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An arginine to glutamine mutation in residue 109 of human ornithine transcarbamylase completely abolishes enzymatic activity in Cos1 cellsCircadian genes in a blind subterranean mammal II: conservation and uniqueness of the three Period homologs in the blind subterranean mole rat, Spalax ehrenbergi superspeciesBiological clock in total darkness: the Clock/MOP3 circadian system of the blind subterranean mole ratMolecular basis of AMP deaminase deficiency in skeletal muscleScanning detection of mutations in human ornithine transcarbamoylase by chemical mismatch cleavageImpaired novelty acquisition and synaptic plasticity in congenital hyperammonemia caused by hepatic glutamine synthetase deficiencyDisparate tissue-specific expression of members of the tissue kallikrein multigene family of the ratAmmonia toxicity to the brain.Neurological implications of urea cycle disordersMice with a deletion in the gene for CCAAT/enhancer-binding protein beta have an attenuated response to cAMP and impaired carbohydrate metabolism.Analysis of genetic variability and mapping of point mutations in influenza virus by the RNase A mismatch cleavage methodDifferent structures in the amino-terminal domain of the ornithine transcarbamylase leader peptide are involved in mitochondrial import and carboxyl-terminal cleavage.Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA.Survey of amino-terminal proteolytic cleavage sites in mitochondrial precursor proteins: leader peptides cleaved by two matrix proteases share a three-amino acid motifThe spfash mouse: a missense mutation in the ornithine transcarbamylase gene also causes aberrant mRNA splicing.Gene expression profiling of astrocytes from hyperammonemic mice reveals altered pathways for water and potassium homeostasis in vivo.Absence of measles viral genomic sequence in intestinal tissues from Crohn's disease by nested polymerase chain reaction.A new imprinted gene cloned by a methylation-sensitive genome scanning methodDetection of single DNA base differences by competitive oligonucleotide primingFunctional characterization of the spf/ash splicing variation in OTC deficiency of mice and man.Experimental and clinical applications of molecular cell biology in nutrition and metabolism.Catabolic ornithine transcarbamylase of Halobacterium halobium (salinarium): purification, characterization, sequence determination, and evolution.Characterization of point mutations in the same arginine codon in three unrelated patients with ornithine transcarbamylase deficiency.An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.Correction of mouse ornithine transcarbamylase deficiency by gene transfer into the germ lineEfficient mitochondrial import of newly synthesized ornithine transcarbamylase (OTC) and correction of secondary metabolic alterations in spf(ash) mice following gene therapy of OTC deficiency.Identification of an embryonic isoform of myelin basic protein that is expressed widely in the mouse embryo.Transgenic mouse model for central nervous system demyelination.Low level of Hox1.3 gene expression does not preclude the use of promoterless vectors to generate a targeted gene disruption. off.Contrasting features of urea cycle disorders in human patients and knockout mouse models.Cytokine gene expression in aortic adventitial inflammation associated with advanced atherosclerosis (chronic periaortitis).Defective ureagenesis in mice carrying a liver-specific disruption of hepatocyte nuclear factor 4alpha (HNF4alpha ). HNF4alpha regulates ornithine transcarbamylase in vivo.The polymerase chain reaction in pathology.Selective amplification of RNA utilizing the nucleotide analog dITP and Thermus thermophilus DNA polymeraseGenetic diversity of Desulfovibrio spp. in environmental samples analyzed by denaturing gradient gel electrophoresis of [NiFe] hydrogenase gene fragments.Origin, structure, and regulation of argK, encoding the phaseolotoxin-resistant ornithine carbamoyltransferase in Pseudomonas syringae pv. phaseolicola, and functional expression of argK in transgenic tobacco.The molecular detection of circulating tumour cellsStructural organization and differential expression of rice alpha-amylase genes.The genetic structure of mouse ornithine transcarbamylase.Oral susceptibility of Aedes albopictus to dengue type 2 virus: a study of infection kinetics, using the polymerase chain reaction for viral detection.
P2860
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P2860
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年学术文章
@wuu
1987年学术文章
@zh-cn
1987年学术文章
@zh-hans
1987年学术文章
@zh-my
1987年学术文章
@zh-sg
1987年學術文章
@yue
1987年學術文章
@zh
1987年學術文章
@zh-hant
name
The molecular basis of the sparse fur mouse mutation.
@ast
The molecular basis of the sparse fur mouse mutation.
@en
type
label
The molecular basis of the sparse fur mouse mutation.
@ast
The molecular basis of the sparse fur mouse mutation.
@en
prefLabel
The molecular basis of the sparse fur mouse mutation.
@ast
The molecular basis of the sparse fur mouse mutation.
@en
P2093
P356
P1433
P1476
The molecular basis of the sparse fur mouse mutation.
@en
P2093
P304
P356
10.1126/SCIENCE.3603027
P407
P577
1987-07-01T00:00:00Z