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Keywords: Programmed cell death
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Journal Articles
Journal: Development
Development (2018) 145 (1): dev150821.
Published: 08 January 2018
... underlying their female-specific generation. We demonstrate that programmed cell death (PCD) eliminates FS-Ilp7 motoneurons in males, and that this requires male-specific splicing of the sex-determination gene fruitless ( fru ) into the Fru MC isoform. However, in females, fru alleles that only generate Fru...
Includes: Supplementary data
Journal Articles
In collection:
Plant development
Journal: Development
Development (2017) 144 (19): 3578–3589.
Published: 01 October 2017
... roots. Consequently, an enhanced phosphoinositide-mediated vacuolar biogenesis correlates with premature programmed cell death (PCD) and secondary cell wall elaboration in xylem cells. By contrast, vacuolar fusion events in protophloem cells trigger the abnormal formation of big vacuoles, preventing...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2015) 142 (4): 672–680.
Published: 15 February 2015
...Idit Eshkar-Oren; Sharon Krief; Napoleone Ferrara; Alison M. Elliott; Elazar Zelzer Blood vessels serve as key regulators of organogenesis by providing oxygen, nutrients and molecular signals. During limb development, programmed cell death (PCD) contributes to separation of the digits...
Journal Articles
Journal: Development
Development (2014) 141 (13): 2724–2734.
Published: 01 July 2014
... mechanosensory neuron and an SDQ interneuron ( Fig. 1 A). Mutations in genes that positively regulate programmed cell-death – e.g. ced-3 – cause Q.pp to survive and to occasionally express the differentiation markers expressed by one of its nieces ( Cordes et al., 2006 ). Mutations in these genes do not affect...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2013) 140 (8): 1830–1842.
Published: 15 April 2013
... product of the gene doublesex promotes programmed cell death of these neuroblasts in females, and is needed for their survival, but not proliferation, in males. These data establish the terminal neuromeres as a model for further investigations into the mechanisms controlling segment- and sex-specific...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2011) 138 (2): 327–338.
Published: 15 January 2011
.... , Steller H. , McCall K. ( 2007 ). The Drosophila caspases Strica and Dronc function redundantly in programmed cell death during oogenesis . Cell Death Differ. 14 , 1508 - 1517 . Brachmann C. B. , Jassim O. W. , Wachsmuth B. D. , Cagan R. L. ( 2000 ). The...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2009) 136 (21): 3669–3678.
Published: 01 November 2009
... ). Retinoic-acid-induced limb-reduction defects: perturbation of zones of programmed cell death as a pathogenetic mechanism. Teratology 40 , 163 -171. Bandyopadhyay, A., Tsuji, K., Cox, K., Harfe, B. D., Rosen, V. and Tabin, C. J. ( 2006 ). Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2009) 136 (12): 2015–2025.
Published: 15 June 2009
..., but its molecular mechanism remains conjectural. Here we report that genetic ablation of the corpus allatum cells of the Drosophila ring gland (the JH source) resulted in JH deficiency, pupal lethality and precocious and enhanced programmed cell death (PCD) of the larval fat body. In the fat body of...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2008) 135 (24): 4153–4164.
Published: 15 December 2008
... ). Widespread programmed cell death in proliferative and postmitotic regions of the fetal cerebral cortex. Development 122 , 1165 -1174. Blaschke, A. J., Weiner, J. A. and Chun, J. ( 1998 ). Programmed cell death is a universal feature of embryonic and postnatal neuroproliferative regions throughout the...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2008) 135 (20): 3435–3445.
Published: 15 October 2008
... (e-mail: technau@uni-mainz.de ) 1 9 2008 © 2008. 2008 Programmed cell death Motoneurons Segment specificity Hox genes CNS Drosophila The body plan of many animals is composed of groups of homologous and morphologically diverse structures, such as comprise the body...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2008) 135 (2): 207–216.
Published: 15 January 2008
...Yukiko Yamada; Keri D. Davis; Clark R. Coffman Primordial germ cell development uses programmed cell death to remove abnormal, misplaced or excess cells. Precise control of this process is essential to maintain the continuity and integrity of the germline, and to prevent germ cells from colonizing...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2007) 134 (24): 4449–4458.
Published: 15 December 2007
... 23 9 2007 © 2007. 2007 Macrophage Angiopoietin Wnt Programmed cell death Vascular regression Cell cycle Macrophages have a critical function in tissue homeostasis because they can rapidly recognize and engulf dead cells( Savill et al., 2002 ). Rapid identification and...
Journal Articles
Journal: Development
Development (2007) 134 (12): 2359–2368.
Published: 15 June 2007
...Sangeeta Pajni-Underwood; Catherine P. Wilson; Cindy Elder; Yuji Mishina; Mark Lewandoski In vertebrate limbs that lack webbing, the embryonic interdigit region is removed by programmed cell death (PCD). Established models suggest that bone morphogenetic proteins (BMPs) directly trigger such PCD...
Journal Articles
Journal: Development
Development (2007) 134 (1): 105–116.
Published: 01 January 2007
...Ana Rogulja-Ortmann; Karin Lüer; Janina Seibert; Christof Rickert; Gerhard M. Technau Although programmed cell death (PCD) plays a crucial role throughout Drosophila CNS development, its pattern and incidence remain largely uninvestigated. We provide here a detailed analysis of the occurrence of...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2006) 133 (21): 4331–4339.
Published: 01 November 2006
... required for the genesis and proper identity specification of tritocerebral neural lineages during embryonic brain development of Drosophila . Drosophila Brain development Neuromere DV patterning ventral nervous system defective Hox gene labial Neuroblast Programmed cell death Here...
Journal Articles
Journal: Development
Development (2006) 133 (14): 2747–2756.
Published: 15 July 2006
... cleavage plane from its normal position, so cell size could affect the frequency at which the anterior daughter of the neuroblast escapes programmed cell death. Thus, increasing the size of the anterior daughter of the HSN/PHB neuroblast may increase the frequency at which this cell escapes programmed cell...
Journal Articles
Journal: Development
Development (2006) 133 (11): 2223–2232.
Published: 01 June 2006
...Youn-Jeong Choi; Gyunghee Lee; Jae H. Park The molecular basis of programmed cell death (PCD) of neurons during early metamorphic development of the central nervous system (CNS) in Drosophila melanogaster are largely unknown, in part owing to the lack of appropriate model systems. Here, we provide...
Journal Articles
Journal: Development
Development (2006) 133 (4): 641–650.
Published: 15 February 2006
...Huarui Liu; Tamara J. Strauss; Malia B. Potts; Scott Cameron Hox genes are crucial determinants of cell fates and of body morphology of animals; mutations affecting these genes result in abnormal patterns of programmed cell death. How Hox genes regulate programmed cell death is an important and...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2004) 131 (7): 1597–1606.
Published: 01 April 2004
...Ken-ichi Kimura; Akitoshi Kodama; Yosihiro Hayasaka; Takumi Ohta At the last step of metamorphosis in Drosophila , the wing epidermal cells are removed by programmed cell death during the wing spreading behavior after eclosion. The cell death was accompanied by DNA fragmentation demonstrated by the...
Includes: Multimedia, Supplementary data
Journal Articles
Journal: Development
Development (2002) 129 (19): 4647–4660.
Published: 01 October 2002
... increased programmed cell death, first in the epithelium and then in the mesenchyme. Programmed cell death was induced primarily in the lateral frontonasal mass with very little cell death medial to the bead. The asymmetric cell death pattern was correlated with a rapid induction of Noggin in the same...