Modular Skeletal Evolution in Sticklebacks Is Controlled by Additive
... armor and trophic traits. We identify .100 quantitative trait loci (QTL) controlling the pattern of serially repeating skeletal elements, including gill rakers, teeth, branchial bones, jaws, median fin spines, and vertebrae. We use this large collection of QTL to address long-standing questions about ...
... armor and trophic traits. We identify .100 quantitative trait loci (QTL) controlling the pattern of serially repeating skeletal elements, including gill rakers, teeth, branchial bones, jaws, median fin spines, and vertebrae. We use this large collection of QTL to address long-standing questions about ...
Periplasmic adaptor protein AcrA has a distinct
... The acrA gene was inactivated by insertion of the aph gene conferring kanamycin resistance. The inserted sequence also includes a ribosomal binding site and an inframe start codon to allow expression of downstream acrB. The mutant was designated L823 (Table 2). The disrupted region was transduced in ...
... The acrA gene was inactivated by insertion of the aph gene conferring kanamycin resistance. The inserted sequence also includes a ribosomal binding site and an inframe start codon to allow expression of downstream acrB. The mutant was designated L823 (Table 2). The disrupted region was transduced in ...
Mutational Analysis of the Drosophila Sister-Chromatid
... were isolated by their failure to complement md' (MIYAZAKI and ORR-WEAVER1992). For all tests requiring a chromosome for which the ord gene was deleted, the deficiency chromosome Df(ZR)W7370 was used (BICKELet al. 1996). The isoX/Y, cv v f car, compound-X and compound-XY stocks were described in KER ...
... were isolated by their failure to complement md' (MIYAZAKI and ORR-WEAVER1992). For all tests requiring a chromosome for which the ord gene was deleted, the deficiency chromosome Df(ZR)W7370 was used (BICKELet al. 1996). The isoX/Y, cv v f car, compound-X and compound-XY stocks were described in KER ...
PCTpc201500834rar1_pap_plantcell 1..16
... showed normal fertility, indicating that the mutations are recessive. Progeny of plants heterozygous for either mutant allele segregated mutant and normal phenotypes in a 1:3 ratio as expected for single Mendelian recessive mutations [cdc20.1-3, 44:141 for mutant/normal, r2(1:3) = 0.145, P > 0.5; cd ...
... showed normal fertility, indicating that the mutations are recessive. Progeny of plants heterozygous for either mutant allele segregated mutant and normal phenotypes in a 1:3 ratio as expected for single Mendelian recessive mutations [cdc20.1-3, 44:141 for mutant/normal, r2(1:3) = 0.145, P > 0.5; cd ...
Arabidopsis Cell Division Cycle 20.1 Is Required for Normal Meiotic
... showed normal fertility, indicating that the mutations are recessive. Progeny of plants heterozygous for either mutant allele segregated mutant and normal phenotypes in a 1:3 ratio as expected for single Mendelian recessive mutations [cdc20.1-3, 44:141 for mutant/normal, r2(1:3) = 0.145, P > 0.5; cd ...
... showed normal fertility, indicating that the mutations are recessive. Progeny of plants heterozygous for either mutant allele segregated mutant and normal phenotypes in a 1:3 ratio as expected for single Mendelian recessive mutations [cdc20.1-3, 44:141 for mutant/normal, r2(1:3) = 0.145, P > 0.5; cd ...
PCTpc201500834rar1_pap_plantcell 1..16
... showed normal fertility, indicating that the mutations are recessive. Progeny of plants heterozygous for either mutant allele segregated mutant and normal phenotypes in a 1:3 ratio as expected for single Mendelian recessive mutations [cdc20.1-3, 44:141 for mutant/normal, r2(1:3) = 0.145, P > 0.5; cd ...
... showed normal fertility, indicating that the mutations are recessive. Progeny of plants heterozygous for either mutant allele segregated mutant and normal phenotypes in a 1:3 ratio as expected for single Mendelian recessive mutations [cdc20.1-3, 44:141 for mutant/normal, r2(1:3) = 0.145, P > 0.5; cd ...
GENETIC AND MOLECULAR ANALYSIS OF THE garnet EYE
... described in Drosophila melanogaster up to 1992 (Lindsley and Zimm 1992). It lists 110 genes; even if pattern and secondary effects are excluded, there are still 85 genes whose primary effect is on eye colour. Nor are these 110 genes likely to be all the genes which affect eye colour. Amongst eight ...
... described in Drosophila melanogaster up to 1992 (Lindsley and Zimm 1992). It lists 110 genes; even if pattern and secondary effects are excluded, there are still 85 genes whose primary effect is on eye colour. Nor are these 110 genes likely to be all the genes which affect eye colour. Amongst eight ...
Effete, a Drosophila chromatin-associated ubiquitin
... their proximity, a phenomenon known as telomere position effect (TPE). This form of transcriptional regulation is conserved from yeast to humans, and has been implicated in numerous human pathologies (reviewed in (Ottaviani et al. 2008). Studies in S. cervisiae have identified more than 50 telomere- ...
... their proximity, a phenomenon known as telomere position effect (TPE). This form of transcriptional regulation is conserved from yeast to humans, and has been implicated in numerous human pathologies (reviewed in (Ottaviani et al. 2008). Studies in S. cervisiae have identified more than 50 telomere- ...
Selective Disruption of Aurora C Kinase Reveals Distinct Functions
... Centromere Protein (INCENP), Survivin, and Borealin [18–20]. Meiotic cells, however, contain another enzymatic subunit, Aurora C kinase (AURKC), that can function in the CPC in place of AURKB [6,21–25]. AURKB and AURKC are members of a conserved serine-threonine protein kinase family, and are highly ...
... Centromere Protein (INCENP), Survivin, and Borealin [18–20]. Meiotic cells, however, contain another enzymatic subunit, Aurora C kinase (AURKC), that can function in the CPC in place of AURKB [6,21–25]. AURKB and AURKC are members of a conserved serine-threonine protein kinase family, and are highly ...
Duplication 12p and PallisterKillian syndrome
... resulting in tetrasomy 12p, which is often present in a tissue limited mosaic state [Peltom€aki et al., 1987]. The PKS phenotype has also been observed in individuals with complete or partial duplications of 12p (trisomy 12p rather than tetrasomy 12p) as the result of an interstitial duplication or ...
... resulting in tetrasomy 12p, which is often present in a tissue limited mosaic state [Peltom€aki et al., 1987]. The PKS phenotype has also been observed in individuals with complete or partial duplications of 12p (trisomy 12p rather than tetrasomy 12p) as the result of an interstitial duplication or ...
Fulltext PDF - Indian Academy of Sciences
... the observation that ts paralytic / lethal trans heterozygous adults showed weaker paralysis than their respective ts paralytic homozygotes (Chandrashekaran and Sarla 1993). The paralytic phenotypes of the 32 possible viable / lethal heteroallelic and four homoallelic combinations of stmA are shown ...
... the observation that ts paralytic / lethal trans heterozygous adults showed weaker paralysis than their respective ts paralytic homozygotes (Chandrashekaran and Sarla 1993). The paralytic phenotypes of the 32 possible viable / lethal heteroallelic and four homoallelic combinations of stmA are shown ...
The importance of genetic influences in asthma REVIEW H. Los* , G.H. Koppelman*
... important in the pathogenesis of asthma. Familial aggregation of asthma was probably first described by Sennertus in 1650 [26]. At the beginning of this century, R. Cooke performed two large studies on the inheritance of atopy, one in 1916 and the other in 1924 [27, 28]. The first study examined ast ...
... important in the pathogenesis of asthma. Familial aggregation of asthma was probably first described by Sennertus in 1650 [26]. At the beginning of this century, R. Cooke performed two large studies on the inheritance of atopy, one in 1916 and the other in 1924 [27, 28]. The first study examined ast ...
THE GENETICS OF CURLY WING IN DROSOPHILA. ANOTHER
... to be present in half of the F1 males which all show the above six recessive first-chromosome characters.Curlythereforeexhibitscompleteindependence of the first or X chromosome (see table 7). If the gene for curly were located in the third chromosome, it would be found to show linkage with other gen ...
... to be present in half of the F1 males which all show the above six recessive first-chromosome characters.Curlythereforeexhibitscompleteindependence of the first or X chromosome (see table 7). If the gene for curly were located in the third chromosome, it would be found to show linkage with other gen ...
Chapter_004 - IHMC Public Cmaps (2)
... Mosby items and derived items © 2010, 2006 by Mosby, Inc., an affiliate of Elsevier Inc. ...
... Mosby items and derived items © 2010, 2006 by Mosby, Inc., an affiliate of Elsevier Inc. ...
Good quality blastocyst from non-/mono
... Although healthy infants have developed from non- and mono-pronuclear zygotes, the transfer of embryos from non- and mono-pronuclear zygotes is not recommended because there are no proper selection criteria. In the present study, we discuss how to select non- and mono-pronuclear embryos with the hig ...
... Although healthy infants have developed from non- and mono-pronuclear zygotes, the transfer of embryos from non- and mono-pronuclear zygotes is not recommended because there are no proper selection criteria. In the present study, we discuss how to select non- and mono-pronuclear embryos with the hig ...
Epigenetic Interactions among Three dTph1
... excision product, because it was isolated from a somatically reverted branch (phenotypic selection for wild-type activity), whereas crosses showed that (germinal) excision of dTph2 from an3-GSm virtually always results in stably inactivated an3 alleles and rarely in An31 revertant alleles (data not ...
... excision product, because it was isolated from a somatically reverted branch (phenotypic selection for wild-type activity), whereas crosses showed that (germinal) excision of dTph2 from an3-GSm virtually always results in stably inactivated an3 alleles and rarely in An31 revertant alleles (data not ...
Genetic characterizations of three male-steriles in wheat, Triticum aestivum L.
... An abnormal 7:1 segregation predominated in most Siete Cerros families with an unexpected high number of nonsegregating headrows. One family of the original 41 segregated for male-sterility as a single recessive allele. The influence of background genotype on the Chancellor male sterility was attrib ...
... An abnormal 7:1 segregation predominated in most Siete Cerros families with an unexpected high number of nonsegregating headrows. One family of the original 41 segregated for male-sterility as a single recessive allele. The influence of background genotype on the Chancellor male sterility was attrib ...
Epigenetic Interactions among Three dTph1 Transposons in Two
... excision product, because it was isolated from a somatically reverted branch (phenotypic selection for wild-type activity), whereas crosses showed that (germinal) excision of dTph2 from an3-GSm virtually always results in stably inactivated an3 alleles and rarely in An31 revertant alleles (data not ...
... excision product, because it was isolated from a somatically reverted branch (phenotypic selection for wild-type activity), whereas crosses showed that (germinal) excision of dTph2 from an3-GSm virtually always results in stably inactivated an3 alleles and rarely in An31 revertant alleles (data not ...
IBS Methods for Affected Pairs Linkage
... possible mapping projects with the certainty that if: (a) a major gene exists for a trait; (b) the trait is reasonably homogeneous; (c) there is sufficient family material available; then a linked marker can be found." ...
... possible mapping projects with the certainty that if: (a) a major gene exists for a trait; (b) the trait is reasonably homogeneous; (c) there is sufficient family material available; then a linked marker can be found." ...
protein 2 gene: study of a cohort of Israeli patients - MRC
... deletion of intron 1 donor splice site are reported. It is shown that various MECP2 mutations had distinct effects on MECP2 expression levels in peripheral blood. The most significant (p,0.001) reduction in the expression of both MECP2 isoforms was related to the presence of the intron 1 donor splic ...
... deletion of intron 1 donor splice site are reported. It is shown that various MECP2 mutations had distinct effects on MECP2 expression levels in peripheral blood. The most significant (p,0.001) reduction in the expression of both MECP2 isoforms was related to the presence of the intron 1 donor splic ...
genetic variability, twin hybrids and constant hybrids, in a case of
... genetic, because MORGANwas able by selection to obtain stocks differing distinctly and consistently in the degree of their beading; in fact (b) he succeeded, by selection, in bringing the extreme and the average intensities of this character both far beyond their original points. These facts too can ...
... genetic, because MORGANwas able by selection to obtain stocks differing distinctly and consistently in the degree of their beading; in fact (b) he succeeded, by selection, in bringing the extreme and the average intensities of this character both far beyond their original points. These facts too can ...
Biology A Chapter 10
... 1. When an area of a chromatid is exchanged with the matching area on a chromatid of its homologous chromosome, _____ occurs. a. crossing over c. hybridization b. mutagenesis d. fertilization 2. Crossing over results in a _____. a. female genotype c. genetic recombination b. male genotype d. phenoty ...
... 1. When an area of a chromatid is exchanged with the matching area on a chromatid of its homologous chromosome, _____ occurs. a. crossing over c. hybridization b. mutagenesis d. fertilization 2. Crossing over results in a _____. a. female genotype c. genetic recombination b. male genotype d. phenoty ...
Meiosis: Chapter 10 - University at Buffalo
... Lisa Nash gave birth to a baby boy, Adam, on August 29, 2000. Adam’s placenta was gathered immediately and all the cord blood saved. Molly started chemotherapy to destroy her bone marrow and received a transfusion of the cord blood cells a month later. Today Molly, Adam, and new little sister Delain ...
... Lisa Nash gave birth to a baby boy, Adam, on August 29, 2000. Adam’s placenta was gathered immediately and all the cord blood saved. Molly started chemotherapy to destroy her bone marrow and received a transfusion of the cord blood cells a month later. Today Molly, Adam, and new little sister Delain ...
Biology 32: Evolutionary Biology Computer simulations of
... lost (frequency=0). Use this program to quantify how the initial frequency of an allele relates to the probability of either its fixation or its loss? Think about how you can use AlleleA1 to determine this. Reset the program to the default values and then change the population size to 100. Run this ...
... lost (frequency=0). Use this program to quantify how the initial frequency of an allele relates to the probability of either its fixation or its loss? Think about how you can use AlleleA1 to determine this. Reset the program to the default values and then change the population size to 100. Run this ...