Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.

瘦(leptin)是肥胖(ob)编码，脂肪细胞分泌一种内源性激，调控体重和脂肪分布。

All the C3 allotype was C3S.The gene frequency was 1.

而且所有第三补体异型均为C3S，而此频率为1。

Gene mutations are alterations in the DNA code.

突变是指DNA 密码改变。

The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.

干细胞白血病(CL)是新发现与白血病发生有关癌。

Without this, you are reducing your chances of concentrating the genes of the linebred ancestor.

没有这种选择，你就正在降低强调在血系内繁殖中祖先机会。

Through similar and supplementary action , polygenes can have important effects on total variability.

通过相同和添加作用，多可以对总变异起重大影响。

That genal genome may lead to better treatment and control of diseaesthe disease.

那些组能带来比较好治疗和疾病控制。

Most of these genes have not been reported to relate to the haematogenesis in ontogeny.

这些大多数在胚胎分化造血发育中作用尚未见报道。

You have good genes from your parents, so you should live a long time.

你从父母那儿获得优良, 所以能够活得很长。

Genes tabA， tabB，tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.

野火氨酸合成有tabA，tabB，talA，dapB等参与，受lemA调控。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与脱辅蛋白结合松弛、易于与之分离辅称为辅。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病，实验动物模型是一个非常好方式。

Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).

而纤毛虫和蚊粘液所表现出整合则是一些例外。

Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.

目前研究热点还包括：-环境相互作用、遗传药理学、咨询等。

There is also GMO zucchini, crookneck squash, papaya, and alfalfa.

也有转南瓜、转葫芦、转木瓜和转苜蓿。

Researchers are gradually deciphering the genetic structure found in the cells of organisms.

研究者正渐渐破译存于有机体细胞内结构。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认型测定结果。

Evidence is accumulating that a defective gene may be responsible for this disease.

越来越多证据表明该疾病是由一种有缺陷引起。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转事物极大潜力。

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫在男性较少见是否由于X染色头感光色变异？

Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.

瘦素(leptin)是肥胖因(ob因)编码，脂肪细胞分泌一种内源性激素，主要调控体重和脂肪分布。

All the C3 allotype was C3S.The gene frequency was 1.

而且所有第三补体异型均为C3S，而此因频率为1。

Gene mutations are alterations in the DNA code.

因突变是指DNA 密码改变。

The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.

干细胞白血病(CL)因是新发现与白血病发生有关因。

Without this, you are reducing your chances of concentrating the genes of the linebred ancestor.

没有这种选择，你就正在降低强调在血系内繁殖中祖先因机会。

Through similar and supplementary action , polygenes can have important effects on total variability.

通过相同和添加作，多因可以对总变异起重大影响。

That genal genome may lead to better treatment and control of diseaesthe disease.

那些因组能带来比较好治疗和疾病控制。

Most of these genes have not been reported to relate to the haematogenesis in ontogeny.

这些因大多数在胚胎分化造血发育中作见报道。

You have good genes from your parents, so you should live a long time.

你从父母那儿获得优良因, 所以能够活得很长。

Genes tabA， tabB，tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.

野火氨酸合成有tabA，tabB，talA，dapB等因参与，受lemA因调控。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与脱辅蛋白结合松弛、易于与之分离辅因子称为辅。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病因，实验动物模型是一个非常好方式。

Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).

而纤毛虫和蚊子粘液素因所表现出因整合则是一些例外。

Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.

目前研究热点还包括：因-环境相互作、遗传药理学、因咨询等。

There is also GMO zucchini, crookneck squash, papaya, and alfalfa.

也有转因南瓜、转因葫芦、转因木瓜和转因苜蓿。

Researchers are gradually deciphering the genetic structure found in the cells of organisms.

研究者正渐渐破译存于有机体细胞内因结构。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采双脱氧DNA链合成终止法进行PCR产物直接测序,确认因型测定结果。

Evidence is accumulating that a defective gene may be responsible for this disease.

越来越多证据表明该疾病是由一种有缺陷因引起。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转因事物极大潜力。

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫在男性较少见是否由于X染色头感光色素因变异？

Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.

瘦素(leptin)是肥胖基(ob基)编码，脂肪细胞分泌一种内源性激素，主要控体重和脂肪分布。

All the C3 allotype was C3S.The gene frequency was 1.

而且所有第三补体异型均为C3S，而此基频率为1。

Gene mutations are alterations in the DNA code.

基突变是指DNA 密码改变。

The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.

干细胞白血病(CL)是新发现与白血病发生有关癌基。

Without this, you are reducing your chances of concentrating the genes of the linebred ancestor.

没有这种选择，你就正降低血系内繁殖中祖先基机会。

Through similar and supplementary action , polygenes can have important effects on total variability.

通过相同和添加作用，基可以对总变异起重影响。

That genal genome may lead to better treatment and control of diseaesthe disease.

那些基组能带来比较好治疗和疾病控制。

Most of these genes have not been reported to relate to the haematogenesis in ontogeny.

这些基数胚胎分化造血发育中作用尚未见报道。

You have good genes from your parents, so you should live a long time.

你从父母那儿获得优良基, 所以能够活得很长。

Genes tabA， tabB，tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.

野火氨酸合成有tabA，tabB，talA，dapB等基参与，受lemA基控。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与脱辅基蛋白结合松弛、易于与之分离辅基子称为辅。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病基，实验动物模型是一个非常好方式。

Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).

而纤毛虫和蚊子粘液素基所表现出基整合则是一些例外。

Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.

目前研究热点还包括：基-环境相互作用、遗传药理学、基咨询等。

There is also GMO zucchini, crookneck squash, papaya, and alfalfa.

也有转基南瓜、转基葫芦、转基木瓜和转基苜蓿。

Researchers are gradually deciphering the genetic structure found in the cells of organisms.

研究者正渐渐破译存于有机体细胞内基结构。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认基型测定结果。

Evidence is accumulating that a defective gene may be responsible for this disease.

越来越证据表明该疾病是由一种有缺陷基引起。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转基事物极潜力。

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫男性较少见是否由于X染色头感光色素基变异？

Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.

瘦素(leptin)是肥胖基因(ob基因)编码，脂肪细胞分泌一种内源性激素，主要调控体重和脂肪分布。

All the C3 allotype was C3S.The gene frequency was 1.

而且所有第三补体型均为C3S，而此基因频率为1。

Gene mutations are alterations in the DNA code.

基因突是指DNA 密码改。

The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.

干细胞白血病(CL)因是新发现与白血病发生有关癌基因。

Without this, you are reducing your chances of concentrating the genes of the linebred ancestor.

没有这种选择，你就正在降低强调在血系内繁殖中祖先基因机会。

Through similar and supplementary action , polygenes can have important effects on total variability.

通过相同和添加作用，多基因可以起重大影响。

That genal genome may lead to better treatment and control of diseaesthe disease.

那些基因组能带来比较好治疗和疾病控制。

Most of these genes have not been reported to relate to the haematogenesis in ontogeny.

这些基因大多数在胚胎分化造血发育中作用尚未见报道。

You have good genes from your parents, so you should live a long time.

你从父母那儿获得优良基因, 所以能够活得很长。

Genes tabA， tabB，tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.

野火氨酸合成有tabA，tabB，talA，dapB等基因参与，受lemA基因调控。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与脱辅基蛋白结合松弛、易于与之分离辅基因子称为辅。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病基因，实验动物模型是一个非常好方式。

Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).

而纤毛虫和蚊子粘液素基因所表现出基因整合则是一些例外。

Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.

目前研究热点还包括：基因-环境相互作用、遗传药理学、基因咨询等。

There is also GMO zucchini, crookneck squash, papaya, and alfalfa.

也有转基因南瓜、转基因葫芦、转基因木瓜和转基因苜蓿。

Researchers are gradually deciphering the genetic structure found in the cells of organisms.

研究者正渐渐破译存于有机体细胞内基因结构。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认基因型测定结果。

Evidence is accumulating that a defective gene may be responsible for this disease.

越来越多证据表明该疾病是由一种有缺陷基因引起。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转基因事物极大潜力。

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫在男性较少见是否由于X染色头感光色素基因？

Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.

瘦素(leptin)是肥胖基因(ob基因)编码，脂肪细胞分泌一种内源性激素，主要调控体重脂肪分布。

All the C3 allotype was C3S.The gene frequency was 1.

而且所有第三补体异型均为C3S，而此基因频率为1。

Gene mutations are alterations in the DNA code.

基因突变是指DNA 密码改变。

The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.

干细胞白血病(CL)因是新发现与白血病发生有关癌基因。

Without this, you are reducing your chances of concentrating the genes of the linebred ancestor.

没有这种选择，你就正在降低强调在血系内繁殖中祖先基因机会。

Through similar and supplementary action , polygenes can have important effects on total variability.

通过相同添加作用，多基因可以对总变异起重大影响。

That genal genome may lead to better treatment and control of diseaesthe disease.

那些基因组能带来比较好治疗疾病控制。

Most of these genes have not been reported to relate to the haematogenesis in ontogeny.

这些基因大多数在胚胎分化造血发育中作用尚未见报道。

You have good genes from your parents, so you should live a long time.

你从父母那儿获得优良基因, 所以能够活得很长。

Genes tabA， tabB，tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.

野火氨酸合成有tabA，tabB，talA，dapB等基因参与，受lemA基因调控。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与脱辅基蛋白结合松弛、易于与之分离辅基因子称为辅。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病基因，实验动物模型是一个非常好方式。

Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).

而纤蚊子粘液素基因所表现出基因整合则是一些例外。

Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.

目前研究热点还包括：基因-环境相互作用、遗传药理学、基因咨询等。

There is also GMO zucchini, crookneck squash, papaya, and alfalfa.

也有转基因南瓜、转基因葫芦、转基因木瓜转基因苜蓿。

Researchers are gradually deciphering the genetic structure found in the cells of organisms.

研究者正渐渐破译存于有机体细胞内基因结构。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认基因型测定结果。

Evidence is accumulating that a defective gene may be responsible for this disease.

越来越多证据表明该疾病是由一种有缺陷基因引起。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转基因事物极大潜力。

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫在男性较少见是否由于X染色头感光色素基因变异？

Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.

瘦素(leptin)是肥胖(ob)编码，脂肪细胞分泌一种内源性激素，主要调控体重和脂肪分布。

All the C3 allotype was C3S.The gene frequency was 1.

而且所有第三补体异型均为C3S，而此频率为1。

Gene mutations are alterations in the DNA code.

突变是指DNA 密码改变。

The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.

干细胞白血病(CL)是新发现与白血病发生有关癌。

Without this, you are reducing your chances of concentrating the genes of the linebred ancestor.

没有这种选择，你就正在降低强调在血系内繁殖中祖先机会。

Through similar and supplementary action , polygenes can have important effects on total variability.

通过相同和添加作用，多可以对总变异起重大影响。

That genal genome may lead to better treatment and control of diseaesthe disease.

那些组能带来比较好治疗和疾病控制。

Most of these genes have not been reported to relate to the haematogenesis in ontogeny.

这些大多数在胚胎分化造血发育中作用尚未见报道。

You have good genes from your parents, so you should live a long time.

你从父母那儿获得优良, 所以能够活得很长。

Genes tabA， tabB，tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.

野火氨酸合成有tabA，tabB，talA，dapB等参与，受lemA调控。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与脱辅蛋白结合松弛、易于与之分离辅子称为辅。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病，物模型是一个非常好方式。

Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).

而纤毛虫和蚊子粘液素所表现出整合则是一些例外。

Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.

目前研究热点还包括：-环境相互作用、遗传药理学、咨询等。

There is also GMO zucchini, crookneck squash, papaya, and alfalfa.

也有转南瓜、转葫芦、转木瓜和转苜蓿。

Researchers are gradually deciphering the genetic structure found in the cells of organisms.

研究者正渐渐破译存于有机体细胞内结构。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认型测定结果。

Evidence is accumulating that a defective gene may be responsible for this disease.

越来越多证据表明该疾病是由一种有缺陷引起。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转事物极大潜力。

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫在男性较少见是否由于X染色头感光色素变异？

Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.

瘦素(leptin)是肥胖(ob)编码，脂肪细胞分泌一种内源性激素，主要调控体重脂肪分布。

All the C3 allotype was C3S.The gene frequency was 1.

而且所有第三补体异型均为C3S，而此频率为1。

Gene mutations are alterations in the DNA code.

突变是指DNA 密码改变。

The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.

干细胞白血病(CL)是新发现与白血病发生有关癌。

Without this, you are reducing your chances of concentrating the genes of the linebred ancestor.

没有这种选择，你就正在降低强调在血系内繁殖中祖先机会。

Through similar and supplementary action , polygenes can have important effects on total variability.

通过相同添加作用，多可以对总变异起重大影响。

That genal genome may lead to better treatment and control of diseaesthe disease.

那些组能带来比较好疾病控制。

Most of these genes have not been reported to relate to the haematogenesis in ontogeny.

这些大多数在胚胎分化造血发育中作用尚未见报道。

You have good genes from your parents, so you should live a long time.

你从父母那儿获得优良, 所以能够活得很长。

Genes tabA， tabB，tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.

野火氨酸合成有tabA，tabB，talA，dapB等参与，受lemA调控。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与脱辅蛋白结合松弛、易于与之分离辅子称为辅。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病，实验动物模型是一个非常好方式。

Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).

而纤毛虫蚊子粘液素所表现出整合则是一些例外。

Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.

目前研究热点还包括：-环境相互作用、遗传药理学、咨询等。

There is also GMO zucchini, crookneck squash, papaya, and alfalfa.

也有转南瓜、转葫芦、转木瓜转苜蓿。

Researchers are gradually deciphering the genetic structure found in the cells of organisms.

研究者正渐渐破译存于有机体细胞内结构。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认型测定结果。

Evidence is accumulating that a defective gene may be responsible for this disease.

越来越多证据表明该疾病是由一种有缺陷引起。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转事物极大潜力。

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫在男性较少见是否由于X染色头感光色素变异？

Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.

瘦素(leptin)是肥胖基因(ob基因)编码，脂肪细胞分泌一种内源性激素，主要调控体重和脂肪分布。

All the C3 allotype was C3S.The gene frequency was 1.

而且所有第三补体异型均为C3S，而此基因频率为1。

Gene mutations are alterations in the DNA code.

基因突变是指DNA 密码改变。

The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.

干细胞白血病(CL)因是新发现与白血病发生有关癌基因。

Without this, you are reducing your chances of concentrating the genes of the linebred ancestor.

没有这种选择，你就正在降低强调在血系内繁殖中祖先基因机。

Through similar and supplementary action , polygenes can have important effects on total variability.

相同和添加作用，多基因可以对总变异起重大影响。

That genal genome may lead to better treatment and control of diseaesthe disease.

那些基因组能带来治疗和疾病控制。

Most of these genes have not been reported to relate to the haematogenesis in ontogeny.

这些基因大多数在胚胎分化造血发育中作用尚未见报道。

You have good genes from your parents, so you should live a long time.

你从父母那儿获得优良基因, 所以能够活得很长。

Genes tabA， tabB，tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.

野火氨酸合成有tabA，tabB，talA，dapB等基因参与，受lemA基因调控。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与脱辅基蛋白结合松弛、易于与之分离辅基因子称为辅。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病基因，实验动物模型是一个非常方式。

Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).

而纤毛虫和蚊子粘液素基因所表现出基因整合则是一些例外。

Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.

目前研究热点还包括：基因-环境相互作用、遗传药理学、基因咨询等。

There is also GMO zucchini, crookneck squash, papaya, and alfalfa.

也有转基因南瓜、转基因葫芦、转基因木瓜和转基因苜蓿。

Researchers are gradually deciphering the genetic structure found in the cells of organisms.

研究者正渐渐破译存于有机体细胞内基因结构。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认基因型测定结果。

Evidence is accumulating that a defective gene may be responsible for this disease.

越来越多证据表明该疾病是由一种有缺陷基因引起。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转基因事物极大潜力。

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫在男性少见是否由于X染色头感光色素基因变异？

Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.

瘦素(leptin)是肥胖基因(ob基因)编码，脂肪细胞分泌一种内源性激素，主要调控体重和脂肪分布。

All the C3 allotype was C3S.The gene frequency was 1.

且所有第三补体异型均为C3S，此基因频率为1。

Gene mutations are alterations in the DNA code.

基因突变是指DNA 密码改变。

The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.

干细胞白血病(CL)因是新发现与白血病发生有关癌基因。

Without this, you are reducing your chances of concentrating the genes of the linebred ancestor.

没有这种选择，你就正在降低强调在血系内繁殖中祖先基因机会。

Through similar and supplementary action , polygenes can have important effects on total variability.

通过相同和添加作用，多基因可以对总变异起重大影响。

That genal genome may lead to better treatment and control of diseaesthe disease.

那些基因组能带来比较好治疗和疾病控制。

Most of these genes have not been reported to relate to the haematogenesis in ontogeny.

这些基因大多数在胚胎分化造血发育中作用尚未见报道。

You have good genes from your parents, so you should live a long time.

你从父母那儿获得优良基因, 所以能够活得很长。

Genes tabA， tabB，tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.

野火氨酸合成有tabA，tabB，talA，dapB等基因参与，受lemA基因调控。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与脱辅基蛋白结合松弛、易于与之分离辅基因子称为辅。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病基因，实验动物模型是一个非常好。

Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).

纤毛虫和蚊子粘液素基因所表现出基因整合则是一些例外。

Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.

目前研究热点还包括：基因-环境相互作用、遗传药理学、基因咨询等。

There is also GMO zucchini, crookneck squash, papaya, and alfalfa.

也有转基因南瓜、转基因葫芦、转基因木瓜和转基因苜蓿。

Researchers are gradually deciphering the genetic structure found in the cells of organisms.

研究者正渐渐破译存于有机体细胞内基因结构。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认基因型测定结果。

Evidence is accumulating that a defective gene may be responsible for this disease.

越来越多证据表明该疾病是由一种有缺陷基因引起。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转基因事物极大潜力。

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫在男性较少见是否由于X染色头感光色素基因变异？