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Journal articles on the topic 'Morphology'

To see the other types of publications on this topic, follow the link: Morphology.

Author: Grafiati

Published: 4 June 2021

Last updated: 6 July 2024

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1

Savazzi, Enrico. "Theoretical shell morphology as a tool in constructional morphology." Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen 195, no. 1-3 (February 14, 1995): 229–40. http://dx.doi.org/10.1127/njgpa/195/1995/229.

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2

Reif, Wolf-Ernst. "The primacy of morphology: pattern cladism, idealistic morphology, and evolution." Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen 228, no. 3 (June 30, 2003): 399–419. http://dx.doi.org/10.1127/njgpa/228/2003/399.

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3

Zwicky, Arnold M., and Geoffrey K. Pullum. "Plain Morphology and Expressive Morphology." Annual Meeting of the Berkeley Linguistics Society 13 (September 10, 1987): 330. http://dx.doi.org/10.3765/bls.v13i0.1817.

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4

Nash, David B. "A general method for morphologic dating of hillslopes." Geology 33, no. 8 (August 1, 2005): 693–95. http://dx.doi.org/10.1130/g21479ar.1.

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Abstract Morphologic dating of hillslopes is the determination of the age of a hillslope by its morphology. Current methods match the observed morphology with the morphology predicted by the diffusion-equation model for hillslope evolution. The morphologic dating method presented here requires no specific model for evolution, but is only applicable to transport-limited hillslopes on which the downslope debris flux is some scale- and time-independent function of slope angle. If these conditions are met, changes in morphology with scale (e.g., height) for a set of hillslopes of a fixed age are identical to changes in morphology with time for a hillslope of a fixed scale. This fact provides the basis for a simple, generally applicable method for morphologically dating such hillslopes with any initial morphology. This new dating method may be applied to a wide variety of vegetated hillslopes in temperate humid regions and is an improvement over previous morphologic dating methods that relied on the diffusion-equation model.

5

Becker, A. E. "Morphology." Current Opinion in Cardiology 1, no. 1 (January 1986): 73–84. http://dx.doi.org/10.1097/00001573-198601000-00014.

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6

Becker, A. E. "Morphology." Current Opinion in Cardiology 2, no. 1 (January 1987): 111–17. http://dx.doi.org/10.1097/00001573-198701010-00022.

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7

Becker, A. E. "Morphology." Current Opinion in Cardiology 3, no. 1 (January 1988): 55–61. http://dx.doi.org/10.1097/00001573-198801000-00010.

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8

Weinberg, Paul M. "Morphology." Current Opinion in Cardiology 4, no. 1 (February 1989): 64–70. http://dx.doi.org/10.1097/00001573-198902000-00014.

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9

Hartroft, W. S. "Morphology." Annals of the New York Academy of Sciences 111, no. 1 (December 15, 2006): 524–34. http://dx.doi.org/10.1111/j.1749-6632.1963.tb36992.x.

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10

Meek, Anna. "Morphology." Missouri Review 24, no. 3 (2001): 25. http://dx.doi.org/10.1353/mis.2001.0134.

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11

Carstairs-McCarthy, Andrew. "Morphology." Lingua 97, no. 1 (September 1995): 89–94. http://dx.doi.org/10.1016/0024-3841(95)90016-0.

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12

Palmaitis, M. L. "Morphology." Kalbotyra 37, no. 4 (December 1, 1986): 45–94. http://dx.doi.org/10.15388/knygotyra.1986.22216.

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13

Goldman, Omer, and Reut Tsarfaty. "Morphology Without Borders: Clause-Level Morphology." Transactions of the Association for Computational Linguistics 10 (2022): 1455–72. http://dx.doi.org/10.1162/tacl_a_00528.

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Abstract Morphological tasks use large multi-lingual datasets that organize words into inflection tables, which then serve as training and evaluation data for various tasks. However, a closer inspection of these data reveals profound cross-linguistic inconsistencies, which arise from the lack of a clear linguistic and operational definition of what is a word, and which severely impair the universality of the derived tasks. To overcome this deficiency, we propose to view morphology as a clause-level phenomenon, rather than word-level. It is anchored in a fixed yet inclusive set of features, that encapsulates all functions realized in a saturated clause. We deliver MightyMorph, a novel dataset for clause-level morphology covering 4 typologically different languages: English, German, Turkish, and Hebrew. We use this dataset to derive 3 clause-level morphological tasks: inflection, reinflection and analysis. Our experiments show that the clause-level tasks are substantially harder than the respective word-level tasks, while having comparable complexity across languages. Furthermore, redefining morphology to the clause-level provides a neat interface with contextualized language models (LMs) and allows assessing the morphological knowledge encoded in these models and their usability for morphological tasks. Taken together, this work opens up new horizons in the study of computational morphology, leaving ample space for studying neural morphology cross-linguistically.

14

Loeb, Keith R., Sindhu Cherian, John M. Pagel, Pamela S. Becker, Frederick R. Appelbaum, and Elihu H. Estey. "Morphology Vs. Multiparameter Flow Cytometry in Evaluation of AML in Cerebrospinal Fluid (CSF)." Blood 120, no. 21 (November 16, 2012): 2499. http://dx.doi.org/10.1182/blood.v120.21.2499.2499.

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Abstract Abstract 2499 Background and Methods: Multiparameter flow cytometry (MFC) is increasingly used in AML diagnostics as a supplement to morphologic examination. Here we retrospectively examine the concordance between MFC and morphologic examination for the detection of AML in CSF. Between 2005 and 2012, CSF from 604 sequential patients with AML or high-risk MDS was obtained at diagnosis or in follow-up of treatment for AML involving the central nervous system. Morphologic examination was done using conventional Wright-Giemsa stained cytospin preparations. MFC was done using a standard single-tube myeloid panel (HLA-DR/CD15/CD33/CD19/CD117/ CD13/ CD38/CD34/CD71/CD45) and/or a panel targeting the prior AML immunophenotype. Results: Results detecting any evidence of AML in the CSF by both techniques is noted in the Table below: The concordance between MFC and morphology (excluding atypical morphology) was high (97%; 539/558), in large part due to the predominance of uninvolved samples using both techniques. However, of the samples positive by MFC, 13% were negative by morphology and another 15% showed atypical cells insufficient for positivity by morphology. Of samples positive by morphology, only a single sample (1.4%) was negative by MFC. In addition, 65% of cases in which morphology was judged atypical were MFC negative, suggesting suboptimal specificity. Patients typically received intrathecal treatment based on positive MFC making it difficult to know whether the disease in the CSF would have expanded without treatment in patients who were MFC positive/morphology negative. Conclusion: Subject to the limitation that the morphology may not have been interpreted entirely independently of the MFC result, the results suggest morphology yields a false negative result in between 13% and 28% of samples and may not be sufficiently sensitive for routine screening of CSF. To follow-up our findings we are examining whether there are features that distinguish patients who were MFC positive/ morphology negative or vice versa and performing a study in which morphology and MFC are being independently assessed. Disclosures: No relevant conflicts of interest to declare.

15

Mall, G., G. Sprinzl, and J. Koebke. "Klinische Morphologie des Brustbeins - Clinical Morphology of the Sternum." Biomedizinische Technik/Biomedical Engineering 36, no. 11 (1991): 288–89. http://dx.doi.org/10.1515/bmte.1991.36.11.288.

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16

Skowron, Andrzej, and Lech Polkowski. "ANALYTICAL MORPHOLOGY: MATHEMATICAL MORPHOLOGY OF DECISION TABLES." Fundamenta Informaticae 27, no. 2,3 (1996): 255–71. http://dx.doi.org/10.3233/fi-1996-272312.

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17

Germing, U. "12 Morphology is dead – long live morphology." Leukemia Research 35 (May 2011): S5. http://dx.doi.org/10.1016/s0145-2126(11)70014-5.

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18

Ju, Jennifer Y., Lorinda A. Soma, Sindhu Cherian, Kerstin L. Edlefsen, Mary-Elizabeth M. Percival, and Ashley M. Eckel. "Assessing the added value of bone marrow morphologic evaluation beyond flow cytometry for disease detection in the setting of acute myeloid leukemia after chemotherapy." American Journal of Clinical Pathology 156, Supplement_1 (October 1, 2021): S16. http://dx.doi.org/10.1093/ajcp/aqab189.028.

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Abstract Complete response after acute myeloid leukemia (AML) therapy historically requires a decrease in bone marrow (BM) blasts to <5% by morphologic assessment. However, accumulating data indicate that measurable residual disease by more sensitive multiparameter flow cytometry (MFC) is a better predictor of outcome than traditional morphologic evaluation. In most cases, morphology alone cannot differentiate between regenerative and neoplastic blasts, raising the question of its added value to more specific MFC. The objective of this study was to assess the value morphologic evaluation adds to MFC for the detection of residual AML in the post-chemotherapy (induction or consolidation) setting. A search of our pathology database identified 47 consecutive nontransplant BM evaluations (41 total patients) in the post-chemotherapy setting between January and March 2020. The morphology portion for each case was reviewed by three independent hematopathologists for evaluation of adequacy (>200 cells), blast count, trilineage hematopoiesis, dysplastic features, focal/patchy disease, and any non-hematopoietic or alternative diagnoses that would not have been discovered by the associated MFC study. The MFC data for each case was separately reviewed by two hematopathologists. Six of the 47 cases showed >5% blasts by morphology (range 8%-70%); in all six cases, >5% abnormal blasts were also identified by MFC (range 23%-78%). Of cases with <5% blasts by morphology (defined as negative by morphology), MFC detected >5% abnormal blasts in four cases and <5% abnormal blasts in five cases (range 0.007-14%). One of these additional nine cases by MFC was identified to have focally clustered blasts by morphology (7% blasts by MFC, <5% overall by morphology). Two of the nine additional cases by MFC were deemed to have inadequate aspirates by morphology. In total, four of the 47 morphology cases had inadequate aspirate smears (9%). Of these four cases, three had adequate particle preparations. Eleven cases overall had corresponding core biopsies submitted, of which five were inadequate (45%). Morphologic examination identified seven cases with dysplastic features; abnormal blasts were identified in four of these cases by MFC (all >5% blasts). In the remaining three cases with dysplasia, ancillary molecular studies supported molecular evidence of residual disease in one case (NPM1 mutation and FLT3-ITD positivity by PCR). No unexpected carcinomas or other findings that would not be detected by the associated MFC study were identified. In conclusion, in our study, morphologic evaluation did not definitively identify any additional cases of residual/recurrent AML that were not identified by MFC. Morphologic evaluation detected dysplasia without abnormal blasts in three cases; however, the significance was unclear without supportive molecular studies. Reducing the number of cases for morphologic evaluation could save resources and improve turnaround time if MFC can provide the relevant details to assess response.

19

Hanson, Curtis A., Paul J. Kurtin, Jerry A. Katzmann, James D. Hoyer, Chin-Yang Li, Janice M. Hodnefield, Cecelia H. Meyers, Thomas M. Habermann, and Thomas E. Witzig. "Immunophenotypic Analysis of Peripheral Blood and Bone Marrow in the Staging of B-Cell Malignant Lymphoma." Blood 94, no. 11 (December 1, 1999): 3889–96. http://dx.doi.org/10.1182/blood.v94.11.3889.

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Abstract This study evaluated the contributing roles of flow cytometric immunophenotyping of blood and bone marrow and immunohistochemical paraffin section staining of bone marrow biopsies in the staging of B-cell malignant lymphoma. Flow immunophenotyping was performed on a marrow specimen in 175 cases; a corresponding blood specimen was also immunophenotyped in 135 of these cases. Morphologic marrow involvement by lymphoma was found in 59 cases; flow immunophenotyping identified 54 cases with a monoclonal B-cell process: morphology-positive/flow-positive (n = 49), morphology-positive/flow-negative (n = 10), morphology-negative/flow-positive (n = 5), and morphology-negative/flow-negative (n = 111). The 10 morphology-positive/flow-negative cases included 5 follicular and 5 large-cell lymphomas with minimal marrow involvement. All 5 morphology-negative/flow-positive cases were from patients with large-cell lymphomas and bulky clinical disease. Because the blood contained the same B-cell clone in 2 of 2 morphology-negative/flow-positive cases studied, blood contamination of marrow may account for these findings. Blood flow cytometric immunophenotyping studies were positive in 32 cases; 30 had marrow involvement by morphology and were from patients with follicular, mantle cell, lymphoplasmacytic, small lymphocytic, or marginal zone lymphomas. From our results, we conclude that (1) bone marrow flow cytometric immunophenotyping is not a cost-effective replacement for good morphologic evaluation in lymphoma staging and that (2) a positive peripheral blood flow cytometric immunophenotyping study when performed in low-grade lymphomas correlates with marrow involvement.

20

Hanson, Curtis A., Paul J. Kurtin, Jerry A. Katzmann, James D. Hoyer, Chin-Yang Li, Janice M. Hodnefield, Cecelia H. Meyers, Thomas M. Habermann, and Thomas E. Witzig. "Immunophenotypic Analysis of Peripheral Blood and Bone Marrow in the Staging of B-Cell Malignant Lymphoma." Blood 94, no. 11 (December 1, 1999): 3889–96. http://dx.doi.org/10.1182/blood.v94.11.3889.423k13_3889_3896.

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Abstract:

This study evaluated the contributing roles of flow cytometric immunophenotyping of blood and bone marrow and immunohistochemical paraffin section staining of bone marrow biopsies in the staging of B-cell malignant lymphoma. Flow immunophenotyping was performed on a marrow specimen in 175 cases; a corresponding blood specimen was also immunophenotyped in 135 of these cases. Morphologic marrow involvement by lymphoma was found in 59 cases; flow immunophenotyping identified 54 cases with a monoclonal B-cell process: morphology-positive/flow-positive (n = 49), morphology-positive/flow-negative (n = 10), morphology-negative/flow-positive (n = 5), and morphology-negative/flow-negative (n = 111). The 10 morphology-positive/flow-negative cases included 5 follicular and 5 large-cell lymphomas with minimal marrow involvement. All 5 morphology-negative/flow-positive cases were from patients with large-cell lymphomas and bulky clinical disease. Because the blood contained the same B-cell clone in 2 of 2 morphology-negative/flow-positive cases studied, blood contamination of marrow may account for these findings. Blood flow cytometric immunophenotyping studies were positive in 32 cases; 30 had marrow involvement by morphology and were from patients with follicular, mantle cell, lymphoplasmacytic, small lymphocytic, or marginal zone lymphomas. From our results, we conclude that (1) bone marrow flow cytometric immunophenotyping is not a cost-effective replacement for good morphologic evaluation in lymphoma staging and that (2) a positive peripheral blood flow cytometric immunophenotyping study when performed in low-grade lymphomas correlates with marrow involvement.

21

Beaulieu, BSc, Marlene, Paul Allard, PhD, Sebastien Hinse, MSc, Martin Simoneau, PhD, and Charles-Hilaire Rivard, MD. "Somatotyping Morphology." Critical Reviews in Physical and Rehabilitation Medicine 17, no. 4 (2005): 317–30. http://dx.doi.org/10.1615/critrevphysrehabilmed.v17.i4.50.

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22

De Belder, Marijke, and Jan Don. "Distributed Morphology." Nederlandse Taalkunde 27, no. 1 (July 1, 2022): 75–104. http://dx.doi.org/10.5117/nedtaa2022.1.007.beld.

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23

McCarroll, Danny, and Olav Slaymaker. "Steepland Morphology." Mountain Research and Development 16, no. 4 (November 1996): 427. http://dx.doi.org/10.2307/3673993.

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24

Jacobs, Malcolm C., and Sergio Scalise. "Generative Morphology." Modern Language Journal 70, no. 1 (1986): 72. http://dx.doi.org/10.2307/328089.

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25

ZAREEN, NUSRAT. "TESTICULAR MORPHOLOGY." Professional Medical Journal 16, no. 02 (June 10, 2009): 289–92. http://dx.doi.org/10.29309/tpmj/2009.16.02.2945.

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Objective: To study the effects of mobile phone induced Electromagnetic fields (EMFs) on testis of young mice. Settings: Department of Anatomy, College of Physicians and Surgeons Pakistan, Regional Centre, Islamabad. Period: January to June, 2008. Study Design: Experimental animal study. Materials & Methods: This study was conducted on two groups of young BALB-c (6 weeks of age) purchased from National Institute of Health Islamabad. These animals were divided into two groups control and treated, each consisting of twenty animals. The treated group was exposed for one month to mobile phone induced EMFs by placing a mobile phone in the floor of the cage. This phone was rung upon from any other line or cell phone twice daily for 15 minutes. The control group was kept under identical conditions except for mobile phone on the cage floor. Results and observations: Histological comparison of testis of the both group animals showed a significant increase, in the number of tubules with sperms in the lumen, increased sub capsular congestion of vessels, presence of vacuolation and giant cells in germinal epithelium and abnormal cells in the lumen of seminiferous tubules of the treated group. Conclusion: The results indicate altered testicular morphology of the EMFs exposed mice.

26

Müntener, Markus. "Morphology 'Today'." CHIMIA International Journal for Chemistry 58, no. 10 (October 1, 2004): 721–22. http://dx.doi.org/10.2533/000942904777677371.

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27

Stump, Gregory T., Andrew Carstairs-McCarthy, P. H. Matthews, and Andrew Spencer. "Current Morphology." Language 69, no. 2 (June 1993): 358. http://dx.doi.org/10.2307/416539.

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28

Lieber, Rochelle, and John T. Stonham. "Combinatorial Morphology." Language 72, no. 1 (March 1996): 130. http://dx.doi.org/10.2307/416798.

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29

Kaye, Alan S., Rajendra Singh, and Rama Kant Agnihotri. "Hindi Morphology." Language 75, no. 3 (September 1999): 625. http://dx.doi.org/10.2307/417098.

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30

Forsberg, Markus, and Aarne Ranta. "Functional morphology." ACM SIGPLAN Notices 39, no. 9 (September 19, 2004): 213–23. http://dx.doi.org/10.1145/1016848.1016879.

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31

Kaufman, Daniel. "Saisiyat Morphology." Oceanic Linguistics 56, no. 1 (2017): 278–93. http://dx.doi.org/10.1353/ol.2017.0013.

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32

Bernecky, Robert. "Array morphology." ACM SIGAPL APL Quote Quad 24, no. 1 (September 1993): 6–16. http://dx.doi.org/10.1145/166198.166200.

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33

Heaton, Raina. "Intransitivizing morphology." Language and Linguistics Compass 12, no. 12 (December 2018): e12305. http://dx.doi.org/10.1111/lnc3.12305.

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34

Marx Adelman,, Marilyn. "Sperm Morphology." Laboratory Medicine 17, no. 1 (January 1, 1986): 32–34. http://dx.doi.org/10.1093/labmed/17.1.32.

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35

Becker, Karl-Friedrich, and Clive R. Taylor. "“Liquid Morphology”." Applied Immunohistochemistry & Molecular Morphology 19, no. 1 (January 2011): 1–9. http://dx.doi.org/10.1097/pai.0b013e3181f50883.

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36

Haralick, R. M., E. Dougherty, J. Ha, T. Kanungo, S. Karasu, C. K. Lee, L. Rystrom, V. Ramesh, and I. Phillips. "Statistical morphology." Journal of Applied Statistics 21, no. 1-2 (January 1994): 341–54. http://dx.doi.org/10.1080/757582979.

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37

Scholtz, Gerhard. "Deconstructing morphology." Acta Zoologica 91, no. 1 (January 2010): 44–63. http://dx.doi.org/10.1111/j.1463-6395.2009.00424.x.

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38

McArthur, J. R. "Morphology Glossary." Hematology 2000, no. 1 (January 1, 2000): 457–74. http://dx.doi.org/10.1182/asheducation-2000.1.457.

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39

Moats, Louisa Cook, and Cheryl Smith. "Derivational Morphology." Language, Speech, and Hearing Services in Schools 23, no. 4 (October 1992): 312–19. http://dx.doi.org/10.1044/0161-1461.2304.312.

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For unclear reasons, current language tests and remedial teaching materials often do not include the explicit evaluation or teaching of derivational morphology. This article reviews recent research on children’s knowledge and acquisition of derivational morphology across studies of listening, speaking, reading, and spelling. We conclude that this dimension of language organization deserves more attention than it now receives in language instruction.

40

Jarmulowicz, Linda, and Valentina L. Taran. "Lexical Morphology." Topics in Language Disorders 33, no. 1 (2013): 57–72. http://dx.doi.org/10.1097/tld.0b013e318280f5c0.

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41

Ray, L. B. "Morphology Central." Science Signaling 2007, no. 392 (June 26, 2007): tw228. http://dx.doi.org/10.1126/stke.3922007tw228.

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42

Bauer, Laurie. "Evaluative Morphology." Studies in Language 21, no. 3 (January 1, 1997): 533–75. http://dx.doi.org/10.1075/sl.21.3.04bau.

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Various claims from the previous literature about the way in which evaluative morphology (particularly diminutives and augmentatives) operates are tested on a large sample of languages. Evaluative morphology is seen as being less morphologically marginal than has been implied in some of the recent literature, but nevertheless as showing some interesting cross-linguistic tendencies.

43

Calderon, Stéphane, and Tamy Boubekeur. "Point morphology." ACM Transactions on Graphics 33, no. 4 (July 27, 2014): 1–13. http://dx.doi.org/10.1145/2601097.2601130.

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44

Gupta, Ajay, and Nawal M. Al-Moosawi. "Lunate morphology." Journal of Biomechanics 35, no. 11 (November 2002): 1451–57. http://dx.doi.org/10.1016/s0021-9290(02)00178-1.

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45

Roerdink, Jos B. T. M. "Group morphology." Pattern Recognition 33, no. 6 (June 2000): 877–95. http://dx.doi.org/10.1016/s0031-3203(99)00152-1.

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46

EGESTEN, A. "Eosinophil Morphology." Respiratory Medicine 94, no. 12 (December 2000): 1256–58. http://dx.doi.org/10.1053/rmed.2000.0978.

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47

SIMON, H. U. "Eosinophil Morphology." Respiratory Medicine 94, no. 12 (December 2000): 1258–59. http://dx.doi.org/10.1053/rmed.2000.0979.

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48

ROSSI, A. G., C. WARD, J. MURRAY, M. C. MARTIN, S. FUJIHARA, I. DRANSFIELD, and C. HASLETT. "Eosinophil Morphology." Respiratory Medicine 94, no. 12 (December 2000): 1259–62. http://dx.doi.org/10.1053/rmed.2000.0980.

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49

DVORAK, A. M. "Eosinophil Morphology." Respiratory Medicine 94, no. 12 (December 2000): 1254–56. http://dx.doi.org/10.1053/rmed.2000.0983.

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50

JACKSON, ROBERT. "MORPHOLOGY REVISITED." International Journal of Dermatology 32, no. 2 (February 1993): 77–81. http://dx.doi.org/10.1111/j.1365-4362.1993.tb01439.x.

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