Results 1 to 10 of about 100,725 (298)
New fusion transcripts identified in normal karyotype acute myeloid leukemia. [PDF]
Genetic aberrations contribute to acute myeloid leukemia (AML). However, half of AML cases do not contain the well-known aberrations detectable mostly by cytogenetic analysis, and these cases are classified as normal karyotype AML.
Hongxiu Wen +14 more
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A chromosome is the structure that organizes DNA and protein in cells. It is a single piece of coiled DNA containing coding and non-coding sequences. Human cells have 23 pairs of chromosomes including 22 pairs of autosomes and one pair of sex chromosome,
Chun-Hung Chou , Muh-Hwa Yang
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Convergent Patterns of Karyotype Evolution Underlying Karyotype Uniformity in Conifers
AbstractKaryotype diversity plays an important role in speciation and diversification. However, gymnosperms, particularly conifers, exhibit remarkable karyotype uniformity. To explore the evolutionary processes shaping karyotypes in gymnosperms, the karyotype evolutionary history is reconstructed through comparative genomic analyses.
Ren‐Gang Zhang +10 more
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CHROMOSOMIC STUDIES IN ZEPHYRANTHES CITRINA BAKER (AMARYLLIDACEAE), A POLYPLOID ORNAMENTAL [PDF]
Zephyranthes citrina is an ornamental American bulbous plant used as an ornamental garden crop for the aesthetic qualities of its yellow perigonium.
Daviña J.R. +5 more
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Chromosomal instability of purebred and crossbred dairy cows
The article presents the results of research on the karyotype characteristics variability in purebred and crossbred dairy cows. The material for the research was peripheral blood samples of purebred firstborn cows of the Ukrainian red-spotted dairy and ...
V. Dzitsiuk, L. Starodub, T. Dyman
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Reconstructing single-cell karyotype alterations in colorectal cancer identifies punctuated and gradual diversification patterns [PDF]
Central to tumor evolution is the generation of genetic diversity. However, the extent and patterns by which de novo karyotype alterations emerge and propagate within human tumors are not well understood, especially at single-cell resolution.
Christopher Kimberley +25 more
core +1 more source
Incidence and risk factors of hearing loss in patients with Turner Syndrome
BackgroundHearing loss (HL) is one of the main medical complications for Turner Syndrome (TS) patients, with an earlier presentation and higher incidence than normal women. However, the etiology of HL in TS is unclear.
Huijia Lin +6 more
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Cytogenetic studies among 809 consecutive patients with essential thrombocythemia (ET; median age 59 years; 65% females) revealed normal karyotype in 754 (93%), loss of chromosome Y only (-Y) in 16 (2%), and abnormalities other than -Y in 39 (4.8%), the ...
Naseema Gangat +7 more
doaj +1 more source
Alterations in the genetic content of a cell are the underlying cause of many human diseases, including cancers. We have developed a method, called digital karyotyping, that provides quantitative analysis of DNA copy number at high resolution. This approach involves the isolation and enumeration of short sequence tags from specific genomic loci ...
Tian-Li, Wang +6 more
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Genetic analysis of Turner syndrome in Tunisian patients: from diagnosis to management
Background/aim Turner syndrome (TS) is a rare sex chromosome abnormality in women, occurring in approximately one in 2500 live births, associated with a wide range of clinical stigmata of which short stature, ovarian dysgenesis, and dysmorphic features ...
Olfa Siala-Sahnoun +7 more
doaj +1 more source

