Gene mutations are alterations in the DNA code.

基因是指DNA 密码改。

Objective To determine the toxicity and mutagenic effect of trichloroacetaldehyde.

了解三氯乙醛毒性和致作用。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微导致致癌倾向综合征着色性干皮病。

Catastrophe theory has become a useful tool in studying incontinuous phenomena since it was established.

摘要理论自问世以来已成为研究现实世界中一些不连续现象有力工具。

Genetic analysis showed that the green-revertible albino trait was controlled by a sin-gle recessive nucleic gene.

遗传分析发现性状受一对隐性核基因控制。

In this review, induction, screening and identification of the mutants of plants in study of photoprotection were summarized.

本文简要介绍了体获得、筛选、，并总结了几类与光破坏防御有关体。

Objective:To observe mutagenicity of siritch vapor condensate(SVC)in mice.

研究胡麻油烟冷凝物对小鼠致作用。

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

研究显示IGRP基因阻断了葡萄糖激酶作为感受器活性。

The study aimed to discuss the optimum conditions of Thermophilic sporotrichum mutant strain TH3-9 for producing cellulase.

探讨嗜热侧孢霉TH3-9株固体发酵产纤维素酶最佳条件。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶基因外显子6区13389G缺失,引起移码。

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

目一痒疹样营养不良型大疱性表皮松解症家系基因,为进一步开展基因诊断和基因治疗奠基础。

Above results showed that minced Cr-containing fish meat has no mutagenic effect and is save for feeding genetic-toxicologically.

上述三项检测结果表明：铬对鱼无致作用，从遗传毒理学角度认为食用是安全。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利用胚胎移植技术对四种无毛小鼠和一种白内障小鼠桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN引起血管疾病，但没有认知异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障碍中作用。

Meanwhile, Anne has been begging Muttonchops and Girlboy to help her take care of the mutant boyfriend from Hell's poultry farm.

同时，安妮已经乞讨Muttonchops和Girlboy帮她照顾男友来自地狱家禽养殖场。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前现存29种洞穴鱼，其眼盲亦与这些有关，但是其基因位置并不相同。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关基因导致眼、皮肤、毛发黑色素沉着减少或缺乏引起一类常染色体隐形遗传疾病总称。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子中ˇ异源双链法、SSCP法与异源双链-SSCP法检出分别为22个(96%)、20个(87%)和23个(100%)。

It is a more important effect that the electromagnetic pollution may accelerate germ plasm aberrance.It leads to the confusion of biothythm and illness.

更重要是可能诱发生物基因，导致生物生长节律混乱和各种恶疾及新生疾病产生。

Gene mutations are alterations in the DNA code.

突是指DNA 密码的改。

Objective To determine the toxicity and mutagenic effect of trichloroacetaldehyde.

了解三氯乙醛的毒性和致突作用。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微突导致致癌倾向综合征着色性干皮病。

Catastrophe theory has become a useful tool in studying incontinuous phenomena since it was established.

摘要突理论自问世以来已成为研究现实世界中一些不连续现象的有力工具。

Genetic analysis showed that the green-revertible albino trait was controlled by a sin-gle recessive nucleic gene.

遗传分析发现该突性状受一对隐性控制。

In this review, induction, screening and identification of the mutants of plants in study of photoprotection were summarized.

本文简要介绍了突体的获得、筛选、鉴定，并总结了几类与光破坏防御有关的突体。

Objective:To observe mutagenicity of siritch vapor condensate(SVC)in mice.

研究胡麻油烟冷凝物对小鼠致突作用。

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

该研究显示突的IGRP阻断了葡萄糖激酶作为感受器的活性。

The study aimed to discuss the optimum conditions of Thermophilic sporotrichum mutant strain TH3-9 for producing cellulase.

探讨嗜热侧孢霉TH3-9突株固体发酵产纤维素酶的最佳条件。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶外显子613389G,引起移码突。

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,为进一步开展诊断和治疗奠定础。

Above results showed that minced Cr-containing fish meat has no mutagenic effect and is save for feeding genetic-toxicologically.

上述三项检测结果表明：铬对鱼无致突作用，从遗传毒理学角度认为食用是安全的。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利用胚胎移植技术对四种突无毛小鼠和一种白内障小鼠的桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、突分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

为ELN突引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合性在视觉空间建构认知障碍中的作用。

Meanwhile, Anne has been begging Muttonchops and Girlboy to help her take care of the mutant boyfriend from Hell's poultry farm.

同时，安妮已经乞讨Muttonchops和Girlboy帮她照顾突男友来自地狱的家禽养殖场。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前现存的29种洞穴鱼，其眼盲亦与这些突有关，但是其突的位置并不相同。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关突导致眼、皮肤、毛发黑色素沉着减少或乏引起的一类常染色体隐形遗传疾病的总称。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子突中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突分别为22个(96%)、20个(87%)和23个(100%)。

It is a more important effect that the electromagnetic pollution may accelerate germ plasm aberrance.It leads to the confusion of biothythm and illness.

更重要的是可能诱发生物的突，导致生物生长节律的混乱和各种恶疾及新生疾病的产生。

Gene mutations are alterations in the DNA code.

突是指DNA 密码的改。

Objective To determine the toxicity and mutagenic effect of trichloroacetaldehyde.

了解三氯乙醛的毒性和致突作用。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微突导致致癌倾向综合征着色性干皮病。

Catastrophe theory has become a useful tool in studying incontinuous phenomena since it was established.

摘要突理论自来已成为研究现实界中一些不连续现象的有力工具。

Genetic analysis showed that the green-revertible albino trait was controlled by a sin-gle recessive nucleic gene.

遗传分析发现该突性状受一对隐性核控制。

In this review, induction, screening and identification of the mutants of plants in study of photoprotection were summarized.

本文简要介绍了突体的获得、筛选、鉴定，并总结了几类与光破坏防御有关的突体。

Objective:To observe mutagenicity of siritch vapor condensate(SVC)in mice.

研究胡麻油烟冷凝物对小鼠致突作用。

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

该研究显示突的IGRP阻断了葡萄糖激酶作为感受器的活性。

The study aimed to discuss the optimum conditions of Thermophilic sporotrichum mutant strain TH3-9 for producing cellulase.

探讨嗜热侧孢霉TH3-9突株固体发酵产纤维素酶的最佳条件。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶外显子6区13389G缺失,引起移码突。

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,为进一步开诊断和治疗奠定础。

Above results showed that minced Cr-containing fish meat has no mutagenic effect and is save for feeding genetic-toxicologically.

上述三项检测结果表明：铬对鱼无致突作用，从遗传毒理学角度认为食用是安全的。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利用胚胎移植技术对四种突无毛小鼠和一种白内障小鼠的桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、突分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

为ELN突引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合性在视觉空间建构认知障碍中的作用。

Meanwhile, Anne has been begging Muttonchops and Girlboy to help her take care of the mutant boyfriend from Hell's poultry farm.

同时，安妮已经乞讨Muttonchops和Girlboy帮她照顾突男友来自地狱的家禽养殖场。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前现存的29种洞穴鱼，其眼盲亦与这些突有关，但是其突的位置并不相同。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关突导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的总称。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子突中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突分别为22个(96%)、20个(87%)和23个(100%)。

It is a more important effect that the electromagnetic pollution may accelerate germ plasm aberrance.It leads to the confusion of biothythm and illness.

更重要的是可能诱发生物的突，导致生物生长节律的混乱和各种恶疾及新生疾病的产生。

Gene mutations are alterations in the DNA code.

基因是指DNA 密码的改。

Objective To determine the toxicity and mutagenic effect of trichloroacetaldehyde.

了解三氯乙醛的毒性和致用。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微导致致癌倾向综合征着色性干皮病。

Catastrophe theory has become a useful tool in studying incontinuous phenomena since it was established.

摘要理论自问世以来已成为研究现实世界中一些不连续现象的有力工具。

Genetic analysis showed that the green-revertible albino trait was controlled by a sin-gle recessive nucleic gene.

遗传分析发现该性状受一对隐性核基因控制。

In this review, induction, screening and identification of the mutants of plants in study of photoprotection were summarized.

本文简要介绍了体的获得、筛选、鉴定，并总结了几类与光破坏防御有关的体。

Objective:To observe mutagenicity of siritch vapor condensate(SVC)in mice.

研究胡麻油烟冷凝物对小鼠致用。

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

该研究显示的IGRP基因阻断了葡酶为感受器的活性。

The study aimed to discuss the optimum conditions of Thermophilic sporotrichum mutant strain TH3-9 for producing cellulase.

探讨嗜热侧孢霉TH3-9株固体发酵产纤维素酶的最佳条件。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶基因外显子6区13389G缺失,引起移码。

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,为进一步开展基因诊断和基因治疗奠定基础。

Above results showed that minced Cr-containing fish meat has no mutagenic effect and is save for feeding genetic-toxicologically.

上述三项检测结果表明：铬对鱼无致用，从遗传毒理学角度认为食用是安全的。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利用胚胎移植技术对四种无毛小鼠和一种白内障小鼠的桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN引起血管的疾病，但没有认知的异常，这些资料暗示了酶1半合性基因在视觉空间建构认知障碍中的用。

Meanwhile, Anne has been begging Muttonchops and Girlboy to help her take care of the mutant boyfriend from Hell's poultry farm.

同时，安妮已经乞讨Muttonchops和Girlboy帮她照顾男友来自地狱的家禽养殖场。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前现存的29种洞穴鱼，其眼盲亦与这些有关，但是其基因的位置并不相同。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关基因导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的总称。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子中ˇ异源双链法、SSCP法与异源双链-SSCP法检出分别为22个(96%)、20个(87%)和23个(100%)。

It is a more important effect that the electromagnetic pollution may accelerate germ plasm aberrance.It leads to the confusion of biothythm and illness.

更重要的是可能诱发生物基因的，导致生物生长节律的混乱和各种恶疾及新生疾病的产生。

Gene mutations are alterations in the DNA code.

基因是指DNA 密码改。

Objective To determine the toxicity and mutagenic effect of trichloroacetaldehyde.

了解三氯乙醛毒性和致作用。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微导致致癌倾向综合征着色性干皮病。

Catastrophe theory has become a useful tool in studying incontinuous phenomena since it was established.

摘要理论自问世以来已成为研究现实世界中一些不连续现象有力工具。

Genetic analysis showed that the green-revertible albino trait was controlled by a sin-gle recessive nucleic gene.

遗传分析发现性状受一对隐性核基因控制。

In this review, induction, screening and identification of the mutants of plants in study of photoprotection were summarized.

本文简要介绍了体获得、筛选、，并总结了几类与光破坏防御有关体。

Objective:To observe mutagenicity of siritch vapor condensate(SVC)in mice.

研究胡麻油烟冷凝物对小鼠致作用。

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

研究显示IGRP基因阻断了葡萄糖激酶作为感受器活性。

The study aimed to discuss the optimum conditions of Thermophilic sporotrichum mutant strain TH3-9 for producing cellulase.

探讨嗜热侧孢霉TH3-9株固体发酵产纤维素酶最佳条件。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶基因外显子6区13389G缺失,引起移码。

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

目一痒疹样营养不良型大疱性表皮松解症家系基因,为进一步开展基因诊断和基因治疗奠基础。

Above results showed that minced Cr-containing fish meat has no mutagenic effect and is save for feeding genetic-toxicologically.

上述三项检测结果表明：铬对鱼无致作用，从遗传毒理学角度认为食用是安全。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利用胚胎移植技术对四种无毛小鼠和一种白内障小鼠桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN引起血管疾病，但没有认知异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障碍中作用。

Meanwhile, Anne has been begging Muttonchops and Girlboy to help her take care of the mutant boyfriend from Hell's poultry farm.

同时，安妮已经乞讨Muttonchops和Girlboy帮她照顾男友来自地狱家禽养殖场。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前现存29种洞穴鱼，其眼盲亦与这些有关，但是其基因位置并不相同。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关基因导致眼、皮肤、毛发黑色素沉着减少或缺乏引起一类常染色体隐形遗传疾病总称。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子中ˇ异源双链法、SSCP法与异源双链-SSCP法检出分别为22个(96%)、20个(87%)和23个(100%)。

It is a more important effect that the electromagnetic pollution may accelerate germ plasm aberrance.It leads to the confusion of biothythm and illness.

更重要是可能诱发生物基因，导致生物生长节律混乱和各种恶疾及新生疾病产生。

Gene mutations are alterations in the DNA code.

基因是指DNA 密的改。

Objective To determine the toxicity and mutagenic effect of trichloroacetaldehyde.

了解三氯乙醛的毒性和致作用。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微导致致癌倾向综合征着色性干皮病。

Catastrophe theory has become a useful tool in studying incontinuous phenomena since it was established.

摘要理论自问世以来已成为研究现实世界中些不连续现象的有力工具。

Genetic analysis showed that the green-revertible albino trait was controlled by a sin-gle recessive nucleic gene.

遗传分析发现该性对隐性核基因控制。

In this review, induction, screening and identification of the mutants of plants in study of photoprotection were summarized.

本文简要介绍了体的获得、筛选、鉴定，并总结了几类与光破坏防御有关的体。

Objective:To observe mutagenicity of siritch vapor condensate(SVC)in mice.

研究胡麻油烟冷凝物对小鼠致作用。

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

该研究显示的IGRP基因阻断了葡萄糖激酶作为感器的活性。

The study aimed to discuss the optimum conditions of Thermophilic sporotrichum mutant strain TH3-9 for producing cellulase.

探讨嗜热侧孢霉TH3-9株固体发酵产纤维素酶的最佳条件。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶基因外显子6区13389G缺失,引起移。

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表皮松解症家系的基因,为进步开展基因诊断和基因治疗奠定基础。

Above results showed that minced Cr-containing fish meat has no mutagenic effect and is save for feeding genetic-toxicologically.

上述三项检测结果表明：铬对鱼无致作用，从遗传毒理学角度认为食用是安全的。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利用胚胎移植技术对四种无毛小鼠和种白内障小鼠的桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障碍中的作用。

Meanwhile, Anne has been begging Muttonchops and Girlboy to help her take care of the mutant boyfriend from Hell's poultry farm.

同时，安妮已经乞讨Muttonchops和Girlboy帮她照顾男友来自地狱的家禽养殖场。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前现存的29种洞穴鱼，其眼盲亦与这些有关，但是其基因的位置并不相同。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关基因导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的类常染色体隐形遗传疾病的总称。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子中ˇ异源双链法、SSCP法与异源双链-SSCP法检出分别为22个(96%)、20个(87%)和23个(100%)。

It is a more important effect that the electromagnetic pollution may accelerate germ plasm aberrance.It leads to the confusion of biothythm and illness.

更重要的是可能诱发生物基因的，导致生物生长节律的混乱和各种恶疾及新生疾病的产生。

Gene mutations are alterations in the DNA code.

基因突是指DNA 密码的改。

Objective To determine the toxicity and mutagenic effect of trichloroacetaldehyde.

了解三氯乙醛的毒性和致突作用。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微突导致致癌倾向综合征着色性干皮病。

Catastrophe theory has become a useful tool in studying incontinuous phenomena since it was established.

摘要突理论自问世以来已成为研究现实世界中一些不连续现象的有力工具。

Genetic analysis showed that the green-revertible albino trait was controlled by a sin-gle recessive nucleic gene.

遗传分析发现该突性状受一隐性核基因控制。

In this review, induction, screening and identification of the mutants of plants in study of photoprotection were summarized.

本文简要介绍了突体的获得、筛选、鉴定，并总结了几类与光破坏防御有关的突体。

Objective:To observe mutagenicity of siritch vapor condensate(SVC)in mice.

研究胡麻油烟冷凝物小鼠致突作用。

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

该研究显示突的IGRP基因阻断了葡萄糖激酶作为感受器的活性。

The study aimed to discuss the optimum conditions of Thermophilic sporotrichum mutant strain TH3-9 for producing cellulase.

探讨嗜热侧孢霉TH3-9突株固体发酵产纤维素酶的最佳条件。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶基因外显子6区13389G缺失,引起移码突。

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,为进一步开展基因诊断和基因治疗奠定基础。

Above results showed that minced Cr-containing fish meat has no mutagenic effect and is save for feeding genetic-toxicologically.

上述三项检测结果表明：铬鱼无致突作用，从遗传毒理学角度认为食用是安全的。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利用胚胎移植技术突无毛小鼠和一白内障小鼠的桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、突分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障碍中的作用。

Meanwhile, Anne has been begging Muttonchops and Girlboy to help her take care of the mutant boyfriend from Hell's poultry farm.

同时，安妮已经乞讨Muttonchops和Girlboy帮她照顾突男友来自地狱的家禽养殖场。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前现存的29洞穴鱼，其眼盲亦与这些突有关，但是其基因突的位置并不相同。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关基因突导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的总称。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子突中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突分别为22个(96%)、20个(87%)和23个(100%)。

It is a more important effect that the electromagnetic pollution may accelerate germ plasm aberrance.It leads to the confusion of biothythm and illness.

更重要的是可能诱发生物基因的突，导致生物生长节律的混乱和各恶疾及新生疾病的产生。

Gene mutations are alterations in the DNA code.

基因是指DNA 密码的改。

Objective To determine the toxicity and mutagenic effect of trichloroacetaldehyde.

了解三氯乙醛的毒性和致作用。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微导致致癌倾向综合征着色性干皮病。

Catastrophe theory has become a useful tool in studying incontinuous phenomena since it was established.

摘要理论自问世以来已成研究实世界中一些不连续象的有力工具。

Genetic analysis showed that the green-revertible albino trait was controlled by a sin-gle recessive nucleic gene.

遗传分析发该性状受一对隐性核基因控制。

In this review, induction, screening and identification of the mutants of plants in study of photoprotection were summarized.

本文简要介绍了的获得、筛选、鉴定，并总结了几类与光破坏防御有关的。

Objective:To observe mutagenicity of siritch vapor condensate(SVC)in mice.

研究胡麻油烟冷凝物对小鼠致作用。

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

该研究显示的IGRP基因阻断了葡萄糖激酶作感受器的活性。

The study aimed to discuss the optimum conditions of Thermophilic sporotrichum mutant strain TH3-9 for producing cellulase.

探讨嗜热侧孢霉TH3-9株固发酵产纤维素酶的最佳条件。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者抗凝血酶基因外显子6区13389G缺失,引起移码。

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皮松解症家系的基因,进一步开展基因诊断和基因治疗奠定基础。

Above results showed that minced Cr-containing fish meat has no mutagenic effect and is save for feeding genetic-toxicologically.

上述三项检测结果明：铬对鱼无致作用，从遗传毒理学角度认食用是安全的。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利用胚胎移植技术对四种无毛小鼠和一种白内障小鼠的桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因ELN引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障碍中的作用。

Meanwhile, Anne has been begging Muttonchops and Girlboy to help her take care of the mutant boyfriend from Hell's poultry farm.

同时，安妮已经乞讨Muttonchops和Girlboy帮她照顾男友来自地狱的家禽养殖场。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前存的29种洞穴鱼，其眼盲亦与这些有关，但是其基因的位置并不相同。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关基因导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色隐形遗传疾病的总称。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子中ˇ异源双链法、SSCP法与异源双链-SSCP法检出分别22个(96%)、20个(87%)和23个(100%)。

It is a more important effect that the electromagnetic pollution may accelerate germ plasm aberrance.It leads to the confusion of biothythm and illness.

更重要的是可能诱发生物基因的，导致生物生长节律的混乱和各种恶疾及新生疾病的产生。

Gene mutations are alterations in the DNA code.

基因突指DNA 密码。

Objective To determine the toxicity and mutagenic effect of trichloroacetaldehyde.

了解三氯乙醛毒性和致突作。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微突导致致癌倾向综合征着色性干皮病。

Catastrophe theory has become a useful tool in studying incontinuous phenomena since it was established.

摘要突理论自问世以来已成为研究现实世界中一些不连续现象有力工具。

Genetic analysis showed that the green-revertible albino trait was controlled by a sin-gle recessive nucleic gene.

遗传分析发现该突性状受一对隐性核基因控制。

In this review, induction, screening and identification of the mutants of plants in study of photoprotection were summarized.

本文简要介绍了突体获得、筛选、鉴定，并总结了几类与光破坏防御有关突体。

Objective:To observe mutagenicity of siritch vapor condensate(SVC)in mice.

研究胡麻油烟冷凝物对小鼠致突作。

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

该研究显示突IGRP基因阻断了葡萄糖激酶作为感受器活性。

The study aimed to discuss the optimum conditions of Thermophilic sporotrichum mutant strain TH3-9 for producing cellulase.

探讨嗜热侧孢霉TH3-9突株固体发酵产纤维素酶最佳条件。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶基因外显子6区13389G缺失,引起移码突。

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

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

Above results showed that minced Cr-containing fish meat has no mutagenic effect and is save for feeding genetic-toxicologically.

上述三项检测结果表明：铬对鱼无致突作，从遗传毒理学角度认为食全。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利胚胎移植技术对四种突无毛小鼠和一种白内障小鼠桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、突分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突引起血管疾病，但没有认知异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障碍中作。

Meanwhile, Anne has been begging Muttonchops and Girlboy to help her take care of the mutant boyfriend from Hell's poultry farm.

同时，妮已经乞讨Muttonchops和Girlboy帮她照顾突男友来自地狱家禽养殖场。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前现存29种洞穴鱼，其眼盲亦与这些突有关，但其基因突位置并不相同。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病由于黑色素合成相关基因突导致眼、皮肤、毛发黑色素沉着减少或缺乏引起一类常染色体隐形遗传疾病总称。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子突中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突分别为22个(96%)、20个(87%)和23个(100%)。

It is a more important effect that the electromagnetic pollution may accelerate germ plasm aberrance.It leads to the confusion of biothythm and illness.

更重要可能诱发生物基因突，导致生物生长节律混乱和各种恶疾及新生疾病产生。

Gene mutations are alterations in the DNA code.

基因突是指DNA 密码改。

Objective To determine the toxicity and mutagenic effect of trichloroacetaldehyde.

了解三氯乙醛毒性和致突作用。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微突导致致癌倾向综合征着色性干皮病。

Catastrophe theory has become a useful tool in studying incontinuous phenomena since it was established.

摘要突理论自问世以来已成为研究现实世界中一些不连续现象有工具。

Genetic analysis showed that the green-revertible albino trait was controlled by a sin-gle recessive nucleic gene.

遗传分析发现该突性状受一对隐性核基因控制。

In this review, induction, screening and identification of the mutants of plants in study of photoprotection were summarized.

本文简要介绍了突体获得、筛选、鉴定，并总结了几类与光破坏防御有关突体。

Objective:To observe mutagenicity of siritch vapor condensate(SVC)in mice.

研究胡麻油烟冷凝物对小鼠致突作用。

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

该研究显示突IGRP基因阻断了葡萄糖激酶作为感受器活性。

The study aimed to discuss the optimum conditions of Thermophilic sporotrichum mutant strain TH3-9 for producing cellulase.

探讨嗜热侧孢霉TH3-9突株固体发酵产纤维素酶最佳条件。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶基因外显子6区13389G缺失,引起移码突。

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

目鉴定一痒疹样营养不良性表皮松解症家系基因突,为进一步开展基因诊断和基因治疗奠定基础。

Above results showed that minced Cr-containing fish meat has no mutagenic effect and is save for feeding genetic-toxicologically.

上述三项检测结果表明：铬对鱼无致突作用，从遗传毒理学角度认为食用是安全。

Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.

方法利用胚胎移植技术对四种突无毛小鼠和一种白内障小鼠桑葚胚进行子宫内移植。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、突分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突引起血管疾病，但没有认知异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障碍中作用。

Meanwhile, Anne has been begging Muttonchops and Girlboy to help her take care of the mutant boyfriend from Hell's poultry farm.

同时，安妮已经乞讨Muttonchops和Girlboy帮她照顾突男友来自地狱家禽养殖场。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前现存29种洞穴鱼，其眼盲亦与这些突有关，但是其基因突位置并不相同。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关基因突导致眼、皮肤、毛发黑色素沉着减少或缺乏引起一类常染色体隐形遗传疾病总称。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子突中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突分别为22个(96%)、20个(87%)和23个(100%)。

It is a more important effect that the electromagnetic pollution may accelerate germ plasm aberrance.It leads to the confusion of biothythm and illness.

更重要是可能诱发生物基因突，导致生物生长节律混乱和各种恶疾及新生疾病产生。