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  3. Homozygous protein C deficiency : identification of a novel missense mutation that causes impaired secretion of the mutant protein C
Homozygous protein C deficiency : identification of a novel missense mutation that causes impaired secretion of the mutant protein C
RDFデータ表示収録DB

Homozygous protein C deficiency : identification of a novel missense mutation that causes impaired secretion of the mutant protein C

利用条件: 著作権あり
人物
山本, 晃士
時間
1992年
所在
国立国会図書館デジタルコレクション

メタデータが似ているアイテム

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Identification of two novel GTP-binding protein α-subunits that lack apparent ADP-ribosylation sites for pertussis toxin

Identification and characterization of novel protein kinases involved in developmental processes

Identification and characterization of novel protein kinases involved in developmental processes

A novel point mutation in leukocyte adhesion deficiency : a Pro-178 was substituted for Leu in the highly conserved region of CD18

A novel point mutation in leukocyte adhesion deficiency : a Pro-178 was substituted for Leu in the highly conserved region of CD18

Isolation and characterization of a Chlamydomonas mutant that has a mutation in the unique gene encoding conventional actin and lacks a subset of inner-arm dynein

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Identification and characterization of novel cdc genes that regulate G1/S transition in fission yeast Schizosaccharomyces pombe

Identification and characterization of novel cdc genes that regulate G1/S transition in fission yeast Schizosaccharomyces pombe

Identification, characterization, and regulation of the proteolytic system that degrades uncomplexed SecY subunit of protein translocase in the Escherichia coli plasma membrane

Identification, characterization, and regulation of the proteolytic system that degrades uncomplexed SecY subunit of protein translocase in the Escherichia coli plasma membrane

Novel missense mutation (W686C) of the phosphofructokinase-M gene in a Japanese Patient with a mild form of glycogenosis 7

Novel missense mutation (W686C) of the phosphofructokinase-M gene in a Japanese Patient with a mild form of glycogenosis 7

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登録日: 2020-12-17

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