Information om | Engelska ordet XXY

Exempel på hur man kan använda XXY i en mening

• The forensic report speculated that Dillema developed from a zygote with an XXY genotype that promptly divided into a half XX, half XY embryo through nondisjunction.
• Male calicoes can happen when a male cat has two X chromosomes (Klinefelter syndrome, with XXY sex chromosomes and generally they are sterile); the condition is a chimera, with two different cell types.
• Because the structure of this motif contains 2 adjacent 3-nucleotide repeats it is believed that −1 frameshifting is described by a tandem slippage model, in which the ribosomal P-site tRNA anticodon re-pairs from XXY to XXX and the A-site anticodon re-pairs from YYH to YYY simultaneously.
• They have provided distribution for many films such as Weekend, Tomboy, XXY, Eyes Wide Open, Four Minutes, The Blossoming of Maximo Oliveros, Transylvania, Cockles and Muscles, Summer Storm, The Guest House and Chemsex.
• It demonstrated that males with XXY tend to be quiet, shy and undemanding; they are less self-confident, less active, and more helpful and obedient than other children their age.
• Very rarely (approximately 1 in 3,000) a male tortoiseshell or calico is born; these typically have an extra X chromosome (XXY), a condition known in humans as Klinefelter syndrome, and their cells undergo an X-inactivation process like in females.
• Because loss of NEMO function is lethal, only heterozygous females or males with XXY karyotype or mosaicism for this gene survive and exhibit symptoms of incontinetia pigmenti, such as skin lesions and abnormalities in hair, teeth, and nails.
• In terms of intersex and film studies, Raphaël Jullien compared Being Impossible to the Argentinian film XXY, also about an intersex youth, saying that XXYs power lies in the suspense of not knowing Alex's troubles, whereas Being Impossible "annihilates any suspense" by placing testimonies from people of non-conforming gender identity at the start of the film.
• Since 2014, noninvasive testing has identified aneuploidies in chromosomes 13, 16, 18, 21, 22, X and Y, including Down syndrome (caused by trisomy 21), Edwards syndrome (caused by trisomy 18), Patau syndrome (caused by trisomy 13), as well as sex chromosome aneuploidies, such as Turner syndrome (45, X) and Klinefelter syndrome (47, XXY).

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