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  1. AU="Grommen, Sylvia V H"
  2. AU="Asemani, Yahya"
  3. AU="Ketomäki, Tuomo"
  4. AU=Cavallini Giorgio
  5. AU="Saha, Aakash"
  6. AU="Noguchi, J"
  7. AU="Löhr, B."
  8. AU="Lokie, Kelsey B"

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  1. Artikel ; Online: The Role of PLAG1 in Mouse Brain Development and Neurogenesis.

    Gasperoni, Jemma G / Tran, Stephanie C / Grommen, Sylvia V H / De Groef, Bert / Dworkin, Sebastian

    Molecular neurobiology

    2024  

    Abstract: The pleomorphic adenoma gene 1 (Plag1) is a transcription factor involved in the regulation of growth and cellular proliferation. Here, we report the spatial distribution and functional implications of PLAG1 expression in the adult mouse brain. We ... ...

    Abstract The pleomorphic adenoma gene 1 (Plag1) is a transcription factor involved in the regulation of growth and cellular proliferation. Here, we report the spatial distribution and functional implications of PLAG1 expression in the adult mouse brain. We identified Plag1 promoter-dependent β-galactosidase expression in various brain structures, including the hippocampus, cortex, choroid plexus, subcommisural organ, ependymal cells lining the third ventricle, medial and lateral habenulae and amygdala. We noted striking spatial-restriction of PLAG1 within the cornu ammonis (CA1) region of the hippocampus and layer-specific cortical expression, with abundant expression noted in all layers except layer 5. Furthermore, our study delved into the role of PLAG1 in neurodevelopment, focusing on its impact on neural stem/progenitor cell proliferation. Loss of Plag1 resulted in reduced proliferation and decreased production of neocortical progenitors in vivo, although ex vivo neurosphere experiments revealed no cell-intrinsic defects in the proliferative or neurogenic capacity of Plag1-deficient neural progenitors. Lastly, we explored potential target genes of PLAG1 in the cortex, identifying that Neurogenin 2 (Ngn2) was significantly downregulated in Plag1-deficient mice. In summary, our study provides novel insights into the spatial distribution of PLAG1 expression in the adult mouse brain and its potential role in neurodevelopment. These findings expand our understanding of the functional significance of PLAG1 within the brain, with potential implications for neurodevelopmental disorders and therapeutic interventions.
    Sprache Englisch
    Erscheinungsdatum 2024-01-19
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 645020-9
    ISSN 1559-1182 ; 0893-7648
    ISSN (online) 1559-1182
    ISSN 0893-7648
    DOI 10.1007/s12035-024-03943-w
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: Crucial Convolution: Genetic and Molecular Mechanisms of Coiling during Epididymis Formation and Development in Embryogenesis

    Wong, Joanne / Gasperoni, Jemma / Fuller, Jarrad / Grommen, Sylvia V. H. / De Groef, Bert / Hogarth, Cathryn / Dworkin, Sebastian

    Journal of developmental biology. 2022 June 14, v. 10, no. 2

    2022  

    Abstract: As embryonic development proceeds, numerous organs need to coil, bend or fold in order to establish their final shape. Generally, this occurs so as to maximise the surface area for absorption or secretory functions (e.g., in the small and large ... ...

    Abstract As embryonic development proceeds, numerous organs need to coil, bend or fold in order to establish their final shape. Generally, this occurs so as to maximise the surface area for absorption or secretory functions (e.g., in the small and large intestines, kidney or epididymis); however, mechanisms of bending and shaping also occur in other structures, notably the midbrain–hindbrain boundary in some teleost fish models such as zebrafish. In this review, we will examine known genetic and molecular factors that operate to pattern complex, coiled structures, with a primary focus on the epididymis as an excellent model organ to examine coiling. We will also discuss genetic mechanisms involving coiling in the seminiferous tubules and intestine to establish the final form and function of these coiled structures in the mature organism.
    Schlagwörter Danio rerio ; absorption ; embryogenesis ; epididymis ; fish ; intestines ; kidneys ; surface area
    Sprache Englisch
    Erscheinungsverlauf 2022-0614
    Erscheinungsort Multidisciplinary Digital Publishing Institute
    Dokumenttyp Artikel
    ZDB-ID 2720870-9
    ISSN 2221-3759
    ISSN 2221-3759
    DOI 10.3390/jdb10020025
    Datenquelle NAL Katalog (AGRICOLA)

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  3. Artikel ; Online: An idea to explore: Genotyping bull sperm to introduce basic molecular biology techniques in an animal science course.

    De Groef, Bert / Grommen, Sylvia V H

    Biochemistry and molecular biology education : a bimonthly publication of the International Union of Biochemistry and Molecular Biology

    2019  Band 47, Heft 6, Seite(n) 708–711

    Abstract: The laboratory exercise described here aims to provide a relevant context for learning basic DNA techniques in an introductory animal science course at tertiary level. In two 4-hr laboratory sessions, students assess the suitability of bulls for ... ...

    Abstract The laboratory exercise described here aims to provide a relevant context for learning basic DNA techniques in an introductory animal science course at tertiary level. In two 4-hr laboratory sessions, students assess the suitability of bulls for inclusion in a gene-assisted selection program for A2 β-casein by genotyping commercial bull sperm. Sperm cells are lysed to extract the genomic DNA, and PCR with primers for the β-casein gene is performed. Using the principle of amplification-created restriction sites, restriction digestion with TaqI can be used to distinguish between the A1 allele and the A2 allele of the gene. Cut PCR amplicons are separated by gel electrophoresis to evaluate the genotype of each bull. Students then write a diagnostic report with accompanying letter to their fictional client, explaining the DNA test, and interpreting the results. © 2019 International Union of Biochemistry and Molecular Biology, 47(6):708-711, 2019.
    Mesh-Begriff(e) Animals ; Caseins/genetics ; Curriculum ; DNA/genetics ; Genotype ; Genotyping Techniques ; Humans ; Laboratories ; Learning ; Male ; Molecular Biology/education ; Molecular Biology/methods ; Science/education ; Spermatozoa/cytology ; Spermatozoa/metabolism ; Students
    Chemische Substanzen Caseins ; DNA (9007-49-2)
    Sprache Englisch
    Erscheinungsdatum 2019-08-30
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 1539-3429
    ISSN (online) 1539-3429
    DOI 10.1002/bmb.21297
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Thyrotropic activity of corticotropin-releasing hormone in an altricial bird species, the zebra finch (Taeniopygia guttata).

    Watanabe, Yugo / Grommen, Sylvia V H / De Groef, Bert

    General and comparative endocrinology

    2018  Band 258, Seite(n) 99–108

    Abstract: In chicken, corticotropin-releasing hormone (CRH) acts as a thyrotropin (TSH)-releasing factor, mediated by the type 2 CRH receptor (CRHR2) on the thyrotropes of the pituitary gland. It is not known whether CRH also controls TSH release in non-precocial ... ...

    Abstract In chicken, corticotropin-releasing hormone (CRH) acts as a thyrotropin (TSH)-releasing factor, mediated by the type 2 CRH receptor (CRHR2) on the thyrotropes of the pituitary gland. It is not known whether CRH also controls TSH release in non-precocial avian species that have a different pattern of thyroidal activity during their life cycle. Therefore, we investigated the TSH-releasing capacity of CRH in an altricial species, the zebra finch (Taeniopygia guttata). Cellular localisation of type 1 CRH receptor (CRHR1) and CRHR2 mRNA in the pituitary was determined by in situ hybridisation, combined with immunohistochemical staining of pituitary thyrotropes. In addition, isolated pituitary glands were stimulated with CRH to determine the effect on TSH release. Lastly, the mRNA levels of hormones and receptors involved in the control of thyroidal and adrenal function were measured by qPCR in zebra finch chicks between hatching and fledging, and in adults. Most of the hypophyseal CRHR2 mRNA co-localised with thyrotropes, whereas CRHR1 mRNA was found inbetween thyrotropes. Pituitary glands stimulated in vitro with CRH showed increased secretion of TSH-like activity. Pituitary CRHR2 mRNA expression decreased while pituitary TSHB mRNA and brain CRH mRNA levels increased towards fledging, similar as seen in chicken hatching. These results suggest that CRHR2 expressed on thyrotropes is likely mediating CRH-induced TSH release in altricial avian species like it does in precocial species, and that the increased thyroid hormone levels towards fledging in altricial birds are the result of increased hypothalamic stimulation, in which the thyrotropic activity of CRH may initially play a role.
    Mesh-Begriff(e) Amino Acid Sequence ; Animals ; Cloning, Molecular ; Corticotropin-Releasing Hormone/pharmacology ; Finches/metabolism ; Open Reading Frames/genetics ; Pituitary Gland/metabolism ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Receptors, Corticotropin-Releasing Hormone/chemistry ; Receptors, Corticotropin-Releasing Hormone/genetics ; Receptors, Corticotropin-Releasing Hormone/metabolism ; Thyrotropin/pharmacology ; Thyrotropin-Releasing Hormone/metabolism ; Thyroxine/pharmacology
    Chemische Substanzen CRF receptor type 1 ; CRF receptor type 2 ; RNA, Messenger ; Receptors, Corticotropin-Releasing Hormone ; Thyrotropin-Releasing Hormone (5Y5F15120W) ; Thyrotropin (9002-71-5) ; Corticotropin-Releasing Hormone (9015-71-8) ; Thyroxine (Q51BO43MG4)
    Sprache Englisch
    Erscheinungsdatum 2018--01
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1851-x
    ISSN 1095-6840 ; 0016-6480
    ISSN (online) 1095-6840
    ISSN 0016-6480
    DOI 10.1016/j.ygcen.2017.10.012
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Crucial Convolution: Genetic and Molecular Mechanisms of Coiling during Epididymis Formation and Development in Embryogenesis.

    Wong, Joanne / Gasperoni, Jemma / Fuller, Jarrad / Grommen, Sylvia V H / De Groef, Bert / Hogarth, Cathryn / Dworkin, Sebastian

    Journal of developmental biology

    2022  Band 10, Heft 2

    Abstract: As embryonic development proceeds, numerous organs need to coil, bend or fold in order to establish their final shape. Generally, this occurs so as to maximise the surface area for absorption or secretory functions (e.g., in the small and large ... ...

    Abstract As embryonic development proceeds, numerous organs need to coil, bend or fold in order to establish their final shape. Generally, this occurs so as to maximise the surface area for absorption or secretory functions (e.g., in the small and large intestines, kidney or epididymis); however, mechanisms of bending and shaping also occur in other structures, notably the midbrain-hindbrain boundary in some teleost fish models such as zebrafish. In this review, we will examine known genetic and molecular factors that operate to pattern complex, coiled structures, with a primary focus on the epididymis as an excellent model organ to examine coiling. We will also discuss genetic mechanisms involving coiling in the seminiferous tubules and intestine to establish the final form and function of these coiled structures in the mature organism.
    Sprache Englisch
    Erscheinungsdatum 2022-06-14
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article ; Review
    ZDB-ID 2720870-9
    ISSN 2221-3759 ; 2221-3759
    ISSN (online) 2221-3759
    ISSN 2221-3759
    DOI 10.3390/jdb10020025
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Effect of in ovo injection of corticotropin-releasing hormone on the timing of hatching in broiler chickens.

    Watanabe, Yugo / Grommen, Sylvia V H / De Groef, Bert

    Poultry science

    2017  Band 96, Heft 9, Seite(n) 3452–3456

    Abstract: In chicken embryos, intravenous injection of corticotropin-releasing hormone (CRH) causes the release of both corticosteroids and thyroid hormones. These hormones initiate and enhance the hatching process, raising the possibility that CRH treatment of ... ...

    Abstract In chicken embryos, intravenous injection of corticotropin-releasing hormone (CRH) causes the release of both corticosteroids and thyroid hormones. These hormones initiate and enhance the hatching process, raising the possibility that CRH treatment of the late chicken embryo could accelerate hatching and/or decrease the spread of hatching. We performed a series of exploratory tests to investigate whether in ovo delivery methods of CRH other than intravenous injection that are more practical in a commercial setting, affect hatching time in broilers. Corticotropin-releasing hormone was injected into the air cell, albumen, or amniotic fluid of broiler breeder eggs, in the last week of embryonic development. Average incubation duration was significantly decreased by 22 h when 2 μg of CRH was injected into the air cell on embryonic day 18 (E18) of Cobb eggs. Acceleration of hatching (but only by 8 h) was also seen for Ross chicks when CRH was injected daily into the albumen between E10 and E18. However, repeats of both experiments did not show consistent effects of CRH on hatching time; in most experiments performed, CRH did not affect hatching time. We speculate that the effectiveness of CRH uptake via these delivery methods and/or the duration and magnitude of the thyroxine and corticosterone response to CRH is not sufficient to have a substantial effect on hatching time. We therefore conclude that in ovo CRH treatment does not seem a feasible option as a practical tool to increase hatchery productivity or to investigate the effects of CRH agonists and antagonists on hatching.
    Mesh-Begriff(e) Animals ; Chick Embryo/drug effects ; Chick Embryo/growth & development ; Chickens/growth & development ; Corticotropin-Releasing Hormone/metabolism ; Embryonic Development ; Injections/veterinary ; Ovum/drug effects
    Chemische Substanzen Corticotropin-Releasing Hormone (9015-71-8)
    Sprache Englisch
    Erscheinungsdatum 2017-06-20
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 242586-5
    ISSN 1525-3171 ; 0032-5791
    ISSN (online) 1525-3171
    ISSN 0032-5791
    DOI 10.3382/ps/pex162
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: Forever young: Endocrinology of paedomorphosis in the Mexican axolotl (Ambystoma mexicanum).

    De Groef, Bert / Grommen, Sylvia V H / Darras, Veerle M

    General and comparative endocrinology

    2018  Band 266, Seite(n) 194–201

    Abstract: The Mexican axolotl (Ambystoma mexicanum) is a salamander species that does not undergo metamorphosis, resulting in the retention of juvenile characteristics in the mature breeding stage (paedomorphosis). Here we review the endocrinological studies ... ...

    Abstract The Mexican axolotl (Ambystoma mexicanum) is a salamander species that does not undergo metamorphosis, resulting in the retention of juvenile characteristics in the mature breeding stage (paedomorphosis). Here we review the endocrinological studies investigating the proximate cause of axolotl paedomorphosis with a focus on the hypothalamo-pituitary-thyroid (HPT) axis. It is well established that axolotl paedomorphosis is a consequence of low activity of the HPT axis. The pituitary hormone thyrotropin (TSH) is capable of inducing metamorphosis in the axolotl, which indicates that all processes and interactions in the HPT axis below the pituitary level are functional, but that TSH release is impaired. In metamorphosing species, TSH secretion is largely controlled by the hypothalamic neuropeptide corticotropin-releasing hormone (CRH), which seems to have lost its thyrotropic activity in the axolotl. However, preliminary experiments have not yet confirmed a role for faulty CRH signalling in axolotl paedomorphosis. Other hypothalamic factors and potential pituitary inhibitors need to be investigated to identify their roles in amphibian metamorphosis and axolotl paedomorphosis.
    Mesh-Begriff(e) Ambystoma mexicanum/physiology ; Animals ; Corticotropin-Releasing Hormone/pharmacology ; Endocrinology ; Metamorphosis, Biological/drug effects ; Signal Transduction/drug effects ; Thyrotropin/pharmacology ; Thyrotropin-Releasing Hormone/metabolism
    Chemische Substanzen Thyrotropin-Releasing Hormone (5Y5F15120W) ; Thyrotropin (9002-71-5) ; Corticotropin-Releasing Hormone (9015-71-8)
    Sprache Englisch
    Erscheinungsdatum 2018-05-16
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Review
    ZDB-ID 1851-x
    ISSN 1095-6840 ; 0016-6480
    ISSN (online) 1095-6840
    ISSN 0016-6480
    DOI 10.1016/j.ygcen.2018.05.016
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: Corticotropin-releasing hormone: Mediator of vertebrate life stage transitions?

    Watanabe, Yugo / Grommen, Sylvia V H / De Groef, Bert

    General and comparative endocrinology

    2016  Band 228, Seite(n) 60–68

    Abstract: Hormones, particularly thyroid hormones and corticosteroids, play critical roles in vertebrate life stage transitions such as amphibian metamorphosis, hatching in precocial birds, and smoltification in salmonids. Since they synergistically regulate ... ...

    Abstract Hormones, particularly thyroid hormones and corticosteroids, play critical roles in vertebrate life stage transitions such as amphibian metamorphosis, hatching in precocial birds, and smoltification in salmonids. Since they synergistically regulate several metabolic and developmental processes that accompany vertebrate life stage transitions, the existence of extensive cross-communication between the adrenal/interrenal and thyroidal axes is not surprising. Synergies of corticosteroids and thyroid hormones are based on effects at the level of tissue hormone sensitivity and gene regulation. In addition, in representative nonmammalian vertebrates, corticotropin-releasing hormone (CRH) stimulates hypophyseal thyrotropin secretion, and thus functions as a common regulator of both the adrenal/interrenal and thyroidal axes to release corticosteroids and thyroid hormones. The dual function of CRH has been speculated to control or affect the timing of vertebrate life history transitions across taxa. After a brief overview of recent insights in the molecular mechanisms behind the synergic actions of thyroid hormones and corticosteroids during life stage transitions, this review examines the evidence for a possible role of CRH in controlling vertebrate life stage transitions.
    Mesh-Begriff(e) Animals ; Corticotropin-Releasing Hormone/metabolism ; Metamorphosis, Biological/physiology ; Vertebrates/growth & development ; Vertebrates/metabolism
    Chemische Substanzen Corticotropin-Releasing Hormone (9015-71-8)
    Sprache Englisch
    Erscheinungsdatum 2016-03-01
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Review
    ZDB-ID 1851-x
    ISSN 1095-6840 ; 0016-6480
    ISSN (online) 1095-6840
    ISSN 0016-6480
    DOI 10.1016/j.ygcen.2016.02.012
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Transcriptional regulation of the chicken CRHR2 gene by pituitary transcription factors.

    Noy, Ellyse B / Watanabe, Yugo / Grommen, Sylvia V H / De Groef, Bert

    General and comparative endocrinology

    2019  Band 284, Seite(n) 113263

    Abstract: Corticotropin-releasing hormone (CRH) is known to act as a potent thyrotropin-releasing factor in non-mammalian species such as chicken and bullfrog. This interaction is mediated by type 2 CRH receptors (CRHR2) expressed by the thyrotropes in the ... ...

    Abstract Corticotropin-releasing hormone (CRH) is known to act as a potent thyrotropin-releasing factor in non-mammalian species such as chicken and bullfrog. This interaction is mediated by type 2 CRH receptors (CRHR2) expressed by the thyrotropes in the pituitary gland. However, the response elements (REs) and their corresponding transcription factors (TFs) that control CRHR2 expression in thyrotropes are not known. Since thyrotrope-specific expression of the β-subunit of thyrotropin is synergistically stimulated by the co-expression of POU1F1 and GATA2, we hypothesised that in non-mammalian vertebrates like chicken, CRHR2 expression is controlled by the same TFs and that their REs are present in the chicken CRHR2 gene promoter. In situ hybridisation and immunohistochemistry suggest that chicken thyrotropes, like those of mammals, express the mRNAs for the TFs GATA2, POU1F1 and PITX1, but not NR5A1. Using luciferase reporter assays, we show that both GATA2 and PITX1 can activate the promoter of CRHR2, but PITX1 requires a functional GATA2 RE to be present. POU1F1 alone did not affect promoter activity, but synergistically increased the effect of GATA2. Promoter deletion analysis and mutagenesis showed that essential GATA2 and PITX1 REs are located between 116 and 198 bp upstream of the start codon. These REs are highly conserved in non-mammalian species. Additionally, NR5A1 (steroidogenic factor 1) suppressed both GATA2- and PITX1-induced promoter activity and may therefore play a role in restricting CRHR2 expression in gonadotropes. We conclude that the expression of CRHR2 in chicken thyrotropes is stimulated by GATA2 with interactions with POU1F1 and PITX1, in the absence of NR5A1.
    Mesh-Begriff(e) Animals ; COS Cells ; Chickens/genetics ; Chlorocebus aethiops ; Conserved Sequence ; Evolution, Molecular ; Gene Expression Regulation ; Luciferases/metabolism ; Mutation/genetics ; Pituitary Gland/metabolism ; Promoter Regions, Genetic ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Receptors, Corticotropin-Releasing Hormone/genetics ; Response Elements/genetics ; Transcription Factors/genetics ; Transcription Factors/metabolism
    Chemische Substanzen CRF receptor type 2 ; RNA, Messenger ; Receptors, Corticotropin-Releasing Hormone ; Transcription Factors ; Luciferases (EC 1.13.12.-)
    Sprache Englisch
    Erscheinungsdatum 2019-08-24
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1851-x
    ISSN 1095-6840 ; 0016-6480
    ISSN (online) 1095-6840
    ISSN 0016-6480
    DOI 10.1016/j.ygcen.2019.113263
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Transcriptome analysis of the epididymis from Plag1 deficient mice suggests dysregulation of sperm maturation and extracellular matrix genes.

    Wong, Joanne / Damdimopoulos, Anastasios / Damdimopoulou, Pauliina / Gasperoni, Jemma G / Tran, Stephanie C / Grommen, Sylvia V H / De Groef, Bert / Dworkin, Sebastian

    Developmental dynamics : an official publication of the American Association of Anatomists

    2020  Band 249, Heft 12, Seite(n) 1500–1513

    Abstract: Background: The transcription factor pleomorphic adenoma gene 1 (PLAG1) is required for male fertility. Mice deficient in PLAG1 exhibit decreased sperm motility and abnormal epididymal tubule elongation and coiling, indicating impaired sperm maturation ... ...

    Abstract Background: The transcription factor pleomorphic adenoma gene 1 (PLAG1) is required for male fertility. Mice deficient in PLAG1 exhibit decreased sperm motility and abnormal epididymal tubule elongation and coiling, indicating impaired sperm maturation during epididymal transit. However, the downstream transcriptomic profile of the Plag1 knockout (KO; Plag1
    Results: In this study, the PLAG1-dependent epididymal transcriptome was characterised using RNA sequencing. Several genes important for the control of sperm maturation, motility, capacitation and the acrosome reaction were dysregulated in Plag1
    Conclusion: Together, these results suggest a defect in the epididymal extracellular matrix in Plag1
    Mesh-Begriff(e) Animals ; DNA-Binding Proteins/genetics ; DNA-Binding Proteins/metabolism ; Epididymis/metabolism ; Extracellular Matrix Proteins/genetics ; Extracellular Matrix Proteins/metabolism ; Gene Expression Profiling ; Male ; Mice ; Mice, Knockout ; Sperm Maturation/genetics ; Transcriptome
    Chemische Substanzen DNA-Binding Proteins ; Extracellular Matrix Proteins ; Plag1 protein, mouse
    Sprache Englisch
    Erscheinungsdatum 2020-10-06
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1102541-4
    ISSN 1097-0177 ; 1058-8388
    ISSN (online) 1097-0177
    ISSN 1058-8388
    DOI 10.1002/dvdy.254
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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