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  1. Article ; Online: H/ACA snoRNA levels are regulated during stem cell differentiation.

    McCann, Kathleen L / Kavari, Sanam L / Burkholder, Adam B / Phillips, Bart T / Hall, Traci M Tanaka

    Nucleic acids research

    2020  Volume 48, Issue 15, Page(s) 8686–8703

    Abstract: H/ACA small nucleolar RNAs (snoRNAs) guide pseudouridylation as part of a small nucleolar ribonucleoprotein complex (snoRNP). Disruption of H/ACA snoRNA levels in stem cells impairs pluripotency, yet it remains unclear how H/ACA snoRNAs contribute to ... ...

    Abstract H/ACA small nucleolar RNAs (snoRNAs) guide pseudouridylation as part of a small nucleolar ribonucleoprotein complex (snoRNP). Disruption of H/ACA snoRNA levels in stem cells impairs pluripotency, yet it remains unclear how H/ACA snoRNAs contribute to differentiation. To determine if H/ACA snoRNA levels are dynamic during differentiation, we comprehensively profiled H/ACA snoRNA abundance in multiple murine cell types and during differentiation in three cellular models, including mouse embryonic stem cells and mouse myoblasts. We determined that the profiles of H/ACA snoRNA abundance are cell-type specific, and we identified a subset of snoRNAs that are specifically regulated during differentiation. Additionally, we demonstrated that a decrease in Snora27 abundance upon differentiation corresponds to a decrease in pseudouridylation of its target site within the E-site transfer RNA (tRNA) binding region of the 28S ribosomal RNA (rRNA) in the large ribosomal subunit. Together, these data point toward a potential model in which H/ACA snoRNAs are specifically regulated during differentiation to alter pseudouridylation and fine tune ribosome function.
    MeSH term(s) Animals ; Base Sequence/genetics ; Cell Differentiation/genetics ; Mice ; Mouse Embryonic Stem Cells ; Myoblasts/metabolism ; Nucleic Acid Conformation ; Pseudouridine/genetics ; RNA, Ribosomal, 28S/genetics ; RNA, Small Nucleolar/genetics ; Ribonucleoproteins, Small Nucleolar/genetics ; Ribosomes/genetics
    Chemical Substances RNA, Ribosomal, 28S ; RNA, Small Nucleolar ; Ribonucleoproteins, Small Nucleolar ; Pseudouridine (1445-07-4)
    Language English
    Publishing date 2020-07-24
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 186809-3
    ISSN 1362-4962 ; 1362-4954 ; 0301-5610 ; 0305-1048
    ISSN (online) 1362-4962 ; 1362-4954
    ISSN 0301-5610 ; 0305-1048
    DOI 10.1093/nar/gkaa612
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Pseudomonas syringae Pathogen Causes Foliar Disease of Upland Cotton in Texas

    Phillips, A. Z / T. Wheeler / J. Woodward / R. S. Bart

    Plant disease. 2018 June, v. 102, no. 6

    2018  

    Abstract: ... has reemerged in the United States since 2011 (Phillips et al. 2017). In 2015, cotton fields near ...

    Abstract Cotton bacterial blight (CBB), caused by Xanthomonas citri pv. malvacearum (Xcm), can cause significant yield losses on susceptible varieties of upland cotton (Gossypium hirsutum L.) (Verma 1986). CBB has reemerged in the United States since 2011 (Phillips et al. 2017). In 2015, cotton fields near Plains, TX, exhibited symptoms of an unknown foliar disease on cotton cultivars that were reported to be resistant to CBB. In June 2016, bacteria were isolated from Fibermax 2007GLT (CBB Resistant) leaves exhibiting CBB-like symptoms. Culture on nutrient-rich NYGA medium with 50 μM cycloheximide revealed two predominant colony morphologies, yellow and white. The yellow colonies were confirmed to be Xcm. Koch’s postulates were used to determine that the white bacteria caused necrotic foliar lesions when infiltrated into cotton leaves alone or in combination with Xcm. Sequencing of the 16s rRNA gene identified this bacterium as Pseudomonas sp. with 99% sequence identity to the Pseudomonas syringae pv. syringae B728a (Gbk 230265-9). Further multilocus sequence analysis using concatenated regions of the gyrB, rpoD, gap1, and gltA on the PAMDB database grouped this pathogen with P. syringae pv. atrofaciens, P. syringae pv. apata, P. syringae pv. pisi, P. syringae pv. syringae, and P. syringae pv. aceris (http://genome.ppws.vt.edu/cgi-bin/MLST/home.pl). Thus, the isolated cotton pathogen is a member of P. syringae. Identification of a pseudomonad cotton pathogen has occurred at least once before in cotton seedlings near Lubbock, TX. This was recorded in the 1994 Cotton Beltwide Conferences Proceedings (ATCC 51506). No other reference to a pseudomonad pathogen of cotton has been found. However, evidence of a Pseudomonas-Xanthomonas disease complex has been found at least once in leafy crucifers (Zhao et al. 2000). Inoculations with a needleless syringe resulted in symptoms that initially appeared as a cell death phenotype but quickly progressed to a spreading necrotic lesion. Foliar disease symptoms were observed after inoculation with a bacterial suspension at OD₆₀₀ of 0.0001 to 0.01. Symptoms appeared as early as 1 day after inoculation. To date, this pathogen has been isolated from 11 different fields in six counties and always in association with Xcm. Additional isolates were identified from symptomatic leaf tissue of at least eight different cultivars at various locations. Four isolates from Donley County, TX, and four cotton cultivars (DP 1454NRB2RF, FM 1320GL, FM 1830GLT, and FM 2484B2F) were screened using the scratch method to identify whether variability existed in the disease response of cultivars. The cultivars were arranged in a split-plot design, with isolate as the main factor and cultivar as the subfactor. Both the main factor and the subfactors were randomized. There were four replications for each isolate/cultivar combination. The test was repeated once. Disease symptoms were less severe on FM 2484B2F (P < 0.05) than the other three cultivars, suggesting that variation exists among cotton germplasm for tolerance to this pathogen. Future phylogenetic analysis will focus on the origin of virulence of this pathogen and its distribution within the cotton production regions in the United States.
    Keywords Brassicaceae ; Gossypium hirsutum ; Pseudomonas syringae ; bacteria ; blight ; cell death ; cotton ; crop production ; cultivars ; cycloheximide ; databases ; experimental design ; foliar diseases ; genes ; germplasm ; leaves ; multilocus sequence typing ; pathogens ; phenotype ; phylogeny ; ribosomal RNA ; seedlings ; virulence ; Texas
    Language English
    Dates of publication 2018-06
    Size p. 1171.
    Publishing place Plant Disease
    Document type Article
    ZDB-ID 754182-x
    ISSN 0191-2917
    ISSN 0191-2917
    DOI 10.1094/PDIS-11-17-1700-PDN
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: Mass spectrometric identification of candidate RNA-binding proteins associated with Transition Nuclear Protein mRNA in the mouse testis.

    Phillips, Bart T / Williams, Jason G / Atchley, Dustin T / Xu, Xiaojiang / Li, Jian-Liang / Adams, Andrea L / Johnson, Katina L / Hall, Traci M Tanaka

    Scientific reports

    2019  Volume 9, Issue 1, Page(s) 13618

    Abstract: Spermatogenesis is a differentiation process that requires dramatic changes to DNA architecture, a process governed in part by Transition Nuclear Proteins 1 and 2 (TNP1 and TNP2). Translation of Tnp1 and Tnp2 mRNAs is temporally disengaged from their ... ...

    Abstract Spermatogenesis is a differentiation process that requires dramatic changes to DNA architecture, a process governed in part by Transition Nuclear Proteins 1 and 2 (TNP1 and TNP2). Translation of Tnp1 and Tnp2 mRNAs is temporally disengaged from their transcription. We hypothesized that RNA regulatory proteins associate specifically with Tnp mRNAs to control the delayed timing of their translation. To identify potential regulatory proteins, we isolated endogenous mRNA/protein complexes from testis extract and identified by mass spectrometry proteins that associated with one or both Tnp transcripts. Five proteins showed strong association with Tnp transcripts but had low signal when Actin mRNA was isolated. We visualized the expression patterns in testis sections of the five proteins and found that each of the proteins was detected in germ cells at the appropriate stages to regulate Tnp RNA expression.
    MeSH term(s) Animals ; Cell Nucleus/metabolism ; Chromosomal Proteins, Non-Histone/metabolism ; Chromosomal Proteins, Non-Histone/physiology ; DNA-Binding Proteins/genetics ; Germ Cells/metabolism ; Male ; Mass Spectrometry/methods ; Mice ; Mice, Inbred DBA ; Nuclear Proteins/metabolism ; RNA/metabolism ; RNA, Messenger/genetics ; RNA-Binding Proteins/metabolism ; Spermatogenesis/genetics ; Testis/metabolism ; Testis/physiology ; Transcription Factors/metabolism
    Chemical Substances Chromosomal Proteins, Non-Histone ; DNA-Binding Proteins ; Nuclear Proteins ; RNA, Messenger ; RNA-Binding Proteins ; Transcription Factors ; spermatid transition proteins ; RNA (63231-63-0)
    Language English
    Publishing date 2019-09-20
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-019-50052-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The elusive spermatogonial stem cell marker?

    Hermann, Brian P / Phillips, Bart T / Orwig, Kyle E

    Biology of reproduction

    2011  Volume 85, Issue 2, Page(s) 221–223

    MeSH term(s) Animals ; Gene Expression Regulation/physiology ; Inhibitor of Differentiation Proteins/metabolism ; Male ; Stem Cells/cytology ; Stem Cells/metabolism
    Chemical Substances Idb4 protein, mouse ; Inhibitor of Differentiation Proteins
    Language English
    Publishing date 2011-05-12
    Publishing country United States
    Document type Editorial ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 1118-6
    ISSN 1529-7268 ; 0006-3363
    ISSN (online) 1529-7268
    ISSN 0006-3363
    DOI 10.1095/biolreprod.111.093146
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Fruitful progress to fertility: male fertility in the test tube.

    Clark, Amander T / Phillips, Bart T / Orwig, Kyle E

    Nature medicine

    2011  Volume 17, Issue 12, Page(s) 1564–1565

    MeSH term(s) Animals ; Antineoplastic Agents/adverse effects ; Cryopreservation/methods ; Fertility ; Fertilization ; Fertilization in Vitro/methods ; Humans ; Infertility, Male/etiology ; Infertility, Male/therapy ; Male ; Models, Animal
    Chemical Substances Antineoplastic Agents
    Language English
    Publishing date 2011-12-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1220066-9
    ISSN 1546-170X ; 1078-8956
    ISSN (online) 1546-170X
    ISSN 1078-8956
    DOI 10.1038/nm.2594
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Nurse Care Management for Opioid Use Disorder Treatment: The PROUD Cluster Randomized Clinical Trial.

    Wartko, Paige D / Bobb, Jennifer F / Boudreau, Denise M / Matthews, Abigail G / McCormack, Jennifer / Lee, Amy K / Qiu, Hongxiang / Yu, Onchee / Hyun, Noorie / Idu, Abisola E / Campbell, Cynthia I / Saxon, Andrew J / Liu, David S / Altschuler, Andrea / Samet, Jeffrey H / Labelle, Colleen T / Zare-Mehrjerdi, Mohammad / Stotts, Angela L / Braciszewski, Jordan M /
    Murphy, Mark T / Dryden, Douglas / Arnsten, Julia H / Cunningham, Chinazo O / Horigian, Viviana E / Szapocznik, José / Glass, Joseph E / Caldeiro, Ryan M / Phillips, Rebecca C / Shea, Mary / Bart, Gavin / Schwartz, Robert P / McNeely, Jennifer / Liebschutz, Jane M / Tsui, Judith I / Merrill, Joseph O / Lapham, Gwen T / Addis, Megan / Bradley, Katharine A / Ghiroli, Megan M / Hamilton, Leah K / Hu, Yong / LaHue, Jennifer S / Loree, Amy M / Murphy, Sean M / Northrup, Thomas F / Shmueli-Blumberg, Dikla / Silva, Angela J / Weinstein, Zoe M / Wong, Mark TinFook / Burganowski, Rachael P

    JAMA internal medicine

    2023  Volume 183, Issue 12, Page(s) 1343–1354

    Abstract: Importance: Few primary care (PC) practices treat patients with medications for opioid use disorder (OUD) despite availability of effective treatments.: Objective: To assess whether implementation of the Massachusetts model of nurse care management ... ...

    Abstract Importance: Few primary care (PC) practices treat patients with medications for opioid use disorder (OUD) despite availability of effective treatments.
    Objective: To assess whether implementation of the Massachusetts model of nurse care management for OUD in PC increases OUD treatment with buprenorphine or extended-release injectable naltrexone and secondarily decreases acute care utilization.
    Design, setting, and participants: The Primary Care Opioid Use Disorders Treatment (PROUD) trial was a mixed-methods, implementation-effectiveness cluster randomized clinical trial conducted in 6 diverse health systems across 5 US states (New York, Florida, Michigan, Texas, and Washington). Two PC clinics in each system were randomized to intervention or usual care (UC) stratified by system (5 systems were notified on February 28, 2018, and 1 system with delayed data use agreement on August 31, 2018). Data were obtained from electronic health records and insurance claims. An implementation monitoring team collected qualitative data. Primary care patients were included if they were 16 to 90 years old and visited a participating clinic from up to 3 years before a system's randomization date through 2 years after.
    Intervention: The PROUD intervention included 3 components: (1) salary for a full-time OUD nurse care manager; (2) training and technical assistance for nurse care managers; and (3) 3 or more PC clinicians agreeing to prescribe buprenorphine.
    Main outcomes and measures: The primary outcome was a clinic-level measure of patient-years of OUD treatment (buprenorphine or extended-release injectable naltrexone) per 10 000 PC patients during the 2 years postrandomization (follow-up). The secondary outcome, among patients with OUD prerandomization, was a patient-level measure of the number of days of acute care utilization during follow-up.
    Results: During the baseline period, a total of 130 623 patients were seen in intervention clinics (mean [SD] age, 48.6 [17.7] years; 59.7% female), and 159 459 patients were seen in UC clinics (mean [SD] age, 47.2 [17.5] years; 63.0% female). Intervention clinics provided 8.2 (95% CI, 5.4-∞) more patient-years of OUD treatment per 10 000 PC patients compared with UC clinics (P = .002). Most of the benefit accrued in 2 health systems and in patients new to clinics (5.8 [95% CI, 1.3-∞] more patient-years) or newly treated for OUD postrandomization (8.3 [95% CI, 4.3-∞] more patient-years). Qualitative data indicated that keys to successful implementation included broad commitment to treat OUD in PC from system leaders and PC teams, full financial coverage for OUD treatment, and straightforward pathways for patients to access nurse care managers. Acute care utilization did not differ between intervention and UC clinics (relative rate, 1.16; 95% CI, 0.47-2.92; P = .70).
    Conclusions and relevance: The PROUD cluster randomized clinical trial intervention meaningfully increased PC OUD treatment, albeit unevenly across health systems; however, it did not decrease acute care utilization among patients with OUD.
    Trial registration: ClinicalTrials.gov Identifier: NCT03407638.
    MeSH term(s) Humans ; Female ; Middle Aged ; Adolescent ; Young Adult ; Adult ; Aged ; Aged, 80 and over ; Male ; Naltrexone/therapeutic use ; Opiate Substitution Treatment/methods ; Leadership ; Opioid-Related Disorders/drug therapy ; Buprenorphine/therapeutic use
    Chemical Substances Naltrexone (5S6W795CQM) ; Buprenorphine (40D3SCR4GZ)
    Language English
    Publishing date 2023-10-30
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 2699338-7
    ISSN 2168-6114 ; 2168-6106
    ISSN (online) 2168-6114
    ISSN 2168-6106
    DOI 10.1001/jamainternmed.2023.5701
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Mass spectrometric identification of candidate RNA-binding proteins associated with Transition Nuclear Protein mRNA in the mouse testis

    Bart T. Phillips / Jason G. Williams / Dustin T. Atchley / Xiaojiang Xu / Jian-Liang Li / Andrea L. Adams / Katina L. Johnson / Traci M. Tanaka Hall

    Scientific Reports, Vol 9, Iss 1, Pp 1-

    2019  Volume 11

    Abstract: Abstract Spermatogenesis is a differentiation process that requires dramatic changes to DNA architecture, a process governed in part by Transition Nuclear Proteins 1 and 2 (TNP1 and TNP2). Translation of Tnp1 and Tnp2 mRNAs is temporally disengaged from ... ...

    Abstract Abstract Spermatogenesis is a differentiation process that requires dramatic changes to DNA architecture, a process governed in part by Transition Nuclear Proteins 1 and 2 (TNP1 and TNP2). Translation of Tnp1 and Tnp2 mRNAs is temporally disengaged from their transcription. We hypothesized that RNA regulatory proteins associate specifically with Tnp mRNAs to control the delayed timing of their translation. To identify potential regulatory proteins, we isolated endogenous mRNA/protein complexes from testis extract and identified by mass spectrometry proteins that associated with one or both Tnp transcripts. Five proteins showed strong association with Tnp transcripts but had low signal when Actin mRNA was isolated. We visualized the expression patterns in testis sections of the five proteins and found that each of the proteins was detected in germ cells at the appropriate stages to regulate Tnp RNA expression.
    Keywords Medicine ; R ; Science ; Q
    Language English
    Publishing date 2019-09-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: A small-molecule PI3Kα activator for cardioprotection and neuroregeneration.

    Gong, Grace Q / Bilanges, Benoit / Allsop, Ben / Masson, Glenn R / Roberton, Victoria / Askwith, Trevor / Oxenford, Sally / Madsen, Ralitsa R / Conduit, Sarah E / Bellini, Dom / Fitzek, Martina / Collier, Matt / Najam, Osman / He, Zhenhe / Wahab, Ben / McLaughlin, Stephen H / Chan, A W Edith / Feierberg, Isabella / Madin, Andrew /
    Morelli, Daniele / Bhamra, Amandeep / Vinciauskaite, Vanesa / Anderson, Karen E / Surinova, Silvia / Pinotsis, Nikos / Lopez-Guadamillas, Elena / Wilcox, Matthew / Hooper, Alice / Patel, Chandni / Whitehead, Maria A / Bunney, Tom D / Stephens, Len R / Hawkins, Phillip T / Katan, Matilda / Yellon, Derek M / Davidson, Sean M / Smith, David M / Phillips, James B / Angell, Richard / Williams, Roger L / Vanhaesebroeck, Bart

    Nature

    2023  Volume 618, Issue 7963, Page(s) 159–168

    Abstract: Harnessing the potential beneficial effects of kinase signalling through the generation of direct kinase activators remains an underexplored area of drug ... ...

    Abstract Harnessing the potential beneficial effects of kinase signalling through the generation of direct kinase activators remains an underexplored area of drug development
    MeSH term(s) Humans ; Neoplasms/drug therapy ; Nerve Regeneration/drug effects ; Protein Isoforms/agonists ; Signal Transduction/drug effects ; Class I Phosphatidylinositol 3-Kinases/chemistry ; Class I Phosphatidylinositol 3-Kinases/drug effects ; Cardiotonic Agents/pharmacology ; Animals ; Biocatalysis/drug effects ; Protein Conformation/drug effects ; Neurites/drug effects ; Reperfusion Injury/prevention & control ; Nerve Crush ; Cell Proliferation/drug effects
    Chemical Substances Protein Isoforms ; PIK3CA protein, human (EC 2.7.1.137) ; Class I Phosphatidylinositol 3-Kinases (EC 2.7.1.137) ; Cardiotonic Agents
    Language English
    Publishing date 2023-05-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 120714-3
    ISSN 1476-4687 ; 0028-0836
    ISSN (online) 1476-4687
    ISSN 0028-0836
    DOI 10.1038/s41586-023-05972-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Spermatogonial stem cell regulation and spermatogenesis.

    Phillips, Bart T / Gassei, Kathrin / Orwig, Kyle E

    Philosophical transactions of the Royal Society of London. Series B, Biological sciences

    2010  Volume 365, Issue 1546, Page(s) 1663–1678

    Abstract: This article will provide an updated review of spermatogonial stem cells and their role in maintaining the spermatogenic lineage. Experimental tools used to study spermatogonial stem cells (SSCs) will be described, along with research using these tools ... ...

    Abstract This article will provide an updated review of spermatogonial stem cells and their role in maintaining the spermatogenic lineage. Experimental tools used to study spermatogonial stem cells (SSCs) will be described, along with research using these tools to enhance our understanding of stem cell biology and spermatogenesis. Increased knowledge about the biology of SSCs improves our capacity to manipulate these cells for practical application. The chapter concludes with a discussion of future directions for fundamental investigation and practical applications of SSCs.
    MeSH term(s) Animals ; Cell Cycle/physiology ; Cell Growth Processes/physiology ; Cell Lineage/physiology ; Humans ; Male ; Spermatogenesis/physiology ; Spermatogonia/cytology ; Spermatogonia/physiology ; Stem Cells/cytology ; Stem Cells/physiology
    Language English
    Publishing date 2010-04-17
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 208382-6
    ISSN 1471-2970 ; 0080-4622 ; 0264-3839 ; 0962-8436
    ISSN (online) 1471-2970
    ISSN 0080-4622 ; 0264-3839 ; 0962-8436
    DOI 10.1098/rstb.2010.0026
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Germline stem cells: toward the regeneration of spermatogenesis.

    Valli, Hanna / Phillips, Bart T / Shetty, Gunapala / Byrne, James A / Clark, Amander T / Meistrich, Marvin L / Orwig, Kyle E

    Fertility and sterility

    2013  Volume 101, Issue 1, Page(s) 3–13

    Abstract: Improved therapies for cancer and other conditions have resulted in a growing population of long-term survivors. Infertility is an unfortunate side effect of some cancer therapies that impacts the quality of life of survivors who are in their ... ...

    Abstract Improved therapies for cancer and other conditions have resulted in a growing population of long-term survivors. Infertility is an unfortunate side effect of some cancer therapies that impacts the quality of life of survivors who are in their reproductive or prereproductive years. Some of these patients have the opportunity to preserve their fertility using standard technologies that include sperm, egg, or embryo banking, followed by IVF and/or ET. However, these options are not available to all patients, especially the prepubertal patients who are not yet producing mature gametes. For these patients, there are several stem cell technologies in the research pipeline that may give rise to new fertility options and allow infertile patients to have their own biological children. We will review the role of stem cells in normal spermatogenesis as well as experimental stem cell-based techniques that may have potential to generate or regenerate spermatogenesis and sperm. We will present these technologies in the context of the fertility preservation paradigm, but we anticipate that they will have broad implications for the assisted reproduction field.
    MeSH term(s) Adult Stem Cells/physiology ; Adult Stem Cells/transplantation ; Animals ; Female ; Germ Cells/physiology ; Germ Cells/transplantation ; Humans ; Male ; Regeneration/physiology ; Reproductive Techniques, Assisted/trends ; Spermatogenesis/physiology ; Spermatozoa/physiology ; Spermatozoa/transplantation
    Language English
    Publishing date 2013-12-05
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 80133-1
    ISSN 1556-5653 ; 0015-0282
    ISSN (online) 1556-5653
    ISSN 0015-0282
    DOI 10.1016/j.fertnstert.2013.10.052
    Database MEDical Literature Analysis and Retrieval System OnLINE

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