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Aicardi-Goutières Syndrome Type 1: A Novel Missense Variant and Review of the Mutational Spectrum.
- Published in:
- Iranian Journal of Child Neurology, 2024, v. 18, n. 3, p. 117, doi. 10.22037/ijcn.v18i3.43274
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- Article
Distinct neurological phenotypes associated with biallelic loss of NOTCH3 function: evidence for recessive inheritance.
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- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09560-z
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- Article
Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy (SMA-PME): three new cases and review of the mutational spectrum.
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- Italian Journal of Pediatrics, 2023, v. 49, n. 1, p. 1, doi. 10.1186/s13052-023-01474-z
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- Article
Long Non-coding RNAs as Regulators of the Mitogen-activated Protein Kinase (MAPK) Pathway in Cancer.
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- Journal of the Czech & Slovak Societies for Oncology / Klinická Onkologie, 2018, v. 31, n. 2, p. 95, doi. 10.14735/amko201895
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- Article
Expression Study and Clinical Correlations of MYC and CCAT2 in Breast Cancer Patients.
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- 2017
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- Publication type:
- journal article
The Role of Long Non-Coding RNAs in Ovarian Cancer.
- Published in:
- Iranian Biomedical Journal, 2017, v. 21, n. 1, p. 1, doi. 10.18869/acadpub.ibj.21.1.3
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- Article
The Role of Long Non-Coding RNAs in Ovarian Cancer.
- Published in:
- 2017
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- Publication type:
- journal article
Comparative expression analysis of hypoxia-inducible factor-alpha and its natural occurring antisense in breast cancer tissues and adjacent noncancerous tissues.
- Published in:
- Cell Biochemistry & Function, 2016, v. 34, n. 8, p. 572, doi. 10.1002/cbf.3230
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- Publication type:
- Article