派博傳思國際中心

標題: Titlebook: Male-Mediated Developmental Toxicity; Andrew F. Olshan,Donald R. Mattison Book 1994 Plenum Press, New York 1994 behavior.cancer.developmen [打印本頁]

作者: 巡洋    時間: 2025-3-21 17:44
書目名稱Male-Mediated Developmental Toxicity影響因子(影響力)




書目名稱Male-Mediated Developmental Toxicity影響因子(影響力)學科排名




書目名稱Male-Mediated Developmental Toxicity網(wǎng)絡公開度




書目名稱Male-Mediated Developmental Toxicity網(wǎng)絡公開度學科排名




書目名稱Male-Mediated Developmental Toxicity被引頻次




書目名稱Male-Mediated Developmental Toxicity被引頻次學科排名




書目名稱Male-Mediated Developmental Toxicity年度引用




書目名稱Male-Mediated Developmental Toxicity年度引用學科排名




書目名稱Male-Mediated Developmental Toxicity讀者反饋




書目名稱Male-Mediated Developmental Toxicity讀者反饋學科排名





作者: pester    時間: 2025-3-21 21:53

作者: 我說不重要    時間: 2025-3-22 01:06
Jennifer M. Ratcliffes structure continually decreases. The extraction of phase information from diffraction experiments is one of several great barriers that crystallographers must overcome on the path to structure solution. One means to overcome this obstacle, the technique of molecular replacement, uses the structura
作者: graphy    時間: 2025-3-22 05:26

作者: 儀式    時間: 2025-3-22 09:12
Robert W. Millerissue. It is generally accepted that FDG reflects the viability of tumour cells. The kinetics of FDG is modulated by several genes, besides the glucose transporters and hexokinases. Additional specific information can be obtained non-invasively by using other tracers specific for cell membrane recep
作者: Flirtatious    時間: 2025-3-22 16:44

作者: 獨特性    時間: 2025-3-22 19:20
Specific-Locus Mutation Tests in Germ Cells of the Mouse: An Assessment of the Screening Procedures y-induced mutation rates, as well as the identification and quantification of factors which affect the sensitivity to mutation induction. Such studies must rely on experiments based on laboratory animals, of which the choice is the house mouse ., due to its small size, short generation time, establi
作者: 子女    時間: 2025-3-22 22:42

作者: panorama    時間: 2025-3-23 03:21
Dominant Mutations in Mice The pioneering studies of Hertwig (1935), Brenneke (1937), and Schaefer (1939) had already indicated that the litters sired during the pre-sterile period of irradiated mice were of reduced size. Since there was no effect on sperm mobility and since the number of fertilized eggs was normal, it was c
作者: Geyser    時間: 2025-3-23 07:03

作者: 油膏    時間: 2025-3-23 12:14

作者: 懶惰人民    時間: 2025-3-23 15:42

作者: 哀悼    時間: 2025-3-23 21:09
Male Mice Receiving Very Low Doses of Ionizing Radiation Transmit an Embryonic Cell Proliferation Di of this ‘chimera assay’ is its exquisite sensitivity for detecting male germ cell exposure to ionizing radiation. Its published detection limit for male germ cell exposure is presently 0.01 Gy exposure of low LET radiation (e.g., x-radiation and gamma radiation). An important feature of the chimera
作者: RAG    時間: 2025-3-23 22:48

作者: Reservation    時間: 2025-3-24 06:05
The Male-Mediated Developmental Toxicity of Cyclophosphamided primarily on the consequences of maternal exposure to teratogens; much less attention has been given to the possible adverse effects on the progeny of paternal exposure to drugs or environmental chemicals. However, a wide range of agents, including environmental pollutants (e.g. lead) and therapeu
作者: Arb853    時間: 2025-3-24 07:35
Male-Mediated Teratogenesis: Ionizing Radiation/Ethylnitrosourea Studiesations result in these defects. Animal experiments anticipated that parental exposure to radiation and chemicals would induce varieties of defects in the offspring, including embryonic deaths, tumors and malformations (Nomura, 1975; 1978; 1982; 1986; Tomatis, 1981). However, these findings have not
作者: GLIDE    時間: 2025-3-24 13:48
Preconception Exposure of Males and Neoplasia in their Progeny: Effects of Metals and Consideration rethane, ethylnitrosourea, 4-nitroquinoline N-oxide, diethylstilbestrol, or cyclophosphamide), have resulted in significant increases in the incidences of tumors in their progeny and sometimes later generations (review in Tomatis et al, 1992; see also Francis et al, 1990; Loktionov et al.; 1992, Tur
作者: murmur    時間: 2025-3-24 16:26

作者: 傳授知識    時間: 2025-3-24 19:17

作者: promote    時間: 2025-3-25 01:29
Male-Mediated Developmental Toxicity: Paternal Exposures and Childhood Canceress of carcinogenesis as it applies to both adults and children. It can also be a frustrating and unrewarding pursuit. The question of the effect of paternal exposure on risk of cancer in an offspring illustrates both the fascination of this field, and its limitations.
作者: Cytology    時間: 2025-3-25 06:54

作者: 整理    時間: 2025-3-25 07:41

作者: MAPLE    時間: 2025-3-25 14:12
Reproductive Outcomes among Men Treated for Cancerrapy with 5-fluorouracil and methotrexate two and a half months and one month before conception and again around the time of conception of a pregnancy. In the fourth month of pregnancy, the obstetricians asked for genetic advice about this couple. The man’s history was also unusual because his fathe
作者: 友好關(guān)系    時間: 2025-3-25 18:26
Genetic Effects of Atomic-Bomb Exposurethree years earlier. He was well prepared for this endeavor, having trained as a physician after receiving his doctoral degree in Drosophila genetics. His work in Japan began when he was assigned by the U.S. Army as Acting Director of the Atomic Bomb Casualty Commission (ABCC), an agency of the Nati
作者: neurologist    時間: 2025-3-25 22:39

作者: Meager    時間: 2025-3-26 00:16

作者: Dedication    時間: 2025-3-26 05:09

作者: tooth-decay    時間: 2025-3-26 09:06

作者: 鞠躬    時間: 2025-3-26 15:35
James W. Allen,Barbara W. Collins,Ronald E. Cannon,Pamela W. McGregor,Arash Afshari,James C. Fuscoe
作者: 苦笑    時間: 2025-3-26 19:42
Lucy M. Anderson,Kazimierz S. Kasprzak,Jerry M. Rice
作者: preservative    時間: 2025-3-26 23:45

作者: 逗留    時間: 2025-3-27 03:11

作者: assent    時間: 2025-3-27 09:14

作者: limber    時間: 2025-3-27 10:08
The Male-Mediated Developmental Toxicity of Cyclophosphamidehemicals may have adverse effects on the fetus by “functionally” altering male germ cells. Paternally-mediated adverse effects on progeny outcome may be manifested as decreased fertility, embryolethality, external or internal malformations evident at the time of birth, or more subtle changes such as
作者: 無情    時間: 2025-3-27 17:26

作者: 有害    時間: 2025-3-27 20:56
Paternal Exposures and Embryonic or Fetal Loss: The Toxicologic and Epidemiologic Evidencedamage to paternal chromosomes, genes and DNA are at a relatively advanced stage of development (National Research Council 1989), other e.g. epigenetic or non-genetic mechanisms have yet to be established.
作者: animated    時間: 2025-3-28 01:48
Book 1994ic investigations have suggested that paternal exposures may be more important than previously suspected. This topic has been termed by some as "male-mediated developmental toxicity. " This is meant to refer to the effects of exposures and other factors relating to the male parent that result in tox
作者: indemnify    時間: 2025-3-28 04:37
pidemiologic investigations have suggested that paternal exposures may be more important than previously suspected. This topic has been termed by some as "male-mediated developmental toxicity. " This is meant to refer to the effects of exposures and other factors relating to the male parent that result in tox978-1-4613-5764-3978-1-4615-1877-8
作者: 庇護    時間: 2025-3-28 08:57
Jonathan Buckleylization methods for membrane proteins are being implemented. These have already been successful and are expected to contribute significantly to the future successes. This chapter will review some basic principles in membrane protein crystallization and give an overview of the current state of the a
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作者: CBC471    時間: 2025-3-28 16:43

作者: Forehead-Lift    時間: 2025-3-28 22:39

作者: 是比賽    時間: 2025-3-29 01:25
Robert W. Milleryr3 octreotide (DOTATOC) in NET. The overexpression of gastrin-releasing peptide (GRP) receptors can be visualised in GIST by using bombesin analogues. These peptides can be labelled by .Ga, which is a generator product and therefore more cost-effective than cyclotron products. .Ga-DOTATOC is a pept
作者: 花爭吵    時間: 2025-3-29 03:21
Book 1994d experimental animal research has focused on the relationship between maternal exposures including medications, tobacco smoke, alcohol, infections, and occupation and the occurrence of spontaneous abortion, low birth weight, and birth defects. The potential role of paternal exposures has not been i
作者: insular    時間: 2025-3-29 10:10

作者: 精密    時間: 2025-3-29 14:18
Paternal Occupation and Birth Defectsunlikely (Brown, 1985). However, recent laboratory and epidemiologic investigations have reinforced earlier animal data suggesting that paternal exposures may be more important than previously suspected. The published literature on paternal occupational exposures and the risk of birth defects in offspring will be reviewed in this chapter.
作者: BILK    時間: 2025-3-29 16:16

作者: 革新    時間: 2025-3-29 21:09

作者: 命令變成大炮    時間: 2025-3-30 02:35

作者: CLAM    時間: 2025-3-30 04:37

作者: 殘暴    時間: 2025-3-30 11:29
Aneuploidy Tests: Cytogenetic Analyses of Mammalian Male Germ Cellsir father (Sherman et al., 1991). In regard to sex chromosome aneuploidies, all of the XYY trisomies, most of the XO monosomies, and half of the XXY trisomies are considered to be of paternal origin (reviewed by May et al., 1990).
作者: 有效    時間: 2025-3-30 16:22
Male-Mediated Reproductive Toxicity: Effects on the Nervous System of Offspringathers to reproductive and developmental toxicants. In both cases, developmental toxicity studies concentrate on maternal exposures both prior to pregnancy and during gestation. Developmental toxicity due to paternal exposure is rarely considered, even in the cases of recognized reproductive toxicants.
作者: 沙文主義    時間: 2025-3-30 17:36
iologic and experimental animal research has focused on the relationship between maternal exposures including medications, tobacco smoke, alcohol, infections, and occupation and the occurrence of spontaneous abortion, low birth weight, and birth defects. The potential role of paternal exposures has
作者: 同來核對    時間: 2025-3-30 23:28
Strategies for the Use of a Multiple-Endpoint System for Mammalian Germ Cell Mutation Testingh fertility is affected by the test compound. Finally, a multiple-endpoint system allows for flexibility. It is clearly an option to add other assays which may become available in the future and to allow selective use of individual endpoints, according to the requirements of a given experiment.
作者: 誘惑    時間: 2025-3-31 01:27

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作者: chalice    時間: 2025-3-31 14:35
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