Functional genetic analysis of mouse chromosome 11 (Q28204984)

Neil Box

7

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Benjamin T. Kile

Benjamin T Kile

1

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Randy L Johnson

9

Randy L Johnson

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Richard R. Behringer

10

Richard R Behringer

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author name string

Kathryn E Hentges

2

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Amander T Clark

3

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Hisashi Nakamura

4

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Andrew P Salinger

5

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David W Stockton

8

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Allan Bradley

11

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Monica J Justice

Initial sequencing and comparative analysis of the mouse genome

12

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language of work or name

English

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publication date

4 September 2003

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published in

Nature

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volume

425

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issue

6953

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page(s)

81-6

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cites work

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Initial sequencing and analysis of the human genome

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Engineering a mouse balancer chromosome

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A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements in mice

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A phenotype-based screen for embryonic lethal mutations in the mouse

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Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis

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Systematic functional analysis of the Caenorhabditis elegans genome using RNAi

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The role of the genome project in determining gene function: insights from model organisms

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Saturation germ line mutagenesis of the murine t region including a lethal allele at the quaking locus

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What cardiovascular defect does my prenatal mouse mutant have, and why?

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Determination of anteroposterior polarity in Drosophila

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Dose-repetition increases the mutagenic effectiveness of N-ethyl-N-nitrosourea in mouse spermatogonia

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Requirement for Lim1 in head-organizer function

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Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

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New member of the winged-helix protein family disrupted in mouse and rat nude mutations

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Mutations affecting the pattern of the larval cuticle inDrosophila melanogaster : I. Zygotic loci on the second chromosome

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Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton

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Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton

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Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis

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Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene

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Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

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Sex and strain-related differences in the peripheral blood cell values of inbred mouse strains

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Quaking is essential for blood vessel development

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