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Stem Cell Reports
|
April 23, 2021
Reprogramming epiblast stem cells into pre-implantation blastocyst cell-like cells
Kiichiro Tomoda, Haiming Hu, Yoshiki Sahara, et al.
Biochemical and Biophysical Research Communications
|
July 3, 2008
Trb2, a mouse homolog of tribbles, is dispensable for kidney and mouse development
Minoru Takasato, Chiyoko Kobayashi, Koji Okabayashi, et al.
The International Journal of Developmental Biology
|
July 23, 2013
Induction of intermediate mesoderm by retinoic acid receptor signaling from differentiating mouse embryonic stem cells
Shiho Oeda, Yohei Hayashi, Techuan Chan, et al.
Journal of the American Society of Nephrology : JASN
|
June 15, 2013
Direct transcriptional reprogramming of adult cells to embryonic nephron progenitors
Caroline E Hendry, Jessica M Vanslambrouck, Jessica Ineson, et al.
Communications Biology
|
May 4, 2023
Cells sorted off hiPSC-derived kidney organoids coupled with immortalized cells reliably model the proximal tubule
Ramin Banan Sadeghian, Ryohei Ueno, Yuji Takata, et al.
Iscience
|
September 17, 2024
Efficient proximal tubule-on-chip model from hiPSC-derived kidney organoids for functional analysis of renal transporters
Cheng Ma, Ramin Banan Sadeghian, Ryosuke Negoro, et al.
STAR Protocols
|
April 23, 2025
Protocol to develop a proximal tubule-on-chip model based on hiPSC-derived kidney organoids for functional analysis of renal transporters
Cheng Ma, Ramin Banan Sadeghian, Ryosuke Negoro, et al.
Mechanisms of Development
|
June 3, 2004
Identification of kidney mesenchymal genes by a combination of microarray analysis and Sall1-GFP knockin mice
Minoru Takasato, Kenji Osafune, Yuko Matsumoto, et al.
Kidney Research and Clinical Practice
|
November 20, 2020
Genetic background, recent advances in molecular biology, and development of novel therapy in Alport syndrome
Kandai Nozu, Yutaka Takaoka, Hirofumi Kai, et al.
Development (Cambridge, England)
|
June 23, 2006
The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development
Masayo Sakaki-Yumoto, Chiyoko Kobayashi, Akira Sato, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 44) with videos related to
Sort By:
Page
of 5
Stem Cell Reports
|
April 23, 2021
Reprogramming epiblast stem cells into pre-implantation blastocyst cell-like cells
Kiichiro Tomoda, Haiming Hu, Yoshiki Sahara, et al.
Biochemical and Biophysical Research Communications
|
July 3, 2008
Trb2, a mouse homolog of tribbles, is dispensable for kidney and mouse development
Minoru Takasato, Chiyoko Kobayashi, Koji Okabayashi, et al.
The International Journal of Developmental Biology
|
July 23, 2013
Induction of intermediate mesoderm by retinoic acid receptor signaling from differentiating mouse embryonic stem cells
Shiho Oeda, Yohei Hayashi, Techuan Chan, et al.
Journal of the American Society of Nephrology : JASN
|
June 15, 2013
Direct transcriptional reprogramming of adult cells to embryonic nephron progenitors
Caroline E Hendry, Jessica M Vanslambrouck, Jessica Ineson, et al.
Communications Biology
|
May 4, 2023
Cells sorted off hiPSC-derived kidney organoids coupled with immortalized cells reliably model the proximal tubule
Ramin Banan Sadeghian, Ryohei Ueno, Yuji Takata, et al.
Iscience
|
September 17, 2024
Efficient proximal tubule-on-chip model from hiPSC-derived kidney organoids for functional analysis of renal transporters
Cheng Ma, Ramin Banan Sadeghian, Ryosuke Negoro, et al.
STAR Protocols
|
April 23, 2025
Protocol to develop a proximal tubule-on-chip model based on hiPSC-derived kidney organoids for functional analysis of renal transporters
Cheng Ma, Ramin Banan Sadeghian, Ryosuke Negoro, et al.
Mechanisms of Development
|
June 3, 2004
Identification of kidney mesenchymal genes by a combination of microarray analysis and Sall1-GFP knockin mice
Minoru Takasato, Kenji Osafune, Yuko Matsumoto, et al.
Kidney Research and Clinical Practice
|
November 20, 2020
Genetic background, recent advances in molecular biology, and development of novel therapy in Alport syndrome
Kandai Nozu, Yutaka Takaoka, Hirofumi Kai, et al.
Development (Cambridge, England)
|
June 23, 2006
The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development
Masayo Sakaki-Yumoto, Chiyoko Kobayashi, Akira Sato, et al.
Page
of 5