A Commemorative Issue in Honor of Professor Merlin G. Butler's Retirement

Contributors: Godler, David E., Veatch, Olivia J.

Subject Terms: DNA methylation, episignature, epigenetics, copy number variant, neurodevelopmental disorder, genomic disorder, FMR1 gene, fragile X syndrome, FMR1 gray zone or intermediate alleles, connective tissue-related disorders, sleep-related breathing disorders, obstructive sleep apnea, polysomnography, growth hormone, before-after comparison, obesity, genetics, monogenic, polygenic, Prader-Willi, syndrome, Prader-Willi syndrome, genotype, phenotype, hypothalamus, brain development, array CGH, CGR, complex genomic rearrangements, chromothripsis, cryptic rearrangement, OGM, optical genome mapping, genome sequencing, DEE, developmental and epileptic encephalopathy, SCN1A, SCN2A, body composition, muscle strength, non-alcoholic fatty liver disease, children, Prader-Willi syndrome (PWS), high-resolution chromosomal microarray, PWS molecular genetic classes, typical 15q11-q13 deletion subtypes, maternal disomy 15 subclasses, atypical PWS genetic findings, DESTINY PWS, Prader–Willi syndrome, hyperphagia, clinical trials, Prader–Willi syndrome (PWS), typical 15q11-q13 Type I, Type II deletions, 15q11.2 BP1-BP2 deletion, clinical findings, autonomic nervous system (ANS), childhood obesity, FMR1, epigenetic boundary, premutation, methylation intellectual disability, Mowat–Wilson syndrome (MWS), case report, review, ZEB2 gene variants, ZEB2 protein domains and defects, ZEB2 functional molecular interactions, Medicine and Nursing

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Access URL: https://directory.doabooks.org/handle/20.500.12854/153161
https://mdpi.com/books/pdfview/book/10424

Microfluidic Synthesis of miR-200c-3p Lipid Nanoparticles: Targeting ZEB2 to Alleviate Chondrocyte Damage in Osteoarthritis

Authors: Zheng D, Chen T, Yang K, Yin G, Chen Y, Gui J, Xu C, Lv S

Source: International Journal of Nanomedicine, Vol Volume 20, Pp 505-521 (2025)

Subject Terms: microfluidic synthesis, mir-200c-3p, lipid nanoparticles, osteoarthritis, zeb2, Medicine (General), R5-920

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Relation: https://www.dovepress.com/microfluidic-synthesis-of-mir-200c-3p-lipid-nanoparticles-targeting-ze-peer-reviewed-fulltext-article-IJN; https://doaj.org/toc/1178-2013

Access URL: https://doaj.org/article/34e8516a468b4f30983f37856558e869

ZEB2 reduction contributes to pre-eclampsia via Wnt/β-Catenin pathway

Authors: Yanxin Zhang, Fangle Gu, Yan Liu, Yujie Sun, Liying Zhang, Dan Lu

Source: Cell Division, Vol 19, Iss 1, Pp 1-12 (2024)

Subject Terms: ZEB2, Pre-eclampsia, Wnt/β-Catenin pathway, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Cytology, QH573-671

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Relation: https://doaj.org/toc/1747-1028

Access URL: https://doaj.org/article/4018a49509494dc1a19bf6726e25d46a

Mowat-Wilson syndrome: unraveling the complexities of diagnosis, treatment, and symptom management

Authors: Yalda Zhoulideh, Jamil Joolideh

Source: Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-10 (2024)

Subject Terms: Hirschsprung, Mowat-Wilson syndrome, MWS, Rare disease, ZEB2, Medicine (General), R5-920, Genetics, QH426-470

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Relation: https://doaj.org/toc/2090-2441

Access URL: https://doaj.org/article/d20f1a85dc874d0e81a7c10571777b83

Molecules at Play in Cancer

Contributors: Iacobas, Dumitru

Subject Terms: Agkistrodon, leucine, membrane, phenylalanine, venom peptides, familial hyperaldosteronism type 3, KCNJ5, adrenal tumor, β-catenin, MALDI-IMS, CYP11B2, PNU-74654, TNF receptor-1, apoptosis, testicular cancer, alveolar epithelial stem cells, ACE2, SARS-CoV-2, COVID-19, RBD of spike glycoprotein, metastatic microenvironment, ovarian cancer, exosomal microRNA, biomarker, early diagnosis, BSG, basigin, CD147, MM, multiple myeloma, survival, AP5M1, BAIAP2L1, CRISPR, ENTPD2, master regulator, LOC145474, MTOR, PRRG1, VIM, WFDC3, circulating tumor cells, non-small-cell lung cancer, single cell next generation sequencing, nematode, microenvironment, cancer, research, ZEB2, prognosis, immune cells, cyclin D1, epidermal growth factor receptor (EGFR), stage I gastric cancer, early gastric cancer, node-negative gastric cancer, B-cell maturation antigen (BCMA), soluble BCMA (sBCMA), multiple myeloma (MM), anti-BCMA CAR-T cell therapy, INDEL, genetic ancestry, Amazon, biomarkers, KIRC, GOT2, multi-omics, epigenetics, immune cell infiltration, arsenic trioxide, Parkin, HeLa, autophagy, salivaomics, breast cancer, saliva, molecular biological subtype, HER2 status, estrogen receptors, progesterone receptors, HPV DNA in breast, nested PCR, gastric cancer, hsa-miR-942-3p, AR, MAPK/ERK signaling pathway, HCC, CTCs, miRNAs, proteomics, fenbendazole, microtubule polymerization, self-administration, EMT, UQCRB, ROS, hypoxia, HIF-1α, deuterium-depleted water (DDW), deuterium-depleted yolk (DDyolk), anticancer drug development, D/H ratio, production of metabolic water, ketogenic diet, NEAT1, liver cancer cell line, drug resistance, SOD2, MAPK, AKT, rhabdomyosarcoma, sarcoma, mouse model, Nf1, Ink4a/Arf, vincristine, Research and information: general, Biology, life sciences

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Access URL: https://directory.doabooks.org/handle/20.500.12854/100114
https://mdpi.com/books/pdfview/book/7207

'Liu-Liang-Chung' syndrome with multiple congenital anomalies and the distinctive craniofacial features caused by dominant ZEB2 gene gain mutation

Authors: Wei-Liang Liu, Fang Li, Wei Chen, Lu Liu, Hai-jian Cheng, Zhi-Xu He, Rong Ai

Source: BMC Pediatrics, Vol 23, Iss 1, Pp 1-6 (2023)

Subject Terms: Liu-Liang-Chung syndrome, ZEB2, Increase of gene dosage, 2q22, Distinctive craniofacial features, Pediatrics, RJ1-570

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Relation: https://doaj.org/toc/1471-2431

Access URL: https://doaj.org/article/e1c1d8e2e28444cfb73740571460d64d

Clinical Characteristics and Novel ZEB2 Gene Mutation Analysis of Three Chinese Patients with Mowat-Wilson Syndrome

Authors: Han X, Zhang Q, Wang C, Han B

Source: Pharmacogenomics and Personalized Medicine, Vol Volume 16, Pp 777-783 (2023)

Subject Terms: mowat-wilson syndrome, zeb2, gene mutation, rehabilitation treatment, long-term follow-up, Therapeutics. Pharmacology, RM1-950

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Relation: https://www.dovepress.com/clinical-characteristics-and-novel-zeb2-gene-mutation-analysis-of-thre-peer-reviewed-fulltext-article-PGPM; https://doaj.org/toc/1178-7066

Access URL: https://doaj.org/article/959f111f1aa3448b82927c6012dc470d

The study of miRNA-200c expression and epithelial-to-mesenchymal transition-related transcription factors in the primary bladder urothelial carcinoma

Authors: Anubhav Narwal, Kalpana Kumari, Seema Kaushal, Amlesh Seth, Brusabhanu Nayak, Yashika Rustagi, Amit Kumar Dinda

Source: Urology Annals, Vol 15, Iss 1, Pp 35-42 (2023)

Subject Terms: bladder carcinoma, mirna-200c, twist, zeb1, zeb2, Diseases of the genitourinary system. Urology, RC870-923

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Relation: http://www.urologyannals.com/article.asp?issn=0974-7796;year=2023;volume=15;issue=1;spage=35;epage=42;aulast=Narwal; https://doaj.org/toc/0974-7796; https://doaj.org/toc/0974-7834

Access URL: https://doaj.org/article/0127d7b10dc0498ab11f9123d943c527

MiR-454-3p promotes apoptosis and autophagy of AML cells by targeting ZEB2 and regulating AKT/mTOR pathway

Authors: Xiao Wang, Liang Zhong, Wenran Dan, Xuan Chu, Xu Luo, Chen Liu, Peng Wan, Yang Lu, Zhenyan Liu, Zhonghui Zhang, Beizhong Liu

Source: Hematology, Vol 28, Iss 1 (2023)

Subject Terms: miR-454-3p, AML, ZEB2, apoptosis, autophagy, AKT/mTOR pathway, Diseases of the blood and blood-forming organs, RC633-647.5

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Relation: https://doaj.org/toc/1607-8454

Access URL: https://doaj.org/article/e89667512df042449bc62ea3a3de514b

A positive feedback loop between ZEB2 and ACSL4 regulates lipid metabolism to promote breast cancer metastasis

Authors: Jiamin Lin, Pingping Zhang, Wei Liu, Guorong Liu, Juan Zhang, Min Yan, Yuyou Duan, Na Yang

Source: eLife, Vol 12 (2023)

Subject Terms: ACSL4, lipid metabolism, lipid droplets, cancer metastasis, EMT, ZEB2, Medicine, Science, Biology (General), QH301-705.5

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Relation: https://elifesciences.org/articles/87510; https://doaj.org/toc/2050-084X

Access URL: https://doaj.org/article/6f23491712fb45748de791946d88ba71

Mowat-Wilson Syndrome as a Differential Diagnosis in Patients with Congenital Heart Defects and Dysmorphic Facies

Authors: Pachajoa H, Gomez-Pineda E, Giraldo-Ocampo S, Lores J

Source: Pharmacogenomics and Personalized Medicine, Vol Volume 15, Pp 913-918 (2022)

Subject Terms: neurodevelopmental disorder, zeb2, genetic disorder, multiple congenital disorder, Therapeutics. Pharmacology, RM1-950

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Relation: https://www.dovepress.com/mowat-wilson-syndrome-as-a-differential-diagnosis-in-patients-with-con-peer-reviewed-fulltext-article-PGPM; https://doaj.org/toc/1178-7066

Access URL: https://doaj.org/article/710e3a0da4fa4e15b35048f5cd50a2d2

miR-215-5p Plays a Key Role in Suppressing Vascular Invasion and Recurrence in Hepatocellular Carcinoma by Blocking Vasculogenic Mimicry

Authors: Heng Zhang, Xi Lan, Liquan Cai, Xunfeng Gao, Feng Gao, Dan Yu, Jinlong Zhang, Jinhui Zhang, Qinwen Tai

Source: Frontiers in Bioscience-Elite, Vol 16, Iss 1, p 6 (2024)

Subject Terms: hepatocellular carcinoma, mir-215-5p, zeb2, vasculogenic mimicry, vascular invasion, recurrent metastasis, Environmental sciences, GE1-350, Microbiology, QR1-502

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Relation: https://www.imrpress.com/journal/FBE/16/1/10.31083/j.fbe1601006; https://doaj.org/toc/1945-0494

Access URL: https://doaj.org/article/35b7c3f1017045f9ae5bcc4b7355e17b

Zinc Finger E-Box Binding Homeobox 2 as a Prognostic Biomarker in Various Cancers and Its Correlation with Infiltrating Immune Cells in Ovarian Cancer

Authors: Hye-Ran Kim, Choong Won Seo, Sang Jun Han, Jae-Ho Lee, Jongwan Kim

Source: Current Issues in Molecular Biology, Vol 44, Iss 3, Pp 1203-1214 (2022)

Subject Terms: ovarian cancer, ZEB2, prognosis, biomarker, immune cells, Biology (General), QH301-705.5

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Relation: https://www.mdpi.com/1467-3045/44/3/79; https://doaj.org/toc/1467-3037; https://doaj.org/toc/1467-3045

Access URL: https://doaj.org/article/3a453a149daa4c6d806e05759f11cd0a

Circular RNA circVAPA contributes to non-small-cell lung cancer progression via miR-342-3p-dependent regulation of ZEB2

Authors: Xiaoyang Liu, Yang Cheng, Yan Wang, Yinhong Zhang

Source: World Journal of Surgical Oncology, Vol 19, Iss 1, Pp 1-13 (2021)

Subject Terms: NSCLC, circVAPA, miR-342-3p, ZEB2, Surgery, RD1-811, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

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Relation: https://doaj.org/toc/1477-7819

Access URL: https://doaj.org/article/e348f3d2bcfb487fa2cdbefb149ede1d

Mowat-Wilson syndrome: literature review and case series

Authors: M. Yu. Bobylova, V. S. Kakaulina, M. O. Abramov, K. Yu. Mukhin

Source: Русский журнал детской неврологии, Vol 16, Iss 3, Pp 10-20 (2021)

Subject Terms: mowat-wilson syndrome, zeb2 gene, epilepsy, electroencephalography, video electroencephalography monitoring, differential diagnosis with angelman syndrome, Neurology. Diseases of the nervous system, RC346-429

File Description: electronic resource

Relation: https://rjdn.abvpress.ru/jour/article/view/370; https://doaj.org/toc/2073-8803; https://doaj.org/toc/2412-9178

Access URL: https://doaj.org/article/c01e639bb6524fe9bcfb8c396003f20f

Physical, language, neurodevelopment and phenotype-genotype correlation of Chinese patients with Mowat-Wilson syndrome

Authors: Lihua Wu, Jianhong Wang, Lei Wang, Qi Xu, Bo Zhou, Zhen Zhang, Qi Li, Hui Wang, Lu Han, Qian Jiang, Lin Wang

Source: Frontiers in Genetics, Vol 13 (2022)

Subject Terms: physical development, language assessment, Mowat-Wilson syndrome, phenotype-genotype correlation, ZEB2, Genetics, QH426-470

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Relation: https://www.frontiersin.org/articles/10.3389/fgene.2022.1016677/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/a648baadf60d467fac1a17cd4482e148

ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function

Authors: Jens Schuster, Joakim Klar, Ayda Khalfallah, Loora Laan, Jan Hoeber, Ambrin Fatima, Velin Marita Sequeira, Zhe Jin, Sergiy V. Korol, Mikael Huss, Ann Nordgren, Britt Marie Anderlid, Caroline Gallant, Bryndis Birnir, Niklas Dahl

Source: Frontiers in Molecular Neuroscience, Vol 15 (2022)

Subject Terms: ZEB2, Mowat-Wilson syndrome, FOXG1, epilepsy, neurodevelopmental disease, GABAergic interneurons, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

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Relation: https://www.frontiersin.org/articles/10.3389/fnmol.2022.988993/full; https://doaj.org/toc/1662-5099

Access URL: https://doaj.org/article/3367a1ecb0fa455a9d3e6d6550ba3e2c

FoXA2 promotes esophageal squamous cell carcinoma progression by ZEB2 activation

Authors: Hanjing Gao, Zheng Yan, Haiyan Sun, Yanfang Chen

Source: World Journal of Surgical Oncology, Vol 19, Iss 1, Pp 1-10 (2021)

Subject Terms: FOXA2, ESCC, Progression, ZEB2, Surgery, RD1-811, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

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Relation: https://doaj.org/toc/1477-7819

Access URL: https://doaj.org/article/baebac792a454c45920013e9af22aa1e

The ZEB2‐dependent EMT transcriptional programme drives therapy resistance by activating nucleotide excision repair genes ERCC1 and ERCC4 in colorectal cancer

Authors: Rahul Sreekumar, Hajir Al‐Saihati, Muhammad Emaduddin, Karwan Moutasim, Massimiliano Mellone, Ashish Patel, Seval Kilic, Metin Cetin, Sule Erdemir, Marta Salgado Navio, Maria Antonette Lopez, Nathan Curtis, Tamer Yagci, John N. Primrose, Brendan D. Price, Geert Berx, Gareth J. Thomas, Eugene Tulchinsky, Alex Mirnezami, A. Emre Sayan

Source: Molecular Oncology, Vol 15, Iss 8, Pp 2065-2083 (2021)

Subject Terms: DNA repair, EMT, ERCC1, oxaliplatin, ZEB2, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

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Relation: https://doaj.org/toc/1574-7891; https://doaj.org/toc/1878-0261

Access URL: https://doaj.org/article/48e36438327a4d3b9ecc9732d773fccf

A Chinese Boy with Mowat–Wilson Syndrome Caused by a 10 bp Deletion in the ZEB2 Gene

Authors: Wei L, Han X, Li X, Han B, Nie W

Source: Pharmacogenomics and Personalized Medicine, Vol Volume 14, Pp 1041-1045 (2021)

Subject Terms: mowat-wilson syndrome, zeb2, gene mutation, phenotype, Therapeutics. Pharmacology, RM1-950

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Relation: https://www.dovepress.com/a-chinese-boy-with-mowatwilson-syndrome-caused-by-a-10-bp-deletion-in--peer-reviewed-fulltext-article-PGPM; https://doaj.org/toc/1178-7066

Access URL: https://doaj.org/article/bf6a3a98ee634dec824dcdedccef5f00