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MDS/MPN-Unclassifiable with t(X;17)(q28;q21) and KANSL1-MTCP1/CMC4 Fusion Gene

期刊: CYTOGENETIC AND GENOME RESEARCH, 2022; 161 (12)

Myelodysplastic/myeloproliferative neoplasm, unclassifiable (MDS/MPN-U) is a poorly characterized entity among overlap myeloid syndromes. Recent studi......

JIF:1.406

Differences in Variants in the Structural Domain of BCR-ABL1 Kinase between Chinese Han and Minority Patients with Chronic Myeloid Leukemia by Sanger Sequencing and Next-Generation Sequencing

期刊: CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (4)

This study aimed to detect differences in BCR-ABL1 kinase domain (KD) variants in patients with chronic myeloid leukemia (CML) who have been warned an......

JIF:1.406

Cohesin RAD21 Gene Promoter Methylation Correlated with Better Prognosis in Breast Cancer Patients

期刊: CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (3)

RAD21 plays multiple roles in numerous cancers. In breast cancer (BC), a high level of RAD21 correlates with poor disease outcomes and resistance to c......

JIF:1.406

Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 Duplication

期刊: CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (1-2)

The 16p11.2 duplication is a well-known cause of developmental delay and autism, but there are only 2 previously reported cases of 16p11.2 triplicatio......

JIF:1.406

Interaction between m6A and ncRNAs and Its Association with Diseases

期刊: CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (4)

Noncoding RNAs (ncRNA) are a kind of endogenous RNA that regulate many vital bioprocesses with limited ability to encode polypeptides. Most of them ar......

JIF:1.406

Comparative Somatic Variant Analysis of a Rare Case with Concurrent Oral Leukoplakia and Oral Submucosal Fibrosis

期刊: CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (4)

Oral leukoplakia (OL) and oral submucosal fibrosis (OSMF) are precancerous conditions with common etiologies but with different risks for oral cancer ......

JIF:1.406

scRepli-Seq: A Powerful Tool to Study Replication Timing and Genome Instability

期刊: CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (4)

Advances in omics technology have made it possible to study a wide range of cellular phenomena at the single-cell level. Recently, we developed single......

JIF:1.406

Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness

期刊: CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (3)

Interstitial 2q24.2q24.3 microdeletions are rare cytogenetic aberrations associated with heterogeneous clinical features depending on the size of the ......

JIF:1.406

Ionizing Radiation-Induced DNA Damage Response in Primary Melanocytes and Keratinocytes of Human Skin

期刊: CYTOGENETIC AND GENOME RESEARCH, 2022; 162 (4)

Currently, our knowledge of how different cell types in a tissue microenvironment respond to low and high linear energy transfer (LET) radiation is hi......

JIF:1.406

Cytogenetic Abnormalities in Multiple Myeloma: Incidence, prognostic significance and geographic heterogeneity in Indian and western population.

期刊: CYTOGENETIC AND GENOME RESEARCH, 2023; ()

Multiple Myeloma(MM) is genetically complex and heterogeneous neoplasm in which cytogenetics is major genetic factor which plays an important role in ......

Insights on the radiation-induced adaptive response at the cellular level and its implications in cancer therapy

期刊: CYTOGENETIC AND GENOME RESEARCH, 2023; ()

Background: Development of resistance upon exposure to small doses of ionizing radiation followed by higher doses is known as radiation-induced adapti......

B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 21

期刊: CYTOGENETIC AND GENOME RESEARCH, 2023; 162 (5)

Pediatric B-cell acute lymphoblastic leukemia (B-ALL) is associated with various specific cytogenetic and molecular markers that significantly influen......

Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions

期刊: CYTOGENETIC AND GENOME RESEARCH, 2023; 162 (5)

We report a patient presenting with neurodevelopmental disorder, cleft palate, micrognathia, relatively mild microcephaly (-2 SD), and ventricular sep......

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