Ecological speciation in phytophagous insects
... differs from previous reviews of ecological speciation in several important ways. First, some topics in the current review were not covered in past reviews. Examples are the individual genetic basis of host plant preference and performance (Tables 2 and 3, respectively), the consideration of alterna ...
... differs from previous reviews of ecological speciation in several important ways. First, some topics in the current review were not covered in past reviews. Examples are the individual genetic basis of host plant preference and performance (Tables 2 and 3, respectively), the consideration of alterna ...
Warren, ST and Ashley, CT: Triplet repeat expansion mutations: The example of fragile X syndrome. Annual Review of Neuroscience 18:77-99 (1995).
... localized this instability to a single 1.0-kb Pst I fragment, pfxa2, that was sequenced and found to contain an unusual CGG trinucleotide repeat of 43 copies. By using the polymerase chain reaction (PCR) and primers flanking the repeat, Kremer et al (1991a) mapped the region of instability in pfxa2 ...
... localized this instability to a single 1.0-kb Pst I fragment, pfxa2, that was sequenced and found to contain an unusual CGG trinucleotide repeat of 43 copies. By using the polymerase chain reaction (PCR) and primers flanking the repeat, Kremer et al (1991a) mapped the region of instability in pfxa2 ...
HLA-A, -B
... Czech Donor Register: Donor age has to be between 18 – 35 years when firstly included into the registr. ...
... Czech Donor Register: Donor age has to be between 18 – 35 years when firstly included into the registr. ...
Alleles of a reelin CGG repeat do not convey
... As so aptly described by Risch [2000], the observation that a disease has a genetic basis, even a substantial one, does not necessarily mean those genetic variants will be easy to find. In fact, the evidence for autism suggests that its genetic basis may be subtle indeed [Risch et al., 1999], and mo ...
... As so aptly described by Risch [2000], the observation that a disease has a genetic basis, even a substantial one, does not necessarily mean those genetic variants will be easy to find. In fact, the evidence for autism suggests that its genetic basis may be subtle indeed [Risch et al., 1999], and mo ...
Document
... Statement of Research Interests for Dr. Aaron M. Rashotte Leaf development and expansion are essential plant processes for which our understanding is incomplete. Plant hormones are known to be implicated in these processes, but only the initial connections necessary for this understanding have been ...
... Statement of Research Interests for Dr. Aaron M. Rashotte Leaf development and expansion are essential plant processes for which our understanding is incomplete. Plant hormones are known to be implicated in these processes, but only the initial connections necessary for this understanding have been ...
What is p53
... the term "p53" appears in the title! This massive interest in a single protein is almost unprecedented and reflects the central place of p53 in the regulation of cell number and the frequency with which abnormalities of p53 occur in human tumours. p53 has been named Molecule of the Year by the edito ...
... the term "p53" appears in the title! This massive interest in a single protein is almost unprecedented and reflects the central place of p53 in the regulation of cell number and the frequency with which abnormalities of p53 occur in human tumours. p53 has been named Molecule of the Year by the edito ...
Ella`s Grace: Microcephalic Osteodysplastic Primordial Dwarfism
... head appeared to glow! Of course, we thought that was impossible and passed it off as nothing. We noticed her head glowing at other times though, too...whenever she was sitting near the light. Just before she reached her nine-month birthday, a CT scan was done. A massive fluid-filled cyst occupied m ...
... head appeared to glow! Of course, we thought that was impossible and passed it off as nothing. We noticed her head glowing at other times though, too...whenever she was sitting near the light. Just before she reached her nine-month birthday, a CT scan was done. A massive fluid-filled cyst occupied m ...
PDF
... the invention of optical tweezers, which manipulate dielectric microscopic objects with the help of a focused light beam [12, 13]. Soon thereafter, magnetic tweezers were invented to allow the manipulation of paramagnetic beads using a gradient of magnetic field [14]. The two techniques have been de ...
... the invention of optical tweezers, which manipulate dielectric microscopic objects with the help of a focused light beam [12, 13]. Soon thereafter, magnetic tweezers were invented to allow the manipulation of paramagnetic beads using a gradient of magnetic field [14]. The two techniques have been de ...
Vitamin D resistant rickets
... transmission), or to an alteration in the FGF23 i.e fibroblast growth factor 23gene on 12p13 (autosomal dominant transmission). Other gene alterations have been suggested, ClCN5 i.e Chloride channel 5 for example which may explain some of the hypophosphatemic rickets with a recessive mode of inherit ...
... transmission), or to an alteration in the FGF23 i.e fibroblast growth factor 23gene on 12p13 (autosomal dominant transmission). Other gene alterations have been suggested, ClCN5 i.e Chloride channel 5 for example which may explain some of the hypophosphatemic rickets with a recessive mode of inherit ...
Identification of the mRNA targets of tRNA
... stability and translational decoding properties, may be central to regulating particular genes, or groups of genes. Mutations in the yeast TRM9 tRNA modification gene drive altered expression of genes enriched in codons targeted by Trm9-modified tRNAs (39). Similarly, mutations in the eukaryotic Elo ...
... stability and translational decoding properties, may be central to regulating particular genes, or groups of genes. Mutations in the yeast TRM9 tRNA modification gene drive altered expression of genes enriched in codons targeted by Trm9-modified tRNAs (39). Similarly, mutations in the eukaryotic Elo ...
Chapter 3: Selection and Adaptation Barry Sinervo © 1997-2007
... are associated with the non-choosy female gene. In addition, all Normal males breed with non-choosy females and thus 100% of the Normal male genes (all of them) are associated with non-choosy females (conversely 0% of the Normal genes are associated with choosy females. Because the combination of el ...
... are associated with the non-choosy female gene. In addition, all Normal males breed with non-choosy females and thus 100% of the Normal male genes (all of them) are associated with non-choosy females (conversely 0% of the Normal genes are associated with choosy females. Because the combination of el ...
- TestbankU
... Answer Location: Genetic Disorders Question Type: MC 48. ______ is a recessive disease that primarily affects descendants of Central and Eastern European Jews. There is no cure for this disease and most die by age 4. a. Tay-Sachs disease b. Cooley’s anemia c. Sickle cell anemia d. Huntington’s Disea ...
... Answer Location: Genetic Disorders Question Type: MC 48. ______ is a recessive disease that primarily affects descendants of Central and Eastern European Jews. There is no cure for this disease and most die by age 4. a. Tay-Sachs disease b. Cooley’s anemia c. Sickle cell anemia d. Huntington’s Disea ...
Product description P003-D1 MLH1-MSH2-v01 - MRC
... syndrome. The analytical sensitivity and specificity for the detection of deletions in the aforementioned genes using mutation negative samples with Lynch syndrome is very high and can be considered >99%. Performance can be compromised by: SNPs or other polymorphisms (e.g. indels) in the DNA target ...
... syndrome. The analytical sensitivity and specificity for the detection of deletions in the aforementioned genes using mutation negative samples with Lynch syndrome is very high and can be considered >99%. Performance can be compromised by: SNPs or other polymorphisms (e.g. indels) in the DNA target ...
Perspectives in Diabetes Glucokinase Gene Structure
... islet, and insulinoma cDNA libraries indicates that different the mRlVA results in an isoform that is missing 17 amino glucokinase isoforms are generated through alternate splic- acids in a region of the protein situated between the putative ing of the glucokinase gene product. One of these isoforms ...
... islet, and insulinoma cDNA libraries indicates that different the mRlVA results in an isoform that is missing 17 amino glucokinase isoforms are generated through alternate splic- acids in a region of the protein situated between the putative ing of the glucokinase gene product. One of these isoforms ...
Association between toluene diisocyanate-induced aspartic acid at position 57
... are consistent with the hypothesis that an immunological mechanism is involved in TDI-induced asthma and that specific genetic factors play a role in conferring susceptibility to or protection against this disease. An immunological mechanism is likely to occur in TDIinduced asthma since the inflamma ...
... are consistent with the hypothesis that an immunological mechanism is involved in TDI-induced asthma and that specific genetic factors play a role in conferring susceptibility to or protection against this disease. An immunological mechanism is likely to occur in TDIinduced asthma since the inflamma ...
Processing the RefSeq and CCDS Annotation Datasets Using the SAS System: Creation of Gene Reference
... of STRAND, either Lines 37-171 or Lines 174-331 are executed. The authors avoided using ELSE IF for two reasons: the computational require of two exclusive IF statements is negligible and indenting made the code more difficult to read on a smaller screen. In either set of IF-THEN-DO-END statements, ...
... of STRAND, either Lines 37-171 or Lines 174-331 are executed. The authors avoided using ELSE IF for two reasons: the computational require of two exclusive IF statements is negligible and indenting made the code more difficult to read on a smaller screen. In either set of IF-THEN-DO-END statements, ...
invited review
... proportional to SGLT1 transport activity, and the area of the particle in the membrane is consistent with TMH 14. The relationship between area and number of TMHs was established by expressing membrane proteins of known structure in oocytes and comparing their area with those obtained from two-dimen ...
... proportional to SGLT1 transport activity, and the area of the particle in the membrane is consistent with TMH 14. The relationship between area and number of TMHs was established by expressing membrane proteins of known structure in oocytes and comparing their area with those obtained from two-dimen ...
Signaling Pathways of Heme Oxygenase
... The toxic effects of CO have been known for many years. Since CO binds hemoglobin with higher affinity than O2, O2 delivery to tissues and organs is blocked by this gaseous molecule. More recently, HO-derived CO has been recognized to be an important cellular messenger with various physiological fun ...
... The toxic effects of CO have been known for many years. Since CO binds hemoglobin with higher affinity than O2, O2 delivery to tissues and organs is blocked by this gaseous molecule. More recently, HO-derived CO has been recognized to be an important cellular messenger with various physiological fun ...
7.Causal - Computer Sciences User Pages
... • Population-based estimates (from a sample of individuals) may not reflect processes within an individual. Jax SysGen: Yandell © 2011 ...
... • Population-based estimates (from a sample of individuals) may not reflect processes within an individual. Jax SysGen: Yandell © 2011 ...
Mice lacking desmocollin 1 show epidermal fragility accompanied
... null mice revealed no abnormalities of the epithelia. Inspection of the oral cavities of null pups revealed no blistering of epithelia. Thus, Dsc1/ mice did not show the type of oral blistering defects responsible for feeding defects and small size in Dsg3/ mice (Koch et al., 1997). Of null anim ...
... null mice revealed no abnormalities of the epithelia. Inspection of the oral cavities of null pups revealed no blistering of epithelia. Thus, Dsc1/ mice did not show the type of oral blistering defects responsible for feeding defects and small size in Dsg3/ mice (Koch et al., 1997). Of null anim ...
Parasitism and Mutualism in Wolbachia: What the
... direction in the evolution of the lifestyles (Anderson and Karr 2001; Fenn et al. 2006) or have expressed caution over certain rooting positions based on statistically weak phylogenetic support (Bandi et al. 1998; Lo et al. 2002; Bordenstein and Rosengaus 2005; Casiraghi et al. 2005). The problems i ...
... direction in the evolution of the lifestyles (Anderson and Karr 2001; Fenn et al. 2006) or have expressed caution over certain rooting positions based on statistically weak phylogenetic support (Bandi et al. 1998; Lo et al. 2002; Bordenstein and Rosengaus 2005; Casiraghi et al. 2005). The problems i ...
Multivariate Analysis of Genotype–Phenotype Association
... can lead to a dramatic loss of statistical power and in fact violate standard rules of statistical inference. Biologically more important, most phenotypes are not determined by single alleles, but by the joint effects, both additive and nonadditive, of a number of alleles at multiple loci. With the ...
... can lead to a dramatic loss of statistical power and in fact violate standard rules of statistical inference. Biologically more important, most phenotypes are not determined by single alleles, but by the joint effects, both additive and nonadditive, of a number of alleles at multiple loci. With the ...
Gene Section MLL (myeloid/lymphoid or mixed lineage leukemia) Atlas of Genetics and Cytogenetics
... This article is an update of: Marschalek R. MLL (myeloid/lymphoid or mixed lineage leukemia). Atlas Genet Cytogenet Oncol Haematol.2003;7(1):16-18. Hess JL, Huret JL. MLL (myeloid/lymphoid or mixed lineage leukemia). Atlas Genet Cytogenet Oncol Haematol.2001;5(1):12-14. Huret JL. MLL (myeloid/lympho ...
... This article is an update of: Marschalek R. MLL (myeloid/lymphoid or mixed lineage leukemia). Atlas Genet Cytogenet Oncol Haematol.2003;7(1):16-18. Hess JL, Huret JL. MLL (myeloid/lymphoid or mixed lineage leukemia). Atlas Genet Cytogenet Oncol Haematol.2001;5(1):12-14. Huret JL. MLL (myeloid/lympho ...
Mapping Polygenes - University of Warwick
... by UNIVERSITY OF WARWICK on 02/23/10. For personal use only. ...
... by UNIVERSITY OF WARWICK on 02/23/10. For personal use only. ...