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Items: 1 to 20 of 64

1.
Role of PAX6, TRPA1, BCL11B, MCOLN2, CUX1, EMX1 in colorectal cancer and osteosarcoma
Jie Zhang, Qiang Gao, Shiyang Hou, Xiaoqian Chi, Meiliang Zheng, Qijun Zhang, Haifeng Shan, Xiaoyu Zhang, Chunbo Kang
Medicine (Baltimore) 2024 Feb 2; 103(5): e37056. Published online 2023 Feb 2. doi: 10.1097/MD.0000000000037056
PMCID:
PMC10843516
ArticlePDF–2.1M
2.
Novel inherited CDX2 variant segregating in a family with diverse congenital malformations of the genitourinary system
Swetha Ramadesikan, Caitlyn M. Colwell, Rachel Supinger, Jesse Hunter, Jessica Thomas, Elizabeth Varga, Elaine R. Mardis, Richard J. Wood, Daniel C. Koboldt
Cold Spring Harb Mol Case Stud. 2023 Dec; 9(4): a006294. doi: 10.1101/mcs.a006294
PMCID:
PMC10815271
ArticlePDF–1.7M
3.
Bacterial clade-specific analysis identifies distinct epithelial responses in inflammatory bowel disease
Gemma L. D’Adamo, Michelle Chonwerawong, Linden J. Gearing, Vanessa R. Marcelino, Jodee A. Gould, Emily L. Rutten, Sean M. Solari, Patricia W.R. Khoo, Trevor J. Wilson, Tamblyn Thomason, Emily L. Gulliver, Paul J. Hertzog, Edward M. Giles, Samuel C. Forster
Cell Rep Med. 2023 Jul 18; 4(7): 101124. Published online 2023 Jul 18. doi: 10.1016/j.xcrm.2023.101124
PMCID:
PMC10394256
ArticlePDF–4.1M
4.
Morphological and Functional Colonic Defects Caused by a Mutated Thyroid Hormone Receptor α
Minjun Kim, Michael Kruhlak, Victoria Hoffmann, Patricia Zerfas, Kevin Bishop, Woo Kyung Lee Doolittle, Elijah F. Edmondson, Yuelin Jack Zhu, Sheue-yann Cheng
Thyroid. February 2023; 33(2): 239–250. Published online 2023 Feb 14. doi: 10.1089/thy.2022.0336
PMCID:
PMC10081711
ArticlePDF–1.4M
5.
Pain triangle phenomenon in possible association with SCN9A: A case report
Maurice Sopacua, Janneke G. J. Hoeijmakers, Anneke J. van der Kooi, Ingemar S. J. Merkies, Catharina G. Faber
Mol Genet Genomic Med. 2022 Oct; 10(10): e2026. Published online 2022 Sep 16. doi: 10.1002/mgg3.2026
PMCID:
PMC9544215
ArticlePDF–427K
6.
A novel SCN9A gene variant identified in a Chinese girl with paroxysmal extreme pain disorder (PEPD): a rare case report
Yi Hua, Di Cui, Lin Han, Lu Xu, Shanshan Mao, Cuiwei Yang, Feng Gao, Zhefeng Yuan
BMC Med Genomics. 2022; 15: 159. Published online 2022 Jul 15. doi: 10.1186/s12920-022-01302-z
PMCID:
PMC9287976
ArticlePDF–1.4M
7.
Colorectal Cancer that Highly Express Both ACE2 and TMPRSS2, Suggesting Severe Symptoms to SARS-CoV-2 Infection
Huai Wang, Jiankang Yang
Pathol Oncol Res. 2021; 27: 612969. Published online 2021 Apr 15. doi: 10.3389/pore.2021.612969
PMCID:
PMC8262219
ArticlePDF–1019K
8.
Currarino syndrome: a comprehensive genetic review of a rare congenital disorder
Gabriel C. Dworschak, Heiko M. Reutter, Michael Ludwig
Orphanet J Rare Dis. 2021; 16: 167. Published online 2021 Apr 9. doi: 10.1186/s13023-021-01799-0
PMCID:
PMC8034116
ArticlePDF–975K
9.
Tissue mRNA for S100A4, S100A6, S100A8, S100A9, S100A11 and S100P Proteins in Colorectal Neoplasia: A Pilot Study
Eva Peterova, Jan Bures, Paula Moravkova, Darina Kohoutova
Molecules. 2021 Jan; 26(2): 402. Published online 2021 Jan 14. doi: 10.3390/molecules26020402
PMCID:
PMC7828666
ArticlePDF–1.1M
10.
Dichorionic twin pregnancy with sirenomelia and chromosomal anomaly in 1 fetus: A case report
Yuan Ting, Li Xue-Lan, Wang Chun-Bao, Zhang Ting, Li Fen, Han Zhen
Medicine (Baltimore) 2021 Jan 8; 100(1): e24229. Published online 2021 Jan 8. doi: 10.1097/MD.0000000000024229
PMCID:
PMC7793322
ArticlePDF–528K
11.
Elevated expression of minichromosome maintenance 3 indicates poor outcomes and promotes G1/S cell cycle progression, proliferation, migration and invasion in colorectal cancer
He Zhou, Yongfu Xiong, Guangjun Zhang, Zuoliang Liu, Lifa Li, Songlin Hou, Tong Zhou
Biosci Rep. 2020 Jul 31; 40(7): BSR20201503. Published online 2020 Jul 9. doi: 10.1042/BSR20201503
PMCID:
PMC7350890
ArticlePDF–3.3M
12.
Novel MNX1 mutations and genotype–phenotype analysis of patients with Currarino syndrome
Lu Han, Zhen Zhang, Hui Wang, Hui Song, Qing Gao, Yuchun Yan, Ran Tao, Ping Xiao, Long Li, Qian Jiang, Qi Li
Orphanet J Rare Dis. 2020; 15: 155. Published online 2020 Jun 22. doi: 10.1186/s13023-020-01442-4
PMCID:
PMC7310025
ArticlePDF–1.5M
13.
Paroxysmal extreme pain disorder in family with c.3892G > T (p.Val1298Phe) in the SCN9A gene mutation – case report
Adam Stępień, Daria Sałacińska, Jacek Staszewski, Marta Durka-Kęsy, Jan Dobrogowski
BMC Neurol. 2020; 20: 182. Published online 2020 May 13. doi: 10.1186/s12883-020-01770-9
PMCID:
PMC7218613
ArticlePDF–4.8M
14.
Night-shift work duration and risk of colorectal cancer according to IRS1 and IRS2 expression
Yan Shi, Li Liu, Tsuyoshi Hamada, Jonathan A Nowak, Marios Giannakis, Yanan Ma, Mingyang Song, Daniel Nevo, Keisuke Kosumi, Mancang Gu, Sun A. Kim, Teppei Morikawa, Kana Wu, Jing Sui, Kyriaki Papantoniou, Molin Wang, Andrew T. Chan, Charles S. Fuchs, Jeffrey A. Meyerhardt, Edward Giovannucci, Shuji Ogino, Eva S. Schernhammer, Reiko Nishihara, Xuehong Zhang
Cancer Epidemiol Biomarkers Prev. Author manuscript; available in PMC 2020 Jul 1.
Published in final edited form as: Cancer Epidemiol Biomarkers Prev. 2020 Jan; 29(1): 133–140. Published online 2019 Oct 30. doi: 10.1158/1055-9965.EPI-19-0325
PMCID:
PMC6954315
ArticlePDF–400K
15.
Downregulation of P2Y2 and HuD during the development of the enteric nervous system in fetal rats with anorectal malformations
Zebing Zheng, Bin Chen, Zhu Jin, Mingjuan Gao, Chengyan Tang, Yuchen Mao, Yan Qu, Yuanmei Liu
Mol Med Rep. 2019 Aug; 20(2): 1297–1305. Published online 2019 Jun 6. doi: 10.3892/mmr.2019.10356
PMCID:
PMC6625457
ArticlePDF–901K
16.
Role of epigenetics in transformation of inflammation into colorectal cancer
Zhen-Hua Yang, Yan-Qi Dang, Guang Ji
World J Gastroenterol. 2019 Jun 21; 25(23): 2863–2877. Published online 2019 Jun 21. doi: 10.3748/wjg.v25.i23.2863
PMCID:
PMC6589733
ArticlePDF–2.7M
17.
Peripheral Lymphocytes of Patients with Inflammatory Bowel Disease Have Altered Concentrations of Key Apoptosis Players: Preliminary Results
Katarzyna Neubauer, Barbara Woźniak-Stolarska, Małgorzata Krzystek-Korpacka
Biomed Res Int. 2018; 2018: 4961753. Published online 2018 Nov 1. doi: 10.1155/2018/4961753
PMCID:
PMC6236662
ArticlePDF–940K
18.
FOXD3/FOXD4 is required for the development of hindgut in the rat model of anorectal malformation
Luo-Jia Wang, Wei-Lin Wang, Hong Gao, Yu-Zuo Bai, Shu-Cheng Zhang
Exp Biol Med (Maywood) 2018 Feb; 243(4): 327–333. Published online 2018 Jan 7. doi: 10.1177/1535370217751073
PMCID:
PMC6022930
ArticlePDF–655K
19.
Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case report
Lucia Cococcioni, Susanna Paccagnini, Elena Pozzi, Luigina Spaccini, Elisa Cattaneo, Serena Redaelli, Francesca Crosti, Gian Vincenzo Zuccotti
Ital J Pediatr. 2018; 44: 59. Published online 2018 May 25. doi: 10.1186/s13052-018-0500-2
PMCID:
PMC5970537
ArticlePDF–862K
20.
Spectrum of MNX1 Pathogenic Variants and Associated Clinical Features in Korean Patients with Currarino Syndrome
Seungjun Lee, Eun Jin Kim, Sung Im Cho, Hyunwoong Park, Soo Hyun Seo, Moon-Woo Seong, Sung Sup Park, Sung-Eun Jung, Seong-Cheol Lee, Kwi-Won Park, Hyun-Young Kim
Ann Lab Med. 2018 May; 38(3): 242–248. Published online 2018 Feb 2. doi: 10.3343/alm.2018.38.3.242
PMCID:
PMC5820069
ArticlePDF–384K

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