Mapping quantitative trait loci and expressed sequence tags related
... 2001, Yang et al. 2002). However, the BPH resistance conferred by these major genes is not durable; for example, Bph1 and bph2 can be overcome by BPH biotypes 2 and 3 (Pathak and Heinrichs 1982, Panda and Khush 1995). In contrast, quantitative trait loci (QTLs) were found to confer more durable BPH ...
... 2001, Yang et al. 2002). However, the BPH resistance conferred by these major genes is not durable; for example, Bph1 and bph2 can be overcome by BPH biotypes 2 and 3 (Pathak and Heinrichs 1982, Panda and Khush 1995). In contrast, quantitative trait loci (QTLs) were found to confer more durable BPH ...
MB206_fhs_lnt_001.1_AT_May09
... The DNA-directed synthesis of RNA is called transcription. Transcription produces RNA molecules that are complimentary copies of one strand of DNA. Only one of the dsDNA strands can serve as template for synthesis of a specific mRNA molecule. mRNAs transmit information from DNA, and each mRN ...
... The DNA-directed synthesis of RNA is called transcription. Transcription produces RNA molecules that are complimentary copies of one strand of DNA. Only one of the dsDNA strands can serve as template for synthesis of a specific mRNA molecule. mRNAs transmit information from DNA, and each mRN ...
HIGH FREQUENCY GENE TARGETING USING INSERTIONAL
... recombination was 1 in 46 (2.2%). This frequency is significantly higher than those reported by two other groups using isogenic DNA sequence replacement constructs (11,12). All three groups were targeting the same region (at and around exon 10 of the Cftr gene), although the replacement targeting co ...
... recombination was 1 in 46 (2.2%). This frequency is significantly higher than those reported by two other groups using isogenic DNA sequence replacement constructs (11,12). All three groups were targeting the same region (at and around exon 10 of the Cftr gene), although the replacement targeting co ...
thesis - Tel Archives ouvertes
... them through the analysis of globozoospermia cases. By this study, we are now focusing our efforts on azoospermia and severe oligozoospermia. The first four chapters describe the background, methods and literature, while following three chapters present an analysis of datas and results. The first ch ...
... them through the analysis of globozoospermia cases. By this study, we are now focusing our efforts on azoospermia and severe oligozoospermia. The first four chapters describe the background, methods and literature, while following three chapters present an analysis of datas and results. The first ch ...
Cloning and Expression of Bovine Sodium/Glucose Cotransporters* J. Dairy Sci. 88:182–194
... (bSGLT1 and bSGLT5) were obtained by rapid amplification of cDNA ends (RACE) using the SMART RACE cDNA amplification kit (Clontech, Palo Alto, CA). The 3′ and 5′ RACE-ready first-strand cDNA were synthesized using 1 µg of poly(A)+ RNA from bovine kidney. For 5′ RACE of bSGLT1, 2 primers, SGLT-R1 and ...
... (bSGLT1 and bSGLT5) were obtained by rapid amplification of cDNA ends (RACE) using the SMART RACE cDNA amplification kit (Clontech, Palo Alto, CA). The 3′ and 5′ RACE-ready first-strand cDNA were synthesized using 1 µg of poly(A)+ RNA from bovine kidney. For 5′ RACE of bSGLT1, 2 primers, SGLT-R1 and ...
Incomplete penetrance of MHC susceptibility genes
... partially penetrant MHC susceptibility genes. One can analyze affected sib pairs (12). If the trait and its genetic markers are rare, ...
... partially penetrant MHC susceptibility genes. One can analyze affected sib pairs (12). If the trait and its genetic markers are rare, ...
Bioinformatics Toolbox
... Interactive programming language — Test your ideas by typing functions that are interpreted interactively with a language whose basic data element is an array. The arrays do not require dimensioning and allow you to solve many technical computing problems, ...
... Interactive programming language — Test your ideas by typing functions that are interpreted interactively with a language whose basic data element is an array. The arrays do not require dimensioning and allow you to solve many technical computing problems, ...
The Association of DRD2 Gene TaqI Polymorphism with Attention
... confirms the role of the dopamine neurotransmitter system in the etiology of ADHD, studies of molecular genetic have mostly focused on genes in these pathways. Because dopamine is involved in a variety of critical functions, therefore many human disorders have been related to dopaminergic dysfunctio ...
... confirms the role of the dopamine neurotransmitter system in the etiology of ADHD, studies of molecular genetic have mostly focused on genes in these pathways. Because dopamine is involved in a variety of critical functions, therefore many human disorders have been related to dopaminergic dysfunctio ...
Major histocompatibility locus genetic markers of beryllium sensitization and disease
... ABSTRACT: Hypersensitivity to beryllium (Be) is found in 1–16% of exposed workers undergoing immunological screening for beryllium disease using the beryllium lymphocyte proliferation test (BeLPT). However, only y50% of BeLPT-positive workers present with lung granulomas (i.e. berylliosis). As beryl ...
... ABSTRACT: Hypersensitivity to beryllium (Be) is found in 1–16% of exposed workers undergoing immunological screening for beryllium disease using the beryllium lymphocyte proliferation test (BeLPT). However, only y50% of BeLPT-positive workers present with lung granulomas (i.e. berylliosis). As beryl ...
Phylogeny, taxonomy, and evolution of the endothelin receptor gene
... EDNR family refer to those recommended by this study, as developed from its gene phylogeny. More generally, the names and symbols of this study also follow the guidelines of the HUGO Gene Nomenclature Committee (Wain et al., 2002). Thus, gene symbols are italicized, whereas gene names and protein sy ...
... EDNR family refer to those recommended by this study, as developed from its gene phylogeny. More generally, the names and symbols of this study also follow the guidelines of the HUGO Gene Nomenclature Committee (Wain et al., 2002). Thus, gene symbols are italicized, whereas gene names and protein sy ...
Overview of the genes of watermelon1
... intermediate between normal and dwarf, and the hypocotyls were somewhat longer than normal vine and considerably longer than dwarf. The dw-1s is recessive to normal plant type. Plants with dw-2 have short internodes due to fewer cells than the normal type, and plants with dw-3 have leaves with fewer ...
... intermediate between normal and dwarf, and the hypocotyls were somewhat longer than normal vine and considerably longer than dwarf. The dw-1s is recessive to normal plant type. Plants with dw-2 have short internodes due to fewer cells than the normal type, and plants with dw-3 have leaves with fewer ...
Chapter 23 Practice Multiple Choice
... In the wild, male house finches (Carpodus mexicanus) vary considerably in the amount of red pigmentation in their head and throat feathers, with colors ranging from pale yellow to bright red. These colors come from carotenoid pigments that are found in the birds' diets; no vertebrates are known to s ...
... In the wild, male house finches (Carpodus mexicanus) vary considerably in the amount of red pigmentation in their head and throat feathers, with colors ranging from pale yellow to bright red. These colors come from carotenoid pigments that are found in the birds' diets; no vertebrates are known to s ...
Direct Deletion Analysis in Two Duchenne Muscular Dystrophy
... skeletal muscle, which results in early muscle degeneration and death. DMD is a common disease that affects 1 : 3500 newborn males (Emery, 1996), while BMD is less frequent. Both of the diseases are caused by mutations, mostly deletions of one or more exons of the dystrophin gene (Den Dunnen et al., ...
... skeletal muscle, which results in early muscle degeneration and death. DMD is a common disease that affects 1 : 3500 newborn males (Emery, 1996), while BMD is less frequent. Both of the diseases are caused by mutations, mostly deletions of one or more exons of the dystrophin gene (Den Dunnen et al., ...
CHAPTER 8 Recombinant DNA Technology
... 6. All copies of a chromosome will contain the same restriction sites, and will be cut into identical fragments. 7. Based on probability, a specific short DNA sequence occurs more frequently than a longer one. a. In a 50% G-C organism with random distribution of bases, the probability of a specific ...
... 6. All copies of a chromosome will contain the same restriction sites, and will be cut into identical fragments. 7. Based on probability, a specific short DNA sequence occurs more frequently than a longer one. a. In a 50% G-C organism with random distribution of bases, the probability of a specific ...
Behavioral Health - PGXL Laboratories
... • All orderable as single genes at the top of the req form ...
... • All orderable as single genes at the top of the req form ...
Training - Tistory
... • There are nine possible dihybrid ratios when both genes show complete dominance Examples: • 9:7 occurs when a homozygous recessive mutation in either or both of two different genes produces the same phenotype • 12:3:1 results when a dominant allele of one gene masks the genotype of a different gen ...
... • There are nine possible dihybrid ratios when both genes show complete dominance Examples: • 9:7 occurs when a homozygous recessive mutation in either or both of two different genes produces the same phenotype • 12:3:1 results when a dominant allele of one gene masks the genotype of a different gen ...
Leukaemia Section t(1;1)(p36;q21) in non Hodgkin lymphoma Atlas of Genetics and Cytogenetics
... mutations are necessary to generate a fully malignant clonal proliferation. Many of these secondary genetic alterations (including chromosome 1) are visible in the clonal karyotype; it is now possible to identify the sequence by which they arise and their influence on clinical behavior by using comp ...
... mutations are necessary to generate a fully malignant clonal proliferation. Many of these secondary genetic alterations (including chromosome 1) are visible in the clonal karyotype; it is now possible to identify the sequence by which they arise and their influence on clinical behavior by using comp ...
Leukaemia Section 8p11 myeloproliferative syndrome (EMS, eight p11 myeloproliferative syndrome)
... 2001). Only interphase cells were available to perform FISH analysis, and the results obtained indicated a breakpoint within or in the vicinity of NUP98 but definite molecular characterization could not be done. Other patient with AML and the same translocation had been reported previously (Larson e ...
... 2001). Only interphase cells were available to perform FISH analysis, and the results obtained indicated a breakpoint within or in the vicinity of NUP98 but definite molecular characterization could not be done. Other patient with AML and the same translocation had been reported previously (Larson e ...
1 Sequential elimination of major-effect contributors
... confounding effects of major loci and epistasis. Therefore, to avoid confounding effects of major loci, epistasis and sample size, we used a targeted backcross mapping strategy that genetically eliminated the effect of a previously identified major QTL underlying high-temperature growth (Htg) in yea ...
... confounding effects of major loci and epistasis. Therefore, to avoid confounding effects of major loci, epistasis and sample size, we used a targeted backcross mapping strategy that genetically eliminated the effect of a previously identified major QTL underlying high-temperature growth (Htg) in yea ...
Real – time fMRI
... • Additionally, except for one, SNPs influencing BMI in normal population didn’t predict BMI in the ANR group, suggesting that their effects are overruled by presence of other, putative genetic risk factors for ANR • Genetic etiology of low BMI in ANR is distinct from that in normal population • It ...
... • Additionally, except for one, SNPs influencing BMI in normal population didn’t predict BMI in the ANR group, suggesting that their effects are overruled by presence of other, putative genetic risk factors for ANR • Genetic etiology of low BMI in ANR is distinct from that in normal population • It ...
Somatic MEN1 gene mutation does not contribute
... with LOH for MEN1 in a sample of 39 sporadic tumours (9). Prezant et al. using dideoxy fingerprinting analysis (which is more sensitive) studied 45 sporadic tumours but failed to reveal any mutations in the coding sequence of MEN1 (10). Recently, in a sample of 31 sporadic tumours, Tanaka et al. det ...
... with LOH for MEN1 in a sample of 39 sporadic tumours (9). Prezant et al. using dideoxy fingerprinting analysis (which is more sensitive) studied 45 sporadic tumours but failed to reveal any mutations in the coding sequence of MEN1 (10). Recently, in a sample of 31 sporadic tumours, Tanaka et al. det ...
Document
... Homozygotes (affected) must have inherited a mutant allele from each parent (barring uniparental disomy or new mutation, which is rare in autosomal recessive disorders). Three types of matings can lead to homozygous affected offspring. The mutant recessive allele is symbolized as r and its normal do ...
... Homozygotes (affected) must have inherited a mutant allele from each parent (barring uniparental disomy or new mutation, which is rare in autosomal recessive disorders). Three types of matings can lead to homozygous affected offspring. The mutant recessive allele is symbolized as r and its normal do ...
Positive Natural Selection in the Human Lineage REVIEW
... provides a review), but they are all based broad- in this manner, few individual genes will give ly on five signatures. Below, we describe the statistically significant signals, after correction involve differences between species, selective nature of each signature, an estimate of the win- for the ...
... provides a review), but they are all based broad- in this manner, few individual genes will give ly on five signatures. Below, we describe the statistically significant signals, after correction involve differences between species, selective nature of each signature, an estimate of the win- for the ...
RNA-Seq
RNA-seq (RNA sequencing), also called whole transcriptome shotgun sequencing (WTSS), is a technology that uses the capabilities of next-generation sequencing to reveal a snapshot of RNA presence and quantity from a genome at a given moment in time.