Helen Lawce | Oregon Health & Science University (original) (raw)
Papers by Helen Lawce
John Wiley & Sons, Inc. eBooks, Mar 4, 2017
John Wiley & Sons, Inc. eBooks, Mar 4, 2017
PubMed, 2019
Interphase fluorescence in situ hybridization (FISH) cutoff values are calculated using various m... more Interphase fluorescence in situ hybridization (FISH) cutoff values are calculated using various mathematical methods to determine whether abnormalities seen are at reportable (statistically significant) levels. However, for interphase FISH studies of samples obtained from oncology patients who have been transplanted or treated, these cutoff values may result in reporting a false negative result due to the small percentage of residual disease that falls below such a cutoff value. Failure to detect the rare abnormal cells may impact patient care and prognosis. For such situations, the two questions are: is the disease still present, and if so, how prevalent is it? The first question is qualitative and the second is quantitative. Traditionally, only the quantitative parameters have been used for determining reportability. Here we propose a method to account for both qualitative and quantitative evaluations of interphase FISH results.
John Wiley & Sons, Inc. eBooks, Mar 4, 2017
John Wiley & Sons, Inc. eBooks, Mar 4, 2017
PubMed, 1975
A male with a karyotype 47,XXXY qs,t(9p-;Xq+) was ascertained utilizing ASG-banding. The karyotyp... more A male with a karyotype 47,XXXY qs,t(9p-;Xq+) was ascertained utilizing ASG-banding. The karyotype was repeated because the original diagnosis of Klinefelter syndrome (47,XXY) was inconsistent with many of the stigmata present. It is suggested that many karyotypes completed prior to the advent of banding techniques will be repeated in an attempt to provide more accurate diagnosis, describe more aberrations, and possibly establish new syndromes.
John Wiley & Sons, Inc. eBooks, Mar 4, 2017
In Vitro Cellular & Developmental Biology – Plant, Feb 1, 1972
Cytogenetic and Genome Research, 1990
Experimental Biology and Medicine, Mar 1, 1981
Transfusion of syngeneic marrow into normal, nonirradiated recipients results only in minimal pro... more Transfusion of syngeneic marrow into normal, nonirradiated recipients results only in minimal proliferation of donor cells. However, irradiated recipients, restored to hematologic normalcy by an initial marrow transfusion, subsequently sustain proliferation which replaces approximately 10% of endogenous marrow after a single transfusion of 4 x 10â· marrow cells of the same strain as the host. Cells from histoincompatible donors proliferate
Prenatal Diagnosis, Mar 1, 1984
45,X/46,XX mosaicism was found in only one of four primary amniotic fluid cultures. Repeat amnioc... more 45,X/46,XX mosaicism was found in only one of four primary amniotic fluid cultures. Repeat amniocentesis revealed 45,X/46,XX mosaicism in all four primary cultures. Mosaicism was confirmed in tissues from the abortus.
John Wiley & Sons, Inc. eBooks, Apr 12, 2017
Experimental Biology and Medicine, 1981
Transfusion of syngeneic marrow into normal, nonirradiated recipients results only in minimal pro... more Transfusion of syngeneic marrow into normal, nonirradiated recipients results only in minimal proliferation of donor cells. However, irradiated recipients, restored to hematologic normalcy by an initial marrow transfusion, subsequently sustain proliferation which replaces approximately 10% of endogenous marrow after a single transfusion of 4 x 10â· marrow cells of the same strain as the host. Cells from histoincompatible donors proliferate
Journal of the Association of Genetic Technologists, Feb 1, 2003
OBJECTIVES Interphase fluorescence in situ hybridization (FISH) cutoff values are calculated usin... more OBJECTIVES Interphase fluorescence in situ hybridization (FISH) cutoff values are calculated using various mathematical methods to determine whether abnormalities seen are at reportable (statistically significant) levels. However, for interphase FISH studies of samples obtained from oncology patients who have been transplanted or treated, these cutoff values may result in reporting a false negative result due to the small percentage of residual disease that falls below such a cutoff value. Failure to detect the rare abnormal cells may impact patient care and prognosis. For such situations, the two questions are: is the disease still present, and if so, how prevalent is it? The first question is qualitative and the second is quantitative. Traditionally, only the quantitative parameters have been used for determining reportability. Here we propose a method to account for both qualitative and quantitative evaluations of interphase FISH results.
This is a case report of an apparently balanced whole arm translocation between the short arms of... more This is a case report of an apparently balanced whole arm translocation between the short arms of chromosomes 5 and 10 in which the centromeric alpha-satellite DNA is split between both derivative chromosomes for both probes, leading to abnormal signal patterns. The patient requested preimplantation genetic testing for the unbalanced products of the translocation. However, using centromeric alpha-satellite DNA probes as controls for the subtelomeric-specific probes in interphase was not informative because of the split signals. The ramifications of such variation in the alpha-satellite regions of chromosomes for other interphase FISH tests are discussed.
Journal of the Association of Genetic Technologists, 2016
Rhesus macaque (Macaca mulatta), because of their similarity to humans, are often used to study c... more Rhesus macaque (Macaca mulatta), because of their similarity to humans, are often used to study complex neurobiology and anatomy, cardiovascular disease, and in vaccine development. While the rhesus genome is studied on its own by primatologists, the grand majority of rhesus macaque research is done with the intention of extrapolating the findings to human diseases and traits. As such, it makes sense that the rhesus genome and karyotype be arranged based on homology to human chromosomes in an effort to ease the comparisons between the two, and aide in interpreting data generated using rhesus macaque model systems. Various approaches have been utilized, including linkage analyses using radiation hybrid markers and human microsatellite loci, and next generation sequencing, to create a comprehensive rhesus genome. Here, we present for the first time, the rhesus macaque karyotype adjusted and renumbered to reflect human homology, and to complement the newly completed sequencing data.
John Wiley & Sons, Inc. eBooks, Mar 4, 2017
John Wiley & Sons, Inc. eBooks, Mar 4, 2017
PubMed, 2019
Interphase fluorescence in situ hybridization (FISH) cutoff values are calculated using various m... more Interphase fluorescence in situ hybridization (FISH) cutoff values are calculated using various mathematical methods to determine whether abnormalities seen are at reportable (statistically significant) levels. However, for interphase FISH studies of samples obtained from oncology patients who have been transplanted or treated, these cutoff values may result in reporting a false negative result due to the small percentage of residual disease that falls below such a cutoff value. Failure to detect the rare abnormal cells may impact patient care and prognosis. For such situations, the two questions are: is the disease still present, and if so, how prevalent is it? The first question is qualitative and the second is quantitative. Traditionally, only the quantitative parameters have been used for determining reportability. Here we propose a method to account for both qualitative and quantitative evaluations of interphase FISH results.
John Wiley & Sons, Inc. eBooks, Mar 4, 2017
John Wiley & Sons, Inc. eBooks, Mar 4, 2017
PubMed, 1975
A male with a karyotype 47,XXXY qs,t(9p-;Xq+) was ascertained utilizing ASG-banding. The karyotyp... more A male with a karyotype 47,XXXY qs,t(9p-;Xq+) was ascertained utilizing ASG-banding. The karyotype was repeated because the original diagnosis of Klinefelter syndrome (47,XXY) was inconsistent with many of the stigmata present. It is suggested that many karyotypes completed prior to the advent of banding techniques will be repeated in an attempt to provide more accurate diagnosis, describe more aberrations, and possibly establish new syndromes.
John Wiley & Sons, Inc. eBooks, Mar 4, 2017
In Vitro Cellular & Developmental Biology – Plant, Feb 1, 1972
Cytogenetic and Genome Research, 1990
Experimental Biology and Medicine, Mar 1, 1981
Transfusion of syngeneic marrow into normal, nonirradiated recipients results only in minimal pro... more Transfusion of syngeneic marrow into normal, nonirradiated recipients results only in minimal proliferation of donor cells. However, irradiated recipients, restored to hematologic normalcy by an initial marrow transfusion, subsequently sustain proliferation which replaces approximately 10% of endogenous marrow after a single transfusion of 4 x 10â· marrow cells of the same strain as the host. Cells from histoincompatible donors proliferate
Prenatal Diagnosis, Mar 1, 1984
45,X/46,XX mosaicism was found in only one of four primary amniotic fluid cultures. Repeat amnioc... more 45,X/46,XX mosaicism was found in only one of four primary amniotic fluid cultures. Repeat amniocentesis revealed 45,X/46,XX mosaicism in all four primary cultures. Mosaicism was confirmed in tissues from the abortus.
John Wiley & Sons, Inc. eBooks, Apr 12, 2017
Experimental Biology and Medicine, 1981
Transfusion of syngeneic marrow into normal, nonirradiated recipients results only in minimal pro... more Transfusion of syngeneic marrow into normal, nonirradiated recipients results only in minimal proliferation of donor cells. However, irradiated recipients, restored to hematologic normalcy by an initial marrow transfusion, subsequently sustain proliferation which replaces approximately 10% of endogenous marrow after a single transfusion of 4 x 10â· marrow cells of the same strain as the host. Cells from histoincompatible donors proliferate
Journal of the Association of Genetic Technologists, Feb 1, 2003
OBJECTIVES Interphase fluorescence in situ hybridization (FISH) cutoff values are calculated usin... more OBJECTIVES Interphase fluorescence in situ hybridization (FISH) cutoff values are calculated using various mathematical methods to determine whether abnormalities seen are at reportable (statistically significant) levels. However, for interphase FISH studies of samples obtained from oncology patients who have been transplanted or treated, these cutoff values may result in reporting a false negative result due to the small percentage of residual disease that falls below such a cutoff value. Failure to detect the rare abnormal cells may impact patient care and prognosis. For such situations, the two questions are: is the disease still present, and if so, how prevalent is it? The first question is qualitative and the second is quantitative. Traditionally, only the quantitative parameters have been used for determining reportability. Here we propose a method to account for both qualitative and quantitative evaluations of interphase FISH results.
This is a case report of an apparently balanced whole arm translocation between the short arms of... more This is a case report of an apparently balanced whole arm translocation between the short arms of chromosomes 5 and 10 in which the centromeric alpha-satellite DNA is split between both derivative chromosomes for both probes, leading to abnormal signal patterns. The patient requested preimplantation genetic testing for the unbalanced products of the translocation. However, using centromeric alpha-satellite DNA probes as controls for the subtelomeric-specific probes in interphase was not informative because of the split signals. The ramifications of such variation in the alpha-satellite regions of chromosomes for other interphase FISH tests are discussed.
Journal of the Association of Genetic Technologists, 2016
Rhesus macaque (Macaca mulatta), because of their similarity to humans, are often used to study c... more Rhesus macaque (Macaca mulatta), because of their similarity to humans, are often used to study complex neurobiology and anatomy, cardiovascular disease, and in vaccine development. While the rhesus genome is studied on its own by primatologists, the grand majority of rhesus macaque research is done with the intention of extrapolating the findings to human diseases and traits. As such, it makes sense that the rhesus genome and karyotype be arranged based on homology to human chromosomes in an effort to ease the comparisons between the two, and aide in interpreting data generated using rhesus macaque model systems. Various approaches have been utilized, including linkage analyses using radiation hybrid markers and human microsatellite loci, and next generation sequencing, to create a comprehensive rhesus genome. Here, we present for the first time, the rhesus macaque karyotype adjusted and renumbered to reflect human homology, and to complement the newly completed sequencing data.