Comparative, Maternal, and Epidemiologic Aspects [electronic resource] / edited by James Wilson.
Erişim Adresi
ISBN
9781461589365
Dil Kodu
İngilizce
Yer Numarası
DK/10556
Basım Bildirimi
1st ed. 1977.
Yayın Bilgisi
New York, NY : Springer US : Imprint: Springer, 1977.
Fiziksel Niteleme
IX, 334 p. online resource.
İçindekiler Notu
Section V: Maternal and Placental Effects -- 1 Maternal and Cytoplasmic Effects in Experimental Teratology -- 2 Factors That Affect Drug Concentrations in Maternal Plasma -- 3 Effects of Placental Pathology on the Embryo and Fetus -- Section VI: Comparative Studies in Man and Other Mammals -- 4 Summary of Comparative Embryology and Teratology -- 5 Comparative Placental Transfer -- Section VII: Epidemiology -- 6 Detection and Evaluation of Pregnancy Wastage -- 7 Value and Methods of Animal Studies in Epidemiology -- 8 Birth Defects Registries and Surveillance -- 9 Correlations of Malformation Frequency with Environmental and Genetic Attributes in Man.
Özet, vb.
Modification of embryonic development by genetic differences in the mother is a well-regcognized phemomenon, but little is known about the genet ics of these maternal traits or the mechanisms by which they act. To illustrate the genetic approach to the problem, examples are given of how differences in embryonic response to a teratogen can be partitioned into those resulting from differences in embryonic genotype (including the possible role of X-linked genes in producing reciprocal cross differences), maternal genotype, and cytoplasmically transmitted factors. The advantages and limitations of analysis by appropriate crosses, in utero treatments, embryo transfers, and in vitro experiments are illustrated. The numerous inbred strains of the mouse, with well-documented physiology, the recently developed recombinant inbred strains, and the existence of easily identified biochemical marker genes offer at tractive opportunities, so far largely unexploited, for causal analysis of mater nal effects on teratological responses. VII. ADDENDUM Since this chapter was written, several relevant papers have appeared. The strain difference between AI] and C57BU6] mice in frequency of cleft-palate response to cortisone was fitted to a model of normally distributed log tolerance (Biddle and Fraser, 1976). Genetic differences, both in maternal uterine environment and embryonic response, can be represented in terms of their effect on the median effective dose required for the cleft-palate re sponse. The maternal effect of AI] dams relative to C57BU6] dams caused a two-fold reduction in embryonic tolerance to cortisone-induced cleft palate.
Konu
Social sciences.
Humanities.
Humanities and Social Sciences.
Humanities.
Humanities and Social Sciences.
Diğer Yazarlar
Kurum Adı
Eseri Alıntıla
Referansları kullanmadan önce gözden geçirmeniz ve varsa gerekli düzeltmeleri yapmanız önerilir.
Dijital Kaynak
MARC Görünümü
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505 0 |aSection V: Maternal and Placental Effects -- 1 Maternal and Cytoplasmic Effects in Experimental Teratology -- 2 Factors That Affect Drug Concentrations in Maternal Plasma -- 3 Effects of Placental Pathology on the Embryo and Fetus -- Section VI: Comparative Studies in Man and Other Mammals -- 4 Summary of Comparative Embryology and Teratology -- 5 Comparative Placental Transfer -- Section VII: Epidemiology -- 6 Detection and Evaluation of Pregnancy Wastage -- 7 Value and Methods of Animal Studies in Epidemiology -- 8 Birth Defects Registries and Surveillance -- 9 Correlations of Malformation Frequency with Environmental and Genetic Attributes in Man.
520 |aModification of embryonic development by genetic differences in the mother is a well-regcognized phemomenon, but little is known about the genet ics of these maternal traits or the mechanisms by which they act. To illustrate the genetic approach to the problem, examples are given of how differences in embryonic response to a teratogen can be partitioned into those resulting from differences in embryonic genotype (including the possible role of X-linked genes in producing reciprocal cross differences), maternal genotype, and cytoplasmically transmitted factors. The advantages and limitations of analysis by appropriate crosses, in utero treatments, embryo transfers, and in vitro experiments are illustrated. The numerous inbred strains of the mouse, with well-documented physiology, the recently developed recombinant inbred strains, and the existence of easily identified biochemical marker genes offer at tractive opportunities, so far largely unexploited, for causal analysis of mater nal effects on teratological responses. VII. ADDENDUM Since this chapter was written, several relevant papers have appeared. The strain difference between AI] and C57BU6] mice in frequency of cleft-palate response to cortisone was fitted to a model of normally distributed log tolerance (Biddle and Fraser, 1976). Genetic differences, both in maternal uterine environment and embryonic response, can be represented in terms of their effect on the median effective dose required for the cleft-palate re sponse. The maternal effect of AI] dams relative to C57BU6] dams caused a two-fold reduction in embryonic tolerance to cortisone-induced cleft palate.
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532 8 |aNo reading system accessibility options actively disabled
532 8 |aPublisher contact for further accessibility information: accessibilitysupport@springernature.com
650 0|aSocial sciences.
650 0|aHumanities.
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245 10|aComparative, Maternal, and Epidemiologic Aspects|h[electronic resource] /|cedited by James Wilson.
250 |a1st ed. 1977.
264 1|aNew York, NY :|bSpringer US :|bImprint: Springer,|c1977.
300 |aIX, 334 p.|bonline resource.
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
347 |atext file|bPDF|2rda
505 0 |aSection V: Maternal and Placental Effects -- 1 Maternal and Cytoplasmic Effects in Experimental Teratology -- 2 Factors That Affect Drug Concentrations in Maternal Plasma -- 3 Effects of Placental Pathology on the Embryo and Fetus -- Section VI: Comparative Studies in Man and Other Mammals -- 4 Summary of Comparative Embryology and Teratology -- 5 Comparative Placental Transfer -- Section VII: Epidemiology -- 6 Detection and Evaluation of Pregnancy Wastage -- 7 Value and Methods of Animal Studies in Epidemiology -- 8 Birth Defects Registries and Surveillance -- 9 Correlations of Malformation Frequency with Environmental and Genetic Attributes in Man.
520 |aModification of embryonic development by genetic differences in the mother is a well-regcognized phemomenon, but little is known about the genet ics of these maternal traits or the mechanisms by which they act. To illustrate the genetic approach to the problem, examples are given of how differences in embryonic response to a teratogen can be partitioned into those resulting from differences in embryonic genotype (including the possible role of X-linked genes in producing reciprocal cross differences), maternal genotype, and cytoplasmically transmitted factors. The advantages and limitations of analysis by appropriate crosses, in utero treatments, embryo transfers, and in vitro experiments are illustrated. The numerous inbred strains of the mouse, with well-documented physiology, the recently developed recombinant inbred strains, and the existence of easily identified biochemical marker genes offer at tractive opportunities, so far largely unexploited, for causal analysis of mater nal effects on teratological responses. VII. ADDENDUM Since this chapter was written, several relevant papers have appeared. The strain difference between AI] and C57BU6] mice in frequency of cleft-palate response to cortisone was fitted to a model of normally distributed log tolerance (Biddle and Fraser, 1976). Genetic differences, both in maternal uterine environment and embryonic response, can be represented in terms of their effect on the median effective dose required for the cleft-palate re sponse. The maternal effect of AI] dams relative to C57BU6] dams caused a two-fold reduction in embryonic tolerance to cortisone-induced cleft palate.
532 8 |aAccessibility summary: This PDF is not accessible. It is based on scanned pages and does not support features such as screen reader compatibility or described non-text content (images, graphs etc). However, it likely supports searchable and selectable text based on OCR (Optical Character Recognition). Users with accessibility needs may not be able to use this content effectively. Please contact us at accessibilitysupport@springernature.com if you require assistance or an alternative format.
532 8 |aInaccessible, or known limited accessibility
532 8 |aNo reading system accessibility options actively disabled
532 8 |aPublisher contact for further accessibility information: accessibilitysupport@springernature.com
650 0|aSocial sciences.
650 0|aHumanities.
650 14|aHumanities and Social Sciences.
700 1 |aWilson, James.|eeditor.|4edt|4http://id.loc.gov/vocabulary/relators/edt
710 2 |aSpringerLink (Online service)
773 0 |tSpringer Nature eBook
776 08|iPrinted edition:|z9780306362439
776 08|iPrinted edition:|z9781461589372
776 08|iPrinted edition:|z9781461589389
856 40|uhttps://doi.org/10.1007/978-1-4615-8936-5
912 |aZDB-2-SHU
912 |aZDB-2-SXH
912 |aZDB-2-BAE
950 |aHumanities, Social Sciences and Law (SpringerNature-11648)
950 |aHistory (R0) (SpringerNature-43722)
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