 
									
								
									Duplicative Transfer of a MADS Box Gene to a Plant Y Chromosome
									
... that dioecy in the genus evolved from gynodioecious ancestors (Desfeux et al. 1996). This is consistent with the fact that, whereas the majority of species in the 80 genera in the family Caryophyllaceae are hermaphroditic, many Silene species are gynodioecious and must carry male sterility factors ( ...
                        	... that dioecy in the genus evolved from gynodioecious ancestors (Desfeux et al. 1996). This is consistent with the fact that, whereas the majority of species in the 80 genera in the family Caryophyllaceae are hermaphroditic, many Silene species are gynodioecious and must carry male sterility factors ( ...
									File - need help with revision notes?
									
... genes on the chromosome: if the loci are far apart (ie. there are more base pairs between the genes) they are more likely to be separated and so this will give a higher frequency of recombination. If the genes are very close to each other on the chromosome, there is less chance that the genes will b ...
                        	... genes on the chromosome: if the loci are far apart (ie. there are more base pairs between the genes) they are more likely to be separated and so this will give a higher frequency of recombination. If the genes are very close to each other on the chromosome, there is less chance that the genes will b ...
									Biology
									
... Breakage of a chromosome can lead to four types of mutations: 1. deletion mutation – a piece breaks off completely 2. duplication mutation – it carries 2 copies 3. inversion mutation – reattachment is reversed 4. translocation mutation – attaches to the wrong ...
                        	... Breakage of a chromosome can lead to four types of mutations: 1. deletion mutation – a piece breaks off completely 2. duplication mutation – it carries 2 copies 3. inversion mutation – reattachment is reversed 4. translocation mutation – attaches to the wrong ...
									Permutation to assess the generalizability of the reduction in error
									
... Permutation to assess the generalizability of the reduction in error rate observed by addition of the ‘histology gene’ To assess whether the reduction seen in error rate was specific to the selected set of 10 discriminatory genes all 1280 genes were ranked by adding the squared values of the Kolmogo ...
                        	... Permutation to assess the generalizability of the reduction in error rate observed by addition of the ‘histology gene’ To assess whether the reduction seen in error rate was specific to the selected set of 10 discriminatory genes all 1280 genes were ranked by adding the squared values of the Kolmogo ...
									CHAPTER 10
									
... same length, same centromere position, and carry genes that control the same inherited traits. • These genes each code for the same trait (ex: earlobe) but maybe not the same type of trait (earlobe) ...
                        	... same length, same centromere position, and carry genes that control the same inherited traits. • These genes each code for the same trait (ex: earlobe) but maybe not the same type of trait (earlobe) ...
									3.2 Probability Student pages
									
... 1. A gene is a section of DNA, with many bases that code for a protein. This results in a trait. 2. Traits are controlled by genes. Genes are found on chromosomes and have a genetic code for a protein. The position of the gene on the chromosome is called the locus. 3. Different versions of a gene fo ...
                        	... 1. A gene is a section of DNA, with many bases that code for a protein. This results in a trait. 2. Traits are controlled by genes. Genes are found on chromosomes and have a genetic code for a protein. The position of the gene on the chromosome is called the locus. 3. Different versions of a gene fo ...
									Molecular Genetics DNA Functions Replication Molecular Genetics
									
... occurred Crossing over frequency used to construct genetic map of chromosomes. o 1 map unit = 1% crossing over between pair of genes DNA sequence information used to explore gene function in other species. ...
                        	... occurred Crossing over frequency used to construct genetic map of chromosomes. o 1 map unit = 1% crossing over between pair of genes DNA sequence information used to explore gene function in other species. ...
									Pedigree Analysis in Human Genetics
									
... • Heterozygotes exhibit the phenotype • Every affected individual has at least one affected parent (except in traits with high mutation rates) • Two affected individuals can have an unaffected child • Usually an affected family member in each generation ...
                        	... • Heterozygotes exhibit the phenotype • Every affected individual has at least one affected parent (except in traits with high mutation rates) • Two affected individuals can have an unaffected child • Usually an affected family member in each generation ...
									Gene Expression
									
... Cells use information in genes to build hundreds of different proteins, each with a specific function. But, not all proteins are required by the cell at any one time. By regulating gene expression, cells are able to control which proteins are made. ...
                        	... Cells use information in genes to build hundreds of different proteins, each with a specific function. But, not all proteins are required by the cell at any one time. By regulating gene expression, cells are able to control which proteins are made. ...
									Genetics Exercises PDF
									
... A description of the process in words: 1) Steroids bind to proteins called “receptors”. 2) Steroid receptors dimerize and bind DNA. 3) Steroid receptors that are bound to DNA recruit other proteins that function as “co-activators”. 4) Coactivators recruit RNA polymerase, which binds to the promote ...
                        	... A description of the process in words: 1) Steroids bind to proteins called “receptors”. 2) Steroid receptors dimerize and bind DNA. 3) Steroid receptors that are bound to DNA recruit other proteins that function as “co-activators”. 4) Coactivators recruit RNA polymerase, which binds to the promote ...
									An introduction to genetic algorithms for neural networks
									
... Figure 5: When genes are far apart on a chromosome, they will tend to be split apart by a single crossover (left). If they are close together, they will tend to stay together (right). The basic chromosome, as mentioned above, can consist of the set of inputs to the network. There are some ways to he ...
                        	... Figure 5: When genes are far apart on a chromosome, they will tend to be split apart by a single crossover (left). If they are close together, they will tend to stay together (right). The basic chromosome, as mentioned above, can consist of the set of inputs to the network. There are some ways to he ...
									The Fluid Mosaic Model of Membranes
									
... – Their children will not have the CF allele, so will not be able to pass on the disorder to their own children. – Although IVF is expensive, in the long term, money will be saved by the NHS as the children born will not have to be treated for CF. Also they will not need a heart–lung ...
                        	... – Their children will not have the CF allele, so will not be able to pass on the disorder to their own children. – Although IVF is expensive, in the long term, money will be saved by the NHS as the children born will not have to be treated for CF. Also they will not need a heart–lung ...
									Homework Assignment #1 - Due September 28th
									
... plain-headed bird is crossed to a homozygous red-feathered, crested-headed bird. What phenotypic and genotypic ratios are expected from testcrossing only the F2 black-crested birds? Hint: Remember to account for the relative frequencies of the different genotypes in this one ...
                        	... plain-headed bird is crossed to a homozygous red-feathered, crested-headed bird. What phenotypic and genotypic ratios are expected from testcrossing only the F2 black-crested birds? Hint: Remember to account for the relative frequencies of the different genotypes in this one ...
									How Inheritance Works In Swine
									
... as black or red coat color) was determined by the order of nucleotides in a segment of the chromosome. This is the gene, the basic unit of inheritance. A chromosome, then, consists of many genes arranged end-to-end. Chromosomes occur in pairs in the nucleus, and each species of farm animals has its ...
                        	... as black or red coat color) was determined by the order of nucleotides in a segment of the chromosome. This is the gene, the basic unit of inheritance. A chromosome, then, consists of many genes arranged end-to-end. Chromosomes occur in pairs in the nucleus, and each species of farm animals has its ...
									Optical Illusions
									
... metabolism Most “single gene disorders” are probably influenced by multiple genes / DNA ...
                        	... metabolism Most “single gene disorders” are probably influenced by multiple genes / DNA ...
									LP - Columbia University
									
... b. Number: There are 2 homologs = 2 of each type of chromosome in diploid cells. One from mom, one from dad. c. Relationship of genes on homologs; alleles. Homologs (except for sex chromosomes) carry homologous DNA. They carry the same genes, in the same order, in corresponding places (loci), but th ...
                        	... b. Number: There are 2 homologs = 2 of each type of chromosome in diploid cells. One from mom, one from dad. c. Relationship of genes on homologs; alleles. Homologs (except for sex chromosomes) carry homologous DNA. They carry the same genes, in the same order, in corresponding places (loci), but th ...
									Name: _ Per: ______ Date: Chapter 14 Test Review Describe how
									
... Any of the chromosomes other than the sex chromosomes (X or Y chromosome, 23rd pair) 3. What are sex-linked genes? X-linked genes? Sex-linked genes are those found on either the X or Y chromosome. X-linked genes are found only on the X. 4. Which gender displays X-linked traits more frequently? Why? ...
                        	... Any of the chromosomes other than the sex chromosomes (X or Y chromosome, 23rd pair) 3. What are sex-linked genes? X-linked genes? Sex-linked genes are those found on either the X or Y chromosome. X-linked genes are found only on the X. 4. Which gender displays X-linked traits more frequently? Why? ...
									Genetics
									
... Mutation and sexual reproduction lead to genetic variation in a population. As a basis for understanding this concept: a. Students know meiosis is an early step in sexual reproduction in which the pairs of chromosomes separate and segregate randomly during cell division to produce gametes containing ...
                        	... Mutation and sexual reproduction lead to genetic variation in a population. As a basis for understanding this concept: a. Students know meiosis is an early step in sexual reproduction in which the pairs of chromosomes separate and segregate randomly during cell division to produce gametes containing ...
									Extensions of Mendel`s Rules
									
... and prevent normal CNS development – 1/15,000 births on average – If affected person consumes a diet low in phenylalanine, then they develop normally – *Mere presence of gene DOES NOT determine phenotype ...
                        	... and prevent normal CNS development – 1/15,000 births on average – If affected person consumes a diet low in phenylalanine, then they develop normally – *Mere presence of gene DOES NOT determine phenotype ...
									answers to review questions chapter 4
									
... a. An autosomal recessive trait is inherited from carriers and affects both sexes. An autosomal dominant trait can be inherited from one parent, who is affected. Autosomal recessive inheritance can skip generations; autosomal dominant inheritance cannot. b. Mendel's first law concerns inheritance of ...
                        	... a. An autosomal recessive trait is inherited from carriers and affects both sexes. An autosomal dominant trait can be inherited from one parent, who is affected. Autosomal recessive inheritance can skip generations; autosomal dominant inheritance cannot. b. Mendel's first law concerns inheritance of ...
X-inactivation
 
                        X-inactivation (also called lyonization) is a process by which one of the two copies of the X chromosome present in female mammals is inactivated. The inactive X chromosome is silenced by its being packaged in such a way that it has a transcriptionally inactive structure called heterochromatin. As nearly all female mammals have two X chromosomes, X-inactivation prevents them from having twice as many X chromosome gene products as males, who only possess a single copy of the X chromosome (see dosage compensation). The choice of which X chromosome will be inactivated is random in placental mammals such as humans, but once an X chromosome is inactivated it will remain inactive throughout the lifetime of the cell and its descendants in the organism. Unlike the random X-inactivation in placental mammals, inactivation in marsupials applies exclusively to the paternally derived X chromosome.
 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									