Wee1 kinase: a potential target to overcome tumor resistance to therapy

F Esposito, R Giuffrida, G Raciti, C Puglisi… - International Journal of …, 2021 - mdpi.com
During the cell cycle, DNA suffers several lesions that need to be repaired prior to entry into
mitosis to preserve genome integrity in daughter cells. Toward this aim, cells have …

[HTML][HTML] The clinical significance of Cyclin B1 and Wee1 expression innon-small-cell lung cancer

T Yoshida, S Tanaka, A Mogi, Y Shitara, H Kuwano - Annals of oncology, 2004 - Elsevier
Background: Cyclin B1 has an important role in the G 2–M phase transition of the cell cycle.
Wee1 delays mitosis by suppressing the activity of the Cyclin B1/cdc2 complex. The …

Coordination of cell cycle exit and differentiation of neuronal progenitors

PK Politis, D Thomaidou, R Matsas - Cell cycle, 2008 - Taylor & Francis
During development, co-ordinate regulation of cell cycle exit and differentiation of neuronal
precursors is essential for generation of appropriate number of neurons and proper wiring of …

[PDF][PDF] Building human genome maps with radiation hybrids

D Slonim, L Kruglyak, L Stein, E Lander - Proceedings of the first annual …, 1997 - dl.acm.org
Genome maps are crucial tools in human genetic research, providing known landmarks for
locating disease genes and frameworks for large-scale sequencing. Radiation hybrid …

A radiation hybrid map of 506 STS markers spanning human chromosome 11

MR James, CW Richard III, JJ Schott, C Yousry… - Nature …, 1994 - nature.com
We present a high resolution radiation hybrid map of human chromosome 11 using 506
sequence tagged sites (STSs) scored on a panel of 86 radiation hybrids. The 506 STSs fall …

Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies

A Pàldi, G Gyapay, J Jami - Current biology, 1995 - cell.com
Background: Meiotic recombination events do not occur randomly along a chromosome, but
appear to be restricted to specific regions. In addition, some regions in the genome undergo …

Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy.

PM Thomas, GJ Cote, DM Hallman… - American journal of …, 1995 - ncbi.nlm.nih.gov
Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare, autosomal
recessive disease of unregulated insulin secretion, defined by elevations in serum insulin …

Activation of extracellular signal-regulated kinase 2 by a novel Abl-binding protein, ST5

M Majidi, AE Hubbs, JH Lichy - Journal of Biological Chemistry, 1998 - ASBMB
The human ST5 gene encodes three proteins with predicted molecular masses of 126, 82,
and 70 kDa. These widely expressed proteins share a C-terminal region that bears …

Double stellate tongue reduction: a new method of treatment for macroglossia in patients with Beckwith-wiedemann syndrome

PC Hettinger, AD Denny - Annals of plastic surgery, 2011 - journals.lww.com
Background: Although multiple methods of tongue reduction have been described, recent
literature suggests that the central reductions may be more favorable in patients with …

Localization of a tumor suppressor gene in 11p15. 5 using the G401 Wilms' tumor assay

LH Reid, A West, DG Gioeli, KK Phillips… - Human molecular …, 1996 - academic.oup.com
Multiple studies have underscored the importance of loss of tumor suppressor genes in the
development of human cancer. To identify these genes, we used somatic cell hybrids in a …