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Correction to: Laminin-derived Ile-Lys-Val-ala-Val: a promising bioactive peptide in neural tissue engineering in traumatic brain injury.

Cell and tissue research

Negah SS, Khooei A, Samini F, Gorji A.
PMID: 29159484
Cell Tissue Res. 2018 Feb;371(2):379-381. doi: 10.1007/s00441-017-2739-0.

There is only one problem with Table 3. The references mentioned in this table were wrong in the final proof.

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Negah SS, Khooei A, Samini F, et al. Correction to: Laminin-derived Ile-Lys-Val-ala-Val: a promising bioactive peptide in neural tissue engineering in traumatic brain injury. Cell Tissue Res. 2018;371(2):379-381doi: 10.1007/s00441-017-2739-0.
Negah, S. S., Khooei, A., Samini, F., & Gorji, A. (2018). Correction to: Laminin-derived Ile-Lys-Val-ala-Val: a promising bioactive peptide in neural tissue engineering in traumatic brain injury. Cell and tissue research, 371(2), 379-381. https://doi.org/10.1007/s00441-017-2739-0
Negah, Sajad Sahab, et al. "Correction to: Laminin-derived Ile-Lys-Val-ala-Val: a promising bioactive peptide in neural tissue engineering in traumatic brain injury." Cell and tissue research vol. 371,2 (2018): 379-381. doi: https://doi.org/10.1007/s00441-017-2739-0
Negah SS, Khooei A, Samini F, Gorji A. Correction to: Laminin-derived Ile-Lys-Val-ala-Val: a promising bioactive peptide in neural tissue engineering in traumatic brain injury. Cell Tissue Res. 2018 Feb;371(2):379-381. doi: 10.1007/s00441-017-2739-0. PMID: 29159484.
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Decellularization of kidney tissue: comparison of sodium lauryl ether sulfate and sodium dodecyl sulfate for allotransplantation in rat.

Cell and tissue research

Keshvari MA, Afshar A, Daneshi S, Khoradmehr A, Baghban M, Muhaddesi M, Behrouzi P, Miri MR, Azari H, Nabipour I, Shirazi R, Mahmudpour M, Tamadon A.
PMID: 34424397
Cell Tissue Res. 2021 Nov;386(2):365-378. doi: 10.1007/s00441-021-03517-5. Epub 2021 Aug 23.

An automatic decellularization device was developed to perfuse and decellularize male rats' kidneys using both sodium lauryl ether sulfate (SLES) and sodium dodecyl sulfate (SDS) and to compare their efficacy in kidney decellularization and post-transplantation angiogenesis. Kidneys were perfused...

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Keshvari MA, Afshar A, Daneshi S, et al. Decellularization of kidney tissue: comparison of sodium lauryl ether sulfate and sodium dodecyl sulfate for allotransplantation in rat. Cell Tissue Res. 2021;386(2):365-378doi: 10.1007/s00441-021-03517-5.
Keshvari, M. A., Afshar, A., Daneshi, S., Khoradmehr, A., Baghban, M., Muhaddesi, M., Behrouzi, P., Miri, M. R., Azari, H., Nabipour, I., Shirazi, R., Mahmudpour, M., & Tamadon, A. (2021). Decellularization of kidney tissue: comparison of sodium lauryl ether sulfate and sodium dodecyl sulfate for allotransplantation in rat. Cell and tissue research, 386(2), 365-378. https://doi.org/10.1007/s00441-021-03517-5
Keshvari, Mohammad Amin, et al. "Decellularization of kidney tissue: comparison of sodium lauryl ether sulfate and sodium dodecyl sulfate for allotransplantation in rat." Cell and tissue research vol. 386,2 (2021): 365-378. doi: https://doi.org/10.1007/s00441-021-03517-5
Keshvari MA, Afshar A, Daneshi S, Khoradmehr A, Baghban M, Muhaddesi M, Behrouzi P, Miri MR, Azari H, Nabipour I, Shirazi R, Mahmudpour M, Tamadon A. Decellularization of kidney tissue: comparison of sodium lauryl ether sulfate and sodium dodecyl sulfate for allotransplantation in rat. Cell Tissue Res. 2021 Nov;386(2):365-378. doi: 10.1007/s00441-021-03517-5. Epub 2021 Aug 23. PMID: 34424397.
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Mechanical stimuli-mediated modulation of bone cell function-implications for bone remodeling and angiogenesis.

Cell and tissue research

Liang W, Wu X, Dong Y, Chen X, Zhou P, Xu F.
PMID: 34665321
Cell Tissue Res. 2021 Dec;386(3):445-454. doi: 10.1007/s00441-021-03532-6. Epub 2021 Oct 19.

Bone remodeling, expressed as bone formation and turnover, is a complex and dynamic process closely related to its form and function. Different events, such as development, aging, and function, play a critical role in bone remodeling and metabolism. The...

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Liang W, Wu X, Dong Y, et al. Mechanical stimuli-mediated modulation of bone cell function-implications for bone remodeling and angiogenesis. Cell Tissue Res. 2021;386(3):445-454doi: 10.1007/s00441-021-03532-6.
Liang, W., Wu, X., Dong, Y., Chen, X., Zhou, P., & Xu, F. (2021). Mechanical stimuli-mediated modulation of bone cell function-implications for bone remodeling and angiogenesis. Cell and tissue research, 386(3), 445-454. https://doi.org/10.1007/s00441-021-03532-6
Liang, Wenqing, et al. "Mechanical stimuli-mediated modulation of bone cell function-implications for bone remodeling and angiogenesis." Cell and tissue research vol. 386,3 (2021): 445-454. doi: https://doi.org/10.1007/s00441-021-03532-6
Liang W, Wu X, Dong Y, Chen X, Zhou P, Xu F. Mechanical stimuli-mediated modulation of bone cell function-implications for bone remodeling and angiogenesis. Cell Tissue Res. 2021 Dec;386(3):445-454. doi: 10.1007/s00441-021-03532-6. Epub 2021 Oct 19. PMID: 34665321.
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A micro-CT-based standard brain atlas of the bumblebee.

Cell and tissue research

Rother L, Kraft N, Smith DB, El Jundi B, Gill RJ, Pfeiffer K.
PMID: 34181089
Cell Tissue Res. 2021 Oct;386(1):29-45. doi: 10.1007/s00441-021-03482-z. Epub 2021 Jun 28.

In recent years, bumblebees have become a prominent insect model organism for a variety of biological disciplines, particularly to investigate learning behaviors as well as visual performance. Understanding these behaviors and their underlying neurobiological principles requires a clear understanding...

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Rother L, Kraft N, Smith DB, et al. A micro-CT-based standard brain atlas of the bumblebee. Cell Tissue Res. 2021;386(1):29-45doi: 10.1007/s00441-021-03482-z.
Rother, L., Kraft, N., Smith, D. B., El Jundi, B., Gill, R. J., & Pfeiffer, K. (2021). A micro-CT-based standard brain atlas of the bumblebee. Cell and tissue research, 386(1), 29-45. https://doi.org/10.1007/s00441-021-03482-z
Rother, Lisa, et al. "A micro-CT-based standard brain atlas of the bumblebee." Cell and tissue research vol. 386,1 (2021): 29-45. doi: https://doi.org/10.1007/s00441-021-03482-z
Rother L, Kraft N, Smith DB, El Jundi B, Gill RJ, Pfeiffer K. A micro-CT-based standard brain atlas of the bumblebee. Cell Tissue Res. 2021 Oct;386(1):29-45. doi: 10.1007/s00441-021-03482-z. Epub 2021 Jun 28. PMID: 34181089; PMCID: PMC8526489.
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Epithelial-mesenchymal transition process during embryo implantation.

Cell and tissue research

Oghbaei F, Zarezadeh R, Jafari-Gharabaghlou D, Ranjbar M, Nouri M, Fattahi A, Imakawa K.
PMID: 35024964
Cell Tissue Res. 2022 Jan 13; doi: 10.1007/s00441-021-03574-w. Epub 2022 Jan 13.

The epithelial to mesenchymal transition (EMT) in endometrial epithelial and trophectoderm cells is essential for the progression of embryo implantation and its impairment could cause implantation failure. Therefore, EMT should be tightly regulated in both embryonic and endometrial cells...

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Oghbaei F, Zarezadeh R, Jafari-Gharabaghlou D, et al. Epithelial-mesenchymal transition process during embryo implantation. Cell Tissue Res. 2022;doi: 10.1007/s00441-021-03574-w.
Oghbaei, F., Zarezadeh, R., Jafari-Gharabaghlou, D., Ranjbar, M., Nouri, M., Fattahi, A., & Imakawa, K. (2022). Epithelial-mesenchymal transition process during embryo implantation. Cell and tissue research, . https://doi.org/10.1007/s00441-021-03574-w
Oghbaei, Farnaz, et al. "Epithelial-mesenchymal transition process during embryo implantation." Cell and tissue research vol. (2022). doi: https://doi.org/10.1007/s00441-021-03574-w
Oghbaei F, Zarezadeh R, Jafari-Gharabaghlou D, Ranjbar M, Nouri M, Fattahi A, Imakawa K. Epithelial-mesenchymal transition process during embryo implantation. Cell Tissue Res. 2022 Jan 13; doi: 10.1007/s00441-021-03574-w. Epub 2022 Jan 13. PMID: 35024964.
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LncRNA KCNQ1OT1 attenuates osteoarthritic chondrocyte dysfunction via the miR-218-5p/PIK3C2A axis.

Cell and tissue research

Liu Y, Zhao D, Wang X, Dong Y, Ding F.
PMID: 33783609
Cell Tissue Res. 2021 Jul;385(1):115-126. doi: 10.1007/s00441-021-03441-8. Epub 2021 Mar 30.

The occurrence of osteoarthritis is closely related to chondrocyte dysfunction caused by cellular inflammatory response and matrix degradation, which seriously affect the quality of life of patients. Therefore, this study aimed to investigate the role of potassium voltage-gated channel...

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Liu Y, Zhao D, Wang X, et al. LncRNA KCNQ1OT1 attenuates osteoarthritic chondrocyte dysfunction via the miR-218-5p/PIK3C2A axis. Cell Tissue Res. 2021;385(1):115-126doi: 10.1007/s00441-021-03441-8.
Liu, Y., Zhao, D., Wang, X., Dong, Y., & Ding, F. (2021). LncRNA KCNQ1OT1 attenuates osteoarthritic chondrocyte dysfunction via the miR-218-5p/PIK3C2A axis. Cell and tissue research, 385(1), 115-126. https://doi.org/10.1007/s00441-021-03441-8
Liu, Yijun, et al. "LncRNA KCNQ1OT1 attenuates osteoarthritic chondrocyte dysfunction via the miR-218-5p/PIK3C2A axis." Cell and tissue research vol. 385,1 (2021): 115-126. doi: https://doi.org/10.1007/s00441-021-03441-8
Liu Y, Zhao D, Wang X, Dong Y, Ding F. LncRNA KCNQ1OT1 attenuates osteoarthritic chondrocyte dysfunction via the miR-218-5p/PIK3C2A axis. Cell Tissue Res. 2021 Jul;385(1):115-126. doi: 10.1007/s00441-021-03441-8. Epub 2021 Mar 30. PMID: 33783609.
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Kidney organoid systems for studies of immune-mediated kidney diseases: challenges and opportunities.

Cell and tissue research

Stein MC, Braun F, Krebs CF, Bunders MJ.
PMID: 34309728
Cell Tissue Res. 2021 Aug;385(2):457-473. doi: 10.1007/s00441-021-03499-4. Epub 2021 Jul 26.

Acute and chronic kidney diseases are major contributors to morbidity and mortality in the global population. Many nephropathies are considered to be immune-mediated with dysregulated immune responses playing an important role in the pathogenesis. At present, targeted approaches for...

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Stein MC, Braun F, Krebs CF, et al. Kidney organoid systems for studies of immune-mediated kidney diseases: challenges and opportunities. Cell Tissue Res. 2021;385(2):457-473doi: 10.1007/s00441-021-03499-4.
Stein, M. C., Braun, F., Krebs, C. F., & Bunders, M. J. (2021). Kidney organoid systems for studies of immune-mediated kidney diseases: challenges and opportunities. Cell and tissue research, 385(2), 457-473. https://doi.org/10.1007/s00441-021-03499-4
Stein, Melissa C, et al. "Kidney organoid systems for studies of immune-mediated kidney diseases: challenges and opportunities." Cell and tissue research vol. 385,2 (2021): 457-473. doi: https://doi.org/10.1007/s00441-021-03499-4
Stein MC, Braun F, Krebs CF, Bunders MJ. Kidney organoid systems for studies of immune-mediated kidney diseases: challenges and opportunities. Cell Tissue Res. 2021 Aug;385(2):457-473. doi: 10.1007/s00441-021-03499-4. Epub 2021 Jul 26. PMID: 34309728; PMCID: PMC8310776.
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Ultrastructural evidence for transepithelial calcium transport in the anterior sternal epithelium of the terrestrial isopod Porcellio scaber (Crustacea) during the formation and resorption of CaCO3 deposits.

Cell and tissue research

Ziegler A.
PMID: 8662354
Cell Tissue Res. 1996 May 20;284(3):459-66. doi: 10.1007/s004410050606.

Before the molt, terrestrial isopods store large amounts of calcium carbonate between the epithelium and the old cuticle of the first four anterior sternites. In order to test whether the anterior sternal epithelium has specific structural differentiations indicative of...

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Ziegler A. Ultrastructural evidence for transepithelial calcium transport in the anterior sternal epithelium of the terrestrial isopod Porcellio scaber (Crustacea) during the formation and resorption of CaCO3 deposits. Cell Tissue Res. 1996;284(3):459-66doi: 10.1007/s004410050606.
Ziegler, A. (1996). Ultrastructural evidence for transepithelial calcium transport in the anterior sternal epithelium of the terrestrial isopod Porcellio scaber (Crustacea) during the formation and resorption of CaCO3 deposits. Cell and tissue research, 284(3), 459-66. https://doi.org/10.1007/s004410050606
Ziegler. "Ultrastructural evidence for transepithelial calcium transport in the anterior sternal epithelium of the terrestrial isopod Porcellio scaber (Crustacea) during the formation and resorption of CaCO3 deposits." Cell and tissue research vol. 284,3 (1996): 459-66. doi: https://doi.org/10.1007/s004410050606
Ziegler A. Ultrastructural evidence for transepithelial calcium transport in the anterior sternal epithelium of the terrestrial isopod Porcellio scaber (Crustacea) during the formation and resorption of CaCO3 deposits. Cell Tissue Res. 1996 May 20;284(3):459-66. doi: 10.1007/s004410050606. PMID: 8662354.
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Early inflammation precedes cardiac fibrosis and heart failure in desmoglein 2 murine model of arrhythmogenic cardiomyopathy.

Cell and tissue research

Ng KE, Delaney PJ, Thenet D, Murtough S, Webb CM, Zaman N, Tsisanova E, Mastroianni G, Walker SLM, Westaby JD, Pennington DJ, Pink R, Kelsell DP, Tinker A.
PMID: 34236518
Cell Tissue Res. 2021 Oct;386(1):79-98. doi: 10.1007/s00441-021-03488-7. Epub 2021 Jul 08.

The study of a desmoglein 2 murine model of arrhythmogenic cardiomyopathy revealed cardiac inflammation as a key early event leading to fibrosis. Arrhythmogenic cardiomyopathy (AC) is an inherited heart muscle disorder leading to ventricular arrhythmias and heart failure due...

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Ng KE, Delaney PJ, Thenet D, et al. Early inflammation precedes cardiac fibrosis and heart failure in desmoglein 2 murine model of arrhythmogenic cardiomyopathy. Cell Tissue Res. 2021;386(1):79-98doi: 10.1007/s00441-021-03488-7.
Ng, K. E., Delaney, P. J., Thenet, D., Murtough, S., Webb, C. M., Zaman, N., Tsisanova, E., Mastroianni, G., Walker, S. L. M., Westaby, J. D., Pennington, D. J., Pink, R., Kelsell, D. P., & Tinker, A. (2021). Early inflammation precedes cardiac fibrosis and heart failure in desmoglein 2 murine model of arrhythmogenic cardiomyopathy. Cell and tissue research, 386(1), 79-98. https://doi.org/10.1007/s00441-021-03488-7
Ng, K E, et al. "Early inflammation precedes cardiac fibrosis and heart failure in desmoglein 2 murine model of arrhythmogenic cardiomyopathy." Cell and tissue research vol. 386,1 (2021): 79-98. doi: https://doi.org/10.1007/s00441-021-03488-7
Ng KE, Delaney PJ, Thenet D, Murtough S, Webb CM, Zaman N, Tsisanova E, Mastroianni G, Walker SLM, Westaby JD, Pennington DJ, Pink R, Kelsell DP, Tinker A. Early inflammation precedes cardiac fibrosis and heart failure in desmoglein 2 murine model of arrhythmogenic cardiomyopathy. Cell Tissue Res. 2021 Oct;386(1):79-98. doi: 10.1007/s00441-021-03488-7. Epub 2021 Jul 08. PMID: 34236518; PMCID: PMC8526453.
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CXCL13 is expressed in a subpopulation of neuroendocrine cells in the murine trachea and lung.

Cell and tissue research

Mahmoud W, Perniss A, Poharkar K, Soultanova A, Pfeil U, Hoek A, Bhushan S, Hain T, Gärtner U, Kummer W.
PMID: 34762185
Cell Tissue Res. 2021 Nov 11; doi: 10.1007/s00441-021-03552-2. Epub 2021 Nov 11.

The conducting airways are lined by distinct cell types, comprising basal, secretory, ciliated, and rare cells, including ionocytes, solitary cholinergic chemosensory cells, and solitary and clustered (neuroepithelial bodies) neuroendocrine cells. Airway neuroendocrine cells are in clinical focus since they...

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Mahmoud W, Perniss A, Poharkar K, et al. CXCL13 is expressed in a subpopulation of neuroendocrine cells in the murine trachea and lung. Cell Tissue Res. 2021;doi: 10.1007/s00441-021-03552-2.
Mahmoud, W., Perniss, A., Poharkar, K., Soultanova, A., Pfeil, U., Hoek, A., Bhushan, S., Hain, T., Gärtner, U., & Kummer, W. (2021). CXCL13 is expressed in a subpopulation of neuroendocrine cells in the murine trachea and lung. Cell and tissue research, . https://doi.org/10.1007/s00441-021-03552-2
Mahmoud, Wafaa, et al. "CXCL13 is expressed in a subpopulation of neuroendocrine cells in the murine trachea and lung." Cell and tissue research vol. (2021). doi: https://doi.org/10.1007/s00441-021-03552-2
Mahmoud W, Perniss A, Poharkar K, Soultanova A, Pfeil U, Hoek A, Bhushan S, Hain T, Gärtner U, Kummer W. CXCL13 is expressed in a subpopulation of neuroendocrine cells in the murine trachea and lung. Cell Tissue Res. 2021 Nov 11; doi: 10.1007/s00441-021-03552-2. Epub 2021 Nov 11. PMID: 34762185.
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Expression of arylalkylamine n-acetyltransferase (AANAT) and acetylserotonin o-methyltransferase (ASMT) in the corpus luteum of pregnant sows and synthesis of melatonin in luteal cells.

Cell and tissue research

Zhang WL, Zhang ZL, Peng J, Yang ST, Chen JX, Wang CX, Tong DW.
PMID: 34816281
Cell Tissue Res. 2021 Nov 24; doi: 10.1007/s00441-021-03556-y. Epub 2021 Nov 24.

In vertebrates, melatonin is mainly synthesized from serotonin in the pineal gland. Many reports have documented that melatonin is also synthesized in the extra-pineal tissues, but the synthesis of melatonin in the corpus luteum (CL) of pregnant sows has...

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Zhang WL, Zhang ZL, Peng J, et al. Expression of arylalkylamine n-acetyltransferase (AANAT) and acetylserotonin o-methyltransferase (ASMT) in the corpus luteum of pregnant sows and synthesis of melatonin in luteal cells. Cell Tissue Res. 2021;doi: 10.1007/s00441-021-03556-y.
Zhang, W. L., Zhang, Z. L., Peng, J., Yang, S. T., Chen, J. X., Wang, C. X., & Tong, D. W. (2021). Expression of arylalkylamine n-acetyltransferase (AANAT) and acetylserotonin o-methyltransferase (ASMT) in the corpus luteum of pregnant sows and synthesis of melatonin in luteal cells. Cell and tissue research, . https://doi.org/10.1007/s00441-021-03556-y
Zhang, W L, et al. "Expression of arylalkylamine n-acetyltransferase (AANAT) and acetylserotonin o-methyltransferase (ASMT) in the corpus luteum of pregnant sows and synthesis of melatonin in luteal cells." Cell and tissue research vol. (2021). doi: https://doi.org/10.1007/s00441-021-03556-y
Zhang WL, Zhang ZL, Peng J, Yang ST, Chen JX, Wang CX, Tong DW. Expression of arylalkylamine n-acetyltransferase (AANAT) and acetylserotonin o-methyltransferase (ASMT) in the corpus luteum of pregnant sows and synthesis of melatonin in luteal cells. Cell Tissue Res. 2021 Nov 24; doi: 10.1007/s00441-021-03556-y. Epub 2021 Nov 24. PMID: 34816281.
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Human umbilical cord mesenchymal stem cells reconstruct the vaginal wall of ovariectomized Sprague-Dawley rats: implications for pelvic floor reconstruction.

Cell and tissue research

Mao M, Li Y, Zhang Y, Kang J, Zhu L.
PMID: 34264376
Cell Tissue Res. 2021 Dec;386(3):571-583. doi: 10.1007/s00441-021-03478-9. Epub 2021 Jul 15.

Vaginal structural defects are involved in pelvic organ prolapse (POP). We tested whether mesenchymal stem cell (MSC) therapy can repair the weakened vaginal wall of POP patients as a novel POP treatment. Ninety-six ovariectomized rats were divided into 4...

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Mao M, Li Y, Zhang Y, et al. Human umbilical cord mesenchymal stem cells reconstruct the vaginal wall of ovariectomized Sprague-Dawley rats: implications for pelvic floor reconstruction. Cell Tissue Res. 2021;386(3):571-583doi: 10.1007/s00441-021-03478-9.
Mao, M., Li, Y., Zhang, Y., Kang, J., & Zhu, L. (2021). Human umbilical cord mesenchymal stem cells reconstruct the vaginal wall of ovariectomized Sprague-Dawley rats: implications for pelvic floor reconstruction. Cell and tissue research, 386(3), 571-583. https://doi.org/10.1007/s00441-021-03478-9
Mao, Meng, et al. "Human umbilical cord mesenchymal stem cells reconstruct the vaginal wall of ovariectomized Sprague-Dawley rats: implications for pelvic floor reconstruction." Cell and tissue research vol. 386,3 (2021): 571-583. doi: https://doi.org/10.1007/s00441-021-03478-9
Mao M, Li Y, Zhang Y, Kang J, Zhu L. Human umbilical cord mesenchymal stem cells reconstruct the vaginal wall of ovariectomized Sprague-Dawley rats: implications for pelvic floor reconstruction. Cell Tissue Res. 2021 Dec;386(3):571-583. doi: 10.1007/s00441-021-03478-9. Epub 2021 Jul 15. PMID: 34264376.
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