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br-j15 | These changes were more marked in the atrophic right kidney than in the left . | <NONE> | <NONE> | [
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br-j15 | In addition , there were 2 small papillary adenomas in the right kidney . | <NONE> | <NONE> | [
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br-j15 | The bone of the vertebral bodies , ribs , and sternum was soft and was easily compressed . | <NONE> | <NONE> | [
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br-j15 | The marrow of the vertebral bodies was pale and showed areas of fatty replacement . | <NONE> | <NONE> | [
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br-j15 | Microscopically , there were many areas of hypercellularity alternating with areas of hypocellularity . | <NONE> | <NONE> | [
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br-j15 | The cells of the erythroid , myeloid , and megakaryocytic series were normal except for their numbers . | <NONE> | <NONE> | [
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br-j15 | There was no evidence of fibrosis . | <NONE> | <NONE> | [
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br-j15 | The muscles of the extremities , chest wall , neck , and abdominal wall were soft , pale , and atrophic . | <NONE> | <NONE> | [
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br-j15 | Microscopic studies of the gastrocnemius , pectoralis major , transversus abdominis , biceps brachii , and diaphragm showed atrophy as well as varying degrees of injury ranging from swelling and vacuolization to focal necrosis of the muscle fibers . | <NONE> | <NONE> | [
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br-j15 | Individual nuclei were usually oval to round , though occasionally elongated , and frequently small and somewhat pyknotic . | <NONE> | <NONE> | [
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br-j15 | Occasionally there were small basophilic fibers that were devoid of myofibrillae and contained many vesicular nuclei with prominent nucleoli (Fig. 5). | <NONE> | <NONE> | [
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br-j15 | These were thought to represent regenerating fibers . | <NONE> | <NONE> | [
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br-j15 | Trichrome stains failed to show fibrosis in the involved muscles . | <NONE> | <NONE> | [
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br-j15 | In all of the sections examined , the arterioles and small arteries were essentially normal . | <NONE> | <NONE> | [
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br-j16 | In attempting to improve specificity of staining , the fluorescein labeled antisera used in both direct and indirect methods were treated in one of several ways: (1) They were passed through Dowex-2-chloride twice and treated with acetone insoluble powders (Coons , 1958) prepared from mouse liver or from healthy sweet clover stems or crown gall tissue produced by Agrobacterium tumefaciens (E. F. Smith + Townsend) Conn , on sweet clover stems . | <NONE> | <NONE> | [
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br-j16 | (2) The conjugates as well as the intermediate sera were absorbed for 30 minutes with 20 - 50 mg of proteins extracted from healthy sweet clover stems . | <NONE> | <NONE> | [
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br-j16 | The proteins were extracted with 3 volumes of * * f in * * f to give a nearly neutral extract and precipitated by 80% saturation with * * f . | <NONE> | <NONE> | [
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br-j16 | (3) In other experiments the indirect conjugate was treated with 3 volumes of ethyl acetate as recommended by Dineen and Ade (1957). | <NONE> | <NONE> | [
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br-j16 | (4) The conjugates were passed through a diethylaminoethyl (DEAE -) cellulose column equilibrated with neutral phosphate buffer (PBS) containing * * f potassium phosphate and * * f . | <NONE> | <NONE> | [
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br-j16 | The sections were then thawed by placing a finger under the slide and dried under a fan for 30 minutes; until used they were stored for as long as 2 weeks . | <NONE> | <NONE> | [
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br-j16 | After drying the sections under the fan , fixing in acetone , and drying at 37 ` as in the indirect method , the sections were treated with conjugated * * f or * * f (undiluted unless mentioned otherwise) for 5 - 30 minutes . | <NONE> | <NONE> | [
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br-j16 | As controls , other sections were similarly treated with * * f or conjugated antiserum to the New York strain of potato yellow-dwarf virus (Wolcyrz and Black , 1956). | <NONE> | <NONE> | [
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br-j16 | In the eyepiece a Wratten 2 B filter was used to filter off residual ultra-violet light . | <NONE> | <NONE> | [
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br-j16 | In the first few experiments * * f was passed through Dowex-2-chloride twice and absorbed twice with 50 - 100 mg sweet clover tissue powder . | <NONE> | <NONE> | [
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br-j16 | The intermediate sera were also similarly absorbed with tissue powder . | <NONE> | <NONE> | [
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br-j16 | Sections of sweet clover stem and root tumors were treated with 1: 10 solution of * * f for 30 minutes , washed in buffered saline for 15 minutes , stained with * * f for 30 minutes , and washed for 15 minutes in PBS . | <NONE> | <NONE> | [
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br-j16 | Such sections showed bright yellow-green specific fluorescence in the cells of the pseudophloem tissue (Lee and Black , 1955). | <NONE> | <NONE> | [
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br-j16 | However , the nonspecific staining by the * * f in tumor sections was considered bright enough to be confused with the staining of small amounts of WTV antigen . | <NONE> | <NONE> | [
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br-j16 | The only treatment by which nonspecific staining could be satisfactorily removed was by passing the conjugate through a DEAE-cellulose column . | <NONE> | <NONE> | [
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br-j16 | In the latter cases an additional treatment of the DEAE cellulose treated * * f with 50 mg of sweet clover stem tissue powder further improved the specificity . | <NONE> | <NONE> | [
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br-j16 | The specificity of staining in WTV tumors with * * f and * * f but not with NS and * * f or with antiserum to potato yellow-dwarf virus and * * f , and the absence of such staining in crown gall tumor tissue from sweet-clover , indicate that an antigen of WTV was being stained . | <NONE> | <NONE> | [
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br-j16 | In later experiments , * * f and * * f were prepared by conjugating 8 mg of FITC per gram of globulin . | <NONE> | <NONE> | [
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br-j16 | The best staining procedure with this purified * * f consisted of staining with the conjugate for 30 minutes and washing in PBS for 15 minutes . | <NONE> | <NONE> | [
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br-j16 | The specificity of staining with * * f was established as follows: * * f specifically stained tumor sections but not sections of healthy sweet clover stems or of crown gall tumor tissue from sweet clover . | <NONE> | <NONE> | [
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br-j16 | Sections of tumors incited by WTV were not similarly stained with conjugated normal serum or conjugated antiserum to potato yellow-dwarf virus . | <NONE> | <NONE> | [
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br-j16 | After passing * * f through DEAE-cellulose , the titer of antibodies to WTV in the specific fraction was 1: 4 of the titer before such passage (precipitin ring tests by R. F. Whitcomb); but mere dilution of the conjugate to 1: 4 did not satisfactorily remove nonspecific staining . | <NONE> | <NONE> | [
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br-j16 | Results of specific staining by the direct and the indirect methods were similar and showed the localization of WTV antigen in certain tissues of tumors . | <NONE> | <NONE> | [
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br-j16 | The virus antigen was concentrated in the pseudophloem tissue . | <NONE> | <NONE> | [
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br-j16 | Within the pseudophloem cells the distribution of WTV antigen was irregular in the cytoplasm . | <NONE> | <NONE> | [
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br-j16 | No antigen was detectable in certain dark spherical areas in most cells . | <NONE> | <NONE> | [
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br-j16 | In all cases studied tissues of the stem on which the tumor had developed did not contain detectable amounts of WTV antigen . | <NONE> | <NONE> | [
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br-j16 | The reason for the failure of these treatments to eliminate nonspecific staining in the conjugates in our system is not known . | <NONE> | <NONE> | [
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br-j16 | The specific staining by both direct and indirect methods showed that WTV antigen was concentrated in the pseudophloem tissue and in a few thick walled cells in the xylem region , but was not detectable in any other tissues of the root and stem tumors . | <NONE> | <NONE> | [
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