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Radioaerosol technique suitable for routine graphic study qf regional ventilation. Pregnancy risk category C. ~100% placental transfer in humans. Use normal adult doses in pregnancy. Due to extensive experience and lack of evidence for teratogenicity, 3TC + AZT are recommended as the dual NRTI backbone of a regimen. Secreted in human breast milk at similar concentrations to those found in serum. trimethoprim increases 3TC AUC 40% adjust 3TC if renal dysfunction, monitor for 3TC toxicity ; 3TC and ddC compete for intracellular phosphorylation in vitro, both cytidine analogues, thus avoid combination. Similarly, avoid coadministration with emtricitabine. See separate Drug Interaction chart. CBC diff, electrolytes, anion gap, serum bicarbonate, amylase, LFTs CBC diff, electrolytes, anion gap, serum bicarbonate, amylase lipase, LFTs q3-6mos Measure serum lactate if low serum bicarbonate or high anion gap and Sx of lactic acidosis. Prodromal Sx include: nausea, anorexia, abdominal pain, vomiting, weight loss, fatigue. Rapidly progressive Sx: tachycardia, tachypnea, hyperventilation, dyspnea, muscular weakness, jaundice, mental status changes. May also progress to multi-organ failure hepatic, pancreatitis, encephalopathy, respiratory ; and death. D C drug: Sx of lactic acidosis, serum lactate 5 mmol L, amylase 200 asymptomatic ; , pancreatitis, LFTs 5xULN, ANC 0.5, painful neuropathy Tablet: 150mg white, diamond-shaped DIN 02192683 300mg gray-blue, diamond-shaped DIN 02247825 Oral Solution: 10mg mL 240mL DIN 02192691; strawberry-banana flavor Combination tablets: Combivir: 300 mg zidovudine 150 mg lamivudine; DIN 02239213 Trizivir: zidovudine 300 mg lamivudine150 mg abacavir 300 mg tablet; DIN 02244757. Kivexa: abacavir 600 mg + 3TC 300 mg tablet; DIN 02269341. Store tabs and solution at room temperature.

ADJUSTMENT.OF.MULTIPLE ORE Patrick.G.Arbogast * , .Vanderbilt versity Hua.Ding, .Vanderbilt versity Wayne.A.Ray, .Vanderbilt versity rdiovascular.risk.factors, .recently-published.large. pharmacoepidemiologic rdiovascular.disease. a rdiovascular.risk ore ; .This. ore.created to.the.outcome.It.is.then summary the andard.error.of.the.exposure timate.and.thus.to.an.excess.of simulation udies ing.this.summary.risk. score.for.large.cohort udies.Results.indicated.that timated andard.errors om.the.regression.models ing.this. summary.risk ore.approximated.their.empirical andard.errors om this.summary.risk. udies. email: .patrick.arbogast vanderbilt.
Clindamycin plus Primaquine vs. Trimethoprim Sulfamethoxazole TMP SMZ ; for Pneumocystis carinii pneumonia in patients with AIDS18. That he was doing the work to identify the meanings related to his distress suggested therapeutic success was likely. The following 2 sessions focused on "catastrophizing, " the cognitive error of constantly anticipating the worst possible outcome. We discussed a variety of situations using the triple column format of examining situations, feelings, and thoughts. In relating his son's newfound interest in the opposite sex, he stated: "If he got a girl pregnant, it would be all over." He quickly labeled the errors in thinking as jumping to a conclusion and catastrophizing, and we worked on finding a more reasonable alternative approach to his thinking. Next, we took on his tendency to compare himself with his brother and then to judge his performance a failure. Together, we reviewed his beliefs about his life and that of his brother, with the aim of finding a more realistic understanding. By the eighth session, Mr. A told me that he and his wife were no longer contemplating divorce. He had written down the issues that.

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Mutagenesis bacterial mutagenic studies have not been performed with sulfamethoxazole and trimethoprim in combination and trimipramine.

Transfer of the amp gene from strain UB1731 using R plasmids. Attempts to transfer the amp gene from E. coli UB1731 to Rstrains of E. coli have always failed limit of detection, 10-9 donor ; . However, a number of R plasmids can mobilize this gene from the chromosome. In a typical example, UB1731 carrying R388 was mated with E. coli JC 6310 in a 2h cross, and the progeny was selected as described above. A total of 100 carbenicillin-resistant colonies were obtained, and all of these were also resistant to trimethoprim when replica plated Table 3 ; . In the absence of R388 no transfer of amp was obtained. R388 therefore allows transfer of the amp gene from UB1731 at a frequency of about one-hundredth the rate found for the transfer of R388 alone. As there is 100% linkage between the penicillin and trimethoprim resistance genes when the initial selection takes place on carbenicillin, the mobilization of the amp gene from the chromosome.
Number Drug name pyridoxine Quinapril Quinine Ranitidine Rifampicin rofecoxib Roxithromycin Salbutamol Salmeterol Selegiline Senna sibutramine sildenafil Simethicone Simvastatin Sodium Aurothiomalate Sodium Citro-Tartrate Sodium Cromoglycate Sodium Valproate Sotalol Spironolactone sulfamethoxazole Sulindac Sulphasalazine Sumatriptan Syringe tadalafil Tamoxifen Citrate Tar with Triethanolamine Sulphate and Fluor Temazepam Tenoxicam Terazosin Hydrochloride Terbinafine Terbutaline Sulphate Thyroxine Tiaprofenic Acid Timolol Tioconazole Tolterodine topical skin Tramadol Tranexamic Acid triamcinolone Acetonide Triamterene Triazolam Trifluoperazine Hydrochloride Trimethoprim Urea Valdecoxib Verapamil Vitamin B Complex Vitamins warfarin sodium Xylometazoline Hydrochloride Zopiclone Lauryl 5 15 67 0.00 0.13 0.02 0.39 topical 250mcg 16mg 20mg Arthritis 2 46 13 Total N-n ; 230 3890 816 % Total % % Total Arthritis N-n ; 0.05 0.07 1.12 0.00 2.32 0.25 0.07 0.00 0.02 0.01 0.05 0.00 0.02 0.05 0.07 Average daily dose Arthritis 100mg 16mg 319mg Total N-n ; 98mg 17mg 280mg and triptorelin.

The benzothiadiazide "thiazide" ; diuretics are widely used for the treatment of hypertension and conditions of fluid retention such as congestive heart failure. All thiazides augment excretion of potassium in the distal tubule and can cause hypokalemma in a patient taking them for a prolonged period 1 ; . Thus, investigation of the cause of hypokalemia may include screening the urine for the presence of thiazides when reliable information cannot be obtained by history. Several methods have been developed to measure qualitatively or quantitatively thiazide diuretics in biological fluids 2-12 ; . An early method involving colorimetric determination of the sulfonamides produced by hydrolysis lacked sensitivity and specificity 5, 12 ; . A simpler spectrophotometric procedure was developed later by Pilsbury and Jackson 3 ; . Although this procedure was in use by our laboratory, it lacked specificity, and the ultraviolet spectra were often difficult to interpret. Alternative methods based on spectrofluorometry 6 ; , thin-layer chromatography 7 ; , paper chromatography 3, 5 ; , and gas-liquid chromatography 8-10 ; have been developed for specific thiazides. Although these methods may give improved specificity, they have not been applied to the measurement of the wide range of thiazides required for a screening test. Liquid-chromatographic methods for hydrochlorothiazide 2, 4 ; , bemetizide 11 ; , and chiorothiazide 12 ; have also been reported. Our attempts to use these methods to screen urines for the presence of thiazides failed, principally because of interfering substances in the extracts. We report.

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Fig. 5 Blood acetaldehyde concentration in rats at the beginning of the different treatments n and acetaldehyde 0 and ethanol con centrations after 14 days of treatment mean SEM ; . Acetaldehyde and ethanol concentrations were determined from tail blood samples taken 30 minutes after the intraperitoneal injection of 1.5 g ethanolAg body weight. Rats received the thiamin-deficient diet combined with one of the five treatments described in the legend to figure 4. * P " 0.05 significance level for differences in changes relative to the initial values compared to the changes in the ad libitum-control group Neuman-Keuls-test and trizivir. News articles on trimethoprim through the lens: january 20 january 26 - jan 27, 2008 the winners: doxycycline, gentamicin and bactrim. Figure 3 Changes in QoL score in RRMS and SPMS patients starting on DMD at time 0. The lower line shows those patients who stopped treatment for clinical reasons within the first three years treatment failures, n0 26 and troleandomycin.
Senator Barrientos was recognized and introduced to the Senate a group of students from Bastrop High School in Bastrop, accompanied by their teacher. The Senate welcomed its guests. MOTION TO ADJOURN On motion of Senator Truan and by unanimous consent, the Senate at 11: 28 a.m. agreed to adjourn, upon completion of the introduction of bills and resolutions on first reading, until 10: 00 a.m. tomorrow. SENATE BILLS ON FIRST READING The following bills were introduced, read first time, and referred to the committees indicated: SB 366 by Madla Relating to the continuation and functions of the Advisory Commission on State Emergency Communications. To Committee on Economic Development. SB 766 by Brown Relating to the issuance of certain permits for the emission of air contaminants. To Committee on Natural Resources. SB 767 by Brown Relating to the treatment of a patient by a physical therapist without a referral from another licensed health care professional. To Committee on Health Services. SB 768 by Madla Relating to the consolidation of emergency communication districts. To Committee on Economic Development. SB 769 by Madla Relating to the creation of an advanced transportation district; authorizing the imposition of a local sales and use tax for advanced transportation and local development. To Committee on Intergovernmental Relations. SB 770 by Shapiro Relating to state agency internal auditing. To Committee on State Affairs. SB 771 by Harris Relating to the legal representation of county officials and employees by district and county attorneys. To Committee on Jurisprudence. SB 772 by Harris Relating to exempting certain persons from requirements related to the sale, exchange, or lease-purchase of a manufactured home. To Committee on State Affairs.

Is self-harm, suicidal or malicious intent suspected? NO Is the home situation of concern e.g., patient lives alone or family caregiver seems unreliable ; ? NO Is patient moderately or severely symptomatic e.g., convulsions, lethargy, abdominal pain, persistent vomiting ; ? NO Have more than 4 hours passed since the ingestion and is the patient asymptomatic? NO Unable to estimate maximum amount ingested? NO Did the patient ingest more than 30 mg kg of camphor, or are there other ingredients in the product at toxic concentrations? NO Observe at home. Consider a follow-up call at 4 hours after exposure. For eye exposures, the eye s ; should be irrigated with room-temperature tap water for 15 minutes. If after irrigation, the patient is having pain, decreased visual acuity, or persistent irritation, referral for an ophthalmologic examination is indicated. For skin exposures, the affected areas should be washed thoroughly with soap and water. If the patient is asymptomatic, it is unlikely that toxicity will occur. If the patient is symptomatic, referral should occur based on the severity of symptoms. It is unlikely that the toxicity will progress in severity once the material has been removed from the skin. YES Refer to emergency department. YES Refer to emergency department. YES Toxicity is unlikely to occur. No referral or treatment is needed. YES Refer to emergency department. YES Refer to emergency department. YES Refer to emergency department and trovafloxacin.

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Hesion to the mHEV cell lines data not shown ; . Furthermore, CD44, which mediates migration of activated lymphocytes into inflammatory sites as well as across cytokine-activated endothelial cells in vitro 20, 21 ; , did not inhibit resting lymphocyte migration across the mHEV cell lines, as determined using an anti-CD44 blocking Ab clone IM7; data not shown ; 11 ; . It also possible that lymphocytes migrate between the endothelial cells on fibronectin. Inhibition of one fibronectin receptor VLA-5 5 1 integrin ; with blocking anti- 5 integrin clone MFR5 ; had no effect on lymphocyte migration data not shown ; . This could not be tested further with CS-1 peptides that block integrin binding to fibronectin, because these peptides also block binding to VCAM-1 22 ; . Furthermore, RGD-containing peptides, which block binding to fibronectin, reversed endothelial cell attachment to the solid support, causing the monolayer to dissociate from Transwells or 96-well plates data not shown ; . In summary, resting lymphocyte 4 integrin binding to VCAM-1 on the mHEV cells was required for lymphocyte migration. Lymphocyte migration across endothelial cell lines requires endothelial cell NADPH oxidase-catalyzed production of ROS The role of VCAM-1 as a receptor for 4 integrin during lymphocyte adhesion has been clearly established 1, 2 ; . However, it is not known whether ligand binding to VCAM-1 initiates intracellular signals in the endothelial cell that are required for endothelial cell promotion of lymphocyte migration. Therefore, our approach was to determine whether inhibitors of signal transduction molecules.
B. Doxycycline 100 mg orally 2 times day for 6 weeks plus streptomycin 1 g intramuscularly for first 1421 days. C. Rifampin 900 mg day orally once for 6 weeks. D. Trimethoprim-sulfamethoxazole 1012 mg kg day of the trimethoprim component ; plus rifampin 1520 mg kg day ; for 6 weeks. 20. A 40-year-old man from Massachusetts was seen in the emergency department with a 1-week history of fever, headache, chills, and fatigue. He reports going hiking in the woods 2 weeks before his illness, but did not recall a tick bite. He has a history of hypertension and splenectomy after trauma when he was 20 years old. He takes metoprolol and has no known drug allergies. His temperature was 37.7C, pulse was 96 beats minute, respiratory rate was 20 breaths minute, and blood pressure was 109 54 mm Hg. Physical examination revealed jaundice and scleral icterus. He had minimal right upper quadrant pain but no hepatomegaly. Laboratory analysis showed a normal white blood cell count, with a mild anemia and thrombocytopenia. Total bilirubin was 14 mg dl, aspartate aminotransferase was 45 IU L, alkaline phosphatase 150 IU L, and lactate dehydrogenase was 900 IU L. Urinalysis showed the presence of hemoglobin. Peripheral blood smear revealed erythrocytes containing Babesia. The patient was diagnosed with babesiosis and started on a combination of clindamycin and quinine. Three days later, he says he can no longer take the regimen because of new-onset diarrhea and ringing in his ears. Which one of the following regimens represents an appropriate alternative therapy for this patient? A. Atovaquone 750 mg orally 2 times day plus azithromycin 500 mg orally on day 1 followed by 250 mg day orally for 6 days. B. Pentamidine 4 mg kg day intramuscularly. C. Chloroquine 500 mg orally every 12 hours for 3 weeks. D. Doxycycline 100 mg orally 2 times day 7 days. 21. A 37-year-old man was seen in the emergency department with a 6-month history of chronic diarrhea, 16-pound weight loss, and new-onset right upper quadrant tenderness. He is positive for the human immunodeficiency virus with a CD4 count of fewer than 100 cells mm3 and viral load of more than 50, 000 copies ml. He currently is not on any therapy for his human immunodeficiency virus and reports no known drug allergies. Physical examination was unremarkable except for right upper quadrant pain. Laboratory analysis reveals an elevated total bilirubin 13 mg dl ; and alkaline phosphatase 300 IU L ; . Biopsy from endoscopy is still pending. The physician suspects bilary cryptosporidiosis. Which one of the following is the best therapy for this patient? A. Paromomycin 500 mg orally 4 times day for 4 weeks. B. Nitazoxanide 500 mg orally 2 times day for 12 weeks. Pharmacotherapy Self-Assessment Program, 5th Edition and truvada.

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Mellaril has not been tested in women to determine its safety in pregnancy. The effects of the medication on the developing fetus in pregnant women are unknown. In animal studies, there was no evidence of harm to and trimethoprim.

Identified for three types of cardiac ion channels 15 ; in human LQT. The most common defects are found in genes encoding the KVLQT1 and HERG potassium channels 13 ; . For the HERG channel, which encodes the pore-forming subunit of the cardiac rapidly activating delayed rectifier potassium channel 1, 6 8 ; , we have recently reported that the loss of channel function can be caused by multiple mechanisms including abnormal protein trafficking, the generation of nonfunctional channels, and altered channel gating 9 ; . In the present experiments, we studied the LQT mutation N470D heterologously expressed in a mammalian cell line. This mutation, when expressed in Xenopus oocytes, has been reported to generate HERG current with reduced amplitude 30% of wild type ; and altered voltage dependence of activation 10 ; . We found that the protein trafficking of N470D mutant is highly temperaturesensitive. In addition, we showed that the defective protein trafficking can be corrected by drugs that selectively block HERG channels and tums. Of chloroform. Vortex-mix and centrifuge as before. Separate and save the aqueous top ; layer, extracting it again with chloroform, then transfer the chloroform bottom ; layers to the acid-extracted chloroform tube. Evaporate the combined acid- and basic-extracted chloroform fractions just to dryness with a gentle stream of dry air in a 40 # bath. water Add 20 LL of the internal standard mepivacaine ; solution. Vortex-mix and inject 2 p.L into the gas chromatograph. For the within-nm precision data we analyzed 12 samples of the standard as rapidly as possible in one day. The results are given in Table 3. Assessing between-run precision from serum in glass. From a 500-mL pool of clear, drug-free, human plasma obtained from the blood bank 2-mL was placed into 15-mL glass-stoppered centrifuge tubes and frozen. One analysis a day was performed for 25 days. The results are given in Table 3. Testing extraction effects and contamination of bloodcollection tubes. We used the following procedure for all the evacuated blood-collection tubes studied. Remove the stopper and add to each tube 5.0 mL of pooled plasma or water along with 0.5 mL of the standard drug mixture. Replace the stopper and mix by inverting several times to imitate the procedure when blood is drawn. Leave the tube standing upright in a rack for 20 h at room temperature. To 2.2 mL of pooled plasma or water add 2.0 mL of 0.5 mol L HC1 to one sample plus 2.0 mL of chloroform, and then add 2.0 mL of 0.5 mol L NaOH and 2.0 mL of chloroform to another portion of the same sample and extract as before. Combine the acid and basic extracts and evaporate just to dryness. Add 20 L of the internal standard solution, vortex-mix, and inject 2 L into the gas chromatograph or the mass spectrometer. The packing in the gas-chromatographic column of the mass spectrometer and the temperature program are the same as specified above for the gas chromatograph.

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Ms is unpredictable; it differs greatly among people diagnosed with the disease: 80% are diagnosed with relapsing remitting disease and about half of these will develop secondary progressive disease 10% are initially diagnosed with a benign form 10% are diagnosed with a primary progressive form of the disease and tysabri.

TABLE 4 ; . This 17-day study of hospitalized patients found a 10-point change of 168 points ; in the Neurobehavioral Rating Scale for patients randomized to citalopram compared with a 2.3-point change for placebo P .001 ; .22 Of the 7 subscales examined, only agitation and lability were significantly improved with citalopram compared with placebo. The trial had a high dropout rate, with more than half of patients in each group failing to complete the study, most commonly due to lack of efficacy. Lyketsos et al31 found sertraline to be effective in the treatment of depression among patients with dementia. However, there was no significant benefit of sertraline on neuropsychiatric symptoms. The authors did report that in subgroup analyses of full responders vs nonresponders in terms of depression symptoms ; , full responders had significantly greater improvement on and trimipramine. Cystis carinii in an infant. Amer. J. Clin. Pathol. 26: 787-793. 3. Donno, L., and V. Sanguineti. 1970. Therapy of natural falciparum malaria with combinations of antifolic drugs in non-immune subjects. Chemotherapy 15: 118-124. 4. Frenkel, J. K., J. T. Good, and J. A. Schultz. 1966. Latent pneumocystis infection in rats, relapse and chemotherapy. Lab. Invest. 15: 1559-1577. 5. Gaylarde, P. M., and I. Sarkany. 1972. Suppression of thymidine uptake of human lymphocytes by co-trimoxazole. Brit. Med. J. 25: 144-146. 6. Ghilchick, M. W., A. S. Morris, and D. S. Reeves. 1970. Immunosuppressive powers of the antibacterial agent trimethoprim. Nature London ; 227: 393-394. 7. Helander, I., H. Arvilommi, S. Lund, and V. K. HopsuHavu, reference in Arvilommi, H. et al., 1972. Immunosuppression by co-trimoxazole. Brit. J. Med. 25: 761-762. 8. Hughes, W. T., H. K. Kim, R. A. Price, and C. Miller. 1973. Attempts at prophylaxis for murine P. carinii pneumonitis. Curr. Ther. Res. 15: 581-587. 9. Hughes, W. T., R. A. Price, H. K. Kim, T. Coburn, D. Grigsby, and S. Feldman. 1973. Pneumocystis carinii pneumonitis in children with malignancies. J. Pediat. 82: 404-415. 10. Lewis, C. 1968. Antiplasmodial activity of halogenated lincomycin analogues in Plasmodium berghei-infected mice. Antimicrob. Ag. Chemother. 1967, p. 537-542. 11. Lunseth, J. H., T. W. Kirmse, A. P. Prezyna, and R. Gerth. 1955. Interstitial plasma cell pneumonia. J. Pediat. 46: 137-145. 12. McMaster, P. R. B., K. G. Powers, J. F. Finerty, and M. H. Lunde. 1973. The effect of two chlorinated lincomycin analogues against acute toxoplasmosis in mice. Amer. J. Trop. Med. Hyg. 22: 14-17. 13. Post, C., T. Fakouhi, W. Dutz, B. Bandarizadeh, and E. E. Kohout. 1971. Prophylaxis of epidemic infantile pneumocystosis with a 20: 1 sulfadoxine plus pyrimethamine combination. Curr. Ther. Res. 13: 273-279. 14. Pyesmany, A. F., and D. L. Cameron. 1973. Septrininduced stimulation of granulocyte metabolism in chronic granulomatous disease. Pediat. Res. 7: 371. 15. Reisberg, B., J. Herzog, and L. Weinstein. 1967. In vitro antibacterial activity of trimethoprim alone and combined with sulfonamides. Antimicrob. Ag. Chemother. 1966, p. 424-429. 16. Remington, J. S., T. Yagura, and W. S. Robinson. 1970. The effect of rifampin on Toxoplasma gondii. Proc. Soc. Exp. Biol. Med. 135: 167-172. 17. Schwartz, D. E., and J. Rieder. 1970. Pharmacokinetics of sulfamethoxazole plus trimethoprim in man and their distribution in the rat. Chemotherapy 15: 337-355. 18. Udall, V. 1969. Toxicology of sulfaphonamide-trimethoprim combinations. Postgrad. Med. J. 45 Suppl ; : 42-. 45. 19. Western, K. A., D. R. Perera, and M. G. Schultz. 1970. Pentamidine isethionate in the treatment of P. carinii pneumonia. Ann. Intern. Med. 73: 695-701 and ubiquinone.

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Plasmids and characterization of the P2 incompatibility group plasmids pMG1 and pMG5. J. Bacteriol. 135: 227-238. Hershfield, V., H. W. Boyer, C. Yanofsky, M. A. Lovett, and D. R. Helinski. 1974. Plasmid Col El as a molecular vehicle for cloning and amplification of DNA. Proc. Natl. Acad. Sci. U.S.A. 71: 3455-3459. Koch, A. L. 1981. Evolution of antibiotic resistance gene function. Microbiol. Rev. 45: 355-378. Low, B. 1968. Formation of merodiploids in matings with a class of rec- recipient strains of Escherichia coli K12. Proc. Natl. Acad. Sci. U.S.A. 60: 160-167. Mandel, M., and A. Higa. 1970. Calcium-dependent bacteriophage DNA infection. J. Mol. Biol. 53: 159-162. Maniatis, T., A. Jeffrey, and D. G. KIeld. 1975. Nucleotide sequence of the rightward operator of phage X. Proc. Natl. Acad. Sci. U.S.A. 72: 1184-1188. MiDler, J. H. 1972. Experiments in molecular genetics. Cold Spring Harbor Laboratories, Cold Spring Harbor, N.Y. Normark, S., and L. G. Burman. 1977. Resistance of Escherichia coli to penicillins: fine structure mapping and dominance of chromosomal beta-lactamase mutations. J. Bacteriol. 132: 1-7. Pattishall, K. H., J. Acar, J. J. Burchall, F. W. Goldstein, and R. J. Harvey. 1977. Two distinct types of trimethoprim-resistant dihydrofolate reductase specified by R-plasmids of different compatibility groups. J. Biol. Chem. 252: 2319-2323. Rosner, J. 1972. Formation, induction and curing of bacteriophage P1 lysogens. Virology 48: 679-684. Schimke, R. T., F. W. Alt, R. E. Kellems, R. J. Kaufman, and J. R. Bertino. 1977. Amplification of dihydrofolate reductase genes in methotrexate-resistant cultured mouse cells. Cold Spring Harbor Symp. Quant. Biol. 42: 649-657. Sheldon, R., and S. Brenner. 1976. Regulatory mutants of dihydrofolate reductase in Escherichia coli K-12. Mol. Gen. Genet. 147: 91-97. Skold, O., and A. Widh. 1974. A new dihydrofolate reductase with low trimethoprim sensitivity induced by an R-factor mediating high resistance to trimethoprim. J. Biol. Chem. 249: 43244325.
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