Kim S. McKim

Cytoplasmic localization and evolutionary conservation of MEI-218, a protein required for meiotic crossing-over in Drosophila.

subito encodes a kinesin-like protein required for meiotic spindle pole formation in Drosophila melanogaster.

mei-P22 encodes a chromosome-associated protein required for the initiation of meiotic recombination in Drosophila melanogaster.

Meiotic recombination and chromosome segregation in Drosophila females.

The Synaptonemal complex component C(2)M regulates meiotic crossing over in Drosophila.

Relationship of DNA double-strand breaks to synapsis in Drosophila.

Meiotic recombination in Drosophila females depends on chromosome continuity between genetically defined boundaries.

Juxtaposition of C(2)M and the transverse filament protein C(3)G within the central region of Drosophila synaptonemal complex.

All paired up with no place to go: pairing, synapsis, and DSB formation in a balancer heterozygote.

When size does not matter: pairing sites during meiosis.

The Drosophila calcipressin sarah is required for several aspects of egg activation.

Kinesin 6 family member Subito participates in mitotic spindle assembly and interacts with mitotic regulators.

When specialized sites are important for synapsis and the distribution of crossovers.

Misregulation of the kinesin-like protein Subito induces meiotic spindle formation in the absence of chromosomes and centrosomes.

Spindle assembly in the oocytes of mouse and Drosophila--similar solutions to a problem.

mei-38 is required for chromosome segregation during meiosis in Drosophila females.

Drosophila PCH2 is required for a pachytene checkpoint that monitors double-strand-break-independent events leading to meiotic crossover formation.

Drosophila hold'em is required for a subset of meiotic crossovers and interacts with the dna repair endonuclease complex subunits MEI-9 and ERCC1.

Cytological analysis of meiosis in fixed Drosophila ovaries.

Chromosome axis defects induce a checkpoint-mediated delay and interchromosomal effect on crossing over during Drosophila meiosis.

Drosophila I-R hybrid dysgenesis is associated with catastrophic meiosis and abnormal zygote formation.

Meiotic checkpoints and the interchromosomal effect on crossing over in Drosophila females.

Drosophila ATM and ATR have distinct activities in the regulation of meiotic DNA damage and repair.

A pathway for synapsis initiation during zygotene in Drosophila oocytes.

Multiple barriers to nonhomologous DNA end joining during meiosis in Drosophila.

The chromosomal passenger complex is required for meiotic acentrosomal spindle assembly and chromosome biorientation.

Microtubule-depolymerizing kinesin KLP10A restricts the length of the acentrosomal meiotic spindle in Drosophila females.

Lateral and End-On Kinetochore Attachments Are Coordinated to Achieve Bi-orientation in Drosophila Oocytes.

Spindle Assembly and Chromosome Segregation Requires Central Spindle Proteins in Drosophila Oocytes.

The microtubule catastrophe promoter Sentin delays stable kinetochore-microtubule attachment in oocytes.

Dynamic and Stable Cohesins Regulate Synaptonemal Complex Assembly and Chromosome Segregation.