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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 2 |
2020 | 1 |
2023 | 1 |
2024 | 2 |
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Page 1
CD109 Attenuates Bleomycin-induced Pulmonary Fibrosis by Inhibiting TGF-β Signaling.
J Immunol. 2024 Apr 1;212(7):1221-1231. doi: 10.4049/jimmunol.2300285.
J Immunol. 2024.
PMID: 38334455
Novel compound heterozygous ATP1A2 variants in a patient with fetal akinesia/hypokinesia sequence.
Furukawa S, Kato M, Nomura T, Sumitomo N, Yoneno S, Nakashima M, Saitsu H.
Furukawa S, et al.
Am J Med Genet A. 2024 Mar;194(3):e63453. doi: 10.1002/ajmg.a.63453. Epub 2023 Oct 23.
Am J Med Genet A. 2024.
PMID: 37870493
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A case of early-onset epileptic encephalopathy with a homozygous TBC1D24 variant caused by uniparental isodisomy.
Nakashima M, Negishi Y, Hori I, Hattori A, Saitoh S, Saitsu H.
Nakashima M, et al.
Am J Med Genet A. 2019 Apr;179(4):645-649. doi: 10.1002/ajmg.a.61056. Epub 2019 Jan 24.
Am J Med Genet A. 2019.
PMID: 30680869
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Low-prevalence mosaicism of chromosome 18q distal deletion identified by exome-based copy number profiling in a child with cerebral hypomyelination.
Shiohama T, Nakashima M, Ikehara H, Kato M, Saitsu H.
Shiohama T, et al.
Congenit Anom (Kyoto). 2020 May;60(3):94-96. doi: 10.1111/cga.12351. Epub 2019 Jul 29.
Congenit Anom (Kyoto). 2020.
PMID: 31328296
No abstract available.
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