Search Results

Identification and characterization of a human MORC2 DNA binding region that is required for gene silencing.

• Authors : Fendler, Nikole L¹ (AUTHOR); Ly, Jimmy^1,2 (AUTHOR); Welp, Luisa^3,4 (AUTHOR)

Subjects: *GENETIC regulation; *GENE silencing; *HUMAN DNA

• Source: Nucleic Acids Research. 2/28/2025, Vol. 53 Issue 4, p1-21. 21p.

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A select inhibitor of MORC2 encapsulated by chimeric membranecoated DNA nanocage target alleviation TNBC progression

• Authors : Xiaohan Su; Yunbo Luo; Yali Wang

Subjects: MORC2; Angoline; Biomimetic nanodrug delivery system

• Source: Materials Today Bio, Vol 31, Iss , Pp 101497- (2025)

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Case Report: Charcot-marie-tooth disease caused by a de novo MORC2 gene mutation - novel insights into pathogenicity and treatment

• Authors : Feng Zhu; Chengcheng Gao; Xiangxiang Zhu

Subjects: MORC2; lower limb weakness; charcot-marie-tooth disease

• Source: Frontiers in Genetics, Vol 15 (2024)

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Oncogenic MORC2 in cancer development and beyond

• Authors : Shan Zhang; Ayao Guo; Huan Wang

Subjects: Cancer development; Hallmarks of cancer; MORC2

• Source: Genes and Diseases, Vol 11, Iss 2, Pp 861-873 (2024)

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High Expression of MORC2 is Associated with Poor Clinical Outcomes and Immune Infiltrates in Colon Adenocarcinoma

• Authors : Zhao P; Ning J; Huang J

Subjects: morc2; colon adenocarcinoma; diagnosis

• Source: International Journal of General Medicine, Vol Volume 16, Pp 4595-4615 (2023)

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De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism

• Authors : Sacoto, Maria J Guillen; Tchasovnikarova, Iva A; Torti, Erin

Subjects: Neurodegenerative; Rare Diseases; Pediatric

• Source: American Journal of Human Genetics. 107(2)

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Intermediate phenotype between CMT2Z and DIGFAN associated with a novel MORC2 variant: a case report

• Authors : Kenta Hanada; Yusuke Osaki; Ryosuke Miyamoto

Subjects: Genetics; QH426-470; Life

• Source: Human Genome Variation, Vol 11, Iss 1, Pp 1-3 (2024)

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MORC2 regulates RBM39-mediated CDK5RAP2 alternative splicing to promote EMT and metastasis in colon cancer

• Authors : Yuxin He; Yangguang Shao; Zhihui Zhou

Subjects: Cytology; QH573-671

• Source: Cell Death and Disease, Vol 15, Iss 7, Pp 1-16 (2024)

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A Novel Heterozygous De Novo MORC2 Missense Variant Causes an Early Onset and Severe Neurodevelopmental Disorder.

• Authors : Arbide, Daniel¹ (AUTHOR); Elkhateeb, Nour² (AUTHOR); Goljan, Ewa³ (AUTHOR)

• Source: Case Reports in Genetics. 1/2/2024, p1-5. 5p.

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Novel Insights into the Role of Chromatin Remodeler MORC2 in Cancer.

• Authors : Chutani, Namita¹ (AUTHOR) ; Ragula, Sandhya² (AUTHOR) ; Syed, Khajamohiddin³ (AUTHOR)

• Source: Biomolecules (2218-273X). Oct2023, Vol. 13 Issue 10, p1527. 12p.

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