A. Kerrebrock

Publications15
h-index14
Citations1,917
Highly Influential Citations110
Claim Author Page
Author pages are created from data sourced from our academic publisher partnerships and public sources.

Recommended Authors

  • E. Lander
  • 789 Publications, 365,832 Citations
  • T. Orr-Weaver
  • 103 Publications, 8,633 Citations
  • M. Ashburner
  • 266 Publications, 72,008 Citations
  • S. Gerbi
  • 148 Publications, 3,733 Citations
  • Publications
  • Influence
The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries
Pudgy (pu) homozygous mice exhibit clear patterning defects at the earliest stages of somitogenesis, resulting in adult mice with severe vertebral and rib deformities. By positional cloning and… Expand
  • 269
  • 23
Disruption of the nuclear hormone receptor RORalpha in staggerer mice.
Homozygous staggerer (sg) mice show a characteristic severe cerebellar ataxia due to a cell-autonomous defect in the development of Purkinje cells. These cells show immature morphology, synaptic… Expand
  • 168
  • 17
Disruption of the nuclear hormone receptor RORα in staggerer mice
HOMOZYGOUS staggerer (sg) mice show a characteristic severe cerebellar ataxia due to a cell-autonomous defect in the development of Purkinje cells1,2. These cells show immature morphology, synaptic… Expand
  • 400
  • 12
Mei-S332, a drosophila protein required for sister-chromatid cohesion, can localize to meiotic centromere regions
Mutations in the Drosophila mei-S332 gene cause premature separation of the sister chromatids in late anaphase of meiosis I. Therefore, the mei-S332 protein was postulated to hold the centromere… Expand
  • 268
  • 12
The Drosophila mei-S332 gene promotes sister-chromatid cohesion in meiosis following kinetochore differentiation.
The Drosophila mei-S332 gene acts to maintain sister-chromatid cohesion before anaphase II of meiosis in both males and females. By isolating and analyzing seven new alleles and a deficiency… Expand
  • 160
  • 12
Serrate2 is disrupted in the mouse limb-development mutant syndactylism
The mouse syndactylism ( sm ) mutation impairs some of the earliest aspects of limb development and leads to subsequent abnormalities in digit formation. In sm homozygotes, the apical ectodermal… Expand
  • 108
  • 8
A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant
Early outgrowth of the vertebrate embryonic limb requires signalling by the apical ectodermal ridge (AER) to the progress zone (PZ), which in response proliferates and lays down the pattern of the… Expand
  • 84
  • 8
The Cohesion Protein MEI-S332 Localizes to Condensed Meiotic and Mitotic Centromeres until Sister Chromatids Separate
The Drosophila MEI-S332 protein has been shown to be required for the maintenance of sister-chromatid cohesion in male and female meiosis. The protein localizes to the centromeres during male meiosis… Expand
  • 127
  • 7
  • PDF
The vibrator Mutation Causes Neurodegeneration via Reduced Expression of PITPα: Positional Complementation Cloning and Extragenic Suppression
The mouse vibrator mutation causes an early-onset progressive action tremor, degeneration of brain stem and spinal cord neurons, and juvenile death. We cloned the vibrator mutation using an in vivo… Expand
  • 172
  • 4
Identification of the Finnish founder mutation for diastrophic dysplasia (DTD)
Diastrophic dysplasia (DTD) is especially prevalent in Finland and the existence of a founder mutation has been previously inferred from the fact that 95% of Finnish DTD chromosomes have a rare… Expand
  • 56
  • 4