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Richardson D, Goldmeier D, Frize G, Lamba H, De Souza C, Kocsis A, Scullard G. Letrozole versus testosterone. a single-center pilot study of HIV-infected men who have sex with men on highly active anti-retroviral therapy HAART ; with hypoactive sexual desire disorder and raised estradiol levels. J Sex Med. 2007 Mar; 4 2 ; : 502-8. Crum NF, Furtek KJ, Olson PE, et al. A Review of Hypogonadism and Erectile Dysfunction among HIV-Infected Men during the Pre- and Post-HAART Eras: Diagnosis, Pathogenesis, and Management. AIDS Patient Care and STDs 2005; 19 10 ; : 665-671.
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In Children These authors identified seventeen prospective studies on ADRs in children following a systematic review of ADRs in hospitalised children and outpatient children, and of ADRs causing paediatric hospital admissions, using MEDLINE and EMBASE. In children who had been hospitalised, the overall incidence of ADRs was 9.5%; 12.3% of the ADRs were classified as severe. The overall rate of paediatric admissions due to ADRs was 2.1%. Of the ADRs causing children to be admitted, 39% were regarded as potentially lifethreatening. For out-patient children, the overall incidence of ADRs was 1.4%. The results show that ADRs in children are a significant public health issue. The completeness and accuracy of prescription reporting as well as clinical information from studies was a rarity, making it difficult for health practitioners to implement evidence based preventative strategies. Further, and methodologically sound, drug surveillance studies are necessary for an effective promotion of a safer use of drugs in children and fexofenadine, for example, estrace estradiol.
Estradiol prevents fatty streak formation in chow-fed atherosclerosis-prone apolipoprotein E ApoE ; -deficient mice. We previously reported that fatty streak development of immunodeficient ApoE recombination activating gene 2 RAG-2 ; double-deficient mice was insensitive to estradiol. In the present work, we demonstrate that the reconstitution of ApoE RAG-2 with bone marrow from immunocompetent ApoE RAG-2 mice restores the protective effect of estradiol on fatty streak constitution. We extended this demonstration to the model of lowdensity lipoprotein receptor-deficient mice, establishing the obligatory role of mature lymphocytes in this process. We then investigated whether the protective effect of estradiol was mediated by a specific lymphocyte subpopulation by studying the hormonal effect on fatty streak constitution in recently developed models of ApoE mice deficient in selective T-lymphocyte subsets either TCR , CD4 , CD8 , or TCR lymphocytes ; or B lymphocytes. In all these specifically immunodeficient mice, estradiol administration to ovariectomized mice conferred protection as in immunocompetent ApoE mice, clearly demonstrating that no single lymphocyte subpopulation was specifically required for this effect. These results point to additional lymphocyte-dependent mechanisms such as modulating the interactions among lymphocytes and between lymphocytes and endothelial and or antigen-presenting cells. J Pathol 2005, 167: 267274.
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There were no significant baseline differences across treatment group by age, sex, ethnicity, BMI, marital status, education level, smoking status, alcohol use, or medication use Table 1; all P 0.05 ; . In both groups, the average age of the subjects was 65 9 y, there were slightly more women than men, and 90% of the subjects were non-Hispanic white. More than one-half of the subjects in each group were currently married, and nearly 50% had college degrees. The average BMI in kg m2 ; both groups of subjects was in the overweight category, 26 27. Few of these subjects 3 6% ; reported being current smokers, and their average alcohol intake was low 6 g to 0.5 drinks d ; . Although the subjects had been screened for serious illness and for use of.
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1. Farthing MJ, Green JRB, Edwards CRW, Dawson AM: Progesterone, prolactin, and gynecomastia in men with liver disease. Gut, 1982; 23: 276-279 Francavilla A, Eagon PK, Di Leo A, Polimeno L, Panella C, Aquilino AM, Ingrosso M, Van Thiel DH, Starzl TE: Sex hormone-related functions in regenerating male rat liver. Gastroenterol, 1986; 91: 1263-1270 Guechot J, Chazouilleres O, Loria A, Hannoun L, Balladur P, Parc R, Giboudeau J, Poupon R: Effect of liver transplantation on sex hormone disordes in male patients with alcohol-induced or post viral hepatitis advanced liver disease. J Hepatol, 1994; 20: 426-430 Krawczuk G: Poziom estradiolu i progesteronu w surowicy krwi w cyklu menstruacyjnym kobiet chorych na ostre wirusowe zapalenie wtroby B. Endokrynol Pol, 1991; 42: 429-435 Krawczuk G, yczak A, Jagieo-Wjtowicz E, Baran E: Poziom PRL, FSH, LH w surowicy krwi w cyklu menstruacyjnym kobiet chorych na ostre wzw A i B. Mat. Nauk. XIII Zjazdu Pol. Tow. Epid. i LChZ, Pozna 1994; 176-178 6. Takahasi H, Ymada S: Studies on changes of thyroid hormones in various liver dieseases: usefulness of free thyroid hormones as liver function test. Jpn J Med, 1989; 28: 297-302 Pawlikowski M: Podstawowe pojcia endokrynologii i mechanizm dziaania hormonw. In: Zarys endokrynologii klinicznej. ed. ; Pawlikowski M. PZWL, Warszawa 1992; 1-18 8. Tilig H, Vogel W, Tratkiewicz J, Aulitzky WE, Herold M, Gruber M: Pilot study of natural human interleukin-2 in patients with chronic hepatitis B. J Hepatol, 1993; 19: 259-267 Weigent DA, Carr DJJ, Blalock JE: Bidirectional communication between the neuroendocrine and immune systems. Common hormones and receptors. In: Decade neuropeptides. Past present and future. Eds. ; Koob GF, Sandman AC, Strand FL. Ann NY Acad of Sci, 1990; 579: 17-27 and flagyl.
Drug Name & Dosage NAPROXEN 500MG TABLET EC NAPROXEN 500MG TABLET EC ESTRADIOL 0.5MG TABLET ESTRADIOL 1MG TABLET ESTRADIOL 2MG TABLET PENICILLIN VK 250MG TABLET PENICILLIN VK 250MG TABLET PENICILLIN VK 250MG TABLET PENICILLIN VK 500MG TABLET PENICILLIN VK 500MG TABLET PENICILLIN VK 500MG TABLET PENICILLIN VK 500MG TABLET NEOMYCIN 500MG TABLET NEOMYCIN 500MG TABLET IMIPRAMINE HCL 10MG TABLET IMIPRAMINE HCL 25MG TABLET IMIPRAMINE HCL 25MG TABLET IMIPRAMINE HCL 50MG TABLET TRIMETHOPRIM 100MG TABLET TRIMETHOPRIM 200MG TABLET METOCLOPRAMIDE 5MG TABLET ALBUTEROL SULFATE 2MG TAB METAPROTERENOL 10MG TABLET METAPROTERENOL 10MG TABLET METAPROTERENOL 20MG TABLET CEPHALEXIN 250MG TABLET AMOXICILLIN 250MG TAB CHEW AMOXICILLIN 250MG CAPSULE AMOXICILLIN 250MG CAPSULE AMOXICILLIN 250MG CAPSULE AMOXICILLIN 500MG CAPSULE AMOXICILLIN 500MG CAPSULE AMPICILLIN TR 250MG CAPSULE AMPICILLIN TR 250MG CAPSULE AMPICILLIN TR 250MG CAPSULE AMPICILLIN TR 500MG CAPSULE AMPICILLIN TR 500MG CAPSULE OXACILLIN 500MG CAPSULE CLOXACILLIN 500MG CAPSULE DICLOXACILLIN 250MG CAPSULE DISOPYRAMIDE 100MG CAPSULE DISOPYRAMIDE 100MG CAPSULE CEPHALEXIN 250MG CAPSULE CEPHALEXIN 250MG CAPSULE CEPHALEXIN 500MG CAPSULE CEPHALEXIN 500MG CAPSULE CEPHRADINE 250MG CAPSULE CEPHRADINE 500MG CAPSULE CEPHRADINE 500MG CAPSULE MINOCYCLINE 50MG CAPSULE MINOCYCLINE 100MG CAPSULE CLINDAMYCIN HCL 150MG CAPS CLINDAMYCIN HCL 150MG CAPS PENICILLIN VK 125MG 5ML LIQ PENICILLIN VK 250MG 5ML LIQ PENICILLIN VK 250MG 5ML LIQ AMOXICILLIN 125MG 5ML SUSP AMOXICILLIN 125MG 5ML SUSP AMOXICILLIN 125MG 5ML SUSP AMOXICILLIN 250MG 5ML SUSP AMOXICILLIN 250MG 5ML SUSP OXACILLIN 250MG 5ML SUSP CLOXACILLIN 125MG 5ML SOLN CEPHALEXIN 125MG 5ML SUSPEN CEPHALEXIN 250MG 5ML SUSPEN CEPHALEXIN 250MG 5ML SUSPEN DILTIAZEM HCL 120MG CAP SA.
Dosing regimen Aspirin should be taken once a day, preferably after a meal to prevent heartburn. Aspirin comes in regular form, buffered to reduce acidity such as Alka-Selzer ; or enteric-coated such as Ascriptin ; . Side-effects Although long-term use of a low dose of aspirin is safe and well tolerated, rare but potentially serious side-effects can occur, and aspirin should therefore only be used under a doctor's supervision. Aspirin may cause gastric and duodenal problems with or without ulcer. These sideeffects are less frequent with buffered or enteric-coated aspirin. Contraindications Active peptic ulcer disease and allergic reactions. 4.4.7 Lipid-lowering drugs The main aim of treatment with lipid-lowering drugs is to reduce the LDL cholesterol level. Drugs available for lowering cholesterol include statins, bile acid sequestrants resins ; , nicotinic acid, fibric acids fibrates ; and omega-3 fatty acids. Although they differ widely in their chemical structure and biomolecular mechanism of action, their way of action is based either on reducing cholesterol synthesis or interfering with cholesterol circulation. The statins are very effective in lowering LDL cholesterol and, to a lesser extent, triglycerides. Bile acid sequestrants lower LDL cholesterol and can be used alone or in combination with statins. Fibric acid derivates are mainly used to treat high triglyceride and low HDL cholesterol. Nicotinic acid lowers LDL cholesterol and triglycerides and raises HDL cholesterol. Even if these drugs are prescribed, treatment with lifestyle measures a healthy diet, weight reduction and adequate physical activity ; must continue. This will keep the drug dose as low as possible and lower the overall risk of coronary heart disease. 4.4.7.1 Statins Names and fluconazole.
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Glucocorticoids GCs ; ' are well established as modulaters of the immune and inflammatory responses in man and in animal models . Most studies of the effects of GCs on the immune responses have demonstrated that GCs are generally immunosuppressive. The suppressive effects include GC-induced rodent thymocyte lysis 1 ; , inhibition of antigen- and mitogen-induced lymphocyte proliferation 2-4 ; , inhibition of production of and response to lymphokines 5, 6 ; , and inhibition of NK activity 7 ; . Recent studies also report that GC inhibits IL-2-R gene expression 8 ; . Conflicting data have been published concerning the effect of GCs on B lymphocytes. The production of polyclonal Ig is significantly enhanced in the presence of GCs in vitro 9-11 ; . The magnitude of the enhancing effect was similar to that observed with other polyclonal B cell activators such as PWM. Since this effect by GCs did not require proliferation, GCs might accelerate B cell maturation and differentiation. However, despite extensive investigation, the precise mechanism of these contrasting effects inhibitory and enhancing ; of GC remains to be clarified. IL-1, a hormone-like polypeptide, functions as a fundamental mediator of immune and inflammatory responses. Although IL-1 has been defined as a thymocyte comitogenic factor 12 ; , it has become evident that IL-1 exhibits a diverse range of biological activities . These include augmentation of B lymphocyte proliferation 13 ; and antibody production 14 ; , fibroblast proliferation 15 ; , acute-phase protein-inducing activity 16 ; , prostaglandin-inducing activity 17 ; , and endogenous pyrogen activity 18 ; . GCs have been reported to suppress both the production and effects of IL-1 . GCs suppress IL-1 production by LPS-stimulated mouse peritoneal macrophages 19, 20 ; . Recently we have extended this observation and shown that GC inhibits the production of both IL-la and IL-1, B by LPS-stimulated human monocytes Lew, W., JJ . Oppenheim, and K. Matsushima, submitted for publication ; . C onsequently, this suppressive effect of GC on IL-1 production may contribute and galantamine.
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And during treatment. At the dose estradiol levels fell by 82.0% and.
The target cell sensitivity of steroid hormones is determined by the concerted action of steroid hormone receptors and steroid-inactivating enzymes or steroid-activating enzymes for review, see Roy, 1992 ; . For estrogen target tissues, this phenomenon has been studied mostly in the human uterus. In the human uterus, inactivation of the most potent natural estrogen, estradiol, to a weakly active estrogen, estrone, is catalyzed by 17 -hydroxysteroid dehydrogenase 17 -HSD, 1 EC 1.1.1.62 ; . In addition, estrogen sulfotransferase EC 2.8.2.15 ; converts estradiol to its inactive sulfoconjugate Liu and Tseng, 1979 ; . In the human uterus, both enzymes are induced by progesterone and their activity is highest during the secretory phase of the menstrual cycle, whereas estradiol receptor levels are lowest during this phase. Together, the lower estradiol receptor levels and the increased intracelThis study was supported in part by Organon N.V., The Netherlands. 1 Abbreviations used are: 17 -HSD, 17 -hydroxysteroid dehydrogenase; ERT, estrogen replacement therapy; E2, estradiol, 1, 3, 5[10]-estratriene-3, -diol; EE, ethynylestradiol, 17 -ethynyl-1, 3, 5[10]-estratriene-3, 17 -diol; MOX, moxestrol, 11 , 17 ; -17-ethynyl-11-1, 3, 5[10]-estratriene11 -methoxy-ethynylestradiol, 3, 17 -diol; ovx, ovariectomized; P4, progesterone; UDP-GT, UDP-glucuronosyl transferase; HPLC, high performance liquid chromatography; E2-3-G, estradiol3 D-glucuronide E1-3-S, estrone-3-sulfate; E1, estrone, 1, 3, 5[10]-estratriene3-ol-17-one; E1-3-G, estrone -D-glucuronide. Send reprint requests to: M. J. Blom, Research Group for Comparative Endocrinology, Graduate School for Developmental Biology, Padualaan 8, 3584 CH Utrecht, The Netherlands. E-mail: m.j.blom bio.uu.nl and glucovance and estradiol.
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The treatment of alopecia and oily skin 139 ; . Hence, we recommend monitoring serum markers of hepatic function at regular intervals during therapy. Other lesser side effects of flutamide include dry skin and a greenish tint to the urine. While doses of 250 mg twice daily are generally used, a single dose of 250 mg day may be effective in some patients 137 ; . Finally, in animal models, flutamide has a feminizing effect in the male fetus 140, 141 ; , and nonsterilized patients of reproductive age should be advised to use effective contraception. 3. Cyproterone acetate. Cyproterone acetate is a 17hydroxyprogesterone acetate derivative with strong progestogenic properties, similar in potency to megesterol acetate 142, 143 ; . The contraceptive properties of CPA occur in part due to gonadotropin suppression. CPA is also categorized as an antiandrogen, since it competes with DHT for binding to the androgen receptor. It produces a decrease in circulating T and androstenedione levels through a reduction in circulating LH and has been used as an effective treatment for hirsutism 144 ; . In a dose ranging study, Barth and colleagues 145 ; noted that an OCP containing 35 mg EE and 2 mg CPA per day was as effective in reducing hirsutism as the same OCP with the addition of 20 mg day or 100 mg day of CPA for the first 10 days of the cycle. Cyproterone acetate in doses of 50 100 mg day, combined with 30 35 mg EE, is as effective as the combination of SPA, 100 mg day, and an OCP in the treatment of hirsutism 146, 147 ; . In another study a triphasic OCP containing CPA, 12.5 mg day for the first 10 days of the cycle plus varying doses of EE ; , was found to be as effective as flutamide, 250 mg day 148 ; . In contrast, an OCP containing CPA, 2 mg day, in combination with EE, 35 mg day, seems less effective than 100 mg day of SPA 149 ; . Few studies investigating the efficacy of CPA in patients with IH are available. Jasonni and colleagues 150 ; treated 11 subjects with IH, defined by normal T and DHS levels and ovulatory cycles, and 15 women with PCOS with CPA, 50 mg day, from days 115 in combination with 0.1 mg day transdermal 17 -estradiol. They reported that the hirsutism score fell by 50% over 6 months, although in reporting their results the investigators did not differentiate between women with IH and PCOS. Peereboom-Wynia and Boekhorst 151 ; treated another 11 well defined women with IH using CPA, 100 200 mg, on days 515 and EE, 50 g, on days 526 of the cycle, and reported a reduction in the hair density and diameter 151 ; . Overall, it would appear that CPA is effective in treating patients with IH, although larger studies are still lacking. This drug is currently not available in the U.S. but has been used for many years in other countries, sold as the OCP Diane-35 or Dianette 2 mg CPA and 35 g EE tablet, Schering AG, Germany ; or Androcur 50 mg tablet, Schering AG, Germany ; . Side effects may include loss of libido. Adrenal insufficiency is a rare complication of CPA therapy, seen primarily in children receiving high doses for the treatment of precocious puberty, and is unlikely to occur in adults 152 ; . As with all antiandrogens, adequate contraception must be used to avoid the possibility of feminizing a male fetus, particularly when CPA is used at low doses in intermittent cycles e.g., 2 mg day for the first 10 days of the cycle and inderal.
By Larry I. Barmat, M.D. from Abington Reproductive Medicine Online Abington's former newsletter ; The field of reproductive endocrinology and infertility has seen tremendous advancements in the last two decades. First and foremost has been the introduction of in vitro fertilization and our greater ability to assist the reproductive process. This has prompted more media coverage and widespread awareness of advanced infertility treatments. As the public becomes increasingly educated about the reproductive technologies a greater number of patients are presenting to fertility specialists to enhance their chances of conception. In addition, the demographics of the reproductive aged population have changed. The post World War II baby boomers have now reached their upper thirties and forties, and approximately one in every five women in the United States is having a first child after 35. Unfortunately, with advancing maternal age there is reduction fertility potential and a variety of fertility treatments are necessary. The physiology of age and infertility is based on the quality and quantity of oocytes eggs ; . A female possesses a maximum of 6 to million eggs at approximately 20 weeks of fetal life. The number of eggs progressively declines to a few million at birth and less than a half million at puberty. The rate of decline then increases again in the mid to late thirties correlating to significant reductions in pregnancy rates and increase in miscarriages. This has been clinically shown in multiple studies. An important aspect of treating an infertility couple is to assess maternal ovarian reserve or biologic ovarian age. This is generally done by checking day 3 FSH and esttradiol levels or via a more provocative Clomiphene Challenge Test CCT ; . If a patient has an elevated day 3 FSH or estradiol, or an elevated day 10 FSH on the CCT this suggests a poor prognosis for multifollicular development with ovulation induction medications and a reduction in pregnancy rates. Based on the results of these hormonal studies and their correlation with other routine fertility tests a couple can make an informed decision of their treatment options. It is a biological fact that there is a reduction in fertility with advancing age, therefore it is important to maximize ones chances of conception in the shortest time interval. The estimated chance of becoming pregnant in any one month is about 20-25% in women under 30, but only 5% in women over 40. After approximately one year of unprotected intercourse these figures significantly decrease to a few percent per month. Therefore, to increase the odds of pregnancy we need to increase the number of gametes sperm and eggs ; present in the women's reproductive tract or actually replace in vitro fertilized embryos into the female's reproductive tract. Clomiphene citrate Clomid ; or injectable gonadotropins FSH ; are the two standard ovulation induction medications used to stimulate multifollicular development. Clomid has a limited ability to enhance pregnancy rates in women over the age of 40. There is little evidence in the literature to suggest any benefit with this mild oral fertility medication. The other option is to use injectable medications containing folliclestimulating hormone FSH ; . The use of FSH in conjunction with intrauterine inseminations may increase the fertility potential in advanced maternal age women with adequate ovarian reserve. Pregnancy rates unfortunately are still relatively low at approximately 5% per cycle. This pregnancy rate continues to decline with each year over 40 such that pregnancy rates in women 43 and older are 1% or less. Therefore, IVF, donor egg, donor embryo, or adoption should in general be recommended for women 43 and older. In vitro fertilization-embryo transfer is often recommended as a frontline, or early, treatment option in women 40 and older because of the disappointingly low pregnancy rates with ovulation induction and intrauterine inseminations. The most recent data generated by the Centers for Disease Control CDC ; and Society of Assisted Reproductive Technologies SART ; published in December 2000 reflecting the 1998 IVF cycles notes a steady decline in pregnancy rates for each year above 40. The pregnancy rates and delivery rates for 40, 41, 42, and above 43 are 21.6%, 15.1%, 18.2%, and 3.3%. The most efficient method to achieve a pregnancy in women 40 and older is with the use of donor oocytes. This assisted reproductive technique has allowed many females with advancing age or premature menopause to conceive and experience the natural bonding process of pregnancy and childbirth. The pregnancy rates of donor egg cycles reflect the age of the donor and approaches 50% in many IVF programs. In addition to donor eggs, some IVF centers offer donor embryos. Pregnancy rates with the use of donor embryos again reflect the age of the female who generated the embryo. The last treatment option is adoption. Adoption, as in all forms of treatment, has its pros and cons. Obviously, the genetic make-up of the child is not of the rearing parents and various in utero exposures cannot always be clearly defined. The benefits are very clear. The time, effort and money invested are essentially guaranteed to result in the desired outcome: a child. The treatment options for women as they advance in age become more and more difficult. It is critical that patients are aware of their weaning fertility potential and counseled about the realistic chances for success with each of the possible treatment options.
Angus-sired heifers were allotted by age mean 4 mo ; , BW mean 135 kg ; , and sire n 4 ; to either a control uninfected, n 10 ; or infected group n 11 ; . Metacercariae of Fasciola hepatica were administered intraruminally, d 0 ; to study effects on interval to puberty, circulating ovarian steroids, serum liver enzymes and BW. Blood samples were collected bimonthly from d 0 to and biweekly from d 60 through 210 for analysis of serum eatradiol 17 E2 ; and progesterone P4 ; concentrations by RIA. At 2-wk intervals, BW was recorded, a blood sample was obtained to quantify serum aspartate-aminotransferase AST ; and -glutamyltranspeptidase GGT ; and a fecal sample was collected to assess excretion of F. hepatica eggs. Puberty was defined by the occurrence of the first luteal phase serum P4 concentrations 1.0 ng ml for a minimum duration of 10 d ; univariate ANOVA using the RANDOM statement in PROC GLM was used to determine significant linear and curvilinear responses to treatment in prepubertal heifers from d 0 to 113 ; for BW, E2 , P4 , AST, and GGT. Treatment effects at d 113 were determined by one way ANOVA. F. hepatica eggs were detected in all infected heifers after day 92. Linear P 0.01 ; and curvilinear P 0.05 ; responses for AST and a linear P 0.05 ; response for GGT concentrations were detected over time in infected heifers. On d 113, mean GGT levels were higher P 0.01 ; in infected than in control heifers 116.4 31.2 vs 20.2 2.8 U L, respectively ; . Mean BW, serum AST, E2 , and P4 concentrations did not differ between treatment groups on d 113. By d 210, 60% six of 10 ; of heifers in the control group and 36% four of 11 ; of heifers in the infected group attained puberty. We conclude that F. hepatica infection induced elevated levels of serum enzymes which are indicative of liver damage, and there was a more persistent elevation in GGT than the elevation in AST levels. Experimental fascioliasis resulted in a lower percentage of heifers that reached puberty within 7 mo of infection as compared to control heifers. Key Words: Heifer, Fascioliasis, Puberty.
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Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndrome. J Cell Biol 1999; 146: 255264. Yang JY, Widmann C. The RasGAP N-terminal fragment generated by caspase cleavage protects cells in a Ras PI3K Akt-dependent manner that does not rely on NF B activation. J Biol Chem 2002; 277: 1464114646. Tomomura M, Fernandez-Gonzales A, Yano R, Yuzaki M. Characterization of the apoptosis-associated tyrosine kinase AATYK ; expressed in the CNS. Oncogene 2001; 20: 10221032. Ozaki T, Nakamura Y, Enomoto H, Hirose M, Sakiyama S. Overexpression of DAN gene product in normal rat fibroblasts causes a retardation of entry into the S phase. Cancer Res 1995; 55: 895900. Larsen M, Ressler SJ, Lu B, Gerdes MJ, McBride L, Dang TD, Rowley DR. Molecular cloning and expression of ps20 growth inhibitor. J Biol Chem 1998; 273: 45744584. Sueoka N, Lee HY, Wiehle S, Cristiano RJ, Fang B, Fi L, Roth JA, Hong WK, Cohen P, Kurie JM. Insulin-like growth factor binding protein-6 activates programmed cell death in non-small cell lung cancer cells. Oncogene 2000; 19: 44324436. Putzer P, Breuer P, Gotz W, Gross M, Kubler B, Scharf JG, Schuller AG, Hartmann H, Braulke T. Mouse insulin-like growth factor binding protein-6: expression, purification, characterization and histochemical localization. Mol Cell Endocrinol 1998; 137: 6978. Kato M, Ishizaki A, Hellman U, Wernstedt C, Kyogoku M, Miyazono K, Heldin CH, Funa K. A human keratinocyte cell line produces two autocrine growth inhibitors, transforming growth factor-beta and insulin-like growth factor binding protein-6, in a calcium- and cell density-dependent manner. J Biol Chem 1995; 270: 1237312379. Westergren-Thorssen G, Norman M, Bjornsson S, Endresen U, Stjernholm Y, Ekman G, Malmstrom A. Differential expressions of mRNA for proteoglycans, collagens and transforming growth factor in the human cervix during pregnancy and involution. Biochim Biophys Acta 1998; 1406: 203213. San Martin S, Zorn TMT. The small proteoglycan biglycan is associated with thick collagen fibrils in the mouse decidua. Cell Mol Biol 2003; 49: 673678. Ameye L, Aria D, Jepsen K, Oldberg A, Xu T, Young MF. Abnormal collagen fibrils in tendons of biglycan fibromodulin-deficient mice lead to gait impairment, ectopic ossification, and osteoarthritis. FASEB J 2002; 16: 673680. Kessler E, Adar R. Type I procollagen C-proteinase from mouse fibroblasts. Purification and demonstration of a 55-kDa enhancer glycoprotein. Eur J Biochem 1989; 186: 115121. Mott JD, Thomas CL, Rosenbach MT, Takahara K, Greenspan DS, Banda MJ. Post-translational proteolytic processing of procollagen Cterminal proteinase enhancer releases a metalloproteinase inhibitor. J Biol Chem 2000; 275: 13841390. Scott IC, Clark TG, Takahara K, Hoffman GG, Greenspan DS. Structural Organization and expression patterns of the human and mouse genes for the type I procollagen COOH-terminal proteinase enhancer protein. Genomics 1999; 55: 229234. Ligon AH, Scott IC, Takahara K, Greenspan DS, Morton CC. PCOLCE deletion and expression analysis in uterine leiomyomata. Cancer Genet Cytogenet 2002; 137: 133137. Layne MD, Yet SF, Maemura K, Hsieh CM, Bernfield M, Perrella MA, Lee ME. Impaired abdominal wall development and deficient wound healing in mice lacking aortic carboxypeptidase-like protein. Mol Cell Biol 2001; 21: 52565261. Layne MD, Endege WO, Jain MK, Yet SF, Hsieh CM, Chin MT, Perralla MA, Blanar MA, Haber E, Lee ME. Aortic carboxypeptidaselike protein, a novel protein with discoidin and carboxypeptidase-like domains, is up-regulated during vascular smooth muscle cell differentiation. J Biol Chem 1998; 273: 1565415660. Norton PA. Pelvic floor disorders: the role of fascia and ligaments. Clin Obstet Gynecol 1993; 36: 926938. Liapis A, Bakas P, Pafiti A, Hassiakos D, Frangos-Plemenos M, Creatsas G. Changes in the quantity of collagen type I in women with genuine stress incontinence. Urol Res 2002; 28: 323326. Jackson S, James M, Abrams P. The effect of estradiol on vaginal collagen metabolism in postmenopausal women with genuine stress incontinence. Br J Obstet Gynaecol 2002; 109: 339344. Ulmsten U, Ekman G, Giertz G, Malmstrom A. Different biochemical composition of connective tissue in continent and stress incontinent women. 1987; 66: 455457. Rechberger T, Donica H, Baranowski W, Jakowicki J. Female urinary and famotidine.
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