177,086 research outputs found

    Idiops mettupalayam Gupta, Ganeshkumar, Das & Siliwal, 2013, sp. nov.

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    <i>Idiops mettupalayam</i> sp. nov. Ganeshkumar and Siliwal <p>(Figs 3 A–H, Table 2)</p> <p> <b>Type specimens.</b> Holotype male. INDIA: Tamil Nadu: Mettupalayam, Coimbatore, [11°32′28′′N & 76°83′43′′E], 29 May 2006, coll. M. Chandrasekaran (WILD-06-ARA-142).</p> <p>Paratypes. INDIA: Tamil Nadu: 2 males, same data as holotype, 2 June 2006, (WILD-06-ARA-143, WILD- 06-ARA-144); male, same data as holotype, 30 May 2006 (WILD-06-ARA-145).</p> <p> <b>Diagnosis.</b> Males of <i>Idiops mettupalayam</i> <b>sp. nov.</b> resemble those of <i>I. bombayensis</i> and <i>I. constructor</i> in having a triangular spine on tibial spur on leg I (Fig. 3 E), but can be distinguished from those species by having mt I strongly incrassate for most of the length (Fig. 3 D) and leg I distinctly longer than leg IV (in <i>I. bombayensis</i> mt I is deeply incrassate in basal 3/4th with indistinct prolateral process; in <i>I. joida,</i> mt I is slender and lacks prolateral process; in <i>I. constructor</i> mt I is strongly incrassate in basal 3/4th and leg I and leg IV equal in length).</p> <p> <b>Etymology.</b> The species epithet is a name in apposition from the type locality, Mettupalayam, located at the foothills of the Western Ghats of Tamil Nadu.</p> <p> <b>Description.</b> Total length 8.53. Carapace 4.53 long, 3.70 wide; chelicerae 1.20 long; abdomen 4.00 long, 2.30 wide. Spinnerets: PMS, 0.27 long, 0.10 wide; PLS, 0.27 basal, 0.47 middle, 0.33 distal; midwidths 0.40, 0.27, 0.20 respectively; 1.07 total length.</p> <p> LEG I LEG II LEG III LEG IV PALP HT*= Holotype, PT= Paratypes <i>Colour in alcohol</i>. Carapace, leg I and palp reddish-brown, other legs yellowish-brown. Abdomen grayishbrown, pattern probably absent (as abdomen have shrunken, pattern not clear). AME encircled with black patch; black patches on caput and few irregular faint patches on rest of carapace.</p> <p> <i>Carapace</i> (Fig. 3 A). Oval, smooth except for few scattered wart-like tubercles along sides of striae; few row of hairs along posterior striae; black patch on caput; fovea deep, procurved.</p> <p> <i>Eyes</i> (Fig. 3 B). Eight in three rows, ALE situated far from AME on clypeal edge; posterior row procurved. Ocular group 1.00 long, 0.67 wide; MOQ almost square, 0.67 front and back width, 0.50 long. Diameter AME 0.28, PME 0.17, ALE 0.33, PLE 0.27; distance between ALE-AME 0.33, AME-AME 0.10, PME-PME 0.20, ALE- PLE 0.10, PLE-PME and ALE-ALE adjacent.</p> <p> <i>Maxillae</i>. 1.20 long anteriorly, 1.47 long posteriorly, 0.67 wide; cuspules absent; anterior lobe distinct, sparsely covered with long and short black bristles.</p> <p> <i>Labium</i>. 0.67 long, 0.60 wide, labiosternal groove shallow, slightly procurved, cuspules absent.</p> <p> <i>Chelicerae</i> (Fig. 3 C). 8 promarginal teeth in single row (size gradually decreasing from anterior to posterior end) on sclerotized ridge and single big tooth on outer margin of row of promarginal teeth; rastellum strong, raised on high triangular mound, consist of 3 large and 8 small thick, spines with 8 spinules on dorso-prolateral edge; many normal pointed spines vertically face and up dorsally on chelicerae; two glabrous bands for length of dorsal surface of chelicerae.</p> <p> <i>Sternum</i>. Broader between posterior coxae; yellowish-brown, elevated in centre, sloping laterally, covered with long black hair; row of long bristles on margins, posterior angle blunt but not separating coxae IV.</p> <p> <i>Sigilla</i>. Posterior sigilla absent; anterior and median pairs not visible due to shrinking of sternum.</p> <p> <i>Legs</i>. Leg I thicker than other legs; ti I inflated with pointed triangular spur facing upward on tubercle and small pointed process below tubercle (Figs 3 D–E); mt prolateraly incrassate 3/4th length, with distinct prolateral process at 1/4th from anterior end (Fig. 3 D); femorae and tibiae III clearly wider than others; metatarsi of all legs longer than tarsi. Legs cylindrical, covered with few scattered hair, bristles and few curved thick thorn-like spines. Two conspicuous glabrous bands for length of femora, patellae and tibiae (not very prominent on leg I). Leg formula 1423.</p> <p> <i>Spines</i>. More on promarginal and retromarginal sides of legs and palp. I: pa, v=3; ti, v=11, p=1+2spur; mt, p=1, v=5, r=5; ta, p=4, r= 9. II: fe, d=7, p=2, r=3; pa, p=2, v=4; ti, p=4+broken, v=9, r=3; mt, p=5, v=10, r=3; ta, p=1, r= 6. III: fe, d=11; pa, p=14, d=7, r=2; ti, p=8, r=d=5, v=7; mt, p=6, v=8, r=6; ta, p=1, r= 3. IV: fe, d=8; pa, p=18, d=5 (many spinules p=110, d=25, r=12); ti, v=7, r=6; mt, v=7, r=2; ta, p=5. Palp: fe, d=4; ti, r=26; ta, d=6.</p> <p> <i>Trichobothria</i>. Clavate absent; ta I, 12 long filiform in each of two zig-zag rows for length; ta II–III, 14 long filiform in 2 zig-zag rows for length; ta IV, 18 long filiform in basal two thirds; palp, 6 short filiform in centre of cymbium. Mt I, 5 short filiform in distal fourth; mt II–IV, 6–7 short filiform in distal fourth.</p> <p> <i>Leg coxae</i>. Coxa I–IV sparsely covered with long and short black bristles, more towards lateral than in centre. Coxae III with central patch without hair or spinules, others sparsely covered with long and short bristles. Coxae IV clearly broader than others, anterior edge curved, sparsely covered long bristles.</p> <p> <i>Claws</i>. Paired claw on leg I–III with unequal three teeth and leg IV with two unequal teeth; unpaired claw on all legs. Both claws (paired as well unpaired) on leg IV larger in size, well developed and prominent than on legs I–III. False claw tufts on each side of paired claws.</p> <p> <i>Scopulae</i>. On all leg tarsi; ta I, few scopuliform hairs in distal half, ta II–IV entire.</p> <p> <i>Abdomen</i> (Fig. 3 A). Grayish-brown covered with short and long black hair; cuticle appears leathery and slightly rough.</p> <p> <i>Spinnerets</i>. PMS digitiform covered with brown hair; PLS covered with brown hair, apical segment domed.</p> <p> <i>Palp</i> (Figs 3 F–H). Tarsi with two unequal lateral processes forming cavity on ventral. Median haematodocha extensive; embolus straight with distally twists about 90o; tip of embolus flat, wedge-like with central notch.</p> <p> <b>Remarks.</b> Paratypes are like the holotype. The paratype specimens are alcohol dried up and therefore only leg morphometry is provided for paratype specimen WILD-06-ARA-144 (Table 2).</p> <p> <b>Natural history.</b> This species was found in dry deciduous habitat, mostly dominated by bamboo. All the males were collected in pit-fall traps, during first monsoon showers. Efforts were made to find females but they could not be located; probably females make vertical burrow on the ground and therefore it was difficult to spot them. The soil was hard and red in colour.</p>Published as part of <i>Gupta, Neha, Ganeshkumar, M., Das, Sanjay Keshari & Siliwal, Manju, 2013, Three new species of Idiops Perty, 1833 (Araneae: Idiopidae) from India, pp. 237-250 in Zootaxa 3635 (3)</i> on pages 244-246, DOI: 10.11646/zootaxa.3635.3.3, <a href="http://zenodo.org/record/216039">http://zenodo.org/record/216039</a&gt

    Idiops oriya Gupta, Ganeshkumar, Das & Siliwal, 2013, sp. nov.

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    <i>Idiops oriya</i> sp. nov. Siliwal <p>(Figs 4 A–E, Table 3)</p> <p> <b>Type specimen.</b> Holotype female. INDIA: Odhisa: Kapilas, Dhenkanal, [19°44′39.1′′N & 83°0 6′34.8′′E], 0 6 August, 2007, elev. 280 m, coll. Saroj Behera (WILD-07-ARA-198).</p> <p> <b>Diagnosis.</b> The new species resembles <i>I. pylorus</i> and <i>I. madrasensis</i> and differs from rest of the South and South-east Asian <i>Idiops</i> sp. in females having leg formula 4123. Females differs from those of <i>I. pylorus</i> by having ocular area longer than wide and those of <i>I. pylorus</i> and <i>I. madrasensis</i> in spermathecae structure being ice-cream cone-shaped (Fig. 4 E).</p> <p> <b>Etymology.</b> The species epithet refers to the vernacular language spoken in the type locality state, Odhisa.</p> <p> <b>Description.</b> Total length 16.66. Carapace 7.38 long, 5.97 wide; chelicerae 33.60 long; abdomen 9.28 long, 6.99 wide. Spinnerets: PMS, 1.02 long, 0.38 wide, 0.17 apart; PLS, 1.09 basal, 0.31 middle, 0.21 distal; midwidths 0.99, 0.77, 0.36 respectively; 1.61 total length.</p> <p> <i>Colour in alcohol.</i> Carapace, patellae, tibiae, metatarsi and tarsi of legs I–II and patella and tarsus of palp blackish-brown, other leg parts reddish-brown. Abdomen dorsally grayish-brown, mottled with yellowish spots; ventrally uniformly yellowish-brown. AME encircled with black patch.</p> <p> <i>Carapace</i> (Fig. 4 A). Glabrous, broader anteriorly (widest between legs II) and gradually narrowing posteriorly, striae prominent; fovea, procurved, deep. Bristles: 2 long and 2 short on caput; 2 short between AME- ALE; 3 short on clypeus edge.</p> <p> <i>Eyes</i> (Fig. 4 B). Eight in three rows, ALE situated far from AME on clypeal edge; posterior row procurved. Ocular group 1.75 long, 1.45 wide; MOQ not square, 0.64 front and 0.82 back width, 0.69 long. Diameter AME 0.22, PME 0.17, ALE 0.25, PLE 0.24; distance between ALE-AME 0.62, AME-AME 0.05, PME-PME 0.06, ALE- PLE 0.90, PLE-PME 0.43 and ALE-ALE adjacent.</p> <p> <i>Maxillae</i> (Fig. 4 C). 2.30 long anteriorly, 2.87 long posteriorly, 1.68 wide; <i>ca.</i> 50 cuspules distributed towards anterior edge; anterior lobe distinct.</p> <p> <i>Labium</i> (Fig. 4 C). 0.99 long, 1.37 wide, shallow labiosternal groove, slightly procurved, 1 large and 4 small cuspules on anterior edge.</p> <p> <i>Chelicerae</i> (Figs 4 C–D). 9 promarginal teeth, 8 retomarginal teeth; rastellum strong, raised on high triangular mound, consist of 16 thick, short spines with many bristles-like spines; two glabrous bands for length of dorsal surface of chelicerae.</p> <p> <i>Sternum</i> (Fig. 4 C). Broader between posterior coxae; reddish-brown, elevated in centre, sloping laterally, covered with long black hair; row of long bristles on margins, posterior angle blunt.</p> <p> <i>Sigilla</i> (Fig. 4 C). Posterior sigilla absent; median pair submarginal, 2.04 apart, 0.30 from margin and anterior pair round, marginal.</p> <p> <i>Legs</i>. Leg III thicker than other legs; femora III clearly wider than others; metatarsi of all legs longer than tarsi. Legs cylindrical except for metatarsi and tarsi of legs I–II and tibiae and tarsi of palp, dorsoventrally flattened, covered with few scattered hair, bristles and few curved, thick, thorn-like spines. Two conspicuous glabrous bands for length of femora, patellae and tibiae. Scopulae absent on all legs and palp. Leg formula 4123.</p> <p> <i>Spines</i>. More on promarginal and retromarginal sides of legs and palp. I: ti, p=18, r=22; mt, p=22, v=2, r=19; ta, p=8, v=3, r= 10. II: ti, p=10, v=8, r=5; mt, p=11, v=7, r=9; ta, p=7, v=3, r= 4. III: pa, p=9, r=2; ti, p=9, v=2, r=7; mt, p=10, v=6, r=7; ta, v= 10. IV: pa, p=11; ti, v=2; mt, v=7; ta, v=9. Palp: pa, v=1; ti, p=11, r=7; ta, p=14, v=5, r=10.</p> <p> <i>Trichobothria</i>. Clavate absent; ta I, 12 long filiform in each of two zig-zag rows for basal 3/4th; ta II, 9 long filiform; ta III–IV, 10 long filiform; palp, 22 short filiform for length. Mt I, 13 short filiform; mt II, 7 short filiform; mt III, 9 filiform; mt IV, 16 short filiform. Trichobothria on tarsi in two zig-zag rows in basal 3/4th and trichobothria on metatarsi for length.</p> <p> <i>Leg coxae</i>. Reddish-brown; coxae I–IV covered with long black bristles, more dense on anterior pairs. Coxae III–IV with central patch glabrous, others sparsely covered with long and short bristles. Coxae IV clearly broader than others, anterior edge curved.</p> <p> <i>Claws</i>. Paired claw on all legs with single tooth and palp with bifid tooth; unpaired claw on leg I–IV; all claws (paired as well as unpaired) leg IV distinctly larger in size than claws on leg I–III. False claw tufts on each side of paired claws.</p> <p> <i>Abdomen</i> (Fig. 4 A). Dorsum, grayish-brown heavily mottled with yellowish spots; uniformly covered with short and long black hairs, cuticle appears leathery and slightly rough. Venter uniformly yellowish-brown, evenly covered with short black hairs, intermixed with few long black hairs.</p> <p> <i>Spinnerets</i>. PMS digitiform covered with brown hair; PLS covered with brown hair, apical segment domed.</p> <p> <i>Spermathecae</i> (Fig. 4 E). Two single lobes facing away from each other; each lobe, distally bulge with notch at tip, resembling teats in mammals, sclerotized, covered with pores, otherwise lobes transparent, gradually narrowing (cone shape) and opens ventrally; transparent sheet of inverted triangular shape covers basal half of lobes.</p> <p> <b>Natural history.</b> The spider was found on a roadside cutting in a deciduous sacred grove. It was found sympatric with <i>Heligmomerus barkudensis</i> (Gravely, 1921) in Kapilas, Odhisa. Only a single female was found and so their population seems to be low as compared to <i>H. barkudensis</i>. More information on habitat can be seen in Siliwal <i>et al</i>. 2010.</p> <p>The burrow of this species was simple tube-like with thick silk linning, measuring about 15.0mm in diameter and 55mm in depth. Burrow was having vertical on the ground with a gentle slope. Like Heligmomerus barkudensis, entrance of the burrow had a hinge door (diameter 13.5mm), inside of which covered with thick layer of silk with claw markings in the center and outer side covered with soil particles and debris.</p>Published as part of <i>Gupta, Neha, Ganeshkumar, M., Das, Sanjay Keshari & Siliwal, Manju, 2013, Three new species of Idiops Perty, 1833 (Araneae: Idiopidae) from India, pp. 237-250 in Zootaxa 3635 (3)</i> on pages 247-249, DOI: 10.11646/zootaxa.3635.3.3, <a href="http://zenodo.org/record/216039">http://zenodo.org/record/216039</a&gt

    Appropriate Similarity Measures for Author Cocitation Analysis

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    We provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis

    "Closing the R&D Gap, Evaluating the Sources of R&D Spending"

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    Both spending and tax policies have been implemented in the United States with the goal of stimulating private sector research and development (R&D). Karier questions whether current R&D policy, especially the research and experimentation tax credit, can contribute to closing the gap between nondefense expenditures on R&D in the United States and such expenditures in other countries, such as Japan and Germany. He also explores possible changes to our current R&D policy to make it more effective.

    Going Beyond Counting First Authors in Author Co-citation Analysis

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    The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed

    Letter from R. R. Zellick, Assistant Trust Officer, Anglo California National Bank of San Francisco, to Joseph R. Goodman, October 2, 1942

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    Letter from R. R. Zellick, Assistant Trust Officer at The Anglo California National Bank of San Francisco, to Joseph R. Goodman, regarding property owned by Dave Tatsuno. Zellick mentions a dispute between current tenants and Tatsuno, and that Tatsuno has asked Goodman to help locate trustworthy tenants.Personal correspondence, organizational records, government documents, publications, and other papers created or collected by Joseph R. Goodman documenting the forced removal and incarceration of Japanese Americans during World War II, as well as organized resistance to incarceration. Included in the collection are records of the Japanese Young Men's Christian Association and the Japanese American Citizens' League in San Francisco, including papers of the Japanese YMCA's executive secretary Lincoln Kanai; Sakai family papers; Goodman's correspondence to and from Japanese American incarcerees, organizations opposing forced removal and incarceration of Japanese Americans, the War Relocation Authority, and others; publications, photographs, and ephemera from the Topaz Relocation Center, where Goodman taught high school; War Relocation Authority records and publications; and newspaper clippings, pamphlets, and reports about forced removal and incarceration created by various government, religious, and civic organizations, in California and nationwide

    Dispelling the Myths Behind First-author Citation Counts

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    We conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more sophisticated methods

    Liftings for noncomplete probability spaces

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    The current state of knowledge concerning liftings for noncomplete probability spaces is discussed. This is a somewhat expanded version of the author's talk given at the 1991 Summer Conference on General Topology and Applications in Honor of Mary Ellen Rudin and Her Work.PT: S; CR: BURKE MR, IN PRESS P AM MATH S BURKE MR, 1991, ISRAEL J MATH, V73, P33 BURKE MR, 1992, ISRAEL J MATH, V79, P289 CARLSON T, THEOREM LIFTING CHRISTENSEN JPR, 1974, TOPOLOGY BOREL STRUC FREMLIN DH, 1989, HDB BOOLEAN ALGEBRAS, P877 INOESCUTULCEA A, 1966, 5TH P BERK S MATH ST, V2 IONESCUTULCEA A, 1967, CONTRIBUTIONS PROB 1, P63 IONESCUTULCEA A, 1969, TOPICS THEORY LIFTIN JECH TJ, 1978, SET THEORY JOHNSON RA, 1980, P AM MATH SOC, V80, P234 JUST W, IN PRESS T AM MATH S KUPKA J, 1983, INDIANA U MATH J, V32, P717 LOSERT V, 1983, LNM, V1080, P95 MAHARAM D, 1958, P AM MATH SOC, V9, P987 SHELAH S, 1983, ISRAEL J MATH, V45, P90 TALAGRAND M, 1982, P AM MATH SOC, V84, P379 VONNEUMANN J, 1931, CRELLES J MATH, V165, P109; NR: 18; TC: 0; J9: ANN N Y ACAD SCI; PG: 4; GA: BZ86BSource type: Electronic(1

    Hansen, Lee (Lee R.). Union, non-union, and managerial pay plan state employees, 2008-2019

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    1 online resource (2 pages)"July 1, 2021."Provides the number of union and non-union state employees in each of the last 14 years. Also provides the number of state employees paid under the state's managerial pay plan during each of those years. Updates OLR research report 2019-R-011

    FOXG1 Regulates PRKAR2B Transcriptionally and Posttranscriptionally via miR200 in the Adult Hippocampus

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    Rett syndrome is a complex neurodevelopmental disorder that is mainly caused by mutations in MECP2. However, mutations in FOXG1 cause a less frequent form of atypical Rett syndrome, called FOXG1 syndrome. FOXG1 is a key transcription factor crucial for forebrain development, where it maintains the balance between progenitor proliferation and neuronal differentiation. Using genome-wide small RNA sequencing and quantitative proteomics, we identified that FOXG1 affects the biogenesis of miR200b/a/429 and interacts with the ATP-dependent RNA helicase, DDX5/p68. Both FOXG1 and DDX5 associate with the microprocessor complex, whereby DDX5 recruits FOXG1 to DROSHA. RNA-Seq analyses of Foxg1cre/+ hippocampi and N2a cells overexpressing miR200 family members identified cAMP-dependent protein kinase type II-beta regulatory subunit (PRKAR2B) as a target of miR200 in neural cells. PRKAR2B inhibits postsynaptic functions by attenuating protein kinase A (PKA) activity; thus, increased PRKAR2B levels may contribute to neuronal dysfunctions in FOXG1 syndrome. Our data suggest that FOXG1 regulates PRKAR2B expression both on transcriptional and posttranscriptional levels.Fil: Weise, Stefan C.. Institute Of Anatomy And Cell Biology; AlemaniaFil: Arumugam, Ganeshkumar. Institute Of Anatomy And Cell Biology; AlemaniaFil: Villarreal, Alejandro. Institute Of Anatomy And Cell Biology; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; ArgentinaFil: Videm, Pavankumar. Universität Freiburg Im Breisgau; AlemaniaFil: Heidrich, Stefanie. Institute Of Anatomy And Cell Biology; AlemaniaFil: Nebel, Nils. Institute Of Anatomy And Cell Biology; AlemaniaFil: Dumit, Veronica Ines. Universität Freiburg Im Breisgau; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Sananbenesi, Farahnaz. Deutsches Zentrum Für Neurodegenerative Erkrankungen E.v.; AlemaniaFil: Reimann, Viktoria. Albert Ludwigs University Of Freiburg; AlemaniaFil: Craske, Madeline. Active Motif Incorporation; Estados UnidosFil: Schilling, Oliver. Universität Freiburg Im Breisgau; AlemaniaFil: Hess, Wolfgang R.. Universität Freiburg Im Breisgau; AlemaniaFil: Fischer, Andre. Universitätsmedizin Göttingen; Alemania. Deutsches Zentrum Für Neurodegenerative Erkrankungen E.v.; AlemaniaFil: Backofen, Rolf. Universidad de Copenhagen; DinamarcaFil: Vogel, Tanja. Universität Freiburg Im Breisgau; Alemani
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