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Artykuły w czasopismach na temat „Seminal vesicles”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 25 lipca 2025

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1

Higgins, S. J., P. Young, J. R. Brody, and G. R. Cunha. "Induction of functional cytodifferentiation in the epithelium of tissue recombinants. I. Homotypic seminal vesicle recombinants." Development 106, no. 2 (1989): 219–34. http://dx.doi.org/10.1242/dev.106.2.219.

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Functional cytodifferentiation of seminal vesicle epithelium was investigated in tissue recombinants. Neonatal rat and mouse seminal vesicles were separated into epithelium and mesenchyme using trypsin. Epithelium and mesenchyme were then recombined in vitro to form interspecific rat/mouse homotypic recombinants. Growth as renal grafts in adult male athymic mice resulted in seminal vesicle morphogenesis in 70% of the recombinants (the remaining 30% failed to grow). Functional cytodifferentiation was judged by the expression of the major androgen-dependent secretory proteins characteristic of t

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2

Nguyen, Thi Trang*1 Trieu Tien Sang2 Nguyen Hoang3 Nguyen Tan Gia Khanh4 &. Tran Trung Duc4. "ASSESSMENT OF THE LEVEL OF SEMINAL ZINC AND FRUCTOSE CONCENTRATION IN SEMINAL PLASMA OF VIETNAMESE INFERTILE MEN." INTERNATIONAL JOURNAL OF RESEARCH SCIENCE & MANAGEMENT 5, no. 7 (2018): 71–82. https://doi.org/10.5281/zenodo.1314131.

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This study assesses the association between the fructose and zinc concentration and various seminal characteristics. Fructose and zinc in semen reflects the secretory function of seminal vesicles. These Tests may help in assessing the diagnosis and the management of male infertility. Gather semial plasma of 180 males with average age of 31.1 ± 3,6 years old. Use the specific complexant to form a stable coloured complex with fructose or zinc. The colour intensity in a determining wavelength is proportional to the amount of fructose or zinc present in the sample. Seminal fructose concentr

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Dalimunthe, Naela Wanda Yusria, Agung Budiyanto, Erna Prawita Setyowati та Agustina Dwi Wijayanti. "Korelasi Berat Badan dan Umur Sapi terhadap Berat, Volume Cairan dan Konsentrasi Prostaglandin F2α pada Vesikula Seminalis". Jurnal Sain Veteriner 35, № 1 (2017): 49. http://dx.doi.org/10.22146/jsv.29291.

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Seminal vesicles were collected from 60 heads of Bulls which butchered in slaughter house (RPH) Yogyakarta. The aims of this study are knowing the relationship between body weight, age, fluids volume and concentration of prostaglandin F2 α (PGF2α) in seminal vesicle of beef cattle. Those seminal vesicles were gathered from bulls which recorded its body weight and age then measured its seminal vesicles for weight, fluids volume and PGF2α levels. The PGF2α level was measured by Enzyme-Linked Immunosorbent Assay. Statistical analysis was performed using one way – analysis of varian, regression an

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Tamano, S., S. Rehm, M. P. Waalkes, and J. M. Ward. "High Incidence and Histogenesis of Seminal Vesicle Adenocarcinoma and Lower Incidence of Prostate Carcinomas in the Lobund-Wistar Prostate Cancer Rat Model Using N-nitrosomethylurea and Testosterone." Veterinary Pathology 33, no. 5 (1996): 557–67. http://dx.doi.org/10.1177/030098589603300511.

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The origin of chemically induced male accessory sex gland tumors was studied in Lobund-Wistar rats. Rats were treated at the age of 3 months with a single intravenous injection of 30 mg N-nitrosomethylurea (NMU)/kg body weight and given subcutaneous silastic implants filled with 40 mg testosterone propionate. Previous reports described a high incidence of prostate carcinomas in these rats with this treatment protocol. Additional animal groups included untreated controls, rats that received only an injection of 30 mg NMU/kg, and rats that were subjected to ablation of the seminal vesicle lobes

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5

Malinowski, Damian, Paweł Grzegółkowski, Katarzyna Piotrowska, Marcin Słojewski, and Marek Droździk. "Membrane Transporters and Carriers in Human Seminal Vesicles." Journal of Clinical Medicine 11, no. 8 (2022): 2213. http://dx.doi.org/10.3390/jcm11082213.

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Seminal vesicles play an important role in the male reproductive system, producing seminal fluid and thus adequate environment for sperm. However, mechanisms underlying secretory functions of the seminal vesicles’ epithelium have not been defined yet. The aim of the present study was to characterize expression and immunolocalization of selected membrane transporters and carriers in the seminal vesicles. The study included biopsy specimens collected from non-affected parts of seminal vesicles from 53 patients of Caucasian origin subjected for prostatectomy. RT-PCR was used to define expression

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6

Eken, Alper, Volkan Izol, I. Atilla Aridogan, Seyda Erdogan, Arbil Acikalin, and Zuhtu Tansug. "An unusual cause of hematospermia: Primary adenocarcinoma of the seminal vesicle." Canadian Urological Association Journal 6, no. 6 (2012): 259. http://dx.doi.org/10.5489/cuaj.127.

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Adenocarcinoma of the seminal vesicles is one of the rare causes of hematospermia. Primary seminal vesicle adenocarcinoma is extremely rare and difficult to diagnose due to frequent invasion of adenocarcinomas of the surrounding organs, especially the prostate. In the present study, a case of a primary seminal vesicle adenocarcinoma will be discussed in the light of the current literature.

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7

Shukri, N. M., F. Grew, and J. G. M. Shire. "Recessive mutation in a standard recombinant-inbred line of mice affects seminal vesicle shape." Genetical Research 52, no. 1 (1988): 27–32. http://dx.doi.org/10.1017/s0016672300027270.

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SummaryA recessive autosomal mutation has been found in the CXBI/ByEss recombinant-inbred line but in neither of the parental strains, C57BL/6ByEss and BALB/cByEss. Its presence in the CXBI/ByJax and CXBI/ByLac sublines suggests an origin early in inbreeding. The locus, seminal vesicle shape (svs), appears to be linked to the albino locus on chromosome 7. The homozygote has seminal vesicles with a smooth tubular external appearance. In segregating crosses homozygotes had slightly lighter seminal vesicles but the weights of other androgen target organs were not reduced. Exogenous testosterone i

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8

HORTON, MICHAEL J., and ROBERT H. GETZENBERG. "Rat Seminal‐Vesicle Secretory Protein SVS II Binds DNA With a Preference for the 5′ Regulatory Region of Secretory Protein SVS IV Gene: Co‐Isolation With Components of the Nuclear Matrix." Journal of Andrology 20, no. 2 (1999): 267–79. http://dx.doi.org/10.1002/j.1939-4640.1999.tb02518.x.

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ABSTRACT: In rats, the ventral prostate and seminal vesicles produce distinct sets of proteins whose functions and tissue‐specific regulation by androgens remain unclear. We have utilized the genes encoding the major secretory protein of seminal vesicles, SVS IV, and the C3 subunit of prostatein of the ventral prostate to study how the nuclear matrix might determine their tissue‐specific gene expression. Nuclear matrix proteins were prepared from purified nuclei with DNase and 2 M NaCl, separated in SDS gels, and transferred onto membranes for DNA‐binding (southwestern) and immunological (west

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9

Hiroyoshi, Satoshi, Takayuki Mitsunaga, Tomoko Ganaha-Kikumura, and Gadi V. P. Reddy. "Effects of Age, Phase Variation and Pheromones on Male Sperm Storage in the Desert Locust, Schistocerca gregaria." Insects 12, no. 7 (2021): 642. http://dx.doi.org/10.3390/insects12070642.

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In general, sperm produced in the testis are moved into the seminal vesicle via the vas deferens in insects, where they are stored. How this sperm movement is controlled is less well understood in locusts or grasshoppers. In this study, the effects of age, phase variation and pheromones on male sperm storage were investigated in the desert locust, Schistocerca gregaria (Forskål). In this locust, a pair of ducts, the vasa deferentia, connect the testes to a pair of the long, slender seminal vesicles that are folded approximately thirty times, and where the sperm are stored. We found that phase

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10

Komori, Koji, Takashi Hirai, Yukihide Kanemitsu, et al. "Pathology Studies of Combined Radical Resection of Seminal Vesicle in the Treatment of Rectal Cancer." International Surgery 96, no. 1 (2011): 51–55. http://dx.doi.org/10.9738/1362.1.

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Abstract To inhibit local recurrence of rectal cancer, it is very important to ensure that there is a sufficient circumferential resection margin. We evaluated pathology studies of combined radical resection of seminal vesicles in the treatment of rectal cancer. We analyzed data from 7 cases of combined radical resection of the seminal vesicle in the treatment of rectal cancer; we also analyzed data from 35 control cases without seminal vesicle resection. The circumferential resection margin averaged 5.97 mm for cases that had combined radical resection of the seminal vesicle, and this was sig

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11

Higgins, S. J., P. Young, and G. R. Cunha. "Induction of functional cytodifferentiation in the epithelium of tissue recombinants. II. Instructive induction of Wolffian duct epithelia by neonatal seminal vesicle mesenchyme." Development 106, no. 2 (1989): 235–50. http://dx.doi.org/10.1242/dev.106.2.235.

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When grown as renal grafts in adult male hosts, the upper (cranial), middle and lower (caudal) portions of fetal mouse and rat Wolffian ducts developed into epididymis, epididymis plus ductus deferens, and seminal vesicle, respectively. In heterotypic tissue recombinants, the epithelia from upper and middle Wolffian ducts were instructively induced to undergo seminal vesicle morphogenesis by neonatal seminal vesicle mesenchyme. Functional cytodifferentiation was examined in these recombinants using antibodies against major androgen-dependent, seminal vesicle-specific secretory proteins. The in

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12

Shah, Rajal B., Min W. Lee, Alvaro A. Giraldo, and Mahul B. Amin. "Histologic and Histochemical Characterization of Seminal Vesicle Intraluminal Secretions." Archives of Pathology & Laboratory Medicine 125, no. 1 (2001): 141–45. http://dx.doi.org/10.5858/2001-125-0141-hahcos.

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Abstract Context.—We have observed intraluminal crystalloid morphology in seminal vesicles that is superficially similar to that seen in prostate neoplasia, but found little information on such morphology in the literature. Design.—Two hundred fifty-three prostate specimens (163 needle biopsies, 75 radical prostatectomies with prostate carcinoma, 11 prostates from autopsy, and 4 cystoprostatectomies without prostate carcinoma) were examined for seminal vesicle secretions, which were categorized as (a) dense platelike inspissated, (b) fluidlike, (c) crystalloid morphology, and (d) absent. Histo

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13

Veyssiere, G., Ch Jean-Faucher, M. Berger, and Cl Jean. "Evidence for reversible and irreversible biochemical defects in accessory sex organs and kidney of neonatally androgenized male mice." Acta Endocrinologica 121, no. 1 (1989): 121–28. http://dx.doi.org/10.1530/acta.0.1210121.

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Abstract. Studies were conducted to evaluate the effects of neonatal administration of supraphysiological doses of testosterone on the growth, hormone responsiveness, DNA and protein content, and protein profiles of the epididymis, vas deferens and seminal vesicles in adult mice. Results indicate that in androgenized males, testicular growth (DNA and protein content), circulating and organ androgen levels, and fertility were significantly depressed. The weights of the epididymis, vas deferens, seminal vesicle and kidney, but not that of the spleen, were significantly diminished subsequently to

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14

Cordeiro, Luiz, Hsiu-Lien Herbie Lin, Anaïs Vitorino Carvalho, Isabelle Grasseau, Rustem Uzbekov, and Elisabeth Blesbois. "First insights on seminal extracellular vesicles in chickens of contrasted fertility." Reproduction 161, no. 5 (2021): 489–98. http://dx.doi.org/10.1530/rep-20-0462.

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Male subfertility causes are very varied and sometimes related to post-gonadic maturation disruption, involving seminal plasma constituents. Among them, extracellular vesicles are involved in key exchanges with sperm in mammals. However, in birds, the existence of seminal extracellular vesicles is still debated. The aim of the present work was first to clarify the putative presence of extracellular vesicles in the seminal plasma of chickens, secondly to characterize their size and protein markers in animals showing different fertility, and finally to make preliminary evaluations of their inter

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15

Noorafshan, Ali, and Saied Karbalay‑Doust. "Curcumin Protects the Seminal Vesicles from Metronidazole‑induced Reduction of Secretion in Mice." Acta Medica (Hradec Kralove, Czech Republic) 55, no. 1 (2012): 32–36. http://dx.doi.org/10.14712/18059694.2015.72.

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Seminal vesicle secretion is important for increasing the stability of sperm chromatin, inhibition of the immune activity in the female reproductive tract and so on. Metronidazole (MTZ), a drug used for treatment of infections caused by anaerobic bacteria and protozoa, may have negative effects on the genital gland including the seminal vesicles. Curcumin exhibits antioxidant as well as anti‑inflammatory properties. The present study aims to evaluate the negative effects of MTZ on the seminal vesicle structure and ameliorative effects of curcumin using stereological methods. Thirty balb/c mice

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Hevia Palacios, M., M. Álvarez-Maestro, J. Gómez Rivas, A. Aguilera Bazan, and L. Martínez-Piñeiro. "Zinner Syndrome with Ectopic Ureter Emptying into Seminal Vesicle." Case Reports in Urology 2021 (January 25, 2021): 1–4. http://dx.doi.org/10.1155/2021/8834127.

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A 66-year-old male patient in follow-up in the urology department for a non-muscle-invasive bladder cancer was detected by ultrasound to have absence of the left kidney and a cystic, multilobed image at the location of the seminal vesicle. Magnetic resonance imaging reveals left renal agenesis and the existence of multiple cysts in the ipsilateral seminal vesicle that reaches a size of 6.9 × 3.7 cm , as well as a ureteral remnant that opens into the seminal vesicle. The patient does not present urinary symptoms, neither pain with ejaculation nor hematuria. A triad of seminal vesicle cyst, ipsi

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17

Salgueiro, Jose Lucas Rodrigues, Otavio Soriano Teruel Pagamisse, Giovanni Pereira Camacho Roque, et al. "AMILOIDOSE DE VESÍCULA SEMINAL: UM RELATO DE CASO." ARACÊ 6, no. 4 (2024): 18745–53. https://doi.org/10.56238/arev6n4-452.

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Amyloidosis is a medical condition of unknown etiology, characterized by the deposition of amyloid proteins in tissues. Urological involvement is rare and occurs mainly in the kidneys and seminal vesicles. Involvement of the seminal vesicle is infrequent, although often asymptomatic, some patients may present symptoms such as hematospermia, suprapubic pain, and obstructive signs. The diagnosis requires imaging tests complemented by transrectal biopsy, and confirmed by the Congo red staining test. The definitive treatment consists of surgical resection, often performed laparoscopicly/minimally

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Tani, Y., A. Suttie, G. P. Flake, A. Nyska, and R. R. Maronpot. "Epithelial-Stromal Tumor of the Seminal Vesicles in the Transgenic Adenocarcinoma Mouse Prostate Model." Veterinary Pathology 42, no. 3 (2005): 306–14. http://dx.doi.org/10.1354/vp.42-3-306.

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The transgenic adenocarcinoma mouse prostate (TRAMP) model, designed for researching human prostatic cancer, was genetically engineered to harbor a transgene composed of the simian virus 40 Large-T/small-t antigen promoted by the rat probasin gene. In addition to prostatic neoplasms, the TRAMP mouse develops tumors in the seminal vesicles. This study was conducted to evaluate the pathology and histogenesis of TRAMP seminal vesicle neoplasms. Tissues of accessory sex organs harvested from 72 TRAMP mice of various ages (11-40 weeks of age) were fixed in neutral buffered formalin and stained with

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Sandeep, Bande, Nerkar Archana, and Bhandarkar Sudhir. "Histological Investigation of Cyclic Variation in Secretory Activity of Seminal Vesicles in Emballonurid Bat, Taphozous kacchensis (Dobson)." International Journal of Zoological Investigations 08, no. 02 (2022): 262–71. http://dx.doi.org/10.33745/ijzi.2022.v08i02.033.

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The present study describes the cyclical changes in the secretory activity of the seminal vesicle in the emballonurid bat, Taphozous kacchensis. The secretory activity in the seminal vesicles during the quiescence cycle was not well marked in T. kacchensis. During the sexually quiescent period (May to August), seminal vesicles were regressed, the tubules were lined by cuboidal to low columnar epithelial cells with round to elongated darkly stained basally to centrally placed nuclei. Cytoplasm was basophilic containing fine or coarse secretory granules in the cytoplasm. The lumina of the tubule

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Li, Sheng-Hsiang, Robert Kuo-Kuang Lee, Ming-Huei Lin, et al. "SSLP-1, a secreted Ly-6 protein purified from mouse seminal vesicle fluid." Reproduction 132, no. 3 (2006): 493–500. http://dx.doi.org/10.1530/rep.1.01183.

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The Ly-6 protein family refers to a group of glycophosphatidyl inositol-anchored membrane proteins with ten conserved cysteines. They are thought to be involved in cellular adhesion and signaling. Recently, a subfamily of secreted Ly-6 proteins has been identified. In the present study, we report a secreted Ly-6 protein, secreted seminal vesicle Ly-6 protein 1 (SSLP-1) purified from mouse seminal vesicles using a series of steps including ion-exchange chromatography on a diethylaminoethyl (DEAE)-Sephacel column, gel filtration on a Sephadex G-75 column, and ion-exchange HPLC on a sulfopropyl c

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Sysoeva, A. P., N. P. Makarova, and E. E. Kraevaya. "The role of seminal plasma extracellular vesicles in changes in the morphofunctional characteristics of human spermatozoa." CLINICAL AND EXPERIMENTAL MORPHOLOGY 10, no. 4 (2021): 5–13. http://dx.doi.org/10.31088/cem2021.10.4.5-13.

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For a long time, the role of seminal plasma during human fertilization remained underestimated. Numerous studies related to the development of different methods for human embryo in vitro cultivation were gener-ally concerned with the quality of male and female gametes. However, in recent years, the development of Omix technologies provided a new insight into great seminal plasma influence on the morphofunctional characteristics of spermatozoa. This is especially true for the regulatory function of extracellular vesicles secreted by male reproductive tract cells. In this work, we attempted to a

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Ferreira, Ríudo De Paiva, Hugo De Azevedo Werneck, Juliana Malta, Aparecida Das Dores Teixeira, Lucio Antonio de Oliveira Campos, and José Eduardo Serrão. "Post-embryonic Development of the Seminal Vesicle in the Stingless Bee Melipona quadrifasciata Lepeletier, 1836 (Apidae: Meliponini)." Sociobiology 66, no. 2 (2019): 287. http://dx.doi.org/10.13102/sociobiology.v66i2.3431.

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The male accessory glands of stingless bees (Apidae: Meliponini) are absent and the morphology of their seminal vesicle indicate probable secretory function by this organ. This study investigated the post-embryonic development of the seminal vesicles in males of the stingless bee Melipona quadrifasciata by histology and histochemistry. White-eyed pupae, pink-eyed pupae, brown-eyed pupae, black-eyed pupae, newly emerged and sexually mature males were studied. Seminal vesicle has a wall with a single layered epithelium onto a thin basement membrane, followed by a well-developed muscle layer. The

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Gupta, Sounak, Loren Herrera-Hernandez, and Lori A. Erickson. "Amyloid Involving the Seminal Vesicles." Mayo Clinic Proceedings 97, no. 6 (2022): 1213–14. http://dx.doi.org/10.1016/j.mayocp.2022.04.010.

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Tjionas, George A., Jonathan I. Epstein, Sean R. Williamson, et al. "Average Weight of Seminal Vesicles." International Journal of Surgical Pathology 23, no. 8 (2015): 617–22. http://dx.doi.org/10.1177/1066896915600519.

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Herts, Brian R. "Calcification of the Seminal Vesicles." Journal of Urology 194, no. 1 (2015): 209–11. http://dx.doi.org/10.1016/j.juro.2015.04.017.

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Panach-Navarrete, J., F. García-Morata, J. A. Hernández-Medina, and J. M. Martínez-Jabaloyas. "When to biopsy seminal vesicles." Actas Urológicas Españolas (English Edition) 39, no. 4 (2015): 203–9. http://dx.doi.org/10.1016/j.acuroe.2015.03.002.

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Ramchandani, Parvati, Marc P. Banner, and Howard M. Pollack. "Imaging of the seminal vesicles." Seminars in Roentgenology 28, no. 1 (1993): 83–91. http://dx.doi.org/10.1016/s0037-198x(05)80115-4.

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Llerena, José, and Janis Letourneau. "Other Prostatic Interventions Seminal Vesicles." Seminars in Interventional Radiology 6, no. 02 (1989): 102–7. http://dx.doi.org/10.1055/s-2008-1075904.

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Alikhan, Mir Basharath, Vera Tesic, Jerome B. Taxy, and Tatjana Antic. "Cytomegalovirus Infection of Seminal Vesicles." International Journal of Surgical Pathology 24, no. 8 (2016): 720. http://dx.doi.org/10.1177/1066896916657592.

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DELİKGÖZ SOYKUT, Ela, and Hatice TATAROĞLU. "Dosimetric evaluation of inclusion of proximal seminal vesicle in target volume in low-risk prostate cancer treated with stereotactic body radiotherapy." Anatolian Current Medical Journal 5, no. 3 (2023): 253–60. http://dx.doi.org/10.38053/acmj.1320219.

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Aims: Ultra hypofractionation using stereotactic body radiotherapy (SBRT) for low-risk PCa is considered a viable treatment option. The target volume for ultra hypofractionated RT was determined as prostate and/or proximal seminal vesicles; however, there are no clear guidelines on when to add a proximal seminal vesicle to the target volume. We aimed to dosimetrically assess the effect of inclusion of the proximal seminal vesicle in the planning target volume (PTV) on the dose distribution of organ at risk (OAR) when SBRT is administered to patients with low-risk PCa. Methods: Low-risk P

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Deshmukh, C. K. I. "341. STUDY OF APHRODISIAC DRUG ACID PHOS ON MALE ALBINO RAT." Reproduction, Fertility and Development 22, no. 9 (2010): 141. http://dx.doi.org/10.1071/srb10abs341.

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The male albino rat, Rattus norvegicus maintained in the laboratory by supplying regularly food and water. Acid phos is a well known aphrodisiac drug from homeopathy medical system. Doses of 200 gm of 30 number globules made from sugar of milk and moistened by 15 mL of acid phos (H3PO3) of 6 potency. Group-I, II and III experimental rats were carried out for 15, 30, and 15 day recovery period respectively. Appreciable behavioral changes and changes in the body weights were noticed. In 15, 30 and in 15 days of recovery period, the acid phosphatase, SGOT and albumin were significant (P < 0.05

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Torry, D. S., C. Thaler, W. Page Faulk, and John A. McIntyre. "Seminal vesicles: A source of TLX in seminal plasma." Human Immunology 23, no. 2 (1988): 152. http://dx.doi.org/10.1016/0198-8859(88)90276-5.

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Gong, Maolei, Fei Wang, Weihua Liu, et al. "Pattern recognition receptor-mediated innate immune responses in seminal vesicle epithelial cell and their impacts on cellular function†." Biology of Reproduction 101, no. 4 (2019): 733–47. http://dx.doi.org/10.1093/biolre/ioz136.

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Abstract The seminal vesicles can be infected by microorganisms, thereby resulting in vesiculitis and impairment in male fertility. Innate immune responses in seminal vesicles cells to microbial infections, which facilitate vesiculitis, have yet to be investigated. The present study aims to elucidate pattern recognition receptor–mediated innate immune responses in seminal vesicles epithelial cells. Various pattern recognition receptors, including Toll-like receptor 3, Toll-like receptor 4, cytosolic ribonucleic acid, and deoxyribonucleic acid sensors, are abundantly expressed in seminal vesicl

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Di Stefano, Andrea F. D., Milko M. Radicioni, Francesca Morano, et al. "Fosfomycin Pharmacokinetic Profile in Plasma and Urine and Quantitative Estimation in Prostate and Seminal Vesicles after One and Two Consecutive Doses of Oral Fosfomycin Trometamol in Healthy Male Volunteers." Antibiotics 11, no. 11 (2022): 1458. http://dx.doi.org/10.3390/antibiotics11111458.

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The present Phase I study investigated, for the first time, fosfomycin pharmacokinetics in humans after two 3 g doses of fosfomycin trometamol administered 27 h apart, according to the dose regimen recommended for the prophylactic indication for transrectal prostate biopsy in adult men. Plasma, urine and seminal plasma concentrations were measured after one and two consecutive doses in 24 healthy men, representative of the target population of the prophylactic indication. Prostate and seminal vesicle concentrations were estimated based on seminal plasma concentrations using a one-step regressi

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Cunha, G. R., P. Young, S. J. Higgins, and P. S. Cooke. "Neonatal seminal vesicle mesenchyme induces a new morphological and functional phenotype in the epithelia of adult ureter and ductus deferens." Development 111, no. 1 (1991): 145–58. http://dx.doi.org/10.1242/dev.111.1.145.

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Mesenchyme from neonatal mouse and rat seminal vesicles (SVM) was grown in association with postnatal (adult) epithelial cells from the ureter (URE) and ductus deferens (DDE) in chimeric tissue recombinants composed of mouse mesenchyme and rat epithelium or vice versa. Functional cytodifferentiation was examined in these SVM + URE and SVM + DDE tissue recombinants with antibodies against major androgen-dependent seminal-vesicle-specific secretory proteins. Adult DDE and URE were induced to express seminal cytodifferentiation and produced the complete spectrum of major seminal vesicle secretory

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Goyal, Shikha, Renu Madan, Urmi Mukherjee, and Rajender Kumar. "Solitary fibrous tumor of the seminal vesicle." Journal of Cancer Research and Therapeutics 19, no. 5 (2023): 1412–14. http://dx.doi.org/10.4103/jcrt.jcrt_525_22.

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ABSTRACT Solitary fibrous tumors (SFTs) are mesenchymal neoplasms with variable clinical behavior depending on age, tumor site, and size, and pathologic factors such as mitoses and necrosis. Imaging features on computed tomography (CT) or magnetic resonance imaging (MRI) are not specific, and the diagnosis relies on histopathology with immunohistochemistry. SFTs arising from seminal vesicles is rare and reported in only eight earlier cases. We discuss the clinical, histopathologic and positron emission tomography (PET) imaging characteristics of a 54-year-old patient with SFT of the seminal ve

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Gur, FM, and S. Timurkaan. "Androgen receptor distribution in the rat prostate gland and seminal vesicles." Veterinární Medicína 61, No. 3 (2016): 148–54. http://dx.doi.org/10.17221/8766-vetmed.

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KISE, HIDEAKI, JUNJI NISHIOKA, KENJI SATOH, TOSHIYUKI OKUNO, JUICHI KAWAMURA, and KOJI SUZUKI. "Measurement of Protein C Inhibitor in Seminal Plasma Is Useful for Detecting Agenesis of Seminal Vesicles or the Vas Deferens." Journal of Andrology 21, no. 2 (2000): 207–12. http://dx.doi.org/10.1002/j.1939-4640.2000.tb02097.x.

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ABSTRACT: Protein C inhibitor (PCI), a plasma serine protease inhibitor of activated protein C, is present at high concentrations in the seminal plasma of normal subjects and is decreased in some infertile patients. We measured the concentrations of PCI, prostate‐specific antigen, and fructose in the seminal plasma of infertile patients (n = 125) and of normal subjects (n = 13). We also measured time‐dependent changes in the concentrations of PCI and fructose in seminal plasma after ejaculation. A weak correlation was found between the levels of PCI and fructose (r =0.268, P = 0.016). The PCI

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Gonzales, Gustavo F., Graciela Kortebani, and Alicia B. Mazzolli. "Leukocytospermia and function of the seminal vesicles on seminal quality." Fertility and Sterility 57, no. 5 (1992): 1058–65. http://dx.doi.org/10.1016/s0015-0282(16)55025-0.

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Scheit, Karl Heinz, Michael Kemme, Gerhard Aumüller, Jürgen Seitz, Gerd Hagendorff, and Michael Zimmer. "The major protein of bull seminal plasma: Biosynthesis and biological function." Bioscience Reports 8, no. 6 (1988): 589–608. http://dx.doi.org/10.1007/bf01117339.

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We isolated the major protein of apparent Mr of 15,000–16,000 from seminal plasma as well as from seminal veiscle secretion of bull and proved by amino acid analysis and tryptic peptide mapping that the two proteins were identical. An antiserum against this major protein was employed to quantitate and identify the major protein in seminal plasma as well as seminal vesicle secretion. The antiserum did not cross-react with proteins from bovine or human plasma or follicular fluid respectively. Cell-free translation of poly(A)RNA from seminal vesicle tissue and immunoprecipitation yielded one majo

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Lin, Ming-Huei, Robert Kuo-Kuang Lee, Yuh-Ming Hwu, et al. "SPINKL, a Kazal-type serine protease inhibitor-like protein purified from mouse seminal vesicle fluid, is able to inhibit sperm capacitation." REPRODUCTION 136, no. 5 (2008): 559–71. http://dx.doi.org/10.1530/rep-07-0375.

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We report a secreted serine protease inhibitor Kazal-type-like (SPINKL) protein. The SPINKL protein was purified from mouse seminal vesicle secretions through a series of steps, including ion-exchange chromatography on a diethylaminoethyl-Sephacel column, gel filtration on a Sephadex G-75 column, and ion-exchange HPLC on a Q strong anion exchange column. Further analysis identified several SPINKL proteins with various N-linked carbohydrates. The SPINKL protein has six conserved cysteine residues that are nearly identical to those of members of the SPINK protein family. It was noted that the SP

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Joo, Ijin, Seung Hyup Kim, and Jeong Yeon Cho. "A comparison of seminal vesicle size on CT between autosomal dominant polycystic kidney disease (ADPKD) patients and normal subjects." Acta Radiologica 51, no. 5 (2010): 569–72. http://dx.doi.org/10.3109/02841851003652583.

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Background: Extrarenal manifestations are common in autosomal dominant polycystic kidney disease (ADPKD). Although seminal vesicles can also be involved in patients with ADPKD, little is known about the size differences of the seminal vesicles between ADPKD patients and normal subjects. Purpose: To determine whether the size of seminal vesicles in ADPKD patients is larger than that in normal subjects with the use of three-dimensional (3D) CT. Material and Methods: Using a retrospective case-control study design, we reviewed the findings of 696 male patients with an age range of 20–69 years who

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Garcia, E. M., J. M. Vazquez, I. Parrilla, et al. "323 EXPRESSION OF PSP-I AND PSP-II IN THE REPRODUCTIVE TRACT OF THE BOAR BY IMMUNOHISTOCHEMISTRY, WESTERN BLOTTING, AND RT-PCR." Reproduction, Fertility and Development 19, no. 1 (2007): 277. http://dx.doi.org/10.1071/rdv19n1ab323.

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In boar seminal plasma, PSP-I and PSP-II form a noncovalent heterodimer, which is known to have a beneficial effect on highly extended boar spermatozoa. These proteins are mainly produced by the seminal vesicles of the male reproductive tract and are mixed with the spermatozoa during ejaculation. This study assessed the epithelial localization and expression of spermadhesin PSP-I and PSP-II subunits using immunohistochemical, western blotting, and RT-PCR methods in porcine testis, epididymis (caput, corpus, and caudal), seminal vesicles, and bulbourethral glands. Tissues were collected from 10

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Secaf, E., R. N. Nuruddin, H. Hricak, R. D. McClure, and B. Demas. "MR imaging of the seminal vesicles." American Journal of Roentgenology 156, no. 5 (1991): 989–94. http://dx.doi.org/10.2214/ajr.156.5.2017966.

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Khmara, T. V., M. O. Ryznychuk, T. B. Sykyrytska, V. D. Moisiuk, Ya P. Stefak, and P. O. Fedirchyk. "Fetal Microscopic Anatomy of Seminal Vesicles." Ukraïnsʹkij žurnal medicini, bìologìï ta sportu 3, no. 1 (2018): 76–79. http://dx.doi.org/10.26693/jmbs03.01.076.

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Lna, J. M., and J. G. Let. "NONINVASIVE IMAGING OF THE SEMINAL VESICLES." INVESTIGATIVE RADIOLOGY 28, no. 12 (1993): 1213. http://dx.doi.org/10.1097/00004424-199312000-00152.

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SMITH, GAIL, CESAR ERCOLE, JOHN C. HULBERT, WILFRIDO R. CASTAÑEDA-ZUÑIGA, and JANIS GISSEL LETOURNEAU. "Transrectal Sonography and the Seminal Vesicles." Journal of Endourology 3, no. 2 (1989): 219–25. http://dx.doi.org/10.1089/end.1989.3.219.

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Castiñerias Fernández, J., C. González Cáliz, J. L. Moyano Calvo, and E. Sánchez Sánchez. "Prostate and seminal vesicles sparing cystectomy." European Urology Supplements 18, no. 11 (2019): e3601. http://dx.doi.org/10.1016/s1569-9056(19)34724-4.

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Kavoussi, Louis R., William W. Schuessler, Thierry G. Vancaillie, and Ralph V. Clayman. "Laparoscopic Approach to the Seminal Vesicles." Journal of Urology 150, no. 2 Part 1 (1993): 417–19. http://dx.doi.org/10.1016/s0022-5347(17)35498-8.

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THIEL, RALF, and PETER EFFERT. "Primary Adenocarcinoma of the Seminal Vesicles." Journal of Urology 168, no. 5 (2002): 1891–96. http://dx.doi.org/10.1016/s0022-5347(05)64260-7.

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