Loss of function of the tuberous sclerosis 2 tumor suppressor gene results in embryonic lethality characterized by disrupted neuroepithelial growth and development

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 26, 1998, Pages 15629-15634

  Rennebeck, Gabriela ^a   Kleymenova, Elena V ^b   Anderson, Rebecca ^b   Yeung, Raymond S ^c   Artzt, Karen ^a   Walker, Cheryl L ^b  

^a UNIVERSITY OF TEXAS AT AUSTIN   (United States)

^b UNIVERSITY OF TEXAS   (United States)

^c UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MESSENGER RNA; TUBERIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; CONTROLLED STUDY; DNA SEQUENCE; EMBRYO; EMBRYO DEATH; EMBRYO DEVELOPMENT; GENE MUTATION; GENOTYPE; IN SITU HYBRIDIZATION; NEUROEPITHELIUM; NONHUMAN; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RAT; SPECIES DIFFERENCE; TUBEROUS SCLEROSIS; TUMOR SUPPRESSOR GENE;

ANIMALS; ECTODERM; EMBRYONIC AND FETAL DEVELOPMENT; EPITHELIUM; EXONS; FETAL DEATH; FETAL RESORPTION; GENES, TUMOR SUPPRESSOR; HOMOZYGOTE; MICE; OLIGONUCLEOTIDE PROBES; POLYMERASE CHAIN REACTION; RATS; RATS, INBRED F344; REPRESSOR PROTEINS; SPECIES SPECIFICITY; TUBEROUS SCLEROSIS; TUMOR SUPPRESSOR PROTEINS;

EID: 0032430266     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.26.15629     Document Type: Article

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