heterozygous in English

adjective

containing a dissimilar pair of genes for any hereditary characteristic (Biology)

Use "heterozygous" in a sentence

Below are sample sentences containing the word "heterozygous" from the English Dictionary. We can refer to these sentence patterns for sentences in case of finding sample sentences with the word "heterozygous", or refer to the context using the word "heterozygous" in the English Dictionary.

1. This is the heterozygous form.

2. If the Alleles are different, the individual is heterozygous.

3. Heterozygous Having two different alleles at a locus.

4. Heterozygous females have transverse black markings, visible only in agoutis.

5. When the two alleles are not identical, they are heterozygous.

6. Certain autosomal translocations in the heterozygous state can be fully viable.

7. Methods: Nine heterozygous mutation carriers and nine healthy controls were investigated.

8. If the Alleles in a matching pair are different, they are called heterozygous Alleles

9. When the two alleles are not identical , they are said to be heterozygous.

10. The transmission frequency of gametes with 6V in heterozygous plants were decreased clearly.

11. Molecular testing (PCR amplification method) revealed a heterozygous mutation responsible for factor V Leiden.

12. 50% are heterozygous for this gene and hatch with a crest of varying sizes.

13. A gene can have many alleles and individuals can have a homozygous or heterozygous genotype.

14. The research deals with functional nano powder, fabrication heterozygous material, 1 - D nano material and devices.

15. Enclosed are the details about the allopurinol challenge test for the detection of heterozygous women and girls.

16. Homozygous and heterozygous carriers of the PTPN 22 1858 T allele had a decreased probability of remission.

17. Horses that are heterozygous carriers of the gene do not develop the condition and are physically healthy.

18. If you have trio data, Codified will search your samples for de-novo and compound-heterozygous variation.

19. Conclusion The proband's hearing loss resulted from the compound heterozygous mutations N392Y and S448X for SLC26A4 gene.

20. Double heterozygote --- An individual who is heterozygous at each of two different loci. Contrast with compound heterozygote.

21. An allele does not care if it is in a half - blooded ( heterozygous ) or pure - blooded ( homozygous ) individual.

22. Other segregants with near-haploid DNA contents were heterozygous at a marker locus indicating that they were aneuploid.

23. When an organism is heterozygous for a trait, the resulting phenotype for that trait expresses only the dominant allele .

24. If an organism is heterozygous for that trait, or possesses one of each Allele, then the dominant trait is expressed.

25. Consider , for the sake of illustration , two heterozygous alleles Aa and Bb which are carried in the same pair of chromosomes .

26. Law or Principle of Dominance: In heterozygous individuals or hybrids, a character is represented by two contrasting factors called alleles or Allelomorphs.

27. In the higher liability classes the probability of an affected individual being heterozygous or homozygous for the major allele was about 0.

28. His speech is heavily saturated with such foreboding words as homozygous, heterozygous, translocations, inversions, haploid, diploid, polyploid, mitosis, meiosis, deoxyribonucleic acid, and the like.

29. That is, the phenotype produced by the two Alleles in heterozygous combination is identical to that produced by one of the two homozygous genotypes

30. 23 Vascular bundle parenchyma cell vacuolated and arranged irregularly. The vascular bundle parenchyma cell of heterozygous plants mixed together and its nucleus were transferred.

31. Dominant allele: an allele, which has the same effect on the phenotype of an organism, whether the organism is homozygous or heterozygous for the gene.

32. In conclusion, our finding is the first to show that a heterozygous missense mutation R689H in SCN5A gene results in the loss of protein function and the Coexistents …

33. The heterozygous abp1/ABP1 insertion mutant has defects in auxin physiology-related responses: higher root slanting angles, longer hypocotyls, agravitropic roots and hypocotyls, Aphototropic hypocotyls, and decreased apical dominance.

34. We found that the heterozygous abp1/ABP1 insertion mutant has defects in auxin physiology-related responses: higher root slanting angles, longer hypocotyls, agravitropic roots and hypocotyls, Aphototropic hypocotyls, and decreased apical …

35. ‘‘Heterozygous’ means having two different Allelomorphs in the two corresponding loci of a pair of chromosomes.’ ‘We do not know at the moment what processes are primarily affected by the Allelomorphs.’

36. As seen in cases of Mendelian diseases, such as sickle cell anemia or thalassemias, heterozygous carriers may have selective advantages, in this particular case a natural resistance against Malaria tropica.

37. READ MORE; along with diet alone or together with other Cholesterol-lowering medicines in adults with high blood Cholesterol levels called primary hyperlipidemia (including a type of high Cholesterol called heterozygous

38. A variety of approaches have been used to address this issue, the most common of which is the study of tumors in women, who are heterozygous for X-linked marker enzymes.

39. ‘‘Heterozygous’ means having two different Allelomorphs in the two corresponding loci of a pair of chromosomes.’ ‘We do not know at the moment what processes are primarily affected by the Allelomorphs.’

40. Bartter syndrome is a heterozygous group of autosomal recessive disorders of electrolyte homeostasis characterized by hypokalemic alkalosis, renal salt wasting that may lead to hypotension, hyper-reninemic hyperaldosteronism, increased urinary prostaglandin excretion, and hypercalciuria with nephrocalcinosis.204,205

41. A number sign (#) is used with this entry because D-Bifunctional protein deficiency can be caused by homozygous or compound heterozygous mutation in the HSD17B4 gene (601860) on chromosome 5q2, which encodes the D-Bifunctional protein (DBP)

42. The segregation of marker bands from at least 44 probes was explained by two alleles per locus, which had to be heterozygous in dihaploid S. acaule and maintained in homozygous condition in homoeologous chromosomes of tetraploid S. acaule.

43. A method of identifying a heterozygous carrier of a recessive black allele in an ovine animal whose white colouration is a result of ubiquitous, dominant expression of a duplicate agouti gene under the control of the itch promoter, comprising the steps of: 1. providing a nucleic acid sample from the ovine animal; and 2. establishing the number of duplicates of the agouti gene in the ovine animal by analysis of the nucleic acid sample, whereby an ovine animal with a single duplicate of the agouti gene is identified as a heterozygous carrier.

44. Mice homozygous recessive at either thea, b ord locus, i.e., with coat color phenotypes of nonagouti, brown or dilute, did not differ significantly on any of the variables from animals heterozygous or homozygous for the corresponding dominant alleles (agouti, black or full color, respectively).

45. Praluent is used together with a low-fat diet, alone or together with other Cholesterol-lowering medicines in adults with high blood Cholesterol levels called primary hyperlipidemia (including a type of high Cholesterol called heterozygous familial hyperCholesterolemia), an inherited type of high Cholesterol

46. It is an allele that expresses its trait even in the presence of an alternative allele. Out of the two alleles or Allelomorphs of a trait, the one which expresses itself in a heterozygous organism in the F1 hybrid is called the dominant trait (dominant allele).

47. It can be shown that the tri - hybrid ratio , that arises from a union in which both parents are heterozygous for three pairs of alleles , leads with dominance , to the combination of three 3 : 1 ratios independently , that is to say , to the ratio of 27 : 9 : 9 : 9 : 3 : 3 : 3 : 1 .

48. A number sign (#) is used with this entry because of evidence that Reis-Bucklers corneal dystrophy (CDRB, or CDB1) is caused by heterozygous mutation in the TGFBI gene on chromosome 5q31.The TGFBI gene is mutant in several other forms of corneal dystrophy, including Thiel-Behnke corneal dystrophy (CDTB, or CDB2; 602082), lattice type I corneal dystrophy (CDL1; 122200), lattice …