@article{2310,
  abstract     = {Loss of the endosomal anion transport protein ClC-5 impairs renal endocytosis and underlies human Dent's disease. ClC-5 is thought to promote endocytosis by facilitating endosomal acidification through the neutralization of proton pump currents. However, ClC-5 is a 2 chloride (Cl-)/proton (H+) exchanger rather than a Cl- channel. We generated mice that carry the uncoupling E211A (unc) mutation that converts CLC-5 into a pure CL- conductor. Adenosine triphosphate (ATP)-dependent acidification of renal endosomes was reduced in mice in which ClC-5 was knocked out, but normal in Clcn5unc mice. However, their proximal tubular endocytosis was also impaired. Thus, endosomal chloride concentration, which is raised by CLC-5 in exchange for protons accumulated by the H+-ATPase, may play a role in endocytosis.},
  author       = {Gaia Novarino and Weinert, Stefanie and Rickheit, Gesa and Jentsch, Thomas J},
  journal      = {Science},
  number       = {5984},
  pages        = {1398 -- 1401},
  publisher    = {American Association for the Advancement of Science},
  title        = {{Endosomal chloride-proton exchange rather than chloride conductance is crucial for renal endocytosis}},
  doi          = {10.1126/science.1188070},
  volume       = {328},
  year         = {2010},
}

@article{2311,
  abstract     = {Inactivation of the mainly endosomal 2Cl-/H+- exchanger ClC-5 severely impairs endocytosis in renal proximal tubules and underlies the human kidney stone disorder Dent's disease. In heterologous expression systems, interaction of the E3 ubiquitin ligasesWWP2and Nedd4-2 with a "PY-motif" in the cytoplasmic C terminus of ClC-5 stimulates its internalization from the plasma membrane and may influence receptor-mediated endocytosis. We asked whether this interaction is relevant in vivo and generated mice in which the PY-motif was destroyed by a point mutation. Unlike ClC-5 knock-out mice, these knock-in mice displayed neither low molecular weight proteinuria nor hyperphosphaturia, and both receptor-mediated and fluid-phase endocytosis were normal. The abundances and localizations of the endocytic receptor megalin and of the Na+-coupled phosphate transporter NaPi-2a (Npt2) were not changed, either. To explore whether the discrepancy in results from heterologous expression studies might be due to heteromerization of ClC-5 with ClC-3 or ClC-4 in vivo, we studied knock-in mice additionally deleted for those related transporters. Disruption of neither ClC-3 nor ClC-4 led to proteinuria or impaired proximal tubular endocytosis by itself, nor in combination with the PY-mutant of ClC-5. Endocytosis of cells lacking ClC-5 was not impaired further when ClC-3 or ClC-4 was additionally deleted. We conclude that ClC-5 is unique among CLC proteins in being crucial for proximal tubular endocytosis and that PY-motif-dependent ubiquitylation of ClC-5 is dispensable for this role.},
  author       = {Rickheit, Gesa and Wartosch, Lena and Schaffer, Sven and Stobrawa, Sandra M and Gaia Novarino and Weinert, Stefanie and Jentsch, Thomas J},
  journal      = {Journal of Biological Chemistry},
  number       = {23},
  pages        = {17595 -- 17603},
  publisher    = {American Society for Biochemistry and Molecular Biology},
  title        = {{Role of ClC-5 in renal endocytosis is unique among ClC exchangers and does not require PY-motif-dependent ubiquitylation}},
  doi          = {10.1074/jbc.M110.115600},
  volume       = {285},
  year         = {2010},
}

@article{232,
  abstract     = {We study the average order of the divisor function, as it ranges over the values of binary quartic forms that are reducible over ℚ.},
  author       = {De La Bretèche, Régis and Browning, Timothy D},
  journal      = {Journal fur die Reine und Angewandte Mathematik},
  number       = {646},
  pages        = {1 -- 44},
  publisher    = {Walter de Gruyter},
  title        = {{Le problème des diviseurs pour des formes binaires de degré 4}},
  doi          = {10.1515/CRELLE.2010.064},
  year         = {2010},
}

@inproceedings{2322,
  author       = {Frank, Rupert L and Lieb, Élliott H and Robert Seiringer},
  pages        = {523 -- 535},
  publisher    = {World Scientific Publishing},
  title        = {{ Equivalence of Sobolev inequalities and Lieb-Thirring inequalities}},
  doi          = {10.1142/9789814304634_0045 },
  year         = {2010},
}

@inproceedings{2323,
  abstract     = {Since the first experimental realization of Bose-Einstein condensation in cold atomic gases in 1995 there has been a surge of activity in this field. Ingenious experiments have allowed us to probe matter close to zero temperature and reveal some of the fascinating effects quantum mechanics has bestowed on nature. It is a challenge for mathematical physicists to understand these various phenomena from first principles, that is, starting from the underlying many-body Schrödinger equation. Recent progress in this direction concerns mainly equilibrium properties of dilute, cold quantum gases. We shall explain some of the results in this article, and describe the mathematics involved in understanding these phenomena. Topics include the ground state energy and the free energy at positive temperature, the effect of interparticle interaction on the critical temperature for Bose-Einstein condensation, as well as the occurrence of superfluidity and quantized vortices in rapidly rotating gases.},
  author       = {Robert Seiringer},
  pages        = {231 -- 245},
  publisher    = {World Scientific Publishing},
  title        = {{Hot topics on cold gases}},
  doi          = {10.1142/9789814304634_0013},
  year         = {2010},
}

@inbook{2324,
  abstract     = {We determine the sharp constant in the Hardy inequality for fractional Sobolev spaces on half-spaces. Our proof relies on a nonlinear and nonlocal version of the ground state representation.},
  author       = {Frank, Rupert L and Robert Seiringer},
  booktitle    = {Around the Research of Vladimir Maz'ya I},
  pages        = {161 -- 167},
  publisher    = {Springer},
  title        = {{Sharp fractional Hardy inequalities in half-spaces}},
  doi          = {10.1007/978-1-4419-1341-8_6},
  volume       = {11},
  year         = {2010},
}

@article{2389,
  abstract     = {We study the eigenvalues of Schrödinger type operators T + λV and their asymptotic behavior in the small coupling limit λ → 0, in the case where the symbol of the kinetic energy, T (p), strongly degenerates on a non-trivial manifold of codimension one.},
  author       = {Hainzl, Christian and Robert Seiringer},
  journal      = {Mathematische Nachrichten},
  number       = {3},
  pages        = {489 -- 499},
  publisher    = {Wiley-Blackwell},
  title        = {{Asymptotic behavior of eigenvalues of Schrödinger type operators with degenerate kinetic energy}},
  doi          = {10.1002/mana.200810195},
  volume       = {283},
  year         = {2010},
}

@article{2392,
  abstract     = {The binding of polarons, or its absence, is an old and subtle topic. Here we prove two things rigorously. First, the transition from many-body collapse to the existence of a thermodynamic limit for N polarons occurs precisely at U=2α, where U is the electronic Coulomb repulsion and α is the polaron coupling constant. Second, if U is large enough, there is no multipolaron binding of any kind. Considering the known fact that there is binding for some U>2α, these conclusions are not obvious and their proof has been an open problem for some time.},
  author       = {Frank, Rupert L and Lieb, Élliott H and Robert Seiringer and Thomas, Lawrence E},
  journal      = {Physical Review Letters},
  number       = {21},
  publisher    = {American Physical Society},
  title        = {{Bipolaron and N-polaron binding energies}},
  doi          = {10.1103/PhysRevLett.104.210402},
  volume       = {104},
  year         = {2010},
}

@article{2409,
  abstract     = {Background: The availability of many gene alignments with overlapping taxon sets raises the question of which strategy is the best to infer species phylogenies from multiple gene information. Methods and programs abound that use the gene alignment in different ways to reconstruct the species tree. In particular, different methods combine the original data at different points along the way from the underlying sequences to the final tree. Accordingly, they are classified into superalignment, supertree and medium-level approaches. Here, we present a simulation study to compare different methods from each of these three approaches.

Results: We observe that superalignment methods usually outperform the other approaches over a wide range of parameters including sparse data and gene-specific evolutionary parameters. In the presence of high incongruency among gene trees, however, other combination methods show better performance than the superalignment approach. Surprisingly, some supertree and medium-level methods exhibit, on average, worse results than a single gene phylogeny with complete taxon information.

Conclusions: For some methods, using the reconstructed gene tree as an estimation of the species tree is superior to the combination of incomplete information. Superalignment usually performs best since it is less susceptible to stochastic error. Supertree methods can outperform superalignment in the presence of gene-tree conflict.},
  author       = {Kupczok, Anne and Schmidt, Heiko and Von Haeseler, Arndt},
  journal      = {Algorithms for Molecular Biology},
  number       = {1},
  publisher    = {BioMed Central},
  title        = {{Accuracy of phylogeny reconstruction methods combining overlapping gene data sets}},
  doi          = {10.1186/1748-7188-5-37},
  volume       = {5},
  year         = {2010},
}

@article{2435,
  abstract     = {We consider a generalization of the van Kampen-Flores Theorem and relate it to the long-standing g-conjecture for simplicial spheres.
},
  author       = {Nevo, Eran and Uli Wagner},
  journal      = {Israel Journal of Mathematics},
  number       = {1},
  pages        = {381 -- 402},
  publisher    = {Springer},
  title        = {{On the embeddability of skeleta of spheres}},
  doi          = {10.1007/s11856-009-0119-5},
  volume       = {174},
  year         = {2010},
}

@article{2442,
  abstract     = {In a new study published in this issue of Developmental Cell, Krouk et al. reveal a surprising mechanism by which plant root systems adapt their architecture for soil exploitation. The dual transporter NRT1.1 uses both nitrate and the plant hormone auxin as substrates, enabling soil nitrate availability to regulate auxin-driven lateral root development.},
  author       = {Beeckman, Tom and Friml, Jirí},
  journal      = {Developmental Cell},
  number       = {6},
  pages        = {877 -- 878},
  publisher    = {Cell Press},
  title        = {{Nitrate Contra Auxin: Nutrient Sensing by roots}},
  doi          = {10.1016/j.devcel.2010.05.020},
  volume       = {18},
  year         = {2010},
}

@article{2503,
  abstract     = {Epilepsy is a devastating and poorly understood disease. Mutations in a secreted neuronal protein, leucine-rich glioma inactivated 1 (LGI1), were reported in patients with an inherited form of human epilepsy, autosomal dominant partial epilepsy with auditory features (ADPEAF). Here, we report an essential role of LGI1 as an antiepileptogenic ligand. We find that loss of LGI1 in mice (LGI1-/-) causes lethal epilepsy, which is specifically rescued by the neuronal expression of LGI1 transgene, but not LGI3. Moreover, heterozygous mice for the LGI1 mutation (LGI1+/-) show lowered seizure thresholds. Extracellularly secreted LGI1 links two epilepsy-related receptors, ADAM22 and ADAM23, in the brain and organizes a transsynaptic protein complex that includes presynaptic potassium channels and postsynaptic AMPA receptor scaffolds. A lack of LGI1 disrupts this synaptic protein connection and selectively reduces AMPA receptor-mediated synaptic transmission in the hippocampus. Thus, LGI1 may serve as a major determinant of brain excitation, and the LGI1 gene-targeted mouse provides a good model for human epilepsy.},
  author       = {Fukata, Yuko and Lovero, Kathryn L and Iwanaga, Tsuyoshi and Watanabe, Atsushi and Yokoi, Norihiko and Tabuchi, Katsuhiko and Ryuichi Shigemoto and Nicoll, Roger A and Fukata, Masaki},
  journal      = {PNAS},
  number       = {8},
  pages        = {3799 -- 3804},
  publisher    = {National Academy of Sciences},
  title        = {{Disruption of LGI1-linked synaptic complex causes abnormal synaptic transmission and epilepsy}},
  doi          = {10.1073/pnas.0914537107},
  volume       = {107},
  year         = {2010},
}

@article{2504,
  abstract     = {We present a method for immunolabeling of multiple species of membrane proteins with high spatial resolution. It allows differentiation of equally sized very small markers with different chemical compositions, which leads to high labeling efficiency and reduces steric hindrance of closely spaced immunolabeled biomolecules. Markers such as CdSe/ZnS semiconductor quantum dots and colloidal gold particles are distinguished by differential contrast in high-angle annular detector dark-field STEM mode or by EDX microanalysis of their elemental contents. This method was tested by observation of labeled AMPA- and NMDA-type glutamate receptors on sodium-dodecyl-sulfate-digested replica prepared from rat hippocampus. To improve particle visibility and detectability, the replica films were made exclusively with carbon to avoid the high background of conventional platinum/carbon replica. Extension of the method is suggested by detection of 1.4 nm nanogold particles and its potential application in the biological imaging research.},
  author       = {Loukanov, Alexandre R and Kamasawa, Naomi and Danev, Radostin S and Ryuichi Shigemoto and Nagayama, Kuniaki},
  journal      = {Ultramicroscopy},
  number       = {4},
  pages        = {366 -- 374},
  publisher    = {Elsevier},
  title        = {{Immunolocalization of multiple membrane proteins on a carbon replica with STEM and EDX}},
  doi          = {10.1016/j.ultramic.2010.01.016},
  volume       = {110},
  year         = {2010},
}

@article{2505,
  abstract     = {Cbln1, secreted from cerebellar granule cells, and the orphan glutamate receptor 52 (GluD2), expressed by Purkinje cells, are essential for synapse integrity between these neurons in adult mice. Nevertheless, no endogenous binding partners for these molecules have been identified. We found that Cblnl binds directly to the N-terminal domain of GluD2. GluD2 expression by postsynaptic cells, combined with exogenously applied Cbln1, was necessary and sufficient to induce new synapses in vitro and in the adult cerebellum in vivo. Further, beads coated with recombinant Cbln1 directly induced presynaptic differentiation and indirectly caused clustering of postsynaptic molecules via GluD2. These results indicate that the Cbln1-GluD2 complex is a unique synapse organizer that acts bidirectionally on both pre- and postsynaptic components.},
  author       = {Matsuda, Keiko and Miura, Eriko and Miyazaki, Taisuke and Kakegawa, Wataru and Emi, Kyoichi and Narumi, Sakae and Fukazawa, Yugo and Ito-lshida, Aya and Kondo, Tetsuro and Ryuichi Shigemoto and Watanabe, Masahiko and Yuzaki, Michisuke},
  journal      = {Science},
  number       = {5976},
  pages        = {363 -- 368},
  publisher    = {American Association for the Advancement of Science},
  title        = {{Cbln1 is a ligand for an orphan glutamate receptor δ2, a bidirectional synapse organizer}},
  doi          = {10.1126/science.1185152},
  volume       = {328},
  year         = {2010},
}

@article{2506,
  abstract     = {Subepithelial fibroblasts of the intestinal villi, which form a contractile cellular network beneath the epithelium, are in close contact with epithelial cells, nerve varicosities, capillaries, smooth muscles and immune cells, and secrete extracellular matrix molecules, growth factors and cytokines, etc. Cultured subepithelial fibroblasts of the rat duodenal villi display various receptors such as endothelins, ATP, substance-P and bradykinin, and release ATP in response to mechanical stimulation. In this study, the presence of functional NK1 receptors (NK1R) was pharmacologically confirmed in primary culture by Ca 2+ measurement, and the effects of substance-P were measured in an acute preparation of epithelium-free duodenal villi from 2- to 3-week-old rats using a two-photon laser microscope. Substance-P elicited an increase in the intracellular Ca 2+ concentration and contraction of the subepithelial fibroblasts in culture and the isolated villi. The localization of NK1R and substance-P in the villi was examined by light and electron microscopic immunohistochemistry. NK1R-like immunoreactivity was intensely localized on the plasma membrane of villous subepithelial fibroblasts in 10-day- to 4-week-old rats and mice and was decreased or absent in adulthood. The pericryptal fibroblasts of the small and large intestine were NK1R immuno-negative. These villous subepithelial fibroblasts form synapse-like structures with both substance-P-immunopositive and -immunonegative nerve varicosities. Here, we propose that the mutual interaction between villous subepithelial fibroblasts and afferent neurons via substance-P and ATP plays important roles in the maturation of the structure and function of the small intestine.},
  author       = {Furuya, Sonoko and Furuya, Kishio and Ryuichi Shigemoto and Sokabe, Masahiro},
  journal      = {Cell and Tissue Research},
  number       = {2},
  pages        = {243 -- 259},
  publisher    = {Springer},
  title        = {{Localization of NK1 receptors and roles of substance-P in subepithelial fibroblasts of rat intestinal villi}},
  doi          = {10.1007/s00441-010-1056-7},
  volume       = {342},
  year         = {2010},
}

@article{2507,
  abstract     = {T-type calcium channels play a pivotal role in regulating neural membrane excitability in the nervous system. However, the precise subcellular distributions of T-type channel subunits and their implication for membrane excitability are not well understood. Here we investigated the subcellular distribution of the α1G subunit of the calcium channel which is expressed highly in the mouse dorsal lateral geniculate nucleus (dLGN). Light microscopic analysis demonstrated that dLGN exhibits intense immunoperoxidase reactivity for the α1G subunit. Electron microscopic observation showed that the labeling was present in both the relay cells and interneurons and was found in the somatodendritic, but not axonal, domains of these cells. Most of the immunogold particles for the α1G subunit were either associated with the plasma membrane or the intracellular membranes. Reconstruction analysis of serial electron microscopic images revealed that the intensity of the intracellular labeling exhibited a gradient such that the labeling density was higher in the proximal dendrite and progressively decreased towards the distal dendrite. In contrast, the plasma membrane-associated particles were distributed with a uniform density over the somatodendritic surface of dLGN cells. The labeling density in the relay cell plasma membrane was about 3-fold higher than that of the interneurons. These results provide ultrastructural evidence for cell-type-specific expression levels and for uniform expression density of the α1G subunit over the plasma membrane of dLGN cells.},
  author       = {Parajuli, Laxmi K and Fukazawa, Yugo and Watanabe, Masahiko and Ryuichi Shigemoto},
  journal      = {Journal of Comparative Neurology},
  number       = {21},
  pages        = {4362 -- 4374},
  publisher    = {Wiley-Blackwell},
  title        = {{Subcellular distribution of α1G subunit of T-type calcium channel in the mouse dorsal lateral geniculate nucleus}},
  doi          = {10.1002/cne.22461},
  volume       = {518},
  year         = {2010},
}

@article{2508,
  abstract     = {The activity patterns of subthalamic nucleus (STN) neurons are intimately linked to motor function and dysfunction and arise through the complex interaction of intrinsic properties and inhibitory and excitatory synaptic inputs. In many neurons, hyperpolarization-activated cyclic nucleotide-gated (HCN) channels play key roles in intrinsic excitability and synaptic integration both under normal conditions and in disease states. However, in STN neurons, which strongly express HCN channels, their roles remain relatively obscure. To address this deficit, complementary molecular and cellular electrophysiological, imaging, and computational approaches were applied to the rat STN. Molecular profiling demonstrated that individual STN neurons express mRNA encoding several HCN subunits, with HCN2 and 3 being the most abundant. Light and electron microscopic analysis showed that HCN2 subunits are strongly expressed and distributed throughout the somatodendritic plasma membrane. Voltage-, current-, and dynamic-clamp analysis, two-photon Ca 2+ imaging, and computational modeling revealed that HCN channels are activated by GABA A receptor-mediated inputs and thus limit synaptic hyperpolarization and deinactivation of low-voltage-activated Ca 2+ channels. Although HCN channels also limited the temporal summation of EPSPs, generated through two-photon uncaging of glutamate, this action was largely shunted by GABAergic inhibition that was necessary for HCN channel activation. Together the data demonstrate that HCN channels in STN neurons selectively counteract GABA A receptor-mediated inhibition arising from the globus pallidus and thus promote single-spike activity rather than rebound burst firing. },
  author       = {Atherton, Jeremy F and Kitano, Katsunori and Baufreton, Jérôme and Fan, Kai and Wokosin, David L and Tkatch, Tatiana and Ryuichi Shigemoto and Surmeier, James D and Bevan, Mark D},
  journal      = {Journal of Neuroscience},
  number       = {47},
  pages        = {16025 -- 16040},
  publisher    = {Society for Neuroscience},
  title        = {{Selective participation of somatodendritic HCN channels in inhibitory but not excitatory synaptic integration in neurons of the subthalamic nucleus}},
  doi          = {10.1523/JNEUROSCI.3898-10.2010},
  volume       = {30},
  year         = {2010},
}

@article{2509,
  abstract     = {Hippocampal CA1 pyramidal cells, which receive γ-aminobutyric acid (GABA)ergic input from at least 18 types of presynaptic neuron, express 14 subunits of the pentameric GABAA receptor. The relative contribution of any subunit to synaptic and extrasynaptic receptors influences the dynamics of GABA and drug actions. Synaptic receptors mediate phasic GABA-evoked conductance and extrasynaptic receptors contribute to a tonic conductance. We used freeze-fracture replica-immunogold labelling, a sensitive quantitative immunocytochemical method, to detect synaptic and extrasynaptic pools of the alpha1, alpha2 and beta3 subunits. Antibodies to the cytoplasmic loop of the subunits showed immunogold particles concentrated on distinct clusters of intramembrane particles (IMPs) on the cytoplasmic face of the plasma membrane on the somata, dendrites and axon initial segments, with an abrupt decrease in labelling at the edge of the IMP cluster. Neuroligin-2, a GABAergic synapse-specific adhesion molecule, co-labels all beta3 subunit-rich IMP clusters, therefore we considered them synapses. Double-labelling for two subunits showed that virtually all somatic synapses contain the alpha1, alpha2 and beta3 subunits. The extrasynaptic plasma membrane of the somata, dendrites and dendritic spines showed low-density immunolabelling. Synaptic labelling densities on somata for the alpha1, alpha2 and beta3 subunits were 78-132, 94 and 79 times higher than on the extrasynaptic membranes, respectively. As GABAergic synapses occupy 0.72% of the soma surface, the fraction of synaptic labelling was 33-48 (alpha1), 40 (alpha2) and 36 (beta3)% of the total somatic surface immunolabelling. Assuming similar antibody access to all receptors, about 60% of these subunits are in extrasynaptic receptors.},
  author       = {Kasugai, Yu and Swinny, Jerome D and Roberts, John D and Dalezios, Yannis and Fukazawa, Yugo and Sieghart, Werner C and Ryuichi Shigemoto and Somogyi, Péter},
  journal      = {European Journal of Neuroscience},
  number       = {11},
  pages        = {1868 -- 1888},
  publisher    = {Wiley-Blackwell},
  title        = {{Quantitative localisation of synaptic and extrasynaptic GABAA receptor subunits on hippocampal pyramidal cells by freeze-fracture replica immunolabelling}},
  doi          = {10.1111/j.1460-9568.2010.07473.x},
  volume       = {32},
  year         = {2010},
}

@article{2510,
  abstract     = {Neurons in the laterocapsular division of the central nucleus of the amygdala (CeC), which is known as the "nociceptive amygdala," receive glutamatergic inputs from the parabrachial nucleus (PB) and the basolateral nucleus of amygdala (BLA), which convey nociceptive information from the dorsal horn of the spinal cord and polymodal information from the thalamus and cortex, respectively. Here, we examined the ultrastructural properties of PB- and BLA-CeC synapses identified with EGFP-expressing lentivirus in rats. In addition, the density of synaptic AMPA receptors (AMPARs) on CeC neurons was studied by using highly sensitive SDS-digested freeze-fracture replica labeling (SDS-FRL). Afferents from the PB made asymmetrical synapses mainly on dendritic shafts (88%), whereas those from the BLA were on dendritic spines (81%). PB-CeC synapses in dendritic shafts were significantly larger (median 0.072 μm 2) than BLA-CeC synapses in spines (median 0.058 μm 2; P = 0.02). The dendritic shafts that made synapses with PB fibers were also significantly larger than those that made synapses with BLA fibers, indicating that the PB fibers make synapses on more proximal parts of dendrites than the BLA fibers. SDS-FRL revealed that almost all excitatory postsynaptic sites have AMPARs in the CeC. The density of AMPAR-specific gold particles in individual synapses was significantly higher in spine synapses (median 510 particles/μm 2) than in shaft synapses (median 427 particles/μm 2; P = 0.01). These results suggest that distinct synaptic impacts from PB- and BLA-CeC pathways contribute to the integration of nociceptive and polymodal information in the CeC.},
  author       = {Dong, Yu-Lin and Fukazawa, Yugo and Wang, Wen and Kamasawa, Naomi and Ryuichi Shigemoto},
  journal      = {Journal of Comparative Neurology},
  number       = {23},
  pages        = {4771 -- 4791},
  publisher    = {Wiley-Blackwell},
  title        = {{Differential postsynaptic compartments in the laterocapsular division of the central nucleus of amygdala for afferents from the parabrachial nucleus and the basolateral nucleus in the rat}},
  doi          = {10.1002/cne.22487},
  volume       = {518},
  year         = {2010},
}

@article{1721,
  author       = {Anna Kicheva and Briscoe, James},
  journal      = {PLoS Biology},
  number       = {7},
  publisher    = {Public Library of Science},
  title        = {{Limbs made to measure}},
  doi          = {10.1371/journal.pbio.1000421},
  volume       = {8},
  year         = {2010},
}