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Journal articles on the topic 'In vitro; Embryology'

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1

Zaninovic, Nikica, and Zev Rosenwaks. "Artificial intelligence in human in vitro fertilization and embryology." Fertility and Sterility 114, no. 5 (2020): 914–20. http://dx.doi.org/10.1016/j.fertnstert.2020.09.157.

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2

Opiela, J., and M. Samiec. "Characterization of mesenchymal stem cells and their application in experimental embryology." Polish Journal of Veterinary Sciences 16, no. 3 (2013): 593–99. http://dx.doi.org/10.2478/pjvs-2013-0084.

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Abstract The efficiency of somatic cell cloning (somatic cell nuclear transfer; SCNT) as well as in vitro fertilization/in vitro embryo production (IVF/IVP) in mammals stay at relatively same level for over a decade. Despite plenty of different approaches none satisfactory break-through took place. In this article, we briefly summarize the implementation of mesenchymal stem cells (MSCs) for experimental embryology. The advantages of using MSCs as nuclear donors in somatic cell cloning and in vitro embryo culture are described. The description of results obtained with these cells in mammalian e
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3

Simopoulou, Mara, Konstantinos Sfakianoudis, Evangelos Maziotis, et al. "Assessing Clinical Embryology Research: A Global Bibliometric Analysis." Medicina 56, no. 5 (2020): 210. http://dx.doi.org/10.3390/medicina56050210.

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Background and Objectives: The evaluative strength of available bibliometric tools in the field of clinical embryology has never been examined in the literature. The aim is to bring insight regarding the identity of clinical embryology research, introducing concerns when solely relying on the methodology of bibliometric analysis. Materials and Methods: An all-inclusive analysis of the most bibliometrically highlighted scientific contributions regarding the cornerstones of clinical embryology was performed employing the Scopus, Web of Science (WoS) and PubMed databases, between 1978–2018. An an
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4

Ghaskadbi, Surendra. "Leela Mulherkar and the teaching of developmental biology." International Journal of Developmental Biology 64, no. 1-2-3 (2020): 41–44. http://dx.doi.org/10.1387/ijdb.200147sg.

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The formal teaching of developmental biology in India began in the late nineteen-fifties at the Department of Zoology of the University of Poona. This was due to the efforts of Leela Mulherkar, who on her return from C.H. Waddington’s laboratory in Edinburgh, took up the teaching of embryology at the Master’s level. Mulherkar began using locally available material to teach how animals develop. They included the embryos of chicken, frog, garden lizard and molluscs, as well as organisms such as hydra and sponges. Her teaching was supported by an active research laboratory that used all these sys
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5

Coticchio, Giovanni, Mariabeatrice Dal-Canto, Maria-Cristina Guglielmo, Mario Mignini-Renzini, and Rubens Fadini. "Human oocyte maturation in vitro." International Journal of Developmental Biology 56, no. 10-11-12 (2012): 909–18. http://dx.doi.org/10.1387/ijdb.120135gv.

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6

Morales, P., V. palma, M. Salgado, and M. Villalon. "Fertilization and early embryology: Sperm interaction with human oviductal cells in vitro." Human Reproduction 11, no. 7 (1996): 1504–9. http://dx.doi.org/10.1093/oxfordjournals.humrep.a019426.

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7

Plachot, Michelle, J. M. Antoine, Sylvia Alvarez, et al. "Fertilization and early embryology: Granulosa cells improve human embryo development in vitro." Human Reproduction 8, no. 12 (1993): 2133–40. http://dx.doi.org/10.1093/oxfordjournals.humrep.a137995.

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8

Krisher, Rebecca L., Adam L. Heuberger, Melissa Paczkowski, et al. "Applying metabolomic analyses to the practice of embryology: physiology, development and assisted reproductive technology." Reproduction, Fertility and Development 27, no. 4 (2015): 602. http://dx.doi.org/10.1071/rd14359.

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The advent of metabolomics technology and its application to small samples has allowed us to non-invasively monitor the metabolic activity of embryos in a complex culture environment. The aim of this study was to apply metabolomics technology to the analysis of individual embryos from several species during in vitro development to gain an insight into the metabolomics pathways used by embryos and their relationship with embryo quality. Alanine is produced by both in vivo- and in vitro-derived human, murine, bovine and porcine embryos. Glutamine is also produced by the embryos of these four spe
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9

Sciorio, Romualdo, Erika Rapalini, and Sandro C. Esteves. "Air quality in the clinical embryology laboratory: a mini-review." Therapeutic Advances in Reproductive Health 15 (January 2021): 263349412199068. http://dx.doi.org/10.1177/2633494121990684.

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The scope of the clinical embryology laboratory has expanded over recent years. It now includes conventional in vitro fertilization (IVF) techniques and complex and time-demanding procedures like blastocyst culture, processing of surgically retrieved sperm, and trophectoderm biopsy for preimplantation genetic testing. These procedures require a stable culture environment in which ambient air quality might play a critical role. The existing data indicate that both particulate matter and chemical pollution adversely affect IVF results, with low levels for better outcomes. As a result, IVF clinic
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10

Ledger, William L. "Medicolegal aspects of reproductive medicine." Clinical Risk 15, no. 5 (2009): 197–200. http://dx.doi.org/10.1258/cr.2009.090061.

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This paper is a review of current techniques and best practice in reproductive medicine, including preimplantation genetic diagnosis and embryo freezing, and management of pregnancy after in vitro fertilization. It discusses medicolegal aspects that can arise from failure to follow best practice including ovarian hyperstimulation syndrome and mistakes occurring in the embryology laboratory.
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11

Lane, Michelle, Megan Mitchell, Kara S. Cashman, Deanne Feil, Sarah Wakefield, and Deirdre L. Zander-Fox. "To QC or not to QC: the key to a consistent laboratory?" Reproduction, Fertility and Development 20, no. 1 (2008): 23. http://dx.doi.org/10.1071/rd07161.

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A limiting factor in every embryology laboratory is its capacity to grow ‘normal’ embryos. In human in vitro fertilisation (IVF), there is considerable awareness that the environment of the laboratory itself can alter the quality of the embryos produced and the industry as a whole has moved towards the implementation of auditable quality management systems. Furthermore, in some countries, such as Australia, an established quality management system is mandatory for clinical IVF practice, but such systems are less frequently found in other embryology laboratories. Although the same challenges of
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12

Turner, Christopher M., and Paul N. Adler. "Morphogenesis of Drosophila pupal wings in vitro." Mechanisms of Development 52, no. 2-3 (1995): 247–55. http://dx.doi.org/10.1016/0925-4773(95)00405-p.

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13

Kanakasabapathy, Manoj Kumar, Prudhvi Thirumalaraju, Charles L. Bormann, et al. "Development and evaluation of inexpensive automated deep learning-based imaging systems for embryology." Lab on a Chip 19, no. 24 (2019): 4139–45. http://dx.doi.org/10.1039/c9lc00721k.

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14

Doyle, Pat. "THE U.K. HUMAN FERTILISATION AND EMBRYOLOGY AUTHORITY." International Journal of Technology Assessment in Health Care 15, no. 1 (1999): 3–10. http://dx.doi.org/10.1017/s0266462399015123.

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The Human Fertilisation and Embryology Act of the United Kingdom was passed in 1990, leading to the formation of the Human Fertilisation and Embryology Authority (HFEA), the first statutory body to regulate and control assisted conception anywhere in the world. The principal function of the HFEA is to license and monitor clinics that carry out in vitro fertilization (IVF), donor insemination (DI), and embryo research. Information on over 135,000 treatment cycles, 20,000 pregnancies, and 25,000 babies following IVF has now been collected as part of the regulatory process, and these data have pe
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15

Telfer, Evelyn E., and Marie Mclaughlin. "Strategies to support human oocyte development in vitro." International Journal of Developmental Biology 56, no. 10-11-12 (2012): 901–7. http://dx.doi.org/10.1387/ijdb.130001et.

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16

Asashima, Makoto. "S08-07 In vitro organogenesis in vertebrate development." Mechanisms of Development 126 (August 2009): S33—S34. http://dx.doi.org/10.1016/j.mod.2009.06.1045.

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17

Greve, Torben, and Henrik Callesen. "Integrating new technologies with embryology and animal production." Reproduction, Fertility and Development 16, no. 2 (2004): 113. http://dx.doi.org/10.1071/rd03084.

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The present review describes a range of selected farm animal embryo technologies used in embryological research and applied in animal breeding and production. Some of the techniques are driven by the breeder’s wish to obtain animals with higher breeding values, whereas others are primarily driven by the curiosity of researchers. The interaction between basic research and practical application in these areas is still a characteristic feature for people who contribute to the International Embryo Transfer Society (IETS) and has been an advantage for both researchers and breeders. One example of s
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18

Lasala, Gina, Donatella Farini, and Massimo De Felici. "Estrogenic in vitro assay on mouse embryonic Leydig cells." International Journal of Developmental Biology 54, no. 4 (2010): 717–22. http://dx.doi.org/10.1387/ijdb.092883gs.

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19

Hyttel, P., K. P. Xu, and T. Greve. "Ultrastructural abnormalities of in vitro fertilization of in vitro matured bovine oocytes." Anatomy and Embryology 178, no. 1 (1988): 47–52. http://dx.doi.org/10.1007/bf00305013.

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20

Vityazeva, I. I., I. I. Barmina, and G. A. Melnichenko. "Historical stages of development of methods of the assisted reproductive technologies based on fertilisation in vitro." Bulletin of Reproductive Health, no. 1 (March 17, 2011): 5–14. http://dx.doi.org/10.14341/brh201115-14.

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This article is devoted, in the first place, to the history of in vitro fertilization method (IVF). The main phase of initiation and further perfection of IVF are elucidated. Correlations of the development knowledge and skills in obstetrics and gynecology, endocrinology, pharmacology are revealed. In a chronological order the main achievements of such reproduction medicine sections as embryology with cryopreservation and PGD analysis, functional diagnostics with ultrasonography are recited. Further practical and scientific perspectives of the artificial reproductive technology's method are de
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21

Li, Wan-Chun, Marko E. Horb, David Tosh, and Jonathan M. W. Slack. "In vitro transdifferentiation of hepatoma cells into functional pancreatic cells." Mechanisms of Development 122, no. 6 (2005): 835–47. http://dx.doi.org/10.1016/j.mod.2005.01.001.

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22

Miyagoe-Suzuki, Yuko, Nami Masubuchi, Kaori Miyamoto, et al. "Reduced proliferative activity of primary POMGnT1-null myoblasts in vitro." Mechanisms of Development 126, no. 3-4 (2009): 107–16. http://dx.doi.org/10.1016/j.mod.2008.12.001.

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23

Qiao, Jizeng, Anya Turetsky, Paul Kemp, and Jeff Teumer. "Hair morphogenesisin vitro: formation of hair structures suitable for implantation." Regenerative Medicine 3, no. 5 (2008): 683–92. http://dx.doi.org/10.2217/17460751.3.5.683.

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24

Iacob, Razvan, Vlad Herlea, Lorand Savu, et al. "Phenotypic assessment of liver-derived cell cultures during in vitro expansion." Regenerative Medicine 16, no. 1 (2021): 33–46. http://dx.doi.org/10.2217/rme-2020-0093.

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Background: Liver cells represent an attractive source of cells for autologous regenerative medicine. The present study assesses the liver cells’ stability during in vitro expansion, as a prerequisite for therapeutic use. Results: The human liver cell cultures in this study were propagated efficiently in vitro for at least 12 passages. No significant changes in morphology, intracellular ultrastructures and characteristic markers expression were found during in vitro expansion of cells from all analyzed donors. However, expanded cells derived from male donors of >60 years old, lost the Y chr
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25

Dumoulin, John C. M., Anton H. J. C. Michiels, Marijke Bras, Math H. E. C. Pieters, Joep P. M. Geraedts, and Johannes L. H. Evers. "Fertilization and early embryology: Temporal effects of ouabain on in-vitro development of mouse zygotes." Human Reproduction 8, no. 9 (1993): 1469–74. http://dx.doi.org/10.1093/oxfordjournals.humrep.a138281.

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26

Tournaye, Herman, Marleen Van der Linden, Etienne Van den Abbeel, Paul Devroey, and Andre Van Steirteghem. "Fertilization and early embryology: Effects of pentoxifylline on in-vitro development of preimplantation mouse embryos." Human Reproduction 8, no. 9 (1993): 1475–80. http://dx.doi.org/10.1093/oxfordjournals.humrep.a138282.

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27

Aboulghar, M. A., R. T. Mansour, G. I. Serour, and Y. M. Amin. "Fertilization and early embryology: The prognostic value of successful in-vitro fertilization in subsequent trials." Human Reproduction 9, no. 10 (1994): 1932–34. http://dx.doi.org/10.1093/oxfordjournals.humrep.a138361.

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28

Rooney, GE, GI Nistor, FB Barry, and HS Keirstead. "In vitro differentiation potential of human embryonic versus adult stem cells." Regenerative Medicine 5, no. 3 (2010): 365–79. http://dx.doi.org/10.2217/rme.10.20.

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29

Kalionis, Bill, and Patrick H. O'Farrell. "A universal target sequence is bound in vitro by diverse homeodomains." Mechanisms of Development 43, no. 1 (1993): 57–70. http://dx.doi.org/10.1016/0925-4773(93)90023-q.

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30

Yeung, Queenie S. Y., Ying Xin Zhang, Jacqueline P. W. Chung, et al. "Practical Considerations in Providing Preimplantation Genetic Testing for Aneuploidies (PGT-A)." Fertility & Reproduction 01, no. 01 (2019): 21–29. http://dx.doi.org/10.1142/s2661318219300046.

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Preimplantation genetic testing for aneuploidies (PGT-A) has been controversial in its application to improve reproductive success, reduce time-to-pregnancy, and serve the intention-to-treat. Nevertheless, many in vitro fertilization (IVF) units have already introduced the service for one reason or another. Given PGT-A is not a stand-alone technique but a clinical service involving several disciplines, this mini review discussed the factors that can influence success rates when PGT-A is applied and highlighted practical issues encountered by clinicians, embryology, and genetics laboratories in
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31

Nieto-Nicolau, Núria, Beatriz Martín-Antonio, Claudia Müller-Sánchez, and Ricardo P. Casaroli-Marano. "In vitro potential of human mesenchymal stem cells for corneal epithelial regeneration." Regenerative Medicine 15, no. 3 (2020): 1409–26. http://dx.doi.org/10.2217/rme-2019-0067.

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Aim: To determine the potential of mesenchymal stem cells (MSC) for corneal epithelial regeneration in vitro. Materials & methods: Bone marrow MSC (BM-MSC) and adipose tissue MSC were analyzed for corneal epithelial and mesenchymal markers, using limbal stem cells and corneal cells as controls. MSC with better potential were cultured with specific mediums for epithelial induction. Transepithelial electric resistance and wound healing assay with human corneal epithelial cells were performed. Results: BM-MSC showed better potential, increased corneal markers, and higher transepithelial elect
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32

Song, Renfang, Graeme Preston, and Ihor V. Yosypiv. "Angiotensin II stimulates in vitro branching morphogenesis of the isolated ureteric bud." Mechanisms of Development 128, no. 7-10 (2011): 359–67. http://dx.doi.org/10.1016/j.mod.2011.07.002.

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33

Eguizabal, Cristina, Maria D. Boyano, Alejandro Diez-Torre, et al. "Interleukin-2 induces the proliferation of mouse primordial germ cells in vitro." International Journal of Developmental Biology 51, no. 8 (2007): 731–38. http://dx.doi.org/10.1387/ijdb.072442ce.

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34

Honda, Arata, Michiko Hirose, Kimiko Inoue, et al. "Large-scale production of growing oocytes in vitro from neonatal mouse ovaries." International Journal of Developmental Biology 53, no. 4 (2009): 605–13. http://dx.doi.org/10.1387/ijdb.082607ah.

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35

Kobayashi, Tohru. "In vitro germ cell differentiation during sex differentiation in a teleost fish." International Journal of Developmental Biology 54, no. 1 (2010): 105–11. http://dx.doi.org/10.1387/ijdb.082836tk.

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36

Hyttel, P. "Bovine cumulus-oocyte disconnection in vitro." Anatomy and Embryology 176, no. 1 (1987): 41–44. http://dx.doi.org/10.1007/bf00309750.

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37

Baldwin, R. "Book Review: Fourth Report of the Voluntary Licensing Authority for Human In Vitro Fertilisation and Embryology." Medicine, Science and the Law 30, no. 2 (1990): 183. http://dx.doi.org/10.1177/002580249003000220.

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38

Hyodo, Masao, Shinji Makino, Yasunori Awaji, et al. "A novel in vitro system for studying cardiomyocyte differentiation with medaka embryonic cells." International Journal of Developmental Biology 53, no. 4 (2009): 615–22. http://dx.doi.org/10.1387/ijdb.092850mh.

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39

Choi, Soon Won, Sigrid Eckardt, Ruhel Ahmad, et al. "Two paternal genomes are compatible with dopaminergic in vitro and in vivo differentiation." International Journal of Developmental Biology 54, no. 11-12 (2010): 1755–62. http://dx.doi.org/10.1387/ijdb.103188sc.

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40

Govindasamy, Niraimathi, Binyamin Duethorn, Hatice O. Oezgueldez, Yung S. Kim, and Ivan Bedzhov. "Test-tube embryos - mouse and human development in vitro to blastocyst stage and beyond." International Journal of Developmental Biology 63, no. 3-4-5 (2019): 203–15. http://dx.doi.org/10.1387/ijdb.180379ib.

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Mammalian embryogenesis is intrauterine and depends on support from the maternal environment. Therefore, in order to directly study and manipulate early mouse and human embryos, fine-tuned culture conditions have to be provided to maintain embryo growth in vitro. Over time, the establishment and implementation of embryo culture methods have come a long way, initially enabling the development of few pre-implantation stages, expanding later to support in vitro embryogenesis from fertilization until blastocyst and even ex utero development beyond the implantation stages. Designing culture conditi
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41

Li, Yan, Chunhui Xu, and Teng Ma. "In vitro organogenesis from pluripotent stem cells." Organogenesis 10, no. 2 (2014): 159–63. http://dx.doi.org/10.4161/org.28918.

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42

Ataliotis, Paris. "Platelet-derived growth factor A modulates limb chondrogenesis both in vivo and in vitro." Mechanisms of Development 94, no. 1-2 (2000): 13–24. http://dx.doi.org/10.1016/s0925-4773(00)00321-x.

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43

Renoncourt, Yannick, Patrick Carroll, Pierre Filippi, Vilma Arce, and Serge Alonso. "Neurons derived in vitro from ES cells express homeoproteins characteristic of motoneurons and interneurons." Mechanisms of Development 79, no. 1-2 (1998): 185–97. http://dx.doi.org/10.1016/s0925-4773(98)00189-0.

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44

Archacka, Karolina, Anna Ajduk, Pawel Pomorski, Katarzyna Szczepanska, Marek Maleszewski, and Maria A. Ciemerych. "Defective calcium release during in vitro fertilization of maturing oocytes of LT/Sv mice." International Journal of Developmental Biology 52, no. 7 (2008): 903–12. http://dx.doi.org/10.1387/ijdb.072397ka.

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45

Ito, Shoko, and Masatoshi Takeichi. "12-P015 In vitro recognition of specific afferent axons by cerebellar granule cell dendrites." Mechanisms of Development 126 (August 2009): S193. http://dx.doi.org/10.1016/j.mod.2009.06.469.

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46

Bouwmeester, Tewis, Stephan Güehmann, Tarek El-Baradi, et al. "Molecular cloning, expression and in vitro functional characterization of Myb-related proteins in Xenopus." Mechanisms of Development 37, no. 1-2 (1992): 57–68. http://dx.doi.org/10.1016/0925-4773(92)90015-c.

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47

Ashfaq, Ramla, Azra Mehmood, Amna Ramzan, Intzar Hussain, Moazzam Nazeer Tarar, and Sheikh Riazuddin. "Antioxidant pretreatment enhances umbilical cord derived stem cells survival in response to thermal stress in vitro." Regenerative Medicine 15, no. 3 (2020): 1441–53. http://dx.doi.org/10.2217/rme-2019-0090.

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Aim: Pretreatment of stem cells with antioxidants accelerates their ability to counter oxidative stress and is associated with the overall therapeutic outcome of their transplantation. Material & methods: Wharton Jelly derived mesenchymal stem cells (WJMSCs) were cultured and pretreated with various doses of antioxidants; Vitamin C (Vit C), Vitamin E (Vit E), Vitamin D3 (Vit D3) and their Cocktail, followed by exposure to in vitro heat injury. Assessment of WJMSCs survival, paracrine release, in vitro wound healing and expression of angiogenic and survival markers was conducted. Results: T
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48

Tournaye, Herman, Marleen Van der Linden, Etienne Van den Abbeel, Paul Devroey, and André Van Steirteghem. "Fertilization and early embryology: The effect of pentoxifylline on mouse in-vitro fertilization and early embryonic development." Human Reproduction 9, no. 10 (1994): 1903–8. http://dx.doi.org/10.1093/oxfordjournals.humrep.a138356.

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49

Yao, Y. Q., W. S. B. Yeung, and P. C. Ho. "Fertilization and early embryology: Human follicular fluid inhibits the binding of human spermatozoa to zona pellucidain vitro." Human Reproduction 11, no. 12 (1996): 2674–80. http://dx.doi.org/10.1093/oxfordjournals.humrep.a019190.

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50

S Zaitseva, Tatiana, Guang Yang, Dimitris Dionyssiou, et al. "Delivery of hepatocyte growth factor mRNA from nanofibrillar scaffolds in a pig model of peripheral arterial disease." Regenerative Medicine 15, no. 6 (2020): 1761–73. http://dx.doi.org/10.2217/rme-2020-0023.

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Background: Chemical modification of mRNA (mmRNA) substantially improves their stability and translational efficiency within cells. Nanofibrillar collagen scaffolds were previously shown to enable the spatially localized delivery and temporally controlled release of mmRNA encoding HGF both in vitro and in vivo. Materials & methods: Herein we developed an improved slow-releasing HGF mmRNA scaffold and tested its therapeutic efficacy in a porcine model of peripheral arterial disease. Results & conclusion: The HGF mmRNA was released from scaffolds in a temporally controlled fashion in vit
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