Sentence examples for abnormality in which from inspiring English sources

Exact(16)

Using S. pombe, we revealed a new activity of Int6 — regulation of the 26S proteasome [ 7], abnormality in which increases levels of cyclin and securin, leading to abnormal mitosis and chromosome instability.

It is a sexual abnormality in which the preferred object of the potential predator is a child, though the pedophile or less frequently used pedophiliac is not required to act on that perversion.

Shed by the yolk sac and fetal liver, alpha-fetoprotein can be used to screen for neural tube defects such as anencephaly and spina bifida (developmental abnormality in which spinal cord is not fully enclosed).

Myopia, also called nearsightedness, visual abnormality in which the resting eye focuses the image of a distant object at a point in front of the retina (the light-sensitive layer of tissue that lines the back and sides of the eye), resulting in a blurred image.

Hyperopia, also called farsightedness, refractive error or abnormality in which the cornea and lens of the eye focus the image of the visual field at an imaginary point behind the retina (the light-sensitive layer of tissue lining the back and sides of the eye).

Bronchial hyper-responsiveness (BHR) describes a lung abnormality in which airways are easily triggered to constrict in response to normally harmless inhaled stimuli, and is a key element of human asthma pathophysiology.

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Similar(44)

Our results suggest that human blastocysts alter the endometrial epithelial adhesion, the initiating event of implantation, via the secretion of miR, abnormalities in which result in implantation failure.

Many human genetic disorders result from unbalanced chromosome abnormalities, in which there is a net gain or loss of genetic material.

Our findings emphasise the important role that human blastocysts have on regulating the very early stages of implantation, adhesion, abnormalities in which lead to implantation failure and infertility.

PCR-based protocols with short tandem repeat markers have recently also been applied in PGD cycles for structural chromosome abnormalities, in which FISH has been traditionally the preferred method [ 31, 32].

As such the findings may not be applicable to children, older cohorts, or individuals with gait abnormalities in which spatiotemporal parameters may vary markedly and faster or slower gait speeds are common [ 25, 34].

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