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。

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

野火氨酸的合成有tabA，tabB，talA，dapB等参与，lemA调控。

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

而纤毛虫和蚊子的粘液素所表现出的整合则是一些例外。

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

目前的研究热点还包括：-环境相互作用、遗传药理学、咨询等。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转事物的极大潜力。

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

瘦素(leptin)是肥胖(ob)编码，脂肪细胞分泌的一内源性激素，主要调控体重和脂肪分布。

Gene mutations are alterations in the DNA code.

突变是指DNA 密码的改变。

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

那些组能带来比较好的治疗和疾病的控制。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的突变,为进一步开展诊断和治疗奠定。

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

从父母那儿获得优良的, 所以能够活得很长。

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的结构。

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

而且所有的第三补体异型均为C3S，而此频率为1。

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的作用尚未见报道。

The ear diametre was inherited in a superdominant fashion with the additive gene as the dominant gene.

穗粗的遗传为超显性遗传,且显性为增效。

But, there were extremely low efficiency of integration, unstable hereditation and expression in transgenic animals by the technique.

但是，这方法存在整合效率低、外源不能在转动物体内稳定遗传及表达的问题。

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

与脱辅蛋白结合松弛、易于与之分离的辅子称为辅。

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

越来越多的证据表明该疾病是由一有缺陷的引起的。

Histones are characterized by numerous posttranslational modifications that influence gene transcription.

组蛋白的特点是大量的翻译后修饰，这些修饰可以影响转录。

Siblings and dizygotic twins share only 50% of their segregating genes.

同卵双生双胞胎和双卵双生双胞胎分享仅50%的。

The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.

而且，位于目的下游的胭脂碱合成酶有表达。

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

也有基因南瓜、基因、基因木瓜和基因苜蓿。

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

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

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

而纤毛虫和蚊子的粘液素基因所表现出的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.

目前的研究热点还包括：基因-环境相互作用、遗传药理学、基因咨询等。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏基因事物的极大潜力。

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，脂肪细胞分泌的一内源性激素，主要调控体重和脂肪分布。

Gene mutations are alterations in the DNA code.

基因突变是指DNA 密码的改变。

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

那些基因组能带来比较好的治疗和疾病的控制。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。

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

你从父母那儿获得优良的基因, 所以能够活得很长。

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

研究者破译存于有机体细胞内的基因结构。

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

而且所有的第三补体异型均为C3S，而此基因频率为1。

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的作用尚未见报道。

The ear diametre was inherited in a superdominant fashion with the additive gene as the dominant gene.

穗粗的遗传为超显性遗传,且显性基因为增效基因。

But, there were extremely low efficiency of integration, unstable hereditation and expression in transgenic animals by the technique.

但是，这方法存在基因整合效率低、外源基因不能在基因动物体内稳定遗传及表达的问题。

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、易于与之分离的辅基因子称为辅。

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

越来越多的证据表明该疾病是由一有缺陷的基因引起的。

Histones are characterized by numerous posttranslational modifications that influence gene transcription.

组蛋白的特点是大量的翻译后修饰，这些修饰可以影响基因录。

Siblings and dizygotic twins share only 50% of their segregating genes.

同卵双生双胞胎和双卵双生双胞胎分享仅50%的基因。

The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.

而且，位于目的基因下游的胭脂碱合成酶基因有表达。

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。

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

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

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

而纤毛虫和蚊子的粘液素基因所现出的基因整合则是外。

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

目前的研究热点还包括：基因-环境相互作用、遗传药理学、基因咨询等。

Some people extoll GM foods’tremendous potential for good.

有人赞赏转基因事物的极大潜力。

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，脂肪细胞分泌的内源性激素，主要调控体重和脂肪分布。

Gene mutations are alterations in the DNA code.

基因突变是指DNA 密码的改变。

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

那基因组能带来比较好的治疗和疾病的控制。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定痒疹样营养不良型大疱性解症家系的基因突变,为进步开展基因诊断和基因治疗奠定基础。

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

你从父母那儿获得优良的基因, 所以能够活得很长。

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的基因结构。

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

而且所有的第三补体异型均为C3S，而此基因频率为1。

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

这基因大多数在胚胎分化造血发育中的作用尚未见报道。

The ear diametre was inherited in a superdominant fashion with the additive gene as the dominant gene.

穗粗的遗传为超显性遗传,且显性基因为增效基因。

But, there were extremely low efficiency of integration, unstable hereditation and expression in transgenic animals by the technique.

但是，这方法存在基因整合效率低、外源基因不能在转基因动物体内稳定遗传及达的问题。

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

与脱辅基蛋白结合弛、易于与之分离的辅基因子称为辅。

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

越来越多的证据明该疾病是由有缺陷的基因引起的。

Histones are characterized by numerous posttranslational modifications that influence gene transcription.

组蛋白的特点是大量的翻译后修饰，这修饰可以影响基因转录。

Siblings and dizygotic twins share only 50% of their segregating genes.

同卵双生双胞胎和双卵双生双胞胎分享仅50%的基因。

The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.

而且，位于目的基因下游的胭脂碱合成酶基因有达。

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。

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

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

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

而纤毛虫和蚊子的粘液素基因所表现出的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.

目前的研究热点还包括：基因-环境相互作用、遗传药理学、基因咨询等。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转基因事物的极大潜力。

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，脂肪细胞分泌的一内源性激素，主要调控体重和脂肪分布。

Gene mutations are alterations in the DNA code.

基因突变是指DNA 密码的改变。

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

那些基因组带来比较好的治疗和疾病的控制。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。

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

你从父母那儿获得优良的基因, 所够活得很长。

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的基因结构。

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

而且所有的第三补体异型均为C3S，而此基因频率为1。

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的作用尚未见报道。

The ear diametre was inherited in a superdominant fashion with the additive gene as the dominant gene.

穗粗的遗传为超显性遗传,且显性基因为增效基因。

But, there were extremely low efficiency of integration, unstable hereditation and expression in transgenic animals by the technique.

但是，这方法存在基因整合效率低、外源基因不在转基因动物体内稳定遗传及表达的问题。

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、易于与之分离的辅基因子称为辅。

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

越来越多的证据表明该疾病是由一有缺陷的基因引起的。

Histones are characterized by numerous posttranslational modifications that influence gene transcription.

组蛋白的特点是大量的翻译后修饰，这些修饰可影响基因转录。

Siblings and dizygotic twins share only 50% of their segregating genes.

同卵双生双胞胎和双卵双生双胞胎分享仅50%的基因。

The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.

而且，位于目的基因下游的胭脂碱合成酶基因有表达。

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。

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

野火氨酸的合成有tabA，tabB，talA，dapB等基参与，受lemA基调控。

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

虫和蚊子的粘液素基所表现出的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.

目前的研究热点还包括：基-环境相互作用、遗传药理学、基咨询等。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转基事物的极大潜力。

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，脂肪细胞分泌的一内源性激素，主要调控体重和脂肪分布。

Gene mutations are alterations in the DNA code.

基突变是指DNA 密码的改变。

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

那些基组能带来比较好的和疾病的控制。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基突变,为进一步开展基诊断和基奠定基础。

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

你从父母那儿获得优良的基, 所以能够活得很长。

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的基结构。

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

且所有的第三补体异型均为C3S，此基频率为1。

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

这些基大多数在胚胎分化造血发育中的作用尚未见报道。

The ear diametre was inherited in a superdominant fashion with the additive gene as the dominant gene.

穗粗的遗传为超显性遗传,且显性基为增效基。

But, there were extremely low efficiency of integration, unstable hereditation and expression in transgenic animals by the technique.

但是，这方法存在基整合效率低、外源基不能在转基动物体内稳定遗传及表达的问题。

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、易于与之分离的辅基子称为辅。

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

越来越多的证据表明该疾病是由一有缺陷的基引起的。

Histones are characterized by numerous posttranslational modifications that influence gene transcription.

组蛋白的特点是大量的翻译后修饰，这些修饰可以影响基转录。

Siblings and dizygotic twins share only 50% of their segregating genes.

同卵双生双胞胎和双卵双生双胞胎分享仅50%的基。

The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.

且，位于目的基下游的胭脂碱合成酶基有表达。

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。

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

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

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

纤毛虫和蚊子的粘液素基因所表现出的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.

目前的研究热点还包括：基因-环境相互作用、遗传药理学、基因咨询等。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转基因事物的极大潜力。

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，脂肪细胞分泌的一内源性激素，主要调控体重和脂肪分布。

Gene mutations are alterations in the DNA code.

基因突变是指DNA 密码的改变。

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

那些基因组能带来比较好的治疗和疾病的控制。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。

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

你从父母那儿获得优良的基因, 所以能够活得很长。

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的基因结构。

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

所有的第三补体异型均为C3S，此基因频率为1。

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的作用尚未见报道。

The ear diametre was inherited in a superdominant fashion with the additive gene as the dominant gene.

穗粗的遗传为超显性遗传,显性基因为增效基因。

But, there were extremely low efficiency of integration, unstable hereditation and expression in transgenic animals by the technique.

但是，这方法存在基因整合效率低、外源基因不能在转基因动物体内稳定遗传及表达的问题。

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、易于与之分离的辅基因子称为辅。

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

越来越多的证据表明该疾病是由一有缺陷的基因引起的。

Histones are characterized by numerous posttranslational modifications that influence gene transcription.

组蛋白的特点是大量的翻译后修饰，这些修饰可以影响基因转录。

Siblings and dizygotic twins share only 50% of their segregating genes.

同卵双生双胞胎和双卵双生双胞胎分享仅50%的基因。

The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.

，位于目的基因下游的胭脂碱合成酶基因有表达。

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

也有因南、因葫芦、因木和因苜蓿。

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

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

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

而纤毛虫和蚊子的粘液素因所表现出的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.

目前的研究热点还包括：因-环境相互作用、遗传药理学、因咨询等。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏因事物的极大潜力。

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，脂肪细胞分泌的一内源性激素，主要调控体重和脂肪分布。

Gene mutations are alterations in the DNA code.

因突变是指DNA 密码的改变。

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

那些因组能带来比较好的治疗和疾病的控制。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的因突变,为进一步开展因诊断和因治疗奠定础。

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

你从父母那儿获得优良的因, 所以能够活得很长。

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

研究者正渐渐破有机体细胞内的因结构。

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

而且所有的第三补体异型均为C3S，而此因频率为1。

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的作用尚未见报道。

The ear diametre was inherited in a superdominant fashion with the additive gene as the dominant gene.

穗粗的遗传为超显性遗传,且显性因为增效因。

But, there were extremely low efficiency of integration, unstable hereditation and expression in transgenic animals by the technique.

但是，这方法在因整合效率低、外源因不能在因动物体内稳定遗传及表达的问题。

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

与脱辅蛋白结合松弛、易与之分离的辅因子称为辅。

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

越来越多的证据表明该疾病是由一有缺陷的因引起的。

Histones are characterized by numerous posttranslational modifications that influence gene transcription.

组蛋白的特点是大量的翻后修饰，这些修饰可以影响因录。

Siblings and dizygotic twins share only 50% of their segregating genes.

同卵双生双胞胎和双卵双生双胞胎分享仅50%的因。

The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.

而且，位目的因下游的胭脂碱合成酶因有表达。

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。

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

野火氨酸的合成有tabA，tabB，talA，dapB等基因参与，受lemA基因。

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

而纤毛虫和蚊子的粘液素基因所表现出的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.

目前的研究热点还包括：基因-环境相互作用、遗传药理学、基因咨询等。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转基因事物的极大潜力。

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，细胞分泌的一内源性激素，主体重和分布。

Gene mutations are alterations in the DNA code.

基因突变是指DNA 密的改变。

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

那些基因组能带来比较好的治疗和疾病的制。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。

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

你从父母那儿获得优良的基因, 所以能够活得很长。

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的基因结构。

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

而且所有的第三补体异型均为C3S，而此基因频率为1。

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的作用尚未见报道。

The ear diametre was inherited in a superdominant fashion with the additive gene as the dominant gene.

穗粗的遗传为超显性遗传,且显性基因为增效基因。

But, there were extremely low efficiency of integration, unstable hereditation and expression in transgenic animals by the technique.

但是，这方法存在基因整合效率低、外源基因不能在转基因动物体内稳定遗传及表达的问题。

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、易于与之分离的辅基因子称为辅。

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

越来越多的证据表明该疾病是由一有缺陷的基因引起的。

Histones are characterized by numerous posttranslational modifications that influence gene transcription.

组蛋白的特点是大量的翻译后修饰，这些修饰可以影响基因转录。

Siblings and dizygotic twins share only 50% of their segregating genes.

同卵双生双胞胎和双卵双生双胞胎分享仅50%的基因。

The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.

而且，位于目的基因下游的胭碱合成酶基因有表达。

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。

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

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

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

而纤毛虫和蚊子的因所表现出的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.

目前的研究热点还包括：因-环境相互作用、遗传药理学、因咨询等。

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转因事物的极大潜力。

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

瘦(leptin)是肥胖因(ob因)编码，脂肪细胞分泌的一内源性激，主要调控体重和脂肪分布。

Gene mutations are alterations in the DNA code.

因突变是指DNA 密码的改变。

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

那些因组能带来比较好的治疗和疾病的控制。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的因突变,为进一步因诊断和因治疗奠定础。

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

你从父母那儿获得优良的因, 所以能够活得很长。

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的因结构。

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

而且所有的第三补体异型均为C3S，而此因频率为1。

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的作用尚未见报道。

The ear diametre was inherited in a superdominant fashion with the additive gene as the dominant gene.

穗粗的遗传为超显性遗传,且显性因为增效因。

But, there were extremely low efficiency of integration, unstable hereditation and expression in transgenic animals by the technique.

但是，这方法存在因整合效率低、外源因不能在转因动物体内稳定遗传及表达的问题。

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

与脱辅蛋白结合松弛、易于与之分离的辅因子称为辅。

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

越来越多的证据表明该疾病是由一有缺陷的因引起的。

Histones are characterized by numerous posttranslational modifications that influence gene transcription.

组蛋白的特点是大量的翻译后修饰，这些修饰可以影响因转录。

Siblings and dizygotic twins share only 50% of their segregating genes.

同卵双生双胞胎和双卵双生双胞胎分享仅50%的因。

The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.

而且，位于目的因下游的胭脂碱合成酶因有表达。