Found: 24
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Stability of Imbalanced Triangles in Gene Regulatory Networks of Cancerous and Normal Cells.
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- Frontiers in Physiology, 2021, v. 11, p. N.PAG, doi. 10.3389/fphys.2020.573732
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- Article
Novel Homozygous Missense Mutation in RYR1 Leads to Severe Congenital Ptosis, Ophthalmoplegia, and Scoliosis in the Absence of Myopathy.
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- Molecular Syndromology, 2017, v. 9, n. 1, p. 25, doi. 10.1159/000481897
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- Article
Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 5, p. 1751, doi. 10.1093/brain/awad427
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- Article
Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 12, p. 5031, doi. 10.1093/brain/awad257
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- Article
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss.
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- Human Genetics, 2024, v. 143, n. 3, p. 311, doi. 10.1007/s00439-024-02649-2
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- Article
Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 2, p. 1, doi. 10.1002/mgg3.2099
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- Article
Whole-exome sequencing deciphers the genetic profile of visual impairments in patients from Southwest Iran.
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- Molecular Genetics & Genomics, 2022, v. 297, n. 5, p. 1289, doi. 10.1007/s00438-022-01917-y
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- Article
Dendrosomal Curcumin Upregulates Expression of the Long Noncoding RNA gene MEG3 in U87MG Glioblastoma Cells.
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- Modares Journal of Medical Sciences: Pathobiology, 2014, v. 17, n. 3, p. 41
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- Article
A novel diblock copolymer of (monomethoxy poly [ethylene glycol]-oleate) with a small hydrophobic fraction to make stable micelles/polymersomes for curcumin delivery to cancer cells.
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- International Journal of Nanomedicine, 2014, v. 9, p. 5541, doi. 10.2147/IJN.S63762
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- Article
Whole exome sequencing identified a novel frameshift variant in the BHLHA9 in an Iranian family with mesoaxial synostotic syndactyly.
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- Congenital Anomalies, 2021, v. 61, n. 6, p. 220, doi. 10.1111/cga.12439
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- Article
Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-44987-6
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- Article
Identification of Three Novel Mutations in the FANCA, FANCC, and ITGA2B Genes by Whole Exome Sequencing.
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- International Journal of Preventive Medicine, 2020, v. 11, n. 1, p. 1, doi. 10.4103/ijpvm.IJPVM_462_19
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- Article
An Insight Into Detection Pathways/Biosensors of Highly Infectious Coronaviruses.
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- Molecular Biotechnology, 2022, v. 64, n. 4, p. 339, doi. 10.1007/s12033-021-00417-5
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- Article
Phenotypic continuum of NFU1‐related disorders.
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- 2022
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- Case Study
HOXC10 is significantly overexpressed in colorectal cancer.
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- Biomedical Reports, 2020, v. 13, n. 3, p. N.PAG, doi. 10.3892/br.2020.1325
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- Article
Putative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three families.
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- Clinical Genetics, 2023, v. 103, n. 3, p. 346, doi. 10.1111/cge.14264
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- Article
Value of Endometrial Echopattern at HCG Administration Day in Predicting IVF Outcome.
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- Archives of Iranian Medicine (AIM), 2017, v. 20, n. 2, p. 101
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- Publication type:
- Article
Clinical Non-penetrance Associated with Biallelic Mutations in the RNase H2 Complex.
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- Journal of Clinical Immunology, 2023, v. 43, n. 4, p. 706, doi. 10.1007/s10875-023-01438-2
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- Article
An analytic treatment of magnetically deformed neutron stars.
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- Astronomische Nachrichten, 2021, v. 342, n. 4, p. 633, doi. 10.1002/asna.202113862
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- Article
Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders.
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- Movement Disorders, 2024, v. 39, n. 9, p. 1624, doi. 10.1002/mds.29883
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- Article
CASC11 and PVT1 spliced transcripts play an oncogenic role in colorectal carcinogenesis.
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- Frontiers in Oncology, 2022, v. 12, p. 1, doi. 10.3389/fonc.2022.954634
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- Article
Identification of new variants in patients with mucopolysaccharidosis in consanguineous Iranian families.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1343094
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- Publication type:
- Article
News and Reports: Identification of the rs797045105 in the SERAC1 Gene by Whole-exome Sequencing in a Patient Suspicious of MEGDEL Syndrome.
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- Basic & Clinical Neuroscience, 2020, v. 11, n. 4, p. 549, doi. 10.32598/bcn.9.10.455
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- Article
Encapsulation of Curcumin in Diblock Copolymer Micelles for Cancer Therapy.
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- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/824746
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- Publication type:
- Article