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Select item 81287751.

Comparing development and regeneration in the submandibular gland highlights distinct mechanisms

Lemonia Chatzeli, Tathyane H. N. Teshima, Mohammad K. Hajihosseini, Marcia Gaete, Gordon B. Proctor, Abigail S. Tucker

J Anat. 2021 Jun; 238(6): 1371–1385. Published online 2021 Jan 16. doi: 10.1111/joa.13387

PMCID:: PMC8128775

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Nonproliferative and Proliferative Lesions of the Rat and Mouse Endocrine System

Annamaria Brändli-Baiocco, Emmanuelle Balme, Marc Bruder, Sundeep Chandra, Juergen Hellmann, Mark J. Hoenerhoff, Takahito Kambara, Christian Landes, Barbara Lenz, Mark Mense, Susanne Rittinghausen, Hiroshi Satoh, Frédéric Schorsch, Frank Seeliger, Takuji Tanaka, Minoru Tsuchitani, Zbigniew Wojcinski, Thomas J. Rosol

J Toxicol Pathol. 2018; 31(3 Suppl): 1S–95S. Published online 2018 Jul 28. doi: 10.1293/tox.31.1S

PMCID:: PMC6108091

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Select item 108131473.

Salivary Gland Bioengineering

Stephen C. Rose, Melinda Larsen, Yubing Xie, Susan T. Sharfstein

Bioengineering (Basel) 2024 Jan; 11(1): 28. Published online 2023 Dec 26. doi: 10.3390/bioengineering11010028

PMCID:: PMC10813147

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The intact parasympathetic nerve promotes submandibular gland regeneration through ductal cell proliferation

Xue Wang, Zhilin Li, Qi Shao, Chunmei Zhang, Jinsong Wang, Zhengxue Han, Songlin Wang, Lizheng Qin

Cell Prolif. 2021 Jul; 54(7): e13078. Published online 2021 Jun 7. doi: 10.1111/cpr.13078

PMCID:: PMC8249781

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Salivary gland function, development, and regeneration

Alejandro M. Chibly, Marit H. Aure, Vaishali N. Patel, Matthew P. Hoffman

Physiol Rev. 2022 Jul 1; 102(3): 1495–1552. Published online 2022 Mar 28. doi: 10.1152/physrev.00015.2021

PMCID:: PMC9126227

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Select item 109792886.

Cell type-specific transforming growth factor-β (TGF-β) signaling in the regulation of salivary gland fibrosis and regeneration

Kevin Muñoz Forti, Gary A. Weisman, Kimberly J. Jasmer

J Oral Biol Craniofac Res. 2024 May-Jun; 14(3): 257–272. Published online 2024 Mar 21. doi: 10.1016/j.jobcr.2024.03.005

PMCID:: PMC10979288

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Analysis of the Clinical Relevance of Histological Classification of Benign Epithelial Salivary Gland Tumours

Henrik Hellquist, António Paiva-Correia, Vincent Vander Poorten, Miquel Quer, Juan C. Hernandez-Prera, Simon Andreasen, Peter Zbären, Alena Skalova, Alessandra Rinaldo, Alfio Ferlito

Adv Ther. 2019; 36(8): 1950–1974. Published online 2019 Jun 17. doi: 10.1007/s12325-019-01007-3

PMCID:: PMC6822986

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Putative effect of chronic renal failure on granular convoluted tubule of submandibular gland in male rats: Immunohistochemical and ultrastructural study

Wafaa Yahia Alghonemy, Fatema Rashed, Mai Badreldin Helal

J Oral Biol Craniofac Res. 2024 Jan-Feb; 14(1): 8–16. Published online 2023 Dec 8. doi: 10.1016/j.jobcr.2023.11.004

PMCID:: PMC10755788

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Characterization of the Arion vulgaris pedal gland system

Sophie Greistorfer, Johannes Suppan, Norbert Cyran, Waltraud Klepal, Robert Farkas, Livia Rudoll, Janek von Byern

J Morphol. 2020 Sep; 281(9): 1059–1071. Published online 2020 Jul 10. doi: 10.1002/jmor.21231

PMCID:: PMC7496283

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Nonproliferative and Proliferative Lesions of the Gastrointestinal Tract, Pancreas and Salivary Glands of the Rat and Mouse

Thomas Nolte, Patricia Brander-Weber, Charles Dangler, Ulrich Deschl, Michael R. Elwell, Peter Greaves, Richard Hailey, Michael W. Leach, Arun R. Pandiri, Arlin Rogers, Cynthia C. Shackelford, Andrew Spencer, Takuji Tanaka, Jerrold M. Ward

J Toxicol Pathol. 2016; 29(1 Suppl): 1S–125S. Published online 2016 Feb 13. doi: 10.1293/tox.29.1S

PMCID:: PMC4765498

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Alx4 relays sequential FGF signaling to induce lacrimal gland morphogenesis

Ankur Garg, Mukesh Bansal, Noriko Gotoh, Gen-Sheng Feng, Jian Zhong, Fen Wang, Ariana Kariminejad, Steven Brooks, Xin Zhang

PLoS Genet. 2017 Oct; 13(10): e1007047. Published online 2017 Oct 13. doi: 10.1371/journal.pgen.1007047

PMCID:: PMC5656309

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International Harmonization of Nomenclature and Diagnostic Criteria (INHAND): Non-proliferative and Proliferative Lesions of the Non-human Primate (M. fascicularis)

Karyn Colman, Rachel N. Andrews, Hannah Atkins, Theresa Boulineau, Alys Bradley, Annamaria Braendli-Baiocco, Raffaella Capobianco, David Caudell, Mark Cline, Takuya Doi, Rainer Ernst, Eric van Esch, Jeffrey Everitt, Pierluigi Fant, Margarita M. Gruebbel, Lars Mecklenburg, Andew D. Miller, Kristen J. Nikula, Shigeru Satake, Julie Schwartz, Alok Sharma, Akihito Shimoi, Cécile Sobry, Ian Taylor, Vimala Vemireddi, Justin Vidal, Charles Wood, John L. Vahle

J Toxicol Pathol. 2021; 34(3 Suppl): 1S–182S. Published online 2021 Sep 28. doi: 10.1293/tox.34.1S

PMCID:: PMC8544165

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The long-term effects of multidrug immunosuppressive protocols based on calcineurin inhibitors and conversion to rapamycin on the morphology, apoptosis, and proliferation of rat salivary glands

Marta Grabowska, Karolina Kędzierska-Kapuza, Andrzej Kram, Kamil Gill, Leszek Teresiński, Olimpia Sipak, Małgorzata Piasecka

Pharmacol Rep. 2023; 75(5): 1240–1253. Published online 2023 Sep 2. doi: 10.1007/s43440-023-00521-0

PMCID:: PMC10539461

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Form and Function of the skin glands in the Himalayan newt Tylototriton verrucosus

Marion Wanninger, Thomas Schwaha, Egon Heiss

Zoological Lett. 2018; 4: 15. Published online 2018 Jun 13. doi: 10.1186/s40851-018-0095-x

PMCID:: PMC5998448

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International Harmonization of Nomenclature and Diagnostic Criteria (INHAND): Nonproliferative and Proliferative Lesions of the Rabbit

Alys E Bradley, Lyn Miller Wancket, Matthias Rinke, Margarita M Gruebbel, Brett H. Saladino, Kenneth Schafer, Osamu Katsuta, Begonya Garcia, Franck Chanut, Katherine Hughes, Keith Nelson, Lauren Himmel, Elizabeth McInnes, Adrienne Schucker, Kazuyuki Uchida

J Toxicol Pathol. 2021; 34(3 Suppl): 183S–292S. Published online 2021 Sep 28. doi: 10.1293/tox.34.183S

PMCID:: PMC8544166

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The evolving landscape of salivary gland tumors

Conor E. Steuer, Glenn J. Hanna, Kartik Viswanathan, James E. Bates, Azeem S. Kaka, Nicole C. Schmitt, Alan L. Ho, Nabil F. Saba

CA Cancer J Clin. Author manuscript; available in PMC 2024 Mar 29.

Published in final edited form as: CA Cancer J Clin. 2023 Nov-Dec; 73(6): 597–619. Published online 2023 Jul 25. doi: 10.3322/caac.21807

PMCID:: PMC10980170

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Structural and bio-functional assessment of the postaxillary gland in Nidirana pleuraden (Amphibia: Anura: Ranidae)

Yuzhou Gong, Yiwei Zeng, Puyang Zheng, Xun Liao, Feng Xie

Zoological Lett. 2020; 6: 7. Published online 2020 Jun 5. doi: 10.1186/s40851-020-00160-w

PMCID:: PMC7275488

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Select item 641174118.

Sweat gland organoids contribute to cutaneous wound healing and sweat gland regeneration

Jinmei Diao, Juan Liu, Shuyong Wang, Mingyang Chang, Xuan Wang, Baolin Guo, Qunfang Yu, Fang Yan, Yuxin Su, Yunfang Wang

Cell Death Dis. 2019 Mar; 10(3): 238. Published online 2019 Mar 11. doi: 10.1038/s41419-019-1485-5

PMCID:: PMC6411741

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Expression patterns of tight junction proteins in porcine major salivary glands: a comparison study with human and murine glands

Xue‐Ming Zhang, Yan Huang, Kuo Zhang, Ling‐Han Qu, Xin Cong, Jia‐Zeng Su, Li‐Ling Wu, Guang‐Yan Yu, Yan Zhang

J Anat. 2018 Aug; 233(2): 167–176. Published online 2018 May 31. doi: 10.1111/joa.12833

PMCID:: PMC6036931

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Select item 511273820.

RNA-seq based transcriptomic map reveals new insights into mouse salivary gland development and maturation

Christian Gluck, Sangwon Min, Akinsola Oyelakin, Kirsten Smalley, Satrajit Sinha, Rose-Anne Romano

BMC Genomics. 2016; 17: 923. Published online 2016 Nov 16. doi: 10.1186/s12864-016-3228-7

PMCID:: PMC5112738

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PMC Images search for granular gland

Figure 1.

Histopathological alterations of the submandibular gland post-irradiation. All submandibular gland tissues were removed on day 7 post-irradiation. (A) Histopathological structure of the control submandibular gland. (B) The irradiated submandibular gland. (C) The phenylephrine-pretreated submandibular gland. Acinar cells are indicated by (a), ductal cells by (d) and granular convoluted tubule cells by (g). Vacuolization of acinar cells (arrow), pyknotic nuclei (arrowhead) and lysis of entire acini and granular convoluted tubules (empty arrow) were shown in the irradiated submandibular gland and mild atrophy and degeneration were shown in the phenylephrine-pretreated submandibular gland. Sections were stained with hematoxylin and eosin (H&E). Light microscopy magnification is ×400.

Mechanism of the protective effect of phenylephrine pretreatment against irradiation-induced damage in the submandibular gland

Exp Ther Med. 2013 Mar;5(3):875-879.
Fig. 2

Case 3. Bilateral lacrimal gland masses on magnetic resonance imaging (A). Case 4. Left lacrimal gland mass on magnetic resonance imaging (B). Case 6. Bilateral lacrimal gland masses on magnetic resonance imaging (C) and weak uptake by bilateral lacrimal gland masses on whole-body 2-[¹⁸F]fluoro-2-deoxy-D-glucose positron emission tomography (FDG-PET) (D). Case 7. Right lacrimal gland mass on magnetic resonance imaging (E) and high uptake on FDG-PET by the right lacrimal gland mass (F). High uptake on FDG-PET by bilateral submandibular glands (arrow, G) and the pancreas (arrow, H). Case 8. Bilateral lacrimal gland masses on magnetic resonance imaging (I) and granular shadows in the lung field (J).

Follow-up with serum IgG4-monitoring in 8 patients with IgG4-related disease diagnosed by a lacrimal gland mass

J Clin Exp Hematop. 2021 Mar;61(1):10-21.
FIGURE 4

Arion vulgaris, scanning electron micrographs of the lateral gland types. In the freeze‐dried tissue samples, (a) three gland types could be observed, which correlate in view of its granular content with the gland types A1l, A3l, and A4l (see Figure for comparison). (b) The granules of gland type A1l are oval and appear sponge‐like. (c) Gland type A3l contains granules of different sizes, while (d) gland type A4l contains roundish, evenly sized granules. Scale bar in image a = 10 μm, in image b to c = 5 μm

Characterization of the Arion vulgaris pedal gland system

J Morphol. 2020 Sep;281(9):1059-1071.
Figure 3The application of common approaches designed to ameliorate non-specific fluorescence in situ hybridization (FISH) probe binding failed to inhibit hybridization to granular gland cells (Gc) and spirocysts (Sp).

Cy3 (A), Cy5-labelled NonEUB338 (B) and Atto 647-labelled Vib-GV (C) FISH probes all hybridized to spirocysts. Blocking solution also failed to prevent non-specific binding of oligonucleotide probes to granular gland cells (D). Scale bars represent 100 µm in (A)–(C) and 50 µm in (D). Abbreviations: Gc, granular gland cell; Sp, spirocysts; and Symb, Symbiodinium.

In situ visualization of bacterial populations in coral tissues: pitfalls and solutions

PeerJ. 2016;4:e2424.