Results 1 to 10 of about 77,861 (207)

Karyotype Analysis

open access: yesBio-Protocol, 2014
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
doaj   +2 more sources

Gross karyotypic and phenotypic alterations among different progenies of the candida glabrata cbs138/atcc2001 reference strain [PDF]

open access: yes, 2012
Peer reviewedPublisher ...
Bader, Oliver   +8 more
core   +11 more sources

New fusion transcripts identified in normal karyotype acute myeloid leukemia. [PDF]

open access: yesPLoS ONE, 2012
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
doaj   +1 more source

Cytogenetic abnormalities in essential thrombocythemia: Clinical and molecular correlates and prognostic relevance in 809 informative cases

open access: yesBlood Cancer Journal, 2022
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

Standardized Karyotype and Idiogram of the Glass Goby Fish (Gobiopterus chuno) (Hamilton, 1822) in Thailand [PDF]

open access: yesScience Technology and Engineering Journal (STEJ), 2020
The standardized karyotype and idiogram of the glass goby fish, Gobiopterus chuno (Hamilton, 1822) from the Chao Phraya Basin in Singburi Province, Thailand, were studied.
Sippakorn Juntaree, Weerayuth Supiwong*
doaj   +1 more source

Digital karyotyping [PDF]

open access: yesProceedings of the National Academy of Sciences, 2002
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 ...
Christoph Lengauer   +6 more
openaire   +3 more sources

Karyotype evolution in Fusarium [PDF]

open access: yesIMA Fungus, 2018
The germ tube burst method (GTBM) was employed to examine karyotypes of 33 Fusarium species representative of 11 species complexes that span the phylogenetic breadth of the genus. The karyotypes revealed that the nucleolar organizing region (NOR), which includes the ribosomal rDNA region, was telomeric in the species where it was discernible.
Waalwijk, C.   +5 more
openaire   +4 more sources

Genomic characterisation of Arachis porphyrocalyx (Valls & C.E. Simpson, 2005) (Leguminosae): Multiple origin of Arachis species with x = 9 [PDF]

open access: yes, 2017
The genus Arachis Linnaeus, 1753 comprises four species with x = 9, three belong to the section Arachis: Arachis praecox (Krapov. W.C. Greg. & Valls, 1994), Arachis palustris (Krapov. W.C. Greg. & Valls, 1994) and Arachis decora (Krapov. W.C.
Lavia, Graciela Inés   +4 more
core   +8 more sources

Genetic identification of bucktooth parrotfish Sparisoma radians (Valenciennes, 1840) (Labridae, Scarinae) by chromosomal and molecular markers [PDF]

open access: yesGenetics and Molecular Biology, 2014
Parrotfishes (Labridae, Scarinae) comprise a large marine fish group of difficult identification, particularly during juvenile phase when the typical morphology and coloration of adults are absent.
Fabilene Gomes Paim   +4 more
doaj   +2 more sources

Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes

open access: yesFrontiers in Neurology, 2020
Ring chromosome 20 [r(20)] syndrome is a rare condition characterized by a non-supernumerary ring chromosome 20 replacing a normal chromosome 20. It is commonly seen in a mosaic state and is diagnosed by means of karyotyping.
Angela Peron   +8 more
doaj   +1 more source

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