Genomics boosts mouse molecular genetics

Trends in Genetics

Volumn 17, Issue 12, 2001, Pages 691-692

  Birchmeier, Carmen ^a   Treier, Mathias ^b  

^a MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

^b EUROPEAN MOLECULAR BIOLOGY LABORATORY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA;

ANIMAL MODEL; CHROMOSOME MAP; CIRCADIAN RHYTHM; CONFERENCE PAPER; DISEASE MODEL; GENE FUNCTION; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MOLECULAR GENETICS; MORPHOGENESIS; NONHUMAN; OSTEOPOROSIS; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ANIMALS; DISEASE MODELS, ANIMAL; DNA TRANSPOSABLE ELEMENTS; EMBRYONIC INDUCTION; GENOMICS; HUMANS; MICE; MICE, MUTANT STRAINS; MOLECULAR BIOLOGY; MUTAGENESIS;

ANIMALIA; RODENTIA;

EID: 0035576884     PISSN: 01689525     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-9525(01)02516-1     Document Type: Conference Paper

References (9)

1. Functional annotation of a full-length mouse cDNA collection
2. Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defect observed in leaden mice
3. Loss of the CIC-7 chloride channel leads to osteopetrosis in mice and man
4. Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
5. Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice
6. Topographic mapping from the retina to the midbrain is controlled by relative but not absolute levels of EphA receptor signaling
7. Efficient chromosomal transposition of a Tc1/mariner- like transposon Sleeping Beauty in mice
8. Transposition and gene disruption in the male germline of the mouse
9. Hybrid vigor, fetal overgrowth, and viability of mice derived by nuclear cloning and tetraploid embryo complementation