Sentence examples for diverse abnormalities from inspiring English sources

The complete reprogramming required for normal development is induced in only a few cases; consequently, faulty epigenetic changes accompanied by diverse abnormalities in the development of somatic/embryonic stem cell nuclear transferred (SECNT) embryos occur very frequently [13], [14], [15], [16], [17], [18].

Therefore, different alterations in pathways controlling microtubule stability may lead to diverse abnormalities in interneuron leading process dynamics.

EEG and MRI data are autonomous sets of variables used to exemplify diverse abnormalities of the region of brain from where seizure initiates.

Surprisingly, SEMA3A is present in both affected networks of MDS-RARS stromal cells (see Additional file 2), suggesting participation of this gene in diverse abnormalities implicated in the modification of hematopoietic cells development and apoptosis in MDS [ 12, 13].

Our study of a cohort of 30 fetuses with diverse abnormalities has allowed us to estimate the current diagnostic yield of exome sequencing for fetal abnormalities as being broadly equivalent to aCGH, which is ∼10% (2– 4).

This condition leads to loss of subcutaneous fat and is associated with diverse metabolic abnormalities such as dyslipidemia, abnormal leptin levels, insulin resistance and overt diabetes.

Next generation sequencing (NGS) analysis of DLBCL has facilitated global identification of numerous and diverse genetic abnormalities in these neoplasms and has shown that GCB and ABC tumours have different mutation profiles.

Although cloned embryos generated by somatic/embryonic stem cell nuclear transfer (SECNT) certainly give rise to viable individuals, they can often undergo embryonic arrest at any stage of embryogenesis, leading to diverse morphological abnormalities.

However, HHV-8-infected patients with diverse immunologic abnormalities [ 3, 4], such as those with the human immunodeficiency virus (HIV) infection, can develop KS.

Fanconi anemia (FA) is an autosomal recessive disorder characterized by diverse developmental abnormalities, progressive bone marrow failure, and a markedly increased incidence of malignancy.

We performed exome sequencing on a cohort of 30 non-aneuploid fetuses and neonates (along with their parents) with diverse structural abnormalities first identified by prenatal ultrasound.