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1: Genetics Worksheet
1: Genetics Worksheet

... A female guinea pig is heterozygous for both fur color and coat texture is crossed with a male that has light fur color and is heterozygous for coat texture. What possible offspring can they produce? Dark fur color is dominant (D) and light fur (d) is recessive. Rough coat texture (R) is dominant, w ...
Repetitive complete hydatidiform mole can be biparental in origin
Repetitive complete hydatidiform mole can be biparental in origin

... which are normally only expressed from the maternally or paternally derived allele. Further evidence that the trophoblastic hyperplasia typical of molar pregnancies results from increased expression of paternally derived genes is provided by studies of the development of reconstituted mouse eggs. Wh ...
Single-Gene Inheritance Single-Gene Inheritance
Single-Gene Inheritance Single-Gene Inheritance

... organisms having some altered form of a normal property. The normal form of any property of an organism is called the wild type, that which is found “in the wild,” or in nature. The genetic modus operandi is to mate an individual showing the property in its wild-type form (for example, a plant with ...
Transduction
Transduction

... There is no meiosis in bacteria so special techniques have been worked out for manipulating genes in bacteria so that mapping experiments, strain construction, and complementation tests can be done. First, we need a way of getting chromosomal DNA from one cell into another. There are several ways to ...
Article The Pseudoautosomal Regions of the U/V Sex
Article The Pseudoautosomal Regions of the U/V Sex

... homozygous sex in these systems. Despite a considerable amount of theoretical work on PAR genetics and evolution, these genomic regions have remained poorly characterized empirically. We show here that although the PARs of the U/V sex chromosomes of the brown alga Ectocarpus recombine at a similar r ...
Prenatal Diagnosis of Rare Familial Unbalanced Translocation of
Prenatal Diagnosis of Rare Familial Unbalanced Translocation of

... karyotype showed a balanced reciprocal translocation of 46, XY, t(7;12)(q34;q24,32). Partner’s brother had an unbalanced form of the translocation with severe learning disability. The diagnosis of the anomaly was based on two- and three-dimensional ultrasound and microarray analysis. Ultrasonography ...
Dissecting plant meiosis using Arabidopsis thaliana mutants
Dissecting plant meiosis using Arabidopsis thaliana mutants

... sequence database that can be queried for knockouts in a gene of interest. An approach has also been developed to allow high throughput screening of chemically mutagenized DNA. In denaturing high power liquid chromatography (DHPLC) plants are treated with a chemical mutagen such as EMS. The gene of ...
Kinds and Rates of Human Heritable Mutations
Kinds and Rates of Human Heritable Mutations

... The genetic code specified in DNA directs the transcription of RNA, which is translated into polypeptide chains; these chains, in turn, are assembled into proteins, which are the body’s tools for the regulation of physiological, biochemical, and behavioral functioning. Mutations, transmissible alter ...
Presentation
Presentation

... First generation parents must be “Aa” because they have normal phenotypes, but affected offspring. ...
the contribution of gene movement to the two rules of speciation
the contribution of gene movement to the two rules of speciation

... contribute to hybrid dysfunction and the Large X-effect depends upon the specific mechanism of gene movement and on details of developmental and reproductive biology of the X. We briefly introduce these mechanisms below, returning to the evidence for each in the next section. There are three mechani ...
Increased sex chromosome expression and epigenetic
Increased sex chromosome expression and epigenetic

... 2006). However, the X and Y chromosomes are continually remodelled during the transition between meiosis and spermiogenesis, and histone modifications associated with transcriptionally active chromatin [e.g. histone acetylation and histone H3 dimethylated on lysine 4 (H3K4me2)] are also enriched on ...
Scientist finds the gene that determines major sensitivity to bitter taste
Scientist finds the gene that determines major sensitivity to bitter taste

... world. Those millions of Europeans, Asians, and individuals from other populations around the world who are non-tasters descended from a common ancestor who emerged from Africa far back in prehistory. Human DNA sequences are overwhelmingly similar, with some small, but sometimes important difference ...
IVRI OB 1809
IVRI OB 1809

... which differed in one recognisable respect: one was tall, the oth<;r dwarf. The first generation, or F I , progeny were all ~tall, but when they were self-pollinated they produced second generation, or F 2 , progeny three-quarters of which were tall and one-quarter dwarf. The dwarfall bred true, and ...
Introduction To Genetics- Chapter 11
Introduction To Genetics- Chapter 11

... crosses between parents with contrasting traits ...
Meiosis I - scecinascience
Meiosis I - scecinascience

... How can two alleles from different genes be inherited together? Alleles of different genes tend to be inherited together from one generation to the next when those genes are located on the same chromosome. ...
ch 11_4
ch 11_4

... How can two alleles from different genes be inherited together? Alleles of different genes tend to be inherited together from one generation to the next when those genes are located on the same chromosome. ...
Inheritance of Aldehyde Oxidase in Drosophila melanogaster
Inheritance of Aldehyde Oxidase in Drosophila melanogaster

... areas of genetic research. The study of genetics focuses on an understanding of the principles which govern the inheritance of specific traits. Initial experiments were concerned with the transmission of hereditary factors from generation to generation and led to the discovery of specific laws which ...
Genome Mapping in the Horse
Genome Mapping in the Horse

... and identify the causative mutation. Further, genome maps can be used for comparative genome mapping in which homologous loci in other species are explored, for evolutionary studies, and also for comparisons of the recombination frequency within and between species. ...
Alu repeat analysis in the complete human genome: trends and
Alu repeat analysis in the complete human genome: trends and

... units separated by a poly ‘A’ stretch. The monomers, homologous to 7SL RNA, are absolutely identical except for a 30 bp insertion in the right monomer (Jelinek et al., 1980; Ullu and Tschudi, 1984). The 3 end of the Alu element has a long stretch of adenine residues, and is flanked by 4–10 bp of di ...
ExomeDepth
ExomeDepth

... optimized set of exomes that are well correlated with that exome. This is what I call the optimized aggregate reference set, which is optimized for each exome sample. So the first step is to select the most appropriate reference sample. This step is demonstrated below. ...
Genetic crosses - thephysicsteacher.ie
Genetic crosses - thephysicsteacher.ie

... Most are like the parents due to genes being linked. A small percentage are unlike the parents due to crossing-over - these are called recombinants. Crossing-over leads to greater variation. Separation of linked genes with crossing-over can result in the same variety of gamete genotypes and offsprin ...
continued
continued

... 10.1 What Is the Physical Basis of Inheritance?  Genes are sequences of nucleotides at specific locations on chromosomes – Inheritance is the process by which the characteristics of individuals are passed to their offspring – A gene is a unit of heredity that encodes information needed to produce ...
Article Why There Are No Essential Genes on
Article Why There Are No Essential Genes on

... chromosomes are probably less likely than plasmids to bear genes coding for conjugation. However, there are other phenotypic traits that also seem to be coded for by plasmidbiased genes. For reasons that have not been fully explained (though see Nogueira et al. 2009), bacteriocin production (Gonzale ...
(2013). Nothing in genetics makes sense except in light of genomic
(2013). Nothing in genetics makes sense except in light of genomic

... Next, suppose that A and B are two alleles at a single locus. If A increases because (a) it was favored by selectionSIL , (b) the forward mutation rate producing it was faster than the back-mutation rate destroying it, (c) immigration brought in the allele faster than emigration removed it, or (d ) ...
A Fine Physical Map of Arabidopsis thaliana Chromosome 5
A Fine Physical Map of Arabidopsis thaliana Chromosome 5

... A fine physical map of Arabidopsis thaliana chromosome 5 was constructed by ordering the clones from YAC, PI, TAC and BAC libraries of the genome using the sequences of a variety of genetic and EST markers and terminal sequences of clones. The markers used were 88 genetic markers, 13 EST markers, 87 ...
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Y chromosome



The Y chromosome is one of two sex chromosomes (allosomes) in mammals, including humans, and many other animals. The other is the X chromosome. Y is the sex-determining chromosome in many species, since it is the presence or absence of Y that determines the male or female sex of offspring produced in sexual reproduction. In mammals, the Y chromosome contains the gene SRY, which triggers testis development. The DNA in the human Y chromosome is composed of about 59 million base pairs. The Y chromosome is passed only from father to son. With a 30% difference between humans and chimpanzees, the Y chromosome is one of the fastest evolving parts of the human genome. To date, over 200 Y-linked genes have been identified. All Y-linked genes are expressed and (apart from duplicated genes) hemizygous (present on only one chromosome) except in the cases of aneuploidy such as XYY syndrome or XXYY syndrome. (See Y linkage.)
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