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Journal articles on the topic 'Tissue imprint'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Mangia, Anita, Annalisa Chiriatti, Patrizia Chiarappa, et al. "Touch Imprint Cytology in Tumor Tissue Banks for the Confirmation of Neoplastic Cellularity and for DNA Extraction." Archives of Pathology & Laboratory Medicine 132, no. 6 (2008): 974–78. http://dx.doi.org/10.5858/2008-132-974-ticitt.

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Abstract Context.—Learning the characteristics of frozen tissue samples stored in tumor banks for biological studies remains a problem. Objective.—To assess the use of touch imprint cytology on fresh tissue samples as a rapid and reliable method of determining the presence and quantity of neoplastic cells before freezing. Design.—Touch imprint cytology was performed on 259 specimens of operable breast cancer. Touch imprints were prepared from fresh tissue specimens before freezing samples for storage. Each tumor sample was imprinted on a glass slide and stained with hematoxylin-eosin. Tumor ce

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2

Gore, CharusheelaRajesh, BikashK Singh, ShirishS Chandanwale, et al. "Imprint cytology: A boon in tissue diagnosis." Medical Journal of Dr. D.Y. Patil University 10, no. 1 (2017): 58. http://dx.doi.org/10.4103/0975-2870.197924.

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3

Liu, Jie, Shuhua Yu, Deborah Litman, Weiping Chen, and Lee S. Weinstein. "Identification of a Methylation Imprint Mark within the Mouse Gnas Locus." Molecular and Cellular Biology 20, no. 16 (2000): 5808–17. http://dx.doi.org/10.1128/mcb.20.16.5808-5817.2000.

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ABSTRACT The imprinted mouse gene Gnas produces the G protein α-subunit GSα and several other gene products by using alternative promoters and first exons. GSα is maternally expressed in some tissues and biallelically expressed in most other tissues, while the gene products NESP55 and XLαs are maternally and paternally expressed, respectively. We investigated the mechanisms of Gnas imprinting. The GSα promoter and first exon are not methylated on either allele. A further upstream region (approximately from positions −3400 to −939 relative to the GSα translational start site) is methylated only

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4

Ricardo-Gonzalez, Roberto R., Steven J. Van Dyken, Christoph Schneider, et al. "Tissue signals imprint ILC2 identity with anticipatory function." Nature Immunology 19, no. 10 (2018): 1093–99. http://dx.doi.org/10.1038/s41590-018-0201-4.

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5

Finkle, Howard I. "Protoplasmic astrocytoma: Cytologic features on tissue imprint preparation." Diagnostic Cytopathology 8, no. 4 (1992): 430–31. http://dx.doi.org/10.1002/dc.2840080425.

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Dayal, Sanjeev, Juliette Murray, Kate Wilson, and Alison Lannigan. "Vastagtű-biopsziás hengerből készített imprint citológia növeli a vékonytű-aspirációs citológia szenzitivitását emlőrákos betegekben." Magyar Sebészet 64, no. 2 (2011): 59–62. http://dx.doi.org/10.1556/maseb.64.2011.2.1.

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Abstract Background: Fine needle aspiration cytology (FNAC) can have high inadequate results. The main objective of this study was to validate the sensitivity of imprint cytology and compare it to that of FNAC across all levels of staff experience. Our other objective was to find out whether handling of a core biopsy to obtain an imprint slide affected its morphology so as to make histopathological reporting from that tissue difficult. This we thought could be of significance while trying to diagnose smaller cancers where just one core could contain tumour. Methods: Patients (n = 56) with a su

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Ifa, Demian R., Amitava Srimany, Livia S. Eberlin, et al. "Tissue imprint imaging by desorption electrospray ionization mass spectrometry." Analytical Methods 3, no. 8 (2011): 1910. http://dx.doi.org/10.1039/c1ay05295k.

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Park, Seok Ju, Ae Ri Kim, Mi Jin Gu, Joon Hyuk Choi, and Duk Seop Shin. "Imprint Cytology of Soft Tissue Myoepithelioma: A Case Study." Korean Journal of Pathology 47, no. 3 (2013): 299. http://dx.doi.org/10.4132/koreanjpathol.2013.47.3.299.

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Choudhary, Prabesh Kumar, Niraj Nepal, Rishab Shrestha, and Utsav Adhikari. "Diagnostic utility of imprint cytology of endoscopic gastric biopsy: A cyto-histo correlation study." Journal of Pathology of Nepal 9, no. 2 (2019): 1542–44. http://dx.doi.org/10.3126/jpn.v9i2.24861.

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Background: Upper gastrointestinal endoscopy is a common procedure done for suspected cases of gastric malignancies. Histopathological examination of gastric tissue has been a gold standard for the diagnosis. Imprint smears of the gastric biopsy specimen is a useful and rapid alternative diagnostic tool. This study was conducted to assess the accuracy of gastric biopsy imprint cytology as compared to the histopathology. Materials and Methods: Imprint smears were made from all cases of gastric biopsy specimens taken from suspected cases of gastric malignancies. They were evaluated by thre

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Bhaker, Poonam, Harsh Mohan, Uma Handa, and Sudhir Kumar. "Role of Intraoperative Pathology Consultation in Skeletal Tumors and Tumor-Like Lesions." Sarcoma 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/902104.

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Early and accurate detection of bone tumors and their staging are important since some of them are highly malignant. Intraoperative pathological consultation in bone tumors and tumor-like conditions is quite complex; however, it allows improvement in prognosis and limb salvage. Present study was conducted on 52 patients who underwent surgical procedure after clinical and radiological diagnosis of bone tumors/tumor-like conditions. Fresh unfixed tissue was quickly inspected grossly, followed by preparation of imprint smears and frozen section which were evaluated by two pathologists separately

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Vijayanarasimha, Divya, Asha Mahadevappa, G. V. Manjunath, and R. Sunila. "Imprint cytology: A diagnostic aid in interpretation of upper gastrointestinal endoscopic biopsies." Journal of Digestive Endoscopy 05, no. 04 (2014): 144–48. http://dx.doi.org/10.4103/0976-5042.150661.

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Abstract Context: Although major advances have occurred in the cytological diagnosis of various organ pathologies, gastrointestinal (GI) cytology has not gained popularity and is only occasionally practiced in the form of brushings and washings. Biopsy touch imprint cytology (IC) is a rapid, simple and inexpensive method of diagnosis of upper GI lesions. Thus, a study to show a correlation of IC and standard histopathology will allow the procedure to be performed routinely as adjunct to histopathology. Aims: To correlate results of imprints made from upper GI biopsies with histopathology in ca

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Neduvanchery, Saheer. "Comparison of intraoperative imprint cytology with frozen section for lymph node metastasis in patients with head and neck cancer." Journal of Clinical Oncology 38, no. 15_suppl (2020): e18548-e18548. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e18548.

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e18548 Background: Intraoperative evaluation of lymph nodal metastasis in head and neck carcinoma assumes importance in deciding the extent of lymph node dissection. Frozen section is the most commonly employed technique. But it requires significant investment in terms of resources, time and personnel. Intraoperative imprint cytology is a rapid, reliable and an inexpensive alternative. So we conducted a prospective diagnostic test accuracy study to assess the diagnostic accuracy of intraoperative imprint cytology and frozen section for lymph node metastasis in Head and neck Cancer when compare

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13

Das, Kaustuv, Catherine Kendall, Martin Isabelle, Clare Fowler, J. Christie-Brown, and Nicholas Stone. "FTIR of touch imprint cytology: A novel tissue diagnostic technique." Journal of Photochemistry and Photobiology B: Biology 92, no. 3 (2008): 160–64. http://dx.doi.org/10.1016/j.jphotobiol.2008.05.012.

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14

Sado, Takashi. "What makes the maternal X chromosome resistant to undergoing imprinted X inactivation?" Philosophical Transactions of the Royal Society B: Biological Sciences 372, no. 1733 (2017): 20160365. http://dx.doi.org/10.1098/rstb.2016.0365.

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In the mouse, while either X chromosome is chosen for inactivation in a random fashion in the embryonic tissue, the paternally derived X chromosome is preferentially inactivated in the extraembryonic tissues. It has been shown that the maternal X chromosome is imprinted so as not to undergo inactivation in the extraembryonic tissues. X-linked noncoding Xist RNA becomes upregulated on the X chromosome that is to be inactivated. An antisense noncoding RNA, Tsix , which occurs at the Xist locus and has been shown to negatively regulate Xist expression in cis, is imprinted to be expressed from the

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Portu, Agustina, Andrés Eugenio Rossini, Silvia Inés Thorp, et al. "Simultaneous Observation of Cells and Nuclear Tracks from the Boron Neutron Capture Reaction by UV-C Sensitization of Polycarbonate." Microscopy and Microanalysis 21, no. 4 (2015): 796–804. http://dx.doi.org/10.1017/s1431927615014348.

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AbstractThe distribution of boron in tissue samples coming from boron neutron capture therapy protocols can be determined through the analysis of its autoradiography image on a nuclear track detector. A more precise knowledge of boron atom location on the microscopic scale can be attained by the observation of nuclear tracks superimposed on the sample image on the detector. A method to produce an “imprint” of cells cultivated on a polycarbonate detector was developed, based on the photodegradation properties of UV-C radiation on this material. Optimal conditions to generate an appropriate mono

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16

Hu, Ji-Fan, Haritha Oruganti, Thanh H. Vu, and Andrew R. Hoffman. "Tissue-Specific Imprinting of the Mouse Insulin-Like Growth Factor II Receptor Gene Correlates with Differential Allele-Specific DNA Methylation." Molecular Endocrinology 12, no. 2 (1998): 220–32. http://dx.doi.org/10.1210/mend.12.2.0062.

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Abstract Imprinted genes may be expressed uniparentally in a tissue- and development-specific manner. The insulin-like growth factor II receptor gene (Igf2r), one of the first imprinted genes to be identified, is an attractive candidate for studying the molecular mechanism of genomic imprinting because it is transcribed monoallelically in the mouse but biallelically in humans. To identify the factors that control genomic imprinting, we examined allelic expression of Igf2r at different ages in interspecific mice. We found that Igf2r is not always monoallelically expressed. Paternal imprinting o

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17

Zuccotti, M., and M. Monk. "The Mouse Xist Gene: a Model for Studying the Gametic Imprinting Phenomenon." Acta geneticae medicae et gemellologiae: twin research 45, no. 1-2 (1996): 199–204. http://dx.doi.org/10.1017/s0001566000001306.

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In mammals, normal embryonic development requires differential genomic imprinting of male and female gametes [1, 2]. Many investigations have been directed towards the understanding of the molecular mechanisms of imprinting and the timing of establishment of the imprint during gametogenesis and its erasure during development.Methylation is the focus of many of these studies as it has been known for some time that this epigenetic modification of the DNA correlates with the status of gene activity. So far, five imprinted genes, expressed from only one of the parental alleles, have been found to

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18

Wong, Newton A. C. S., Radu Mihai, Edward Alexander Sheffield, Caroline Jane Calder, and John Richard Farndon. "Imprint Cytology of Parathyroid Tissue in Relation to Other Tissues of the Neck and Mediastinum." Acta Cytologica 44, no. 2 (2000): 109–13. http://dx.doi.org/10.1159/000326346.

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Dasgupta, Senjuti, SujitKumar Dutta, NirmalKumar Bhattacharyya, Parul Jain, Debdas Bose, and PranabKumar Biswas. "Comparative study of imprint cytology and histopathology of soft tissue tumors." Indian Journal of Medical and Paediatric Oncology 38, no. 4 (2017): 461. http://dx.doi.org/10.4103/ijmpo.ijmpo_132_16.

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Sandhu, Azmat Kaur, Ruchita Tyagi, Amit Mittal, et al. "Rapid Intra-operative Diagnosis of CNS Lymphoma on Squash & Imprint Smears – A Boon for the Surgeon: Case Report." Annals of Pathology and Laboratory Medicine 7, no. 9 (2020): C115–118. http://dx.doi.org/10.21276/apalm.2849.

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Primary CNS Lymphoma [PCNL] accounts for 3% of all brain tumors. Diagnosing PCNL on squash and imprint cytology is a challenge for the pathologist but a boon for the operating surgeon as the knowledge of the nature of the lesion determines the nature of surgery. We report a case of 59 years old immunocompetent male who presented with right hemiparesis and headache. MRI Brain was suggestive of Left frontal Glioma. Intra-operatively, squash cytology and imprint smears of tissue from the lesion showed scattered lymphoid cells which also exhibited perivascular cuffing. Cytology was suggestive of l

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Zauderer, Marjorie Glass, Hira Rizvi, Mariel A. DuBoff, et al. "Association of BAP1 alterations with malignant pleural mesothelioma treated with trimodality therapy." Journal of Clinical Oncology 37, no. 15_suppl (2019): 8552. http://dx.doi.org/10.1200/jco.2019.37.15_suppl.8552.

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8552 Background: Trimodality therapy with pleurectomy/decortication, cytotoxic chemotherapy, and adjuvant pleural intensity modulated radiation therapy (IMPRINT) is an emerging standard of care for locally advanced epithelioid mesothelioma (Rimner, Zauderer et al. JCO 2016). Some patients, however, progress rapidly and we therefore sought to identify potential predictive markers of response to this treatment. Given the putative role of BAP1 in DNA damage repair, we hypothesized that alteration in BAP1 would be associated with improved local control after radiation therapy. Methods: We identifi

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Coombes, Candice, Philippe Arnaud, Emma Gordon, et al. "Epigenetic Properties and Identification of an Imprint Mark in the Nesp-Gnasxl Domain of the Mouse Gnas Imprinted Locus." Molecular and Cellular Biology 23, no. 16 (2003): 5475–88. http://dx.doi.org/10.1128/mcb.23.16.5475-5488.2003.

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ABSTRACT The Gnas locus in the mouse is imprinted with a complex arrangement of alternative transcripts defined by promoters with different patterns of monoallelic expression. The Gnas transcript is subject to tissue-specific imprinted expression, Nesp is expressed only from the maternal allele, and Gnasxl is expressed only from the paternal allele. The mechanisms controlling these expression patterns are not known. To identify potential imprinting regulatory regions, particularly for the reciprocally expressed Nesp and Gnasxl promoters, we examined epigenetic properties of the locus in gamete

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23

Horii, T., M. Kimura, S. Morita, Y. Nagao, and I. Hatada. "222 LOSS OF IMPRINTS OF PARTHENOGENETIC EMBRYONIC STEM CELLS IN MURINE CHIMERAS." Reproduction, Fertility and Development 19, no. 1 (2007): 228. http://dx.doi.org/10.1071/rdv19n1ab222.

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Mammalian parthenotes with the 2 maternal genomes cannot develop to term. By contrast, chimeras produced by parthenogenetic and normal embryos can develop to term. However, parthenogenetic cells contribute to restricted cells and body weights of the chimeras are reduced. These effects are due to aberrant expressions of imprinted genes, with complete methylation of the maternally methylated genes and complete loss of the paternally methylated genes. On the other hand, parthenogenetic ES (PGES) chimeras show more normal tissue contribution of donor cells and body weight compared to parthenogenet

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Müller, Thomas, Sheran Oradu, Demian R. Ifa, R. Graham Cooks, and Bernhard Kräutler. "Direct Plant Tissue Analysis and Imprint Imaging by Desorption Electrospray Ionization Mass Spectrometry." Analytical Chemistry 83, no. 14 (2011): 5754–61. http://dx.doi.org/10.1021/ac201123t.

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25

Carreira, Vinicius Soares, Heitor Flávio Ferrari, Ingeborg Maria Langohr, et al. "Leishmaniasp. Amastigotes Identification in Canine Transmissible Venereal Tumor." Case Reports in Veterinary Medicine 2014 (2014): 1–4. http://dx.doi.org/10.1155/2014/603852.

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Leishmaniasis is a vector-borne disease withLeishmania chagasibeing the etiological agent of canine visceral leishmaniasis in South America. Canine venereal tumor is a transplantable round cell tumor of histiocytic origin which is mostly observed in sexually active male and female intact dogs. It has been shown thatLeishmaniaamastigotes have higher tropism for the canine male genital tract tissues and venereal leishmaniasis transmission has been documented in dogs but, to date, a canine venereal tumor-dependent transmission route has not been fully demonstrated. In this report, a 10-year-old,

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Van de Pette, Mathew, Simon J. Tunster, and Rosalind M. John. "Loss of Imprinting of Cdkn1c Protects against Age and Diet-Induced Obesity." International Journal of Molecular Sciences 19, no. 9 (2018): 2734. http://dx.doi.org/10.3390/ijms19092734.

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Cyclin dependent kinase inhibitor 1c (Cdkn1c) is a maternally expressed imprinted gene with roles in embryonic development, post-natal metabolism and behaviour. Using mouse models with altered dosages of Cdkn1c, we have previously identified a role for the gene in promoting brown adipose tissue formation. Here, we use these transgenic mouse lines to model the loss of imprinting of Cdkn1c in adulthood. We demonstrate that only a two-fold increase in the expression of Cdkn1c during development is sufficient to protect against age-related weight gain in addition to glucose and insulin intolerance

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MacDonald, William A., Saqib S. Sachani, Carlee R. White, and Mellissa R. W. Mann. "A role for chromatin topology in imprinted domain regulation." Biochemistry and Cell Biology 94, no. 1 (2016): 43–55. http://dx.doi.org/10.1139/bcb-2015-0032.

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Recently, many advancements in genome-wide chromatin topology and nuclear architecture have unveiled the complex and hidden world of the nucleus, where chromatin is organized into discrete neighbourhoods with coordinated gene expression. This includes the active and inactive X chromosomes. Using X chromosome inactivation as a working model, we utilized publicly available datasets together with a literature review to gain insight into topologically associated domains, lamin-associated domains, nucleolar-associating domains, scaffold/matrix attachment regions, and nucleoporin-associated chromati

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Guntara, Dicky, and Putri Welda Utami Ritonga. "Perbedaan teknik pencetakan two step dengan spacer coping metal dan polyethylene sheet terhadap cacat permukaan dan akurasi dimensi model kerja gigi tiruan cekatDifference between two step printing techniques with spacer coping metal and polyethylene sheet to surface defects and dimensional accuracy of fixed denture working models." Padjadjaran Journal of Dental Researchers and Students 3, no. 2 (2019): 120. http://dx.doi.org/10.24198/pjdrs.v3i2.23798.

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Pendahuluan: Pencetakan merupakan hasil dari cetakan gigi dan struktur jaringan pendukung. Untuk mendapatkan hasil cetakan yang baik, maka diperlukan teknik cetakan yang mampu menghasilkan permukaan cetakan yang halus dan akurasi dimensi yang tepat sehingga meningkatkan keberhasilan pembuatan gigi tiruan cekat. Salah satu teknik pencetakan untuk mendapatkan hasil cetakan yang baik adalah teknik two step dengan spacer. Tujuan penelitian ini untuk mengetahui cacat permukaan dan perbedaan nilai akurasi dimensi model kerja gigi tiruan cekat pada pencetakan two–step dengan spacer coping metal 1 mm,

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Koo, Chae H., Henry Rappaport, Khalil Sheibani, Gerassimos A. Pangalis, Bharat N. Nathwani, and Carl D. Winberg. "Imprint cytology of non-Hodgkin's lymphomas based on a study of 212 immunologically characterized cases: Correlation of touch imprints with tissue sections." Human Pathology 20, no. 12 (1989): 1–26. http://dx.doi.org/10.1016/0046-8177(89)90287-6.

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Weinstein, Lee S., Jie Liu, Akio Sakamoto, Tao Xie, and Min Chen. "Minireview: GNAS: Normal and Abnormal Functions." Endocrinology 145, no. 12 (2004): 5459–64. http://dx.doi.org/10.1210/en.2004-0865.

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Abstract GNAS is a complex imprinted gene that uses multiple promoters to generate several gene products, including the G protein α-subunit (Gsα) that couples seven-transmembrane receptors to the cAMP-generating enzyme adenylyl cyclase. Somatic activating Gsα mutations, which alter key residues required for the GTPase turn-off reaction, are present in various endocrine tumors and fibrous dysplasia of bone, and in a more widespread distribution in patients with McCune- Albright syndrome. Heterozygous inactivating Gsα mutations lead to Albright hereditary osteodystrophy. Gsα is imprinted in a ti

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Sakhautdinova, R. R., M. P. Sutunkova, I. A. Minigalieva, and Tatyana V. Bushueva. "A CYTOLOGICAL STUDY OF IMPRINT SMEARS (TOUCH PREPARATION CYTOLOGY) TO EVALUATE THE TOXICITY OF METAL-CONTAINING NANOPARTICLES IN EXPERIMENTAL ANIMALS." Hygiene and sanitation 99, no. 1 (2020): 120–24. http://dx.doi.org/10.33029/0016-9900-2020-99-1-120-124.

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Introduction. Touch preparation cytology is a well-known technique widely used in clinical practice. It can be also applied for an express assessment of cyto-morphological effects of metal-containing nanoparticles in experimental animals. Material and methods. We’ve studied 144 imprint smears (of the liver, kidneys, lungs, tracheobronchial and mesenteric lymph nodes) taken from 52 rats, weighed 280-300 g, aged 3.5 months. This was done following a subchronic intraperitoneal administration of TiO2, Al2O3, and SiO2 nanoparticles, in a range of doses, and a subacute (5-times) inhalational exposur

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Wu, Qian, Stanislav S. Rubakhin, and Jonathan V. Sweedler. "Quantitative Imprint Mass Spectrometry Imaging of Endogenous Ceramides in Rat Brain Tissue with Kinetic Calibration." Analytical Chemistry 92, no. 9 (2020): 6613–21. http://dx.doi.org/10.1021/acs.analchem.0c00392.

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Xue, Peng-Peng, Jian-dong Yuan, Qing Yao, Ying-Zheng Zhao, and He-Lin Xu. "Bioactive Factors-imprinted Scaffold Vehicles for Promoting Bone Healing: The Potential Strategies and the Confronted Challenges for Clinical Production." BIO Integration 1, no. 1 (2020): 37–54. http://dx.doi.org/10.15212/bioi-2020-0010.

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Abstract Wound repair of bone is a complicated multistep process orchestrated by inflammation, angiogenesis, callus formation, and bone remodeling. Many bioactive factors (BFs) including cytokine and growth factors (GFs) have previously been reported to be involved in regulating wound healing of bone and some exogenous BFs such as bone morphogenetic proteins (BMPs) were proven to be helpful for improving bone healing. In this regard, the BFs reported for boosting bone repair were initially categorized according to their regulatory mechanisms. Thereafter, the challenges including short half-lif

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Abouzid, A. M., J. Freitas-Astua, D. E. Purcifull, et al. "Serological Studies Using Polyclonal Antisera Prepared Against the Viral Coat Protein of Four Begomoviruses Expressed in Escherichia coli." Plant Disease 86, no. 10 (2002): 1109–14. http://dx.doi.org/10.1094/pdis.2002.86.10.1109.

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Polyclonal rabbit antisera were produced to the coat protein of Bean golden mosaic virus Brazil isolate (BGMV), Cabbage leaf curl virus (CabLCV), Tomato yellow leaf curl virus (TYLCV), and Tomato mottle virus (ToMoV), all expressed in Escherichia coli by the pETh expression vector. The expressed coat protein of each virus was purified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis for use as an immunogen. The antisera to BGMV, CabLCV, TYLCV, and ToMoV reacted in indirect (plate-trapping) enzyme-linked immunosorbent assay (ELISA) with extracts from begomovirus-infected tissue. The

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Rekhtman, Natasha, Sofia Kazi, JinJuan Yao, et al. "Depletion of Core Needle Biopsy Cellularity and DNA Content as a Result of Vigorous Touch Preparations." Archives of Pathology & Laboratory Medicine 139, no. 7 (2014): 907–12. http://dx.doi.org/10.5858/arpa.2014-0392-oa.

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Context Touch preparations (TP) of core needle biopsies (CNBs) are used at some institutions for on-site assessment of CNB adequacy. In our clinical practice, we have encountered instances in which TPs resulted in substantial depletion of CNB cellularity. Objective To examine the effect of increasingly vigorous TPs on cellularity and DNA content of CNBs. Design Ex vivo CNBs (n = 56) were performed on resected lung and kidney tumor specimens. For each specimen, CNBs were performed in quadruplicate on tumor and nontumor tissue and subjected to 1 of 4 TP methods: imprint, 1-cm drag, 2-cm drag, or

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Yamagami, Takuji, Rika Yoshimatsu, Kenji Kajiwara, et al. "Effectiveness of combined use of imprint cytological and histological examination in CT-guided tissue-core biopsy." European Radiology 24, no. 5 (2014): 1127–34. http://dx.doi.org/10.1007/s00330-014-3104-2.

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Bauer, Henrik C. F., Andris Kreicbergs, and Bernhard Tribukait. "DNA microspectrophotometry of bone sarcomas in tissue sections as compared to imprint and flow DNA analysis." Cytometry 7, no. 6 (1986): 544–50. http://dx.doi.org/10.1002/cyto.990070608.

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Zhang, Shunchao, and Zhihan Lv. "Diagnosis and Exercise Rehabilitation of Knee Joint Anterior Cruciate Ligament Injury Based on 3D-CT Reconstruction." Complexity 2020 (September 28, 2020): 1–13. http://dx.doi.org/10.1155/2020/3690124.

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The joint capsule of the knee joint is attached to the edges of various articular surfaces and is thin and loose. Therefore, ligament reinforcement is needed to protect the knee joint and increase the stability of the joint. It plays a vital role in human activities. In this paper, a 3D-CT three-dimensional reconstruction method is used to reconstruct the ACL natural femoral imprint and double-bone tract. The relative positional relationship between the two center points is compared, and the law is summarized to guide the improvement of ACL anatomic double-beam reconstruction under arthroscopy

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Arima, Takahiro, Kenichiro Hata, Satoshi Tanaka, et al. "Loss of the maternal imprint in Dnmt3Lmat−/− mice leads to a differentiation defect in the extraembryonic tissue." Developmental Biology 297, no. 2 (2006): 361–73. http://dx.doi.org/10.1016/j.ydbio.2006.05.003.

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Machado, Gisele Fabrino, Rosemeri de Oliveira Vasconcelos, Maria Cecília Rui Luvizotto, and Terezinha Cristina Cândido. "Fungal pyogranulomatous encephalitis in a dog with leishmaniosis." Ciência Rural 36, no. 4 (2006): 1325–27. http://dx.doi.org/10.1590/s0103-84782006000400047.

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A case of pyogranulomatous micotic encephalitis in a one-year old, female, Fila Brasileiro dog is reported. Gross examination of the cerebrum revealed a softened haemorrhagic area in the right frontal cortex and on the cut surface of the left hemisphere, which affected the white matter and deep cortical areas. The diagnosis of multifocal mycotic pyogranulomatous encephalitis was obtained by the histopathological examination, which showed the presence of macrophages, giant cells, haemorrhage and brownish septate hyphae diffusely distributed within the tissue and invading vessel lumina. Identifi

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Li, Nainong, Ying Chen, Wei He, et al. "Anti-CD3 preconditioning separates GVL from GVHD via modulating host dendritic cell and donor T-cell migration in recipients conditioned with TBI." Blood 113, no. 4 (2009): 953–62. http://dx.doi.org/10.1182/blood-2008-06-165522.

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Abstract Host dendritic cells (DCs) play a critical role in initiating graft-versus-host disease (GVHD) and graft-versus-leukemia (GVL), and separation of GVL from GVHD remains a major challenge in the treatment of hematologic malignancies by allogeneic hematopoietic cell transplantation (HCT). Here, we show that preconditioning with anti-CD3 monoclonal antibody before conditioning with total body irradiation (TBI) prevents GVHD but retains GVL in a HCT model of major histocompatibility complex (MHC)–mismatched C57BL/6 donor to BALB/c host. Prevention of GVHD is associated with inhibition of d

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Roh, Jong-Lyel, William H. Westra, Joseph A. Califano, David Sidransky, and Wayne M. Koch. "Tissue imprint for molecular mapping of deep surgical margins in patients with head and neck squamous cell carcinoma." Head & Neck 34, no. 11 (2012): 1529–36. http://dx.doi.org/10.1002/hed.21982.

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Newman, Shelley J., Stephen A. Smith, and Kurt Zimmerman. "Mammary carcinoma arising in an adenoma in a ewe." Journal of Veterinary Diagnostic Investigation 33, no. 3 (2021): 566–71. http://dx.doi.org/10.1177/1040638721993061.

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A large, firm, multi-cystic mammary gland mass grew slowly over 4 y in a 12-y-old, female Finn–Shetland cross sheep. A diagnosis of epithelial malignancy was suspected following fine-needle aspiration cytology at 30 mo after initial observation. The sheep was euthanized when the flock was downsized 18 mo later. A field postmortem examination revealed a large mammary mass, but an absence of metastases to internal organs. Imprint cytology of the mammary tissue supported a benign proliferative process. Histologically, mammary tissue was obliterated by cystic, tubular, and papillary adenomatous ar

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Perez Sanchez, V. M., M. C. Angel, C. V. Judith, et al. "HER-2/neu amplification detected by fluorescence in situ hybridization in touch imprint cytology in comparison with tissue sections." European Journal of Cancer Supplements 6, no. 7 (2008): 139. http://dx.doi.org/10.1016/s1359-6349(08)70623-2.

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Milovancev, Milan, Kaitlin L. Townsend, Elena Gorman, Shay Bracha, Katie Curran, and Duncan S. Russell. "Shaved margin histopathology and imprint cytology for assessment of excision in canine mast cell tumors and soft tissue sarcomas." Veterinary Surgery 46, no. 6 (2017): 879–85. http://dx.doi.org/10.1111/vsu.12668.

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Shin, Dong-Myung, Ewa K. Zuba-Surma, Mariusz Z. Ratajczak, and Magdalena Kucia. "The Unique Pattern of Somatic Imprint in Oct-4+ Very Small Embryonic Like (VSEL) Stem Cells Isolated from Adult Tissues Further Supports Both Their Epiblast/Germ Line Origin and Explains Quiescent Status: Potential Modification of Somatic Imprint as a Key to Longevity?" Blood 112, no. 11 (2008): 385. http://dx.doi.org/10.1182/blood.v112.11.385.385.

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Abstract Recently, we identified a population of very small embryonic like (VSEL) SCs in adult bone marrow (BM) (Leukemia2006:20;857). These VSELs are: very small in size (~3.6 um); Oct-4+CXCR4+SSEA-1+Sca-1+CD45−lin−; possessing large nuclei containing unorganized chromatin (euchromatin); and we learned that in co-cultures with C2C12 cells, VSELs form embryoid body-like spheres (VSEL-DSs) that contain primitive SCs capable to differentiate into all three germ layers (e.g., myocardium, neural tissue, and pancreas). To better characterize this intriguing population of SCs, we employed bisulfite

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Lumia, V., G. Pasquini, and M. Barba. "Sensitive Detection of Artichoke Latent Virus in Globe Artichoke Field Samples by One-step RT-PCR or Tissue Imprint Hybridization." Journal of Phytopathology 151, no. 7-8 (2003): 477–79. http://dx.doi.org/10.1046/j.1439-0434.2003.00753.x.

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Ruby, Stephen G., and Anne C. McNally. "Quality Control of Imprint and Tissue Section DNA Ploidy Analysis in Image Analysis Systems Utilizing Cell Culture-Based Control Materials." American Journal of Clinical Pathology 104, no. 2 (1995): 167–71. http://dx.doi.org/10.1093/ajcp/104.2.167.

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Nakamura, Shigeo, Takashi Koshikawa, Sadayuki Kaba, Yoshiro Tokoro, Taizan Suchi, and Soji Kurita. "Imprint cytology of low-grade B-cell lymphoma of mucosa-associated lymphoid tissue arising in the thymus: A case report." Diagnostic Cytopathology 9, no. 6 (1993): 665–67. http://dx.doi.org/10.1002/dc.2840090612.

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Reik, Wolf, Fatima Santos, Kohzoh Mitsuya, Hugh Morgan, and Wendy Dean. "Epigenetic asymmetry in the mammalian zygote and early embryo: relationship to lineage commitment?" Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 358, no. 1436 (2003): 1403–9. http://dx.doi.org/10.1098/rstb.2003.1326.

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Epigenetic asymmetry between parental genomes and embryonic lineages exists at the earliest stages of mammalian development. The maternal genome in the zygote is highly methylated in both its DNA and its histones and most imprinted genes have maternal germline methylation imprints. The paternal genome is rapidly remodelled with protamine removal, addition of acetylated histones, and rapid demethylation of DNA before replication. A minority of imprinted genes have paternal germline methylation imprints. Methylation and chromatin reprogramming continues during cleavage divisions, but at the blas

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