Mitochondrial genes in the colourless alga Prototheca wickerhamii
... the filamentous fungus Podospora anserina and up to seven introns in various strains of the yeast Saccharomyces cerevisiae, but none in the common laboratory strain of Neurospora crassa (5, 6, 7, 8). So far, only few introns have been detected in mitochondria from angiosperms and gymnosperms and all ...
... the filamentous fungus Podospora anserina and up to seven introns in various strains of the yeast Saccharomyces cerevisiae, but none in the common laboratory strain of Neurospora crassa (5, 6, 7, 8). So far, only few introns have been detected in mitochondria from angiosperms and gymnosperms and all ...
12q14 microdeletions
... 12q14 microdeletions A 12q14 microdeletion is a very rare genetic condition in which a tiny piece is missing from one of the 46 chromosomes – chromosome 12. Chromosomes are made up mostly of DNA and are the structures in the nucleus of the body’s cells that carry genetic information (known as genes ...
... 12q14 microdeletions A 12q14 microdeletion is a very rare genetic condition in which a tiny piece is missing from one of the 46 chromosomes – chromosome 12. Chromosomes are made up mostly of DNA and are the structures in the nucleus of the body’s cells that carry genetic information (known as genes ...
Affymetrix Chips
... expression data maintained by European Bioinformatics Institute. ChipDB - A searchable database of gene expression Gene Expression Atlas - A database for gene expression profile from 91 normal human and mouse samples across a diverse array of tissues, organs, and cell lines. Gene Expression Database ...
... expression data maintained by European Bioinformatics Institute. ChipDB - A searchable database of gene expression Gene Expression Atlas - A database for gene expression profile from 91 normal human and mouse samples across a diverse array of tissues, organs, and cell lines. Gene Expression Database ...
SPT3 interacts with TFIID to allow normal transcription in
... function in vivo. To study further the sptlS-21 defect, extragenic suppressors of this mutation were isolated and analyzed. All of the extragenic suppressors of sptlS-21 are mutations in the previously identified SPT3 gene. Suppression of sptlS-21 by these spt3 mutations is allele-specific, suggesti ...
... function in vivo. To study further the sptlS-21 defect, extragenic suppressors of this mutation were isolated and analyzed. All of the extragenic suppressors of sptlS-21 are mutations in the previously identified SPT3 gene. Suppression of sptlS-21 by these spt3 mutations is allele-specific, suggesti ...
Document
... with a carrier incidence of 1 in 40. Canavan disease is a central nervous system disease that is usually fatal in childhood, with a few people surviving to adulthood. This disease is the result of a substance that destroys the central nervous system over time. There is presently no effective treatme ...
... with a carrier incidence of 1 in 40. Canavan disease is a central nervous system disease that is usually fatal in childhood, with a few people surviving to adulthood. This disease is the result of a substance that destroys the central nervous system over time. There is presently no effective treatme ...
achondroplasia
... chance that the child will inherit one abnormal gene from each parent and have severe skeletal abnormalities that lead to early death. A child who does not inherit the gene will be completely free of the condition, and cannot pass it on to his or her own children. ...
... chance that the child will inherit one abnormal gene from each parent and have severe skeletal abnormalities that lead to early death. A child who does not inherit the gene will be completely free of the condition, and cannot pass it on to his or her own children. ...
predominant expression of at cell receptor v,6 gene subfamily
... and V,18 .2 bands . T cell clone PJpR-6 .2 has deleted all of the members of the V,38 gene subfamily on one chromosome and has a rearrangement to V08.2 on the other, leaving one germline copy of the V08.3 gene on that chromosome (Fig . 3 a) . With a J,I-specific probe, it was shown that this clone u ...
... and V,18 .2 bands . T cell clone PJpR-6 .2 has deleted all of the members of the V,38 gene subfamily on one chromosome and has a rearrangement to V08.2 on the other, leaving one germline copy of the V08.3 gene on that chromosome (Fig . 3 a) . With a J,I-specific probe, it was shown that this clone u ...
The CNS midline cells and spitz class genes are required for proper
... group gives rise to a NB (Campos-Ortega, 1993). Although the establishment of NB and VE fate. The sim gene product is known mechanisms for NB formation are relatively well understood, the to be a nuclear protein containing a basic helix-loop-helix motif molecular mechanisms leading to the determinat ...
... group gives rise to a NB (Campos-Ortega, 1993). Although the establishment of NB and VE fate. The sim gene product is known mechanisms for NB formation are relatively well understood, the to be a nuclear protein containing a basic helix-loop-helix motif molecular mechanisms leading to the determinat ...
File
... This makes for a lot of genetic diversity. This trick is accomplished through independent assortment and crossing-over. ...
... This makes for a lot of genetic diversity. This trick is accomplished through independent assortment and crossing-over. ...
Exercise II - GEP Community Server
... ii. inaccurate transcriptional start and termination sites and therefore inaccurate 5’- and 3’untranslated regions (caused by difficulties predicting first and last exons due to transcriptional start and termination sites not following easily discernable patterns). 8. The Augustus gene prediction ha ...
... ii. inaccurate transcriptional start and termination sites and therefore inaccurate 5’- and 3’untranslated regions (caused by difficulties predicting first and last exons due to transcriptional start and termination sites not following easily discernable patterns). 8. The Augustus gene prediction ha ...
The E-Class PPR Protein MEF3 of Arabidopsis
... Fig. 1 An ecotype-specific difference in RNA editing is observed at a conserved nucleotide in mitochondrial RNAs. (A) The editing site at nucleotide 89 in the mRNA of the atp4 gene (atp4-89) in mitochondria of Arabidopsis thaliana is processed to nearly 100% in ecotypes Columbia (Col) and C24, but o ...
... Fig. 1 An ecotype-specific difference in RNA editing is observed at a conserved nucleotide in mitochondrial RNAs. (A) The editing site at nucleotide 89 in the mRNA of the atp4 gene (atp4-89) in mitochondria of Arabidopsis thaliana is processed to nearly 100% in ecotypes Columbia (Col) and C24, but o ...
Meiosis - DiBiasioScience
... Telophase I • Each pole now has haploid set of chromosomes. • Cytokinesis occurs and two haploid daughter cells are formed. ...
... Telophase I • Each pole now has haploid set of chromosomes. • Cytokinesis occurs and two haploid daughter cells are formed. ...
PDF
... Xun Huang1,2, James T. Warren3, JoAnn Buchanan4, Lawrence I. Gilbert3 and Matthew P. Scott1,* Mutations in either of the two human Niemann-Pick type C (NPC) genes, NPC1 and NPC2, cause a fatal neurodegenerative disease associated with abnormal cholesterol accumulation in cells. npc1a, the Drosophila ...
... Xun Huang1,2, James T. Warren3, JoAnn Buchanan4, Lawrence I. Gilbert3 and Matthew P. Scott1,* Mutations in either of the two human Niemann-Pick type C (NPC) genes, NPC1 and NPC2, cause a fatal neurodegenerative disease associated with abnormal cholesterol accumulation in cells. npc1a, the Drosophila ...
Introduction to Genetics
... Let PL / pl denote that in the parent, one chromosome carries the P and L alleles (at the flower color and pollen shape loci, respectively), while the other chromosome carries the p and l alleles. Unless there is a recombination event, one of the two parental chromosome types (PL or pl) are passed o ...
... Let PL / pl denote that in the parent, one chromosome carries the P and L alleles (at the flower color and pollen shape loci, respectively), while the other chromosome carries the p and l alleles. Unless there is a recombination event, one of the two parental chromosome types (PL or pl) are passed o ...
Clinical Laboratory Reports in Molecular Pathology
... then the level of DNA or housekeeping RNA in the blood might also be low). The expected result in a normal individual should be stated. This is expressed as a normal range for a quantitative test, along with the units of measurement. Interassay reproducibility is an important parameter that allows a ...
... then the level of DNA or housekeeping RNA in the blood might also be low). The expected result in a normal individual should be stated. This is expressed as a normal range for a quantitative test, along with the units of measurement. Interassay reproducibility is an important parameter that allows a ...
P.Point Lecture Template - Green River Community College
... How many genetically unique gametes are possible for the following genotypes? List the genotypes of all possible gametes for #’s 1-5, below. ...
... How many genetically unique gametes are possible for the following genotypes? List the genotypes of all possible gametes for #’s 1-5, below. ...
meiosis
... Telophase II – The only difference from mitotic division is that chromosomes do not replicate before they divide at centromeres. ...
... Telophase II – The only difference from mitotic division is that chromosomes do not replicate before they divide at centromeres. ...
PDF
... results provide strong support for the view that all melanoblasts are affected and the host tissue plays an important role in determining the pattern of spotting. However, there appear to be some indications that all melanoblasts may not be affected to the same degree. INTRODUCTION ...
... results provide strong support for the view that all melanoblasts are affected and the host tissue plays an important role in determining the pattern of spotting. However, there appear to be some indications that all melanoblasts may not be affected to the same degree. INTRODUCTION ...
Text S1 unc-46 The unc-46 gene encodes a protein required for the
... brenneri CRE appeared to be functionally equivalent to its C. elegans counterpart. We did not observe any ectopic expression. ...
... brenneri CRE appeared to be functionally equivalent to its C. elegans counterpart. We did not observe any ectopic expression. ...
The PTPN22 R620W mutation is independent of HLA
... Due to the rarity of IIM, difficulties will always be encountered when trying to recruit a sufficient number of cases for analysis in genetic association studies that examine SNPs with a modest effect size. The present study was not powered to detect associations after stratification by disease or ...
... Due to the rarity of IIM, difficulties will always be encountered when trying to recruit a sufficient number of cases for analysis in genetic association studies that examine SNPs with a modest effect size. The present study was not powered to detect associations after stratification by disease or ...
PDF
... Maternal effects are defined by mutations that affect the next generation when they are maternally inherited. To date, most indepth studies of maternal effects in plants have attributed their origin to genomic imprinting that restricts expression to the maternal allele. The DNA glycosylase DEMETER ( ...
... Maternal effects are defined by mutations that affect the next generation when they are maternally inherited. To date, most indepth studies of maternal effects in plants have attributed their origin to genomic imprinting that restricts expression to the maternal allele. The DNA glycosylase DEMETER ( ...
Analysis of the mitochondrial COI gene and its
... The mitochondrial cytochrome oxidase subunit 1 (COI) gene is one of the most popular markers used in molecular systematics. Portions of this gene are often used to infer phylogenies. In addition, COI is currently the focus of considerable interest, especially its 5' portion, which is used by the DNA ...
... The mitochondrial cytochrome oxidase subunit 1 (COI) gene is one of the most popular markers used in molecular systematics. Portions of this gene are often used to infer phylogenies. In addition, COI is currently the focus of considerable interest, especially its 5' portion, which is used by the DNA ...
ISEcp1 pneumoniae Research Article
... very well shown by some of the isolates in this study with phenotypic negative result yet positive for PCR. In PCR based identification 49.5% positive strains for blaCTX-M were identified which is quite higher percentage. Most prevalent cluster among these isolates was found out by RFLP study that i ...
... very well shown by some of the isolates in this study with phenotypic negative result yet positive for PCR. In PCR based identification 49.5% positive strains for blaCTX-M were identified which is quite higher percentage. Most prevalent cluster among these isolates was found out by RFLP study that i ...
Controlling Soil-borne cereal mosaic virus in the UK by developing
... prepared from triplicate samples taken at 5, 7, 9, 12, and 14 days after planting and the results normalised against an RNA specific control. These results demonstrated C sub A9 increased in expression after 14 days in both uninfected and infected soil, suggesting C sub A9 is not involved in SBCMV r ...
... prepared from triplicate samples taken at 5, 7, 9, 12, and 14 days after planting and the results normalised against an RNA specific control. These results demonstrated C sub A9 increased in expression after 14 days in both uninfected and infected soil, suggesting C sub A9 is not involved in SBCMV r ...