Guanqing, Hayashi, Tomohito, Xenophontos, Stavroulla L., Veldhuisen, Barbera, Saris, Jasper J., Reynolds, David M., Cai, Yiqiang, Gabow, Patricia A., Pierides, Alkis, Kimberling, William J., Breuning, Martijn H., Deltas, C. Constantinou, Dorien J. M. Peters, Somlo, Stefan

Volltext

Forkhead transcription factors, Fkh1p and Fkh2p, collaborate with Mcm1p to control transcription required for M-phase von Kumar, Raman, Reynolds, David M, Shevchenko, Andrej, Shevchenko, Anna, Goldstone, Sherilyn D, Dalton, Stephen

Volltext

Amnion as a surrogate tissue reporter of the effects of maternal preeclampsia on the fetus von Suzuki, Masako, Maekawa, Ryo, Patterson, Nicole E, Reynolds, David M, Calder, Brent R, Reznik, Sandra E, Heo, Hye J, Einstein, Francine Hughes, Greally, John M

Volltext

Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease von REYNOLDS, D. M, HAYASHI, T, FOSSDAL, R, COTO, E, GUANQINGWU, BREUNING, M. H, GERMINO, G. G, PETERS, D. J. M, SOMLO, S, YIQIANG CAI, VELDHUISEN, B, WATNICK, T. J, LENS, X. M, MOCHIZUKI, T, QIAN, F, MAEDA, Y, LI LI

Volltext

Characterization of the Exon Structure of the Polycystic Kidney Disease 2 Gene (PKD2) von Hayashi, Tomohito, Mochizuki, Toshio, Reynolds, David M., Wu, Guanqing, Cai, Yiqiang, Somlo, Stefan

Volltext

Rapid screening of SNPs in metastatic colorectal cancer (mCRC) utilizing multiplex sequencing technology (Sequenom) von Maitra, Radhashree, Nayak, Jay B., Basu-Mallick, Atrayee, Sood, Arjun, Augustine, Titto A, Mariadason, John, Reynolds, David M, Goel, Sanjay

Volltext

Evidence for a third genetic locus for autosomal dominant polycystic kidney disease von Daoust, Martin C., Reynolds, David M., Bichet, Daniel G., Somlo, Stefan

Volltext

Mosaic Epigenetic Dysregulation of Ectodermal Cells in Autism Spectrum Disorder: e1004402 von Berko, Esther R, Suzuki, Masako, Beren, Faygel, Lemetre, Christophe, Alaimo, Christine M, Calder, R Brent, Ballaban-Gil, Karen, Gounder, Batya, Kampf, Kaylee, Kirschen, Jill, Maqbool, Shahina B, Momin, Zeineen, Reynolds, David M, Russo, Natalie, Shulman, Lisa, Stasiek, Edyta, Tozour, Jessica, Valicenti-McDermott, Maria, Wang, Shenglong, Abrahams, Brett S, Hargitai, Joseph, Inbar, Dov, Zhang, Zhengdong, Buxbaum, Joseph D, Molholm, Sophie, Foxe, John J, Marion, Robert W, Auton, Adam, Greally, John M

Volltext

Identification of PKD2L, a human pkd2-related gene : Tissue-specific expression and mapping to chromosome 10q25 von GUANQING WU, HAYASHI, T, PARK, J.-H, DIXIT, M, REYNOLDS, D. M, LI LI, MAEDA, Y, YIQIANG CAI, COCA-PRADOS, M, SOMLO, S

Volltext

Identification ofPKD2L,a HumanPKD2-Related Gene: Tissue-Specific Expression and Mapping to Chromosome 10q25 von Wu, Guanqing, Hayashi, Tomohito, Park, Jong-Hoon, Dixit, Mehul, Reynolds, David M., Li, Li, Maeda, Yoshiko, Cai, Yiqiang, Coca-Prados, Miguel, Somlo, Stefan

Volltext

Multidimensional digital experience analysis von Perpetua, Jr., Dennis Anthony, Reynolds, David M

Volltext bestellen

MULTIDIMENSIONAL DIGITAL EXPERIENCE ANALYSIS von Perpetua, JR., Dennis Anthony, Reynolds, David M

Volltext bestellen

Novel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) gene von VIRIBAY, M, HAYASHI, T, SAN MILLAN, J. L, TELLERIA, D, MOCHIZUKI, T, REYNOLDS, D. M, ALONSO, R, LENS, X. M, MORENO, F, HARRIS, P. C, SOMLO, S

Volltext