Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 9 of 9 entries
Sorted by: Best Match Show Resources per page
Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores.

Human genetics

Miyoshi T, Belyantseva IA, Kitajiri SI, Miyajima H, Nishio SY, Usami SI, Kim BJ, Choi BY, Omori K, Shroff H, Friedman TB.
PMID: 34232383
Hum Genet. 2021 Jul 07; doi: 10.1007/s00439-021-02304-0. Epub 2021 Jul 07.

Stereocilia protrude up to 100 µm from the apical surface of vertebrate inner ear hair cells and are packed with cross-linked filamentous actin (F-actin). They function as mechanical switches to convert sound vibration into electrochemical neuronal signals transmitted to...

Cite
Miyoshi T, Belyantseva IA, Kitajiri SI, et al. Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores. Hum Genet. 2021;doi: 10.1007/s00439-021-02304-0.
Miyoshi, T., Belyantseva, I. A., Kitajiri, S. I., Miyajima, H., Nishio, S. Y., Usami, S. I., Kim, B. J., Choi, B. Y., Omori, K., Shroff, H., & Friedman, T. B. (2021). Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores. Human genetics, . https://doi.org/10.1007/s00439-021-02304-0
Miyoshi, Takushi, et al. "Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores." Human genetics vol. (2021). doi: https://doi.org/10.1007/s00439-021-02304-0
Miyoshi T, Belyantseva IA, Kitajiri SI, Miyajima H, Nishio SY, Usami SI, Kim BJ, Choi BY, Omori K, Shroff H, Friedman TB. Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores. Hum Genet. 2021 Jul 07; doi: 10.1007/s00439-021-02304-0. Epub 2021 Jul 07. PMID: 34232383.
Copy Download .nbib Format: NLM
Variants of human CLDN9 cause mild to profound hearing loss.

Human mutation

Ramzan M, Philippe C, Belyantseva IA, Nakano Y, Fenollar-Ferrer C, Tona R, Yousaf R, Basheer R, Imtiaz A, Faridi R, Munir Z, Idrees H, Salman M, Nambot S, Vitobello A, Kartti S, Zarrik O, Witmer PD, Sobreria N, Ibrahimi A, Banfi B, Moutton S, Friedman TB, Naz S.
PMID: 34265170
Hum Mutat. 2021 Oct;42(10):1321-1335. doi: 10.1002/humu.24260. Epub 2021 Aug 01.

Hereditary deafness is clinically and genetically heterogeneous. We investigated deafness segregating as a recessive trait in two families. Audiological examinations revealed an asymmetric mild to profound hearing loss with childhood or adolescent onset. Exome sequencing of probands identified a...

Cite
Ramzan M, Philippe C, Belyantseva IA, et al. Variants of human CLDN9 cause mild to profound hearing loss. Hum Mutat. 2021;42(10):1321-1335doi: 10.1002/humu.24260.
Ramzan, M., Philippe, C., Belyantseva, I. A., Nakano, Y., Fenollar-Ferrer, C., Tona, R., Yousaf, R., Basheer, R., Imtiaz, A., Faridi, R., Munir, Z., Idrees, H., Salman, M., Nambot, S., Vitobello, A., Kartti, S., Zarrik, O., Witmer, P. D., Sobreria, N., Ibrahimi, A., Banfi, B., Moutton, S., Friedman, T. B., & Naz, S. (2021). Variants of human CLDN9 cause mild to profound hearing loss. Human mutation, 42(10), 1321-1335. https://doi.org/10.1002/humu.24260
Ramzan, Memoona, et al. "Variants of human CLDN9 cause mild to profound hearing loss." Human mutation vol. 42,10 (2021): 1321-1335. doi: https://doi.org/10.1002/humu.24260
Ramzan M, Philippe C, Belyantseva IA, Nakano Y, Fenollar-Ferrer C, Tona R, Yousaf R, Basheer R, Imtiaz A, Faridi R, Munir Z, Idrees H, Salman M, Nambot S, Vitobello A, Kartti S, Zarrik O, Witmer PD, Sobreria N, Ibrahimi A, Banfi B, Moutton S, Friedman TB, Naz S. Variants of human CLDN9 cause mild to profound hearing loss. Hum Mutat. 2021 Oct;42(10):1321-1335. doi: 10.1002/humu.24260. Epub 2021 Aug 01. PMID: 34265170; PMCID: PMC8435009.
Copy Download .nbib Format: NLM
Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin.

Current biology : CB

McGrath J, Tung CY, Liao X, Belyantseva IA, Roy P, Chakraborty O, Li J, Berbari NF, Faaborg-Andersen CC, Barzik M, Bird JE, Zhao B, Balakrishnan L, Friedman TB, Perrin BJ.
PMID: 33400922
Curr Biol. 2021 Mar 22;31(6):1141-1153.e7. doi: 10.1016/j.cub.2020.12.006. Epub 2021 Jan 04.

Stereocilia on auditory sensory cells are actin-based protrusions that mechanotransduce sound into an electrical signal. These stereocilia are arranged into a bundle with three rows of increasing length to form a staircase-like morphology that is required for hearing. Stereocilia...

Cite
McGrath J, Tung CY, Liao X, et al. Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin. Curr Biol. 2021;31(6):1141-1153.e7doi: 10.1016/j.cub.2020.12.006.
McGrath, J., Tung, C. Y., Liao, X., Belyantseva, I. A., Roy, P., Chakraborty, O., Li, J., Berbari, N. F., Faaborg-Andersen, C. C., Barzik, M., Bird, J. E., Zhao, B., Balakrishnan, L., Friedman, T. B., & Perrin, B. J. (2021). Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin. Current biology : CB, 31(6), 1141-1153.e7. https://doi.org/10.1016/j.cub.2020.12.006
McGrath, Jamis, et al. "Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin." Current biology : CB vol. 31,6 (2021): 1141-1153.e7. doi: https://doi.org/10.1016/j.cub.2020.12.006
McGrath J, Tung CY, Liao X, Belyantseva IA, Roy P, Chakraborty O, Li J, Berbari NF, Faaborg-Andersen CC, Barzik M, Bird JE, Zhao B, Balakrishnan L, Friedman TB, Perrin BJ. Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin. Curr Biol. 2021 Mar 22;31(6):1141-1153.e7. doi: 10.1016/j.cub.2020.12.006. Epub 2021 Jan 04. PMID: 33400922.
Copy Download .nbib Format: NLM
'Candidatus Chloroploca mongolica' sp. nov. a new mesophilic filamentous anoxygenic phototrophic bacterium.

FEMS microbiology letters

Bryantseva IA, Grouzdev DS, Krutkina MS, Ashikhmin AA, Kostrikina NA, Koziaeva VV, Gorlenko VM.
PMID: 34390245
FEMS Microbiol Lett. 2021 Aug 26;368(16). doi: 10.1093/femsle/fnab107.

A mesophilic filamentous anoxygenic phototrophic bacterium, designated M50-1, was isolated from a microbial mat of the Chukhyn Nur soda lake (northeastern Mongolia) with salinity of 5-14 g/L and pH 8.0-9.3. The organism is a strictly anaerobic phototrophic bacterium, which...

Cite
Bryantseva IA, Grouzdev DS, Krutkina MS, et al. 'Candidatus Chloroploca mongolica' sp. nov. a new mesophilic filamentous anoxygenic phototrophic bacterium. FEMS Microbiol Lett. 2021;368(16)doi: 10.1093/femsle/fnab107.
Bryantseva, I. A., Grouzdev, D. S., Krutkina, M. S., Ashikhmin, A. A., Kostrikina, N. A., Koziaeva, V. V., & Gorlenko, V. M. (2021). 'Candidatus Chloroploca mongolica' sp. nov. a new mesophilic filamentous anoxygenic phototrophic bacterium. FEMS microbiology letters, 368(16), . https://doi.org/10.1093/femsle/fnab107
Bryantseva, Irina A, et al. "'Candidatus Chloroploca mongolica' sp. nov. a new mesophilic filamentous anoxygenic phototrophic bacterium." FEMS microbiology letters vol. 368,16 (2021). doi: https://doi.org/10.1093/femsle/fnab107
Bryantseva IA, Grouzdev DS, Krutkina MS, Ashikhmin AA, Kostrikina NA, Koziaeva VV, Gorlenko VM. 'Candidatus Chloroploca mongolica' sp. nov. a new mesophilic filamentous anoxygenic phototrophic bacterium. FEMS Microbiol Lett. 2021 Aug 26;368(16). doi: 10.1093/femsle/fnab107. PMID: 34390245.
Copy Download .nbib Format: NLM
Genome Sequence of .

Microbiology resource announcements

Grouzdev DS, Gaisin VA, Krutkina MS, Bryantseva IA, Lunina ON, Savvichev AS, Gorlenko VM.
PMID: 30533845
Microbiol Resour Announc. 2018 Nov 29;7(21). doi: 10.1128/MRA.01415-18. eCollection 2018 Nov.

Draft genome sequences of green-colored and brown-colored green sulfur bacteria (GSB),

Cite
Grouzdev DS, Gaisin VA, Krutkina MS, et al. Genome Sequence of . Microbiol Resour Announc. 2018;7(21)doi: 10.1128/MRA.01415-18.
Grouzdev, D. S., Gaisin, V. A., Krutkina, M. S., Bryantseva, I. A., Lunina, O. N., Savvichev, A. S., & Gorlenko, V. M. (2018). Genome Sequence of . Microbiology resource announcements, 7(21), . https://doi.org/10.1128/MRA.01415-18
Grouzdev, Denis S, et al. "Genome Sequence of ." Microbiology resource announcements vol. 7,21 (2018). doi: https://doi.org/10.1128/MRA.01415-18
Grouzdev DS, Gaisin VA, Krutkina MS, Bryantseva IA, Lunina ON, Savvichev AS, Gorlenko VM. Genome Sequence of . Microbiol Resour Announc. 2018 Nov 29;7(21). doi: 10.1128/MRA.01415-18. eCollection 2018 Nov. PMID: 30533845; PMCID: PMC6284733.
Copy Download .nbib Format: NLM
Heliorestis daurensis, gen. nov. Sp. Nov., An alkaliphilic rod-to-coiled-shaped phototrophic heliobacterium from a siberian soda lake .

Archives of microbiology

Bryantseva IA, Gorlenko VM, Kompantseva EI, Achenbach LA, Madigan MT.
PMID: 10460887
Arch Microbiol. 1999 Sep;172(3):167-74. doi: 10.1007/s002030050756.

A novel alkaliphilic heliobacterium was isolated from microbial mats of a low-salt alkaline Siberian soda lake. Cells of the new organism were tightly coiled when grown in coculture with a rod-shaped bacterium, but grew as short filaments when finally...

Cite
Bryantseva IA, Gorlenko VM, Kompantseva EI, et al. Heliorestis daurensis, gen. nov. Sp. Nov., An alkaliphilic rod-to-coiled-shaped phototrophic heliobacterium from a siberian soda lake . Arch Microbiol. 1999;172(3):167-74doi: 10.1007/s002030050756.
Bryantseva, I. A., Gorlenko, V. M., Kompantseva, E. I., Achenbach, L. A., & Madigan, M. T. (1999). Heliorestis daurensis, gen. nov. Sp. Nov., An alkaliphilic rod-to-coiled-shaped phototrophic heliobacterium from a siberian soda lake . Archives of microbiology, 172(3), 167-74. https://doi.org/10.1007/s002030050756
Bryantseva, et al. "Heliorestis daurensis, gen. nov. Sp. Nov., An alkaliphilic rod-to-coiled-shaped phototrophic heliobacterium from a siberian soda lake ." Archives of microbiology vol. 172,3 (1999): 167-74. doi: https://doi.org/10.1007/s002030050756
Bryantseva IA, Gorlenko VM, Kompantseva EI, Achenbach LA, Madigan MT. Heliorestis daurensis, gen. nov. Sp. Nov., An alkaliphilic rod-to-coiled-shaped phototrophic heliobacterium from a siberian soda lake . Arch Microbiol. 1999 Sep;172(3):167-74. doi: 10.1007/s002030050756. PMID: 10460887.
Copy Download .nbib Format: NLM
Draft genome sequences of '.

Standards in genomic sciences

Grouzdev DS, Rysina MS, Bryantseva IA, Gorlenko VM, Gaisin VA.
PMID: 30338027
Stand Genomic Sci. 2018 Oct 11;13:24. doi: 10.1186/s40793-018-0329-8. eCollection 2018.

'

Cite
Grouzdev DS, Rysina MS, Bryantseva IA, et al. Draft genome sequences of '. Stand Genomic Sci. 2018;13:24doi: 10.1186/s40793-018-0329-8.
Grouzdev, D. S., Rysina, M. S., Bryantseva, I. A., Gorlenko, V. M., & Gaisin, V. A. (2018). Draft genome sequences of '. Standards in genomic sciences, 1324. https://doi.org/10.1186/s40793-018-0329-8
Grouzdev, Denis S, et al. "Draft genome sequences of '." Standards in genomic sciences vol. 13 (2018): 24. doi: https://doi.org/10.1186/s40793-018-0329-8
Grouzdev DS, Rysina MS, Bryantseva IA, Gorlenko VM, Gaisin VA. Draft genome sequences of '. Stand Genomic Sci. 2018 Oct 11;13:24. doi: 10.1186/s40793-018-0329-8. eCollection 2018. PMID: 30338027; PMCID: PMC6180586.
Copy Download .nbib Format: NLM
Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma cultures.

Cell reports

Miyoshi T, Zhang Q, Miyake T, Watanabe S, Ohnishi H, Chen J, Vishwasrao HD, Chakraborty O, Belyantseva IA, Perrin BJ, Shroff H, Friedman TB, Omori K, Watanabe N.
PMID: 33535030
Cell Rep. 2021 Feb 02;34(5):108708. doi: 10.1016/j.celrep.2021.108708.

Fast-dissociating, specific antibodies are single-molecule imaging probes that transiently interact with their targets and are used in biological applications including image reconstruction by integrating exchangeable single-molecule localization (IRIS), a multiplexable super-resolution microscopy technique. Here, we introduce a semi-automated screen...

Cite
Miyoshi T, Zhang Q, Miyake T, et al. Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma cultures. Cell Rep. 2021;34(5):108708doi: 10.1016/j.celrep.2021.108708.
Miyoshi, T., Zhang, Q., Miyake, T., Watanabe, S., Ohnishi, H., Chen, J., Vishwasrao, H. D., Chakraborty, O., Belyantseva, I. A., Perrin, B. J., Shroff, H., Friedman, T. B., Omori, K., & Watanabe, N. (2021). Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma cultures. Cell reports, 34(5), 108708. https://doi.org/10.1016/j.celrep.2021.108708
Miyoshi, Takushi, et al. "Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma cultures." Cell reports vol. 34,5 (2021): 108708. doi: https://doi.org/10.1016/j.celrep.2021.108708
Miyoshi T, Zhang Q, Miyake T, Watanabe S, Ohnishi H, Chen J, Vishwasrao HD, Chakraborty O, Belyantseva IA, Perrin BJ, Shroff H, Friedman TB, Omori K, Watanabe N. Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma cultures. Cell Rep. 2021 Feb 02;34(5):108708. doi: 10.1016/j.celrep.2021.108708. PMID: 33535030; PMCID: PMC7904085.
Copy Download .nbib Format: NLM
Variants of human CLDN9 cause mild to profound hearing loss.

Human mutation

Ramzan M, Philippe C, Belyantseva IA, Nakano Y, Fenollar-Ferrer C, Tona R, Yousaf R, Basheer R, Imtiaz A, Faridi R, Munir Z, Idrees H, Salman M, Nambot S, Vitobello A, Kartti S, Zarrik O, Witmer PD, Sobreria N, Ibrahimi A, Banfi B, Moutton S, Friedman TB, Naz S.
PMID: 34265170
Hum Mutat. 2021 Oct;42(10):1321-1335. doi: 10.1002/humu.24260. Epub 2021 Aug 01.

Hereditary deafness is clinically and genetically heterogeneous. We investigated deafness segregating as a recessive trait in two families. Audiological examinations revealed an asymmetric mild to profound hearing loss with childhood or adolescent onset. Exome sequencing of probands identified a...

Cite
Ramzan M, Philippe C, Belyantseva IA, et al. Variants of human CLDN9 cause mild to profound hearing loss. Hum Mutat. 2021;42(10):1321-1335doi: 10.1002/humu.24260.
Ramzan, M., Philippe, C., Belyantseva, I. A., Nakano, Y., Fenollar-Ferrer, C., Tona, R., Yousaf, R., Basheer, R., Imtiaz, A., Faridi, R., Munir, Z., Idrees, H., Salman, M., Nambot, S., Vitobello, A., Kartti, S., Zarrik, O., Witmer, P. D., Sobreria, N., Ibrahimi, A., Banfi, B., Moutton, S., Friedman, T. B., & Naz, S. (2021). Variants of human CLDN9 cause mild to profound hearing loss. Human mutation, 42(10), 1321-1335. https://doi.org/10.1002/humu.24260
Ramzan, Memoona, et al. "Variants of human CLDN9 cause mild to profound hearing loss." Human mutation vol. 42,10 (2021): 1321-1335. doi: https://doi.org/10.1002/humu.24260
Ramzan M, Philippe C, Belyantseva IA, Nakano Y, Fenollar-Ferrer C, Tona R, Yousaf R, Basheer R, Imtiaz A, Faridi R, Munir Z, Idrees H, Salman M, Nambot S, Vitobello A, Kartti S, Zarrik O, Witmer PD, Sobreria N, Ibrahimi A, Banfi B, Moutton S, Friedman TB, Naz S. Variants of human CLDN9 cause mild to profound hearing loss. Hum Mutat. 2021 Oct;42(10):1321-1335. doi: 10.1002/humu.24260. Epub 2021 Aug 01. PMID: 34265170; PMCID: PMC8435009.
Copy Download .nbib Format: NLM
Showing 1 to 9 of 9 entries