1923
DOI: 10.5962/bhl.title.31181
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Outline of genetics : with special reference to plant material / by Merle C. Coulter.

Abstract: been the actual history of the case, for, with the beginning of the twentieth century, the study of evolution culminated in, and became diverted into, genetics, the experimental study of inheritance. Of course genetics has not answered all of the questions that have presented themselves in connection with evolution, but many critical and suggestive findings have been made, as will be seen in the following chapters; and unquestionably genetics will contribute a great deal more in the next few decades. CHAPTER I… Show more

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Cited by 9 publications
(13 citation statements)
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“…The bond angles in the base are quite similar to the values observed in 4-thiouridine (Saenger & Scheit, 1969), thymidine (Young, Tollin & Wilson, 1969) and the other 5-substituted bases such as 5-methyluridine (Hunt & Sabramanian, 1969), 5-fluoro-2'-deoxyuridine (Harris & Maclntyre, 1964) and 5-chlorouridine (Coulter, 1969). The exocyclic angles involving the C-S bond are remarkably close to the values found in the corresponding keto compounds.…”
Section: Bond Lengthssupporting
confidence: 71%
“…The bond angles in the base are quite similar to the values observed in 4-thiouridine (Saenger & Scheit, 1969), thymidine (Young, Tollin & Wilson, 1969) and the other 5-substituted bases such as 5-methyluridine (Hunt & Sabramanian, 1969), 5-fluoro-2'-deoxyuridine (Harris & Maclntyre, 1964) and 5-chlorouridine (Coulter, 1969). The exocyclic angles involving the C-S bond are remarkably close to the values found in the corresponding keto compounds.…”
Section: Bond Lengthssupporting
confidence: 71%
“…Similar values for the same angle were observed in 6-methyluridine, 69.6 and 69.4 ° (Suck & Saenger, 1972), 3',5'-diacetyl-2'-deoxy-2'-fluorouridine, 68.5 o (Suck et al, 1974) and cytidine-2',3'-cyclophosphate, 62.9 and 74.5 ° (Coulter, 1973); in 4-thiouridine this angle is increased considerably to 92.9 ° (Saenger & Scheit, 1970). In Table 8 these torsion angles are listed together with the conformational angles within the ribose moieties.…”
Section: Discussionsupporting
confidence: 68%
“…Clearly the C(3')-endo envelope, which dominates in anti-nucleosides, is not preferred in syn-nucleosides but is replaced by a C(3')-endo,C(4')-exo twist form and by the C(2')-endo envelope which both appear to avoid unfavourable contacts between 0(2) and the H atom attached to C(3'). The ribose puckering for cytidine-2',3'-cyclophosphate (Coulter, 1973) differs from that of the other syn-nucleosides in Table 8, probably as a consequence of the fused phosphodiester group.…”
Section: Discussionmentioning
confidence: 92%
See 1 more Smart Citation
“…The experiment reported herein takes~dvantage of the high pcnetrntlng puwer of 800 MeV protons and pluces samples, one with an imposed cyclic stress, the other with no stress, In line along the proton baam to as~iureiden~ical irradiation hictories In both samples (Fig. 1) [4]. For Al, the damage energy cross section was found to be 63 barn-keV, and since the threshold displacement energy is 17 keV, the damage rate is (1) where dpa is displacements per atorn.…”
Section: Introdijctionmentioning
confidence: 99%