Browse By Person: Pennisi, David

Wang, Zhen, Chan, Hsiu Wen, Gambarotta, Giovanna, Smith, Nicola J., Purdue, Brooke W., Pennisi, David J., Porrello, Enzo R., O'Brien, Shannon L., Reichelt, Melissa E., Thomas, Walter G., & Paravicini, Tamara M. (2021) Stimulation of the four isoforms of receptor tyrosine kinase ErbB4, but not ErbB1, confers cardiomyocyte hypertrophy. Journal of Cellular Physiology, 236(12), pp. 8160-8170.

5

5

Dutta, Sanjay, Leo, Paul, Kulasinghe, Arutha, Monkman, James, Pennisi, David, Roberts, Kate E., Ladwa, Rahul, & O'Byrne, Ken (2021) Genetic mutations and signatures in lung cancer - findings from a whole exome sequencing platform. Lung Cancer, 156(Supplement 1), S1.

Seabrook, Amanda J., Harris, Jessica E., Velosa, Sofia B., Kim, Edward, McInerney-Leo, Aideen M., Dwight, Trisha, Hockings, Jason I., Hockings, Nicholas G., Kirk, Judy, Leo, Paul J., Love, Amanda J., Luxford, Catherine, Marshall, Mhairi, Mete, Ozgur, Pennisi, David J., Brown, Matthew A., Gill, Anthony J., Hockings, Gregory I., Clifton-Bligh, Roderick J., & Duncan, Emma L. (2021) Multiple Endocrine Tumors Associated with Germline MAX Mutations: Multiple Endocrine Neoplasia Type 5? Journal of Clinical Endocrinology and Metabolism, 106(4), e1163-e1182.

74

12

Demeshko, Anastassia, Pennisi, David J., Narayan, Sushil, Gray, Stacy W., Brown, Matthew A., & McInerney-Leo, Aideen M. (2020) Factors influencing cancer genetic somatic mutation test ordering by cancer physician. Journal of Translational Medicine, 18(1), Article number: 431.

44

13

Tam, Oliver, Pennisi, David, Wilkinson, Lorine, Little, Melissa, Wazin, Fatima, Wan, Victor, & Lovicu, Frank (2018) Crim1 is required for maintenance of the ocular lens epithelium. Experimental Eye Research, 170, pp. 58-66.

12

11

Blum, Stefan, Ji, Ying, Pennisi, David, Li, Zhixiu, Leo, Paul, McCombe, Pamela, & Brown, Matt (2018) Genome-wide association study in Guillain-Barre syndrome. Journal of Neuroimmunology, 323, pp. 109-114.

275

16

18

Iyer, Swati, Chhabra, Yash, Harvey, Tracey, Wang, Richard, Chiu, Han Sheng, Smith, A., Thomas, Walter, Pennisi, David, & Piper, Michael (2017) CRIM1 is necessary for coronary vascular endothelial cell development and homeostasis. Journal of Molecular Histology, 48(1), pp. 53-61.

11

Li, Zhixiu, Haynes, Katelin, Pennisi, David, Anderson, Lisa, Song, Xiaoxia, Thomas, Gethin, Kenna, Tony, Leo, Paul, & Brown, Matt (2017) Epigenetic and gene expression analysis of ankylosing spondylitis-associated loci implicate immune cells and the gut in the disease pathogenesis. Genes and Immunity, 18(3), pp. 135-143.

24

21

Wang, Xiaobing, Ellis, Jonathan, Pennisi, David, Song, Sharon, Batra, Jyotsna, Hollis, Kelly, Bradbury, Linda, Li, Zhixiu, Kenna, Tony, & Brown, Matt (2017) Transcriptome analysis of ankylosing spondylitis patients before and after TNF-a inhibitor therapy reveals the pathways affected. Genes and Immunity, 18, pp. 184-190.

181

24

Iyer, Swati, Chou, Fang Yu, Wang, Richard, Chiu, Han Sheng, Sundar Raju, Vinay, Little, Melissa, Thomas, Walter, Piper, Michael, & Pennisi, David (2016) Crim1 has cell-autonomous and paracrine roles during embryonic heart development. Scientific Reports, 6, Article number: 19832 1-15.

133

11

12

Iyer, Swati, Pennisi, David, & Piper, Michael (2016) Crim1-, a regulator of developmental organogenesis. Histology and Histopathology, 31(10), pp. 1049-1057.

165

9

Pennisi, David (2016) Towards consensus on coronary vessel development: Coronary arterial endothelial cells derive primarily from the sinus venosus during embryogenesis (Editorial). Circulation Research, 118(12), pp. 1861-1862.

2

Phua, Yu Leng, Martel, Nick, Pennisi, David J., Little, Melissa H., & Wilkinson, Lorine (2013) Distinct sites of renal fibrosis in Crim1 mutant mice arise from multiple cellular origins. Journal of Pathology, 229(5), pp. 685-696.

35

32

Pennisi, David, Kinna, Genevieve, Chiu, Han Sheng, Simmons, David, Wilkinson, L., & Little, Melissa (2012) Crim1 has an essential role in glycogen trophoblast cell and sinusoidal-trophoblast giant cell development in the placenta. Placenta, 33(3), pp. 175-182.

19

Chiu, Han Sheng, York, J. Philippe, Wilkinson, Lorine, Zhang, Pumin, Little, Melissa, & Pennisi, David (2012) Production of a mouse line with a conditional Crim1 mutant allele. Genesis: The Journal of Genetics and Development, 50(9), pp. 711-716.

18

Little, Melissa, Georgas, Kylie, Pennisi, David, & Wilkinson, Lorine (2010) Kidney development: Two tales of tubulogenesis. Current Topics in Developmental Biology, 90, pp. 193-229.

91

83

Pennisi, David & Mikawa, Takashi (2009) FGFR-1 is required by epicardium-derived cells for myocardial invasion and correct coronary vascular lineage differentiation. Developmental Biology, 328(1), pp. 148-159.

47

46

Wilkinson, Lorine, Gilbert, Thierry, Sipos, Arnold, Toma, Ildiko, Pennisi, David, Peti-Peterdi, Janos, & Little, Melissa (2009) Loss of renal microvascular integrity in postnatal Crim1 hypomorphic transgenic mice. Kidney International, 76(11), pp. 1161-1171.

31

29

Pennisi, David, Wilkinson, Lorine, Kolle, Gabriel, Sohaskey, Michael, Gillinder, Kevin, Piper, Michael, McAvoy, John, Lovicu, Frank, & Little, Melissa (2007) Crim1KST264/KST264 mice display a disruption of the Crim1 gene resulting in perinatal lethality with defects in multiple organ systems. Developmental Dynamics, 236(2), pp. 502-511.

56

53

Mikawa, Takashi, Gourdie, Robert G., Takebayashi-Suzuki, Kimiko, Kanzawa, Nobuyuki, Pennisi, David J., Poma, Clifton P., & Shulimovich, Maxim (2005) Induction and patterning of the Purkinje fiber network. In Runge, Marschall S. & Patterson, Cam (Eds.) Principles of Molecular Cardiology. Humana Press, Totowa, NJ, pp. 311-321.

Mikawa, Takashi, Gourdie, Robert G., Poma, Clifton P., Shulimovich, Maxim, Hall, Christopher, Hewett, Kenneth W., Justus, Chip, Reckova, Maria, Sedmera, David, Tobita, Kiminasa, Hurtado, Romulo, Pennisi, David J., Kanzawa, Nobuyuki, & Takebayashi-Suzuki, Kimiko (2005) Induction and patterning of the impulse conducting Purkinje fiber network. In Artman, Michael, Benson, D. Woodrow, Srivastava, Deepak, & Nakazawa, Makoto (Eds.) Cardiovascular Development and Congenital Malformations: Molecular and Genetic Mechanisms. Blackwell, Oxford, UK, pp. 91-94.

Pennisi, David J. & Mikawa, Takashi (2005) Normal patterning of the coronary capillary plexus is dependent on the correct transmural gradient of FGF expression in the myocardium. Developmental Biology, 279(2), pp. 378-390.

31

27

Hatcher, Cathy J., Kim, Min-Su, Pennisi, David J., Song, Yan, Diman, Nata, Goldstein, Marsha M., Mikawa, Takashi, & Basson, Craig T. (2005) TBX5 regulates cardiac cell behavior during cardiogenesis. In Artman, Michael, Benson, D. Woodrow, Srivastava, Deepak, & Nakazawa, Makoto (Eds.) Cardiovascular Development and Congenital Malformations: Molecular and Genetic Mechanisms. Blackwell, Oxford, UK, pp. 27-30.

Hatcher, Cathy J., Diman, Nata Y.S.-G., Kim, Min-Su, Pennisi, David J., Song, Yan, Goldstein, Marsha M., Mikawa, Takashi, & Basson, Craig T. (2004) A role for Tbx5 in proepicardial cell migration during cardiogenesis. Physiological Genomics, 18(2), pp. 129-140.

84

78

Hall, Christopher E., Hurtado, Romulo, Hewett, Kenneth W., Shulimovich, Maxim, Poma, Clifton P., Reckova, Maria, Justus, Chip, Pennisi, David J., Tobita, Kiminasa, Sedmera, David, Gourdie, Robert G., & Mikawa, Takashi (2004) Hemodynamic-dependent patterning of endothelin converting enzyme 1 expression and differentiation of impulse-conducting Purkinje fibers in the embryonic heart. Development, 131(3), pp. 581-592.

96

88

Pennisi, David J., Ballard, Victoria L.T., & Mikawa, Takashi (2003) Epicardium is required for the full rate of myocyte proliferation and levels of expression of myocyte mitogenic factors FGF2 and its receptor, FGFR-1, but not for transmural myocardial patterning in the embryonic chick heart. Developmental Dynamics, 228(2), pp. 161-172.

89

Mikawa, T., Gourdie, R.G., Takebayashi-Suzuki, K., Kanzawa, N., Hyer, J., Pennisi, D.J., Poma, C.P., Shulimovich, M., Diaz, K.G., Layliev, J., & Prasad, A. (2003) Induction and patterning of the Purkinje fibre network. Novartis Foundation Symposium, 250, pp. 142-153.

15

Pennisi, D.J., Rentschler, S., Gourdie, R.G., Fishman, G.I., & Mikawa, T. (2002) Induction and patterning of the cardiac conduction system. International Journal of Developmental Biology, 46(6), pp. 765-775.

74

60

Hosking, Brett M., Wyeth, Jason R., Pennisi, David J., Wang, S-C. Mary, Koopman, Peter, & Muscat, George E. O. (2001) Cloning and functional analysis of the Sry-related HMG box gene, Sox18. Gene, 262(1-2), pp. 239-247.

41

39

Pennisi, D. J., Bowles, Josephine, Nagy, Andras, Muscat, George, & Koopman, Peter (2000) Mice null for Sox18 are viable and display a mild coat defect. Molecular and Cellular Biology, 20(24), pp. 9331-9336.

107

Pennisi, David J., Gardner, Jennifer, Chambers, Doreen, Hosking, Brett, Peters, Josephine, Muscat, George, Abbott, Catherine, & Koopman, Peter (2000) Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice. Nature Genetics, 24(4), pp. 434-437.

208

191

Pennisi, David J., James, Kristy M., Hosking, Brett, Muscat, George E.O., & Koopman, Peter (2000) Structure, mapping, and expression of human SOX18. Mammalian Genome, 11(12), pp. 1147-1149.

14

13

Greenfield, Andy, Carrel, Laura, Pennisi, David J., Philippe, Christophe, Quaderi, Nandita, Siggers, Pamela, Steiner, Kirsten, Tam, Patrick P. L., Monaco, Anthony P., Willard, Huntington F., & Koopman, Peter (1998) The UTX gene escapes X inactivation in mice and humans. Human Molecular Genetics, 7(4), pp. 737-742.

223

213

Greenfield, Andy, Scott, Diane, Pennisi, David J., Ehrmann, Ingrid, Ellis, Pamela, Cooper, Leanne, Simpson, Elizabeth, & Koopman, Peter (1996) An H–YDb epitope is encoded by a novel mouse Y chromosome gene. Nature Genetics, 14(4), pp. 474-478.

167

157

Monkley, S.J., Delaney, S.J., Pennisi, D.J., Christiansen, J.H., & Wainwright, B.J. (1996) Targeted disruption of the Wnt2 gene results in placentation defects. Development, 122(11), pp. 3343-3353.

98

327

316

Export as	Atom RSS 1.0 RSS 2.0