Results 31 to 40 of about 409,247 (302)

Establishment of a novel human lymphoblastic cell strain with the long arm of chromosome 11 aberration without MLL rearrangement

open access: yesScientific Reports, 2017
At present, all cell strains derived from acute lymphoblastic leukemia (ALL) patients with the long arm of chromosome 11 aberration are accompanied with mixed lineage leukemia (MLL) gene rearrangement.
Qian Wang   +14 more
doaj   +1 more source

Y CHROMOSOME ABNORMALITY IN PATIENTS WITH AMBIGUOUS GENITALIA [PDF]

open access: yes, 2008
Background. Ambiguous genitalia is an abnormality signing by the presence of atypical appearance of external genitalia as male or female, or appear as combination of both male and female appearance.
Wasilah , Siti   +2 more
core   +1 more source

Molecular cytogenetic characterization of partial trisomy of the long arm of chromosome 11 in a patient with multiple congenital anomalies

open access: yesMolecular Cytogenetics, 2022
Background Partial trisomy of the long arm of chromosome 11 is a rare cytogenetic abnormality. It has been characterized by variable sized duplications that lead to a range of phenotypes including growth retardation, developmental delay/intellectual ...
Austin Walker   +7 more
doaj   +1 more source

X chromosome inactivation during Drosophila spermatogenesis [PDF]

open access: yes, 2007
Genes with male- and testis-enriched expression are under-represented on the Drosophila melanogaster X chromosome. There is also an excess of retrotransposed genes, many of which are expressed in testis, that have “escaped” the X chromosome and moved to ...
Baines, J.   +11 more
core   +2 more sources

Chromosome Abnormalities

open access: yesVeterinary Clinics of North America: Food Animal Practice, 1993
Chromosome abnormalities have been described in food animals since 1964. Some are self-limiting because they cause sterility or other developmental defects incompatible with normal growth and development, making them unacceptable for production systems.
openaire   +2 more sources

Cytomolecular identification of individual wheat-wheat chromosome arm associations in wheat-rye hybrids [PDF]

open access: yes, 2013
Chromosome pairing in the meiotic metaphase I of wheatrye hybrids has been characterized by sequential genomic and fluorescent in situ hybridization allowing not only the discrimination of wheat and rye chromosomes, but also the identification of the
Megyeri, Mária   +2 more
core   +1 more source

Sex chromosome aneuploidy in cytogenetic findings of referral patients from south of Iran [PDF]

open access: yesIranian Journal of Reproductive Medicine, 2012
Background: Chromosome abnormality (CA) including Sex chromosomes abnormality (SCAs) is one of the most important causes of disordered sexual development and infertility.
Najmeh Jouyan   +4 more
doaj  

Pengaruh Kejutan Suhu Panas dan Lama Waktu Setelah Pembuahan Terhadap Daya Tetas dan Abnormalitas Larva Ikan Nila (Oreochromis niloticus)
[The Thermal Temperature Shock and Time After Fertilization In Hatching Rate and Abnormality Of Nile Fish (Oreochromis niloticus) ]

open access: yesJurnal Ilmiah Perikanan dan Kelautan, 2009
The chromosome manipulation in fish is one of the strategy that will be used to produce of the high generation and good quality in its genetics, as follow fast to grow, disease resistant, high survival, tolerate with environment exchange and easy to be ...
Akhmad Taufiq Mukti   +2 more
doaj   +1 more source

Chromosome breakpoint distribution of damage induced in peripheral blood lymphocytes by densely ionising radiation [PDF]

open access: yes, 2006
Purpose: To assess the chromosomal breakpoint distribution in human peripheral blood lymphocytes (PBL) after exposure to a low dose of high linear energy transfer (LET) α-particles using the technique of multiplex fluorescence in situ hybridisation (m ...
Anderson, RM   +3 more
core   +1 more source

Neuropsychological and Educational Outcomes in Shwachman–Diamond Syndrome—A Report From the North American Shwachman–Diamond Syndrome Registry

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Shwachman–Diamond syndrome (SDS) is a rare autosomal recessive ribosomopathy characterized by bone marrow failure and multisystem involvement, with emerging evidence of associated neurocognitive impairment. Methods We conducted a retrospective study of 240 individuals with biallelic Shwachman–Bodian–Diamond syndrome (SBDS) mutations
Jane Koo   +11 more
wiley   +1 more source

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