NCBI Bibliography
https://www.ncbi.nlm.nih.gov/myncbi/ariel.pani.1/bibliography/public/
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Gordon KL*, Payne SG*, Linden-High LM*, Pani AM, Goldstein B, Hubbard JA, Sherwood DR (2019) Ectopic germ cells can induce niche-like enwrapment by body wall muscle. Current Biology 29: 828-833.e5
Pani AM, Goldstein B (2018) Direct visualization of a native Wnt in vivoreveals that a long-range Wnt gradient forms by extracellular dispersal. eLife7:e38325 DOI: 10.7554/eLife.38325 (recommended by F1000)
Heppert JK, Pani AM, Roberts AM, Dickinson DJ, Goldstein B (2018) A CRISPR tagging-based screen reveals localized players in Wnt-directed asymmetric cell division. Genetics 208: 1147-1164 (cover image)
Darras S, Fritzenwanker J, Uhlinger K, Farrelly E, Pani AM, Hurley I, Norris R, Osowitz M, Terasaki M, Wu M, Aronowicz J, Kirschner M, Gerhart J, Lowe CJ (2018) Anteroposterior patterning by early canonical Wnt signaling during hemichordate development. PLoS Biology 16: e2003698
Naegeli KM, Hastie E, Garde A, Wang Z, Keeley DP, Gordon KL, Pani AM, Kelley LC, Morrissey M, Chi Q, Goldstein B, Sherwood DR (2017) Cell invasion in vivo via rapid exocytosis of a transient lysosome-derived membrane domain. Developmental Cell 43: 403-417
Highlighted by – Wang S, Yamada KM (2017) Localized lysosome exocytosis helps breach tissue barriers. Developmental Cell 43: 377-378
Linden LM, Gordon KL, Pani AM, Payne SG, Garde A, Burkholder D, Chi Q, Goldstein B, Sherwood DR (2017) Identification of regulators of germ stem cell enwrapment by its niche in C. elegans. Developmental Biology 429: 271-284.
Heppert JK, Dickinson DJ, Pani AM, Higgins CD, Steward A, Ahringer J, Kuhn JR, Goldstein B (2016) Comparative assessment of fluorescent proteins for in vivoimaging in an animal model system. Molecular Biology of the Cell 27: 3385-3394.
Marston DJ*, Higgins CD*, Peters KA, Cupp TD, Dickinson DJ, Pani AM, Moore RP, Cox AH, Kiehart DP, Goldstein B (2016) MRCK-1 drives apical constriction in C. elegansby linking developmental patterning to force generation. Current Biology 26: 2079-2089.
Yao Y, Minor PJ, Zhao YT, Jeong Y, Pani AM, King AN, Symmons O, Gan L, Cardoso WV, Spitz F, Lowe CJ, Epstein DJ (2016) Cis-regulatory architecture of a brain signaling center predates the origin of chordates. Nature Genetics 48: 575-580.
Simakov O, Kawashima T, Marletaz F, Jenkins J, Koyanagi R, et. al. 23 of 52 authors (2015) Hemichordate genomes and deuterostome origins. Nature 527: 459-465.
Highlighted by – Dunn CW (2015) Genomics: Acorn worms in a nutshell. Nature 527: 448-449
Dickinson DJ, Pani AM, Heppert J, Higgins CD, Goldstein B (2015) Streamlined genome engineering with a self-excising drug selection cassette. Genetics200: 1035-1049. (original and SapTrap based plasmids at Addgene) (C. elegans genome engineering protocols)
Pani AM, Mullarkey E*, Aronowicz J*, Assimacopoulos S, Grove EA, Lowe CJ (2012) Ancient deuterostome origins of vertebrate brain signalling centres. Nature 483: 289-294.
Highlighted by – Gee H (2012) Developmental biology: a brainy background. Nature 483: 280.
Lowe CJ, Pani AM (2011) Animal evolution: a soap opera of unremarkable worms. Current Biology 21: 151-153
Sobreira TJP, Marlétaz F, Simões-Costa M, Schechtman D, Pereira AC, Brunet F, Sweeney S, Pani A, Aronowicz J, Lowe CJ, Davidson B, Laudet V, Bronner M, de Oliveira PSL, Schubert M, Xavier-Neto J (2010) Structural shifts of aldehyde dehydrogenase enzymes were instrumental for the early evolution of retinoid-dependent axial patterning in metazoans. Proc Natl Acad Sci USA 108: 226-231.
Pani AM, Hobart HH, Morris CA, Mervis CB, Bray-Ward P, Kimberley KW, Rios CM, Clark RC, Gulbronson MD, Gowans GC, Gregg RG (2010) Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome. PLoS One 5: e12349.
Morris CA, Pani AM, Mervis CB, Rios CM, Kistler DJ, Gregg RG. (2010) Alpha-1-Antitrypsin deficiency alleles are associated with joint dislocation and scoliosis in Williams syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics 154C; 299-306.
Hobart HH, Morris CA, Mervis CB, Pani AM, Kistler DJ, Rios CM, Kimberley KW, Gregg RG, Bray-Ward P (2010) Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics 154C: 220-228.
Marshall C*, Young E*, Pani AM, Morris C, Freckmann M-L, Lacassie Y, Howard C, Fitzgerald KK, Peippo M, Morris CA, Shane K, Priolo M, Morimoto M, Kondo I, Manquoqlu E, Berker-Karauzum S, Edery P, Hobart HH, Mervis CB, Zuffardi O, Reymond A, Kaplan P, Tassabehji M, Gregg RG, Scherer SW, Osborne LR. (2008) Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11. American Journal of Human Genetics 83: 106-111.
* equal contributions
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