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... Nishida, 1997; Stolfi et al., 2010) by observing formation of the BWM by time-lapse imaging. We found that, indeed, the BWM formed as an extension of the ASM (supplementary material Movie 1). Thus, the absence of the BWM in Ci-Hox1-deficient juveniles is likely to be due to disruption of ASM formati ...
... Nishida, 1997; Stolfi et al., 2010) by observing formation of the BWM by time-lapse imaging. We found that, indeed, the BWM formed as an extension of the ASM (supplementary material Movie 1). Thus, the absence of the BWM in Ci-Hox1-deficient juveniles is likely to be due to disruption of ASM formati ...
Resistance genes in barley - Journal of Applied Genetics
... The number of named and mapped resistance genes in barley increased significantly in the last decade (Table 1). At present a catalogue of gene symbols for barley is not available. There is a “Catalogue of gene symbols for wheat”, which has been published and is also updated on-line, initiated about ...
... The number of named and mapped resistance genes in barley increased significantly in the last decade (Table 1). At present a catalogue of gene symbols for barley is not available. There is a “Catalogue of gene symbols for wheat”, which has been published and is also updated on-line, initiated about ...
Thalassemias
... Although, the NRBC seen in the blood film are from both the BM and the extramedullary erythropoiesis. ...
... Although, the NRBC seen in the blood film are from both the BM and the extramedullary erythropoiesis. ...
The msh2 Gene of Schizosaccharomyces pombe Is
... homology to the Msh2 subgroup. msh2 disruption gives rise to increased mitotic mutation rates and increased levels of postmeiotic segregation of genetic markers. In bandshift assays performed with msh2D cell extracts, a general mismatch-binding activity is absent. By complementation assays, we showe ...
... homology to the Msh2 subgroup. msh2 disruption gives rise to increased mitotic mutation rates and increased levels of postmeiotic segregation of genetic markers. In bandshift assays performed with msh2D cell extracts, a general mismatch-binding activity is absent. By complementation assays, we showe ...
The Nucleotide Sequence Determination of Catalases of Three
... amplified showed that those fragments contained sequences homologous with the known Candida catalases, indicating the usefulness of the designed primers. We determined the nucleotide sequences of the open reading frames and respective 5’ untranscribed regions of these yeasts and compared each sequen ...
... amplified showed that those fragments contained sequences homologous with the known Candida catalases, indicating the usefulness of the designed primers. We determined the nucleotide sequences of the open reading frames and respective 5’ untranscribed regions of these yeasts and compared each sequen ...
CHEK2*1100delC Genotyping for Clinical Assessment of Breast
... CHEK2 (cell cycle checkpoint kinase 2) acts as a tumor suppressor in the nucleus, where it blocks cell proliferation and initiates DNA repair in response to DNA double-strand breakage.1,2 A dysfunctional variant, CHEK2*1100delC, has lost this ability. CHEK2*1100delC is primarily present in individua ...
... CHEK2 (cell cycle checkpoint kinase 2) acts as a tumor suppressor in the nucleus, where it blocks cell proliferation and initiates DNA repair in response to DNA double-strand breakage.1,2 A dysfunctional variant, CHEK2*1100delC, has lost this ability. CHEK2*1100delC is primarily present in individua ...
Insulin-like growth factor (IGF) signalling is required for early dorso
... zebrafish IGF-1Rs in the vertebrate IGF-1R clade, distinct from the insulin receptor or insulin-related receptor clades. IGF-1Ra and IGF-1Rb mRNAs and proteins are expressed in overlapping spatial domains in vivo, but exhibit distinct temporal expression patterns in specific tissues and organs. Stro ...
... zebrafish IGF-1Rs in the vertebrate IGF-1R clade, distinct from the insulin receptor or insulin-related receptor clades. IGF-1Ra and IGF-1Rb mRNAs and proteins are expressed in overlapping spatial domains in vivo, but exhibit distinct temporal expression patterns in specific tissues and organs. Stro ...
Linking Cognitive Neuroscience and Molecular Genetics: New Perspectives from Williams... Ursula Bellugi and Marie St. George (Eds.)
... phenotype is unknown. The current report will illustrate the structure of the flanking duplications and suggest a possible relationship to the WMS breakpoints. In the current work, we will describe the construction of a working physical map of the WMS region including the flanking duplications. Comb ...
... phenotype is unknown. The current report will illustrate the structure of the flanking duplications and suggest a possible relationship to the WMS breakpoints. In the current work, we will describe the construction of a working physical map of the WMS region including the flanking duplications. Comb ...
Role of 1-aminocyclopropane-1-carboxylate (ACC) Synthases
... RhETR1 (similar to AtERS1) transcripts. Results showed that expression levels of RhETR1 were distinctly higher in ‘Bronze’, suggesting that modulation of receptor levels may contribute to ethylene perception and sensitivity. Thus, short flower life in ‘Bronze’ expressing high levels of RhETR1 transc ...
... RhETR1 (similar to AtERS1) transcripts. Results showed that expression levels of RhETR1 were distinctly higher in ‘Bronze’, suggesting that modulation of receptor levels may contribute to ethylene perception and sensitivity. Thus, short flower life in ‘Bronze’ expressing high levels of RhETR1 transc ...
Price, DK, Zhang, F, Ashley, CT and Warren, ST: The chicken FMR1 gene is highly conserved containing a CTT 5\' untranslated repeat and encodes an RNA-binding protein. Genomics 31:3-12 (1996).
... this type of mutation, fragile X syndrome, is the most frequent inherited form of mental retardation. Fragile X syndrome segregates as an X-linked dominant disorder with reduced penetrance and has been mapped to the fragile X mental retardation (FMR1) gene located at human Xq27.3 (Warren and Ashley, ...
... this type of mutation, fragile X syndrome, is the most frequent inherited form of mental retardation. Fragile X syndrome segregates as an X-linked dominant disorder with reduced penetrance and has been mapped to the fragile X mental retardation (FMR1) gene located at human Xq27.3 (Warren and Ashley, ...
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS)
... Preeclampsia is a potentially life-threatening disease that occurs exclusively in pregnant women during late gestation (>20 weeks). The two hallmark symptoms are hypertension and proteinuria, complicating at least 5% of pregnancies and are usually resolved upon delivery of the placenta (Lain and Rob ...
... Preeclampsia is a potentially life-threatening disease that occurs exclusively in pregnant women during late gestation (>20 weeks). The two hallmark symptoms are hypertension and proteinuria, complicating at least 5% of pregnancies and are usually resolved upon delivery of the placenta (Lain and Rob ...
1q21 microdeletions
... (array-CGH). This shows gains and losses of tiny amounts of DNA throughout the genome (also called duplications and deletions) and can show whether particular genes are present or not. A deletion so small that it can only be identified in this way is called a microdeletion. ...
... (array-CGH). This shows gains and losses of tiny amounts of DNA throughout the genome (also called duplications and deletions) and can show whether particular genes are present or not. A deletion so small that it can only be identified in this way is called a microdeletion. ...
1q21 microdeletions
... chromosomes of both parents. The parents’ chromosomes should be checked even if they are themselves completely healthy with no developmental problems at all. If one parent has the same microdeletion, it has been inherited. If both parents have normal chromosomes, the 1q21.1 microdeletion is a new oc ...
... chromosomes of both parents. The parents’ chromosomes should be checked even if they are themselves completely healthy with no developmental problems at all. If one parent has the same microdeletion, it has been inherited. If both parents have normal chromosomes, the 1q21.1 microdeletion is a new oc ...
Vegetative incompatibility in filamentous fungi: Podospora and
... fact that incompatibility associated with mating type is suppressed by mutations in the tol (for tolerant) gene, but tol mutations do not disrupt the sexual cycle [11,12•]. Another example is the het-c locus of P. anserina — het-c is involved in the het-c/het-e and het-c/het-d non-allelic incompatib ...
... fact that incompatibility associated with mating type is suppressed by mutations in the tol (for tolerant) gene, but tol mutations do not disrupt the sexual cycle [11,12•]. Another example is the het-c locus of P. anserina — het-c is involved in the het-c/het-e and het-c/het-d non-allelic incompatib ...
A, B, a
... • Experimentally determined from frequency of recombinant phenotypes in testcrosses • Roughly proportional to physical length of DNA between loci • Greater physical distance between two loci, greater chance of recombination by crossing-over ...
... • Experimentally determined from frequency of recombinant phenotypes in testcrosses • Roughly proportional to physical length of DNA between loci • Greater physical distance between two loci, greater chance of recombination by crossing-over ...
Gene Name
... Caucasians could be related to the absence of the mitochondrial isozyme. This gene encodes a cytosolic isoform, which has a high affinity for aldehydes. Same as BMPR1A or bone morphogenetic protein receptor, type IA. The bone morphogenetic protein (BMP) receptors are a family of transmembrane serine ...
... Caucasians could be related to the absence of the mitochondrial isozyme. This gene encodes a cytosolic isoform, which has a high affinity for aldehydes. Same as BMPR1A or bone morphogenetic protein receptor, type IA. The bone morphogenetic protein (BMP) receptors are a family of transmembrane serine ...
T1 transgenic tobacco plants
... folowing: (1) maize weevils (Sitophilus zeamais Motsch); (2) the attributes/ characters of plant defensines; and (3) Transgenic engineering in maize plants. Maize weevil is a popular destructive species and protopathic pest. It is distributed globally, mainly in warm areas and especially in Asia, Me ...
... folowing: (1) maize weevils (Sitophilus zeamais Motsch); (2) the attributes/ characters of plant defensines; and (3) Transgenic engineering in maize plants. Maize weevil is a popular destructive species and protopathic pest. It is distributed globally, mainly in warm areas and especially in Asia, Me ...
Chapter 15
... being JH III (Darrouzet et al., 1997; Richard et al., 1989; Riddiford, 1994). D. melanogaster produces both JH III and JHB3, both of which have endocrine function in dipterans (Riddiford, 1993; Yin et al., 1995). Whereas the effects of JH III are better known, JHB3 appears to be the major product of ...
... being JH III (Darrouzet et al., 1997; Richard et al., 1989; Riddiford, 1994). D. melanogaster produces both JH III and JHB3, both of which have endocrine function in dipterans (Riddiford, 1993; Yin et al., 1995). Whereas the effects of JH III are better known, JHB3 appears to be the major product of ...
Package `BitSeq`
... seed=NULL, samples=NULL, optLimit=1e-5, optMethod="FR", procN=4, verbose=FALSE, veryVerbose=FALSE, pretend=FALSE) ...
... seed=NULL, samples=NULL, optLimit=1e-5, optMethod="FR", procN=4, verbose=FALSE, veryVerbose=FALSE, pretend=FALSE) ...
Factor V Leiden Information for Patients and Families
... • Serious illness, casts and surgery can increase your chances of developing blood clots. When you need health care or go to the hospital, tell your health care team that you have Factor V Leiden, so that they can plan the care you need. You may be treated with blood thinners until the risk has pass ...
... • Serious illness, casts and surgery can increase your chances of developing blood clots. When you need health care or go to the hospital, tell your health care team that you have Factor V Leiden, so that they can plan the care you need. You may be treated with blood thinners until the risk has pass ...
O4 M.A. Rouf Mian
... collected from Wooster for identifying the source of aphid resistance. The SSR genotyping was performed using standard protocols. A mapping population from a cross between Ohio adapted cultivar ‘Wyandot’ and PI 243540 was used for mapping the gene. The phenotypic data were analyzed using SAS (SAS In ...
... collected from Wooster for identifying the source of aphid resistance. The SSR genotyping was performed using standard protocols. A mapping population from a cross between Ohio adapted cultivar ‘Wyandot’ and PI 243540 was used for mapping the gene. The phenotypic data were analyzed using SAS (SAS In ...
Functions of the nonsense-mediated RNA decay pathway in Drosophila development. PLoS Genetics 2 , 2143-2154.
... production of truncated, potentially harmful proteins that can interfere with normal cellular processes (e.g., [3]). The NMD pathway has also been found to influence expression of a variety of wild-type transcripts (reviewed in [4]), implying that the pathway has regulatory roles beyond its surveill ...
... production of truncated, potentially harmful proteins that can interfere with normal cellular processes (e.g., [3]). The NMD pathway has also been found to influence expression of a variety of wild-type transcripts (reviewed in [4]), implying that the pathway has regulatory roles beyond its surveill ...