Homeobox Gene meaning in Urdu
Homeobox Gene Synonym
Homeobox Gene Definitions
1) Homeobox Gene, Homeobox : جنین کے جین : (noun) one of various similar homeotic genes that are involved in bodily segmentation during embryonic development.
Useful Words
Homeotic Gene : جنین کی نشوونما کرنے والا جین , Holandric Gene : کروموسوم کا جین , Genetic : جینیاتی , Heterozygosity : مختلف نسب کا , Homozygosity : ایک جیسے دو جینز ملاپ , Ada-Scid : مدافعتی نظام کی خرابی , Homozygote : ایک جیسے دو جینز والی , Heterozygote : مختلف نسب کا , Activator : تحریک کار , Mesothelium : میان مخاطیہ , Monogenic Disease : ایک خاندانی بیماری , Abnormalcy : جسمانی معذوری , Chromosome : لون جسم , Edward Lawrie Tatum : امریکی جاندار اشیا کی کیمیا کا ماہر , Jacques Lucien Monod : حیاتی کیمیا کا فرانسیسی ماہر , Histocompatibility Complex : چھٹے انسانی کروموسوم کی جین , Avoirdupois : موٹا , Humoral : جسم کی رطوبتوں کے بارے میں , Injure : زخمی کرنا , Body Forth : مجسم کرنا , Contractile Organ : سکڑنے والا , Defect : خرابی , Embonpoint : موٹاپا , Crud : بیماری , Bodied : جسمانی , Lie Detector : جھوٹ پکڑنے کا آلہ , Ablate : بدن کےکسی عضو کو کاٹ دینا , Acathexia : اکتھیکسیا بیماری , Figure : انسانی جسم کا نمونہ , Abdominousness : شکمی حالت , Scrawniness : دبلا پن
Useful Words Definitions
Homeotic Gene: one the genes that are involved in embryologic development.
Holandric Gene: a gene located on a Y chromosome.
Genetic: of or relating to or produced by or being a gene.
Heterozygosity: the state of being heterozygous; having two different alleles of the same gene.
Homozygosity: the state of being homozygous; having two identical alleles of the same gene.
Ada-Scid: SCID resulting from mutation of a gene that codes for adenosine deaminase.
Homozygote: (genetics) an organism having two identical alleles of a particular gene and so breeding true for the particular characteristic.
Heterozygote: (genetics) an organism having two different alleles of a particular gene and so giving rise to varying offspring.
Activator: (biology) any agency bringing about activation; a molecule that increases the activity of an enzyme or a protein that increases the production of a gene product in DNA transcription.
Mesothelium: epithelium originating in the embryonic mesoderm; lines the primordial body cavity.
Monogenic Disease: an inherited disease controlled by a single pair of genes.
Abnormalcy: an abnormal physical condition resulting from defective genes or developmental deficiencies.
Chromosome: a threadlike strand of DNA in the cell nucleus that carries the genes in a linear order.
Edward Lawrie Tatum: United States biochemist who discovered how genes act by regulating definite chemical events (1909-1975).
Jacques Lucien Monod: French biochemist who (with Francois Jacob) explained how genes are activated and suggested the existence of messenger RNA (1910-1976).
Histocompatibility Complex: a family of fifty or more genes on the sixth human chromosome that code for proteins on the surfaces of cells and that play a role in the immune response.
Avoirdupois: excess bodily weight.
Humoral: of or relating to bodily fluids.
Injure: cause injuries or bodily harm to.
Body Forth: represent in bodily form.
Contractile Organ: a bodily organ that contracts.
Defect: an imperfection in a bodily system.
Embonpoint: the bodily property of being well rounded.
Crud: an ill-defined bodily ailment.
Bodied: possessing or existing in bodily form.
Lie Detector: a polygraph that records bodily changes sometimes associated with lying.
Ablate: remove an organ or bodily structure.
Acathexia: an inability to retain bodily secretions.
Figure: a model of a bodily form (especially of a person).
Abdominousness: the bodily property of a protruding belly.
Scrawniness: the bodily property of lacking flesh.