Pages that link to "Q52500623"

The following pages link to A gene controlling condensation of heterochromatin in Drosophila melanogaster (Q52500623):

Displaying 26 items.

• The cellular basis of hybrid dysgenesis and Stellate regulation in Drosophila (Q26785476) (← links)
• BRCT domain-containing protein TopBP1 functions in DNA replication and damage response (Q28200771) (← links)
• TopBP1 localises to centrosomes in mitosis and to chromosome cores in meiosis (Q28261299) (← links)
• Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome (Q33592534) (← links)
• Mutations in genes encoding essential mitotic functions in Drosophila melanogaster (Q33951102) (← links)
• Identification of genomic regions required for DNA replication during Drosophila embryogenesis. (Q33961893) (← links)
• Mutagen sensitivity and suppression of position-effect variegation result from mutations in mus209, the Drosophila gene encoding PCNA. (Q34322170) (← links)
• Systematic, RNA-interference-mediated identification of mus-101 modifier genes in Caenorhabditis elegans (Q34572464) (← links)
• The Drosophila mus101 gene, which links DNA repair, replication and condensation of heterochromatin in mitosis, encodes a protein with seven BRCA1 C-terminus domains (Q34610522) (← links)
• A large-scale screen for mutagen-sensitive loci in Drosophila. (Q34644806) (← links)
• Trans-acting amplification mutants and other eggshell mutants of the third chromosome in Drosophila melanogaster (Q35605443) (← links)
• Sequence-directed curvature of repetitive AluI DNA in constitutive heterochromatin of Artemia franciscana (Q36263066) (← links)
• Looking at Drosophila mitotic chromosomes (Q36699171) (← links)
• DNA Repair in Drosophila: Mutagens, Models, and Missing Genes (Q39116605) (← links)
• Somatic cell hybridization of roberts syndrome and normal lymphoblasts resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypes (Q41145920) (← links)
• Morphology and Structure of Polytene Chromosomes (Q41624502) (← links)
• Polytene Chromosomes, Heterochromatin, and Position Effect Variegation (Q41628631) (← links)
• Loss of Drosophila Myb interrupts the progression of chromosome condensation (Q47070245) (← links)
• Broad‐Complex function during oogenesis in Drosophila melanogaster (Q48194221) (← links)
• Heteropycnosis of an underreplicating chromosome (Q49030435) (← links)
• Molecular studies on interspersed repetitive and unique sequences in the region of the complementation group uncoordinated on the X chromosome of Drosophila melanogaster (Q52455937) (← links)
• 7 Genetic Analysis of Cell Division in Drosophila (Q63481303) (← links)
• Antibodies to defined histone epitopes reveal variations in chromatin conformation and underacetylation of centric heterochromatin in human metaphase chromosomes (Q67535242) (← links)
• Nucleotide variation and molecular structure of the heterochromatic repetitive AluI DNA in the brine shrimp Artemia franciscana (Q67976950) (← links)
• Biochemical formulations of embryonic gene control (Q72091118) (← links)
• The processivity factor Pol32 mediates nuclear localization of DNA polymerase delta and prevents chromosomal fragile site formation in Drosophila development (Q92113016) (← links)