1. Gene mutations are alterations in the DNA code.

2. Gene mutations occur spontaneously and can be induced by mutagenic agents such has high temperature, mustard gas, and radiation.

3. Other workers have found ras gene mutations in between 39% and 47% of colorectal cancers.

4. K-ras gene mutations, by contrast with p53, clearly occur at an earlier stage in the neoplastic sequence.

5. Conclusion Abore point mutation is an inherited gene mutation.

6. AIM:To investigate gene mutation of patient with oligodontia.

7. Conclusion PTEN gene mutation might play important role in tumor genesis and development of bladder cancer.

8. Objective : To analyze G 6 PD gene mutation in 168 Cantonese G 6 PD deficient male infants.

9. Variations of flower color are related to gene mutation and pollination pattern and so on.

10. Conclusion: E2 of NF2 gene mutation might be one of the critical factor in the tumorogenesis of acoustic neuromas .

11. Objective To establish TK gene mutation assay using human lymphoblastoid cell line TK6 and to study the genotoxic mechanism of Vinblastine(VBL).

12. Objective: To exclude known gene mutation, 21 exon of SOS1 which had been certified by foreign country form 2 families with hereditary gingival fibromatosis .

13. Objective To study the gene mutation and clinical characteristics of hereditary spinocerebellar ataxia type 7 (SCA7).

14. The variegation of petals originates chiefly from gene mutation and viral infection.

15. Ras gene mutation in childhood AML was mainly found in M 2 , M 4 , M 5 subtypes.

16. HBV gene mutation along different types of TCM syndrome are detected by microarray assay.

17. Objective To study the gene mutation in a pedigree with Dowling - Meara type epidermolysis bullosa simplex ( DM - EBS ).

18. Conclusion There is K 14 1 A domain gene mutation in this DM - EBS pedigree.

19. Objective To explore SCA3 gene mutation in the patients with inherited spinocerebellar ataxia.

20. Conclusion Maybe there is no association with E237G gene mutation between asthma and atopy.

21. Enough premalignant cells are present in the bulk of stool to permit the analysis of tumour suppressor gene mutations by this technique.

22. In order to explore the effect of precedent mutation on the sensitivity to mutagens the mutants resistant to 6 thioguanine (6 TG) were selected by 6 TG using gene mutation assay in V79 cells.

23. Absreact: This experiment was conducted to study the influence of growth hormone receptor(GHR) gene mutation on the semen quality of sex-linked dwarf chicken.

24. Single strand conformation polymorphism (SSCP) essay and sequence analysis of the PCR product were used to ascertain the gene mutation.

25. Conclusion The assumable reasons for the dominance of heterozygous ADH2 genotype were a relatively small size of samples or gene mutation etc, which needed further researches to be confirmed.

26. Each of them has its advantages. Selecting appropriate method would provide much better approaches for gene mutation analysis.

26. try its best to gather and create good sentences.

27. Conclusbo : It'suggsts that ras gene aed p 53 gene mutation may be related with L - form infedtbo.

28. Objective:To assess the roles of single stranded conformation polymorphism(SSCP)and heteroduplex polymorphism(HET)in screening gene mutation.

29. Hypoxanthine guanine Phosphoribosyl Transferase(HPRT) is a classical gene locus in the research of single gene mutation.

30. Objective To detect the activity of transglutaminase 1 ( TGM 1 ) and gene mutation in a family with lamellar ichthyosis.

31. These gene mutation distributing in all over the whole coding section of ATM gene. Every Exon exist the gene mutated site and no obvious hot mutated site be discovered.

32. Objective To study the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7 (SCA7).

33. Objetive : To detect the gene mutation of a patient with anhidrotic ectodermal dysplasia.

34. The two mutants arose from new gene mutation characterized by transformation and will be very useful in identification of new gene controlling peroxisome assembly from yeast.

35. Conclusion The loss of cell cycle check points and the disfunction of DNA repair caused by ATM gene mutation may be responsible for high radiosensitivity of AT5BIVA cells.

36. Change the time, the gene mutation that future generations of Apple's become very tall, please Apple.

37. Methods HPRT gene mutation frequency (Mf) was examined by the technique of multinuclear cell assay.

38. Objective : To study the effects of propolis against gene mutation induced by powerful mutagens in mice.

39. To investigate the relationship between isoniazid - resistance and Kat G gene mutation or deletion.

40. Cells with Ras gene mutation or transformed by Ras become resistant to p 53 dependent apoptosis.

41. According to comparing the zymograms of isoelectrofocusing, the relationship of enzyme activity and energy metabolism, and the relationship of enzyme activity and gene mutation were studied.

42. Objective To study a Chinese pedigree Hailey - Hailey disease - mine the ATP 2 C 1 gene mutation in this family.

43. Methods HPRT gene mutation frequency was examined by the technique of multinuclear cell assay.

44. These changes encompass a diverse set of biological end points, such as kari-otypic abnormalities, gene mutation and amplification, and delayed reproductive cell death etc.

45. How can a single gene mutation lead to a complex psychiatric phenotype?

46. Our Studies suggest that all the gene mutation may le ad to jaundice of the newborn, acute hemolytic anaemia, and have some relation to viral hepatitis, leukaemia, lymphoma.

47. ConclusionG 71 R gene mutation combined with G 6 PDdeficiency aggravates the degree of neonatal jaundice.

48. Objective To study the gene mutation and clinical characteristics of hereditary spinocerebellar ataxia type 7.

49. It has been widely applied gene analysis, detection of gene mutation and genetic disease.

50. Take the gene mutation that causes phenylketonuria or PKU. People with the disease can't break down the amino acid phenylalanine a problem that can lead to severe cognitive damage.

51. Gene mutation analysis was performed for patients with BH4 deficiency and their parents.

52. Objective To identity the ABCD1 gene mutation in a Chinese family with X-linked adrenoleukodystrophy(ALD).

53. Multiple allele specific polymerase chain reaction (MASPCR) was used for targeted DNA amplification and gene mutation analysis.

54. The couples were put into three groups depending on the DNA of the men: men without the gene mutation, men with one copy of the mutant gene and men with both copies of the mutation.

55. Conclusions FH is an euchromosome dominant genetic disease that is caused by the defective LDLR resulted from gene mutation.

56. Methods: Polymerase chain reaction-single strand conformation polymorphism(PCR-SSCP) was used to exclude known gene mutation of HGF from 2 familial gingival fibromatosis .

56. is a online sentence dictionary, on which you can find good sentences for a large number of words.

57. In this article, the growth regulating mechanism of chicken is discussed, The sex-linked dwarfism in chickens is due to the GHR gene mutation and point mutation and deletion are two main forms.

58. Objective : To identify gene mutation in a family with Weber - Cockayne type epidermolysis bullosa simplex ( WC - EBS ).

59. If the suppressor gene mutation may lead to disorders and cancerous cell growth.

60. BRAF gene mutation has been confirmed to be closely related to the dedifferentiation of papillary thyroid carcinoma.

61. Objective : To detect ED 1 gene mutation in three hypohidrotic ectodermal dysplasia ( HED ) nuclear families.

62. Mass spectrometry analysis, biotinidase activity determination and gene mutation analysis may be helpful in the definite diagnosis of this disorder.

63. Objective : To identify gene mutation in a family with Weber - Cockayne type epidermolysis bullosa simplex ( EBS - WC ).