Relevant bibliographies by topics / Lynch-like syndrome

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Lynch-like syndrome'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Lynch-like syndrome"

1

Carethers, John M. "Differentiating Lynch-Like From Lynch Syndrome." Gastroenterology 146, no. 3 (2014): 602–4. http://dx.doi.org/10.1053/j.gastro.2014.01.041.

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2

Semyanikhina, A. V., A. O. Rasulov, and L. N. Lyubchenko. "Clinical and genetic aspects of differential diagnostics of hereditary non-polyposis colorectal cancer." Advances in molecular oncology 6, no. 2 (2019): 21–27. http://dx.doi.org/10.17650/2313-805x-2019-6-2-21-27.

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Lynch syndrome was synonymous with hereditary non-polyposis colorectal cancer for a long time, however, mapping of the DNA mismatch repair (MMR) genes has led to distinguish Lynch syndrome as an independent syndromic unit from a number of Lynch-like syndromes that phenotypically mimic with the most frequent hereditary variant of colon cancer but genetically representing quite a heterogeneous group. This article presents up to date clinical and genetic characteristics of Lynch syndrome and Lynch-like conditions.
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Yamamoto, Azusa, Tatsuro Yamaguchi, Okihide Suzuki, et al. "Prevalence and molecular characteristics of DNA mismatch repair deficient endometrial cancer in a Japanese hospital-based population." Japanese Journal of Clinical Oncology 51, no. 1 (2020): 60–69. http://dx.doi.org/10.1093/jjco/hyaa142.

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Abstract Background The prevalence and molecular characteristics of defective DNA mismatch repair endometrial cancers in the Japanese population have been underexplored. Data supporting clinical management of patients with Lynch-like syndrome and germline variant of uncertain significance of mismatch repair genes are still lacking. Methods Immunohistochemistry of mismatch repair proteins (MLH1, MSH2, MSH6 and PMS2) was performed on formalin-fixed paraffin-embedded sections prepared from resected primary endometrial cancers in 395 women with a median age of 59 years. Genetic and/or epigenetic a
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4

Picó, María Dolores, Adela Castillejo, Óscar Murcia, et al. "Clinical and Pathological Characterization of Lynch-Like Syndrome." Clinical Gastroenterology and Hepatology 18, no. 2 (2020): 368–74. http://dx.doi.org/10.1016/j.cgh.2019.06.012.

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Antelo, Marina, Mariano Golubicki, Enrique Roca, et al. "Lynch-like syndrome is as frequent as Lynch syndrome in early-onset nonfamilial nonpolyposis colorectal cancer." International Journal of Cancer 145, no. 3 (2019): 705–13. http://dx.doi.org/10.1002/ijc.32160.

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Faisal, Muhammad Salman, Carol A. Burke, Mohammad A. Abbass, et al. "S0205 Association of Cancer With Comorbid Inflammatory Diseases in Lynch Syndrome and Lynch-Like Syndrome Individuals." American Journal of Gastroenterology 115, no. 1 (2020): S68. http://dx.doi.org/10.14309/01.ajg.0000702868.94370.a1.

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Picó, Maria Dolores, Rodrigo Jover, Oscar Murcia, et al. "1071 - Clinical and Molecular Characterization of Lynch-Like Syndrome." Gastroenterology 154, no. 6 (2018): S—206—S—207. http://dx.doi.org/10.1016/s0016-5085(18)31086-2.

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8

Xicola, Rosa M., Julia R. Clark, Timothy Carroll, et al. "Implication of DNA repair genes in Lynch-like syndrome." Familial Cancer 18, no. 3 (2019): 331–42. http://dx.doi.org/10.1007/s10689-019-00128-6.

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9

Mas-Moya, Jenny, Beth Dudley, Randall E. Brand, et al. "Clinicopathological comparison of colorectal and endometrial carcinomas in patients with Lynch-like syndrome versus patients with Lynch syndrome." Human Pathology 46, no. 11 (2015): 1616–25. http://dx.doi.org/10.1016/j.humpath.2015.06.022.

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10

Chika, Noriyasu, Hidetaka Eguchi, Kensuke Kumamoto, et al. "Prevalence of Lynch syndrome and Lynch-like syndrome among patients with colorectal cancer in a Japanese hospital-based population." Japanese Journal of Clinical Oncology 47, no. 2 (2016): 108–17. http://dx.doi.org/10.1093/jjco/hyw178.

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Dissertations / Theses on the topic "Lynch-like syndrome"

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Vargas, Parra Gardenía María. "Elucidating the molecular basis of Lynch-Like syndrome." Doctoral thesis, Universitat de Barcelona, 2016. http://hdl.handle.net/10803/386467.

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BACKGROUND: MMR deficiency is a hallmark of tumors from Lynch syndrome LS) patients, who harbor germline mutations in MMR genes. No germline alterations are detected in a significant proportion of suspected LS now known as Lynch-like syndrome (LLS) cases. HYPOTHESIS: In LS-suspected patients there may be other responsible causes for the MMR-deficiency in tumors, such as unidentified germline mutations or epimutations in MMR genes, or mutations in other CRC-associated genes (germline or somatic). AIMS: To elucidate the molecular basis of MMR deficiency in LS-suspected cases without identifi
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2

Cooper, Julia Nicole. "Genetics Clinic Re-contact of Patients with Unexplained Defective Mismatch Repair." The Ohio State University, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1554401645266717.

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El, Jamal Noura. "Homéostasie de l’intestin et de la peau : cibles et modèles pour étudier l’inflammation et la carcinogenèse." Thesis, Lille 2, 2012. http://www.theses.fr/2012LIL2S023/document.

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L’homéostasie des muqueuses intestinale et cutanée dépend des interactions complexes entre le microbiote, l’épithélium et le système immunitaire de l’hôte. Des mécanismes régulateurs divers coopèrent afin de maintenir l’équilibre physiologique, et un défaut dans ces mécanismes entrainent des situations pathologiques. Le glucagon like peptide 2 (GLP-2) est un neuropeptide caractérisé par des propriétés prolifératives et anti-inflammatoires. Le potentiel thérapeutique des analogues de GLP-2 est actuellement évalué dans des essais cliniques pour des maladies digestives. Les effets du GLP-2 dans l
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Book chapters on the topic "Lynch-like syndrome"

1

Vargas-Parra, Gardenia, Matilde Navarro, Marta Pineda, and Gabriel Capellá. "The Molecular Basis of Lynch-like Syndrome." In Hereditary Colorectal Cancer. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-74259-5_2.

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Conference papers on the topic "Lynch-like syndrome"

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Golubicki, Mariano, Laia Bonjoch, José G. Acuña-Ochoa, et al. "Abstract 2366: Germline biallelic mutations inMCM8are associated with early-onset Lynch-like syndrome." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-2366.

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Buchanan, Daniel D., Mark Clendenning, Harindra Jayasekara, et al. "Abstract 4266: Double somatic mutations as a cause of tumor mismatch repair-deficiency in population-based colorectal and endometrial cancer with Lynch-like syndrome." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-4266.

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