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Collection of 2429 constrained headshots of 277 volunteers for deep learning.
Aoto S, Hangai M, Ueno-Yokohata H, Ueda A, Igarashi M, Ito Y, Tsukamoto M, Jinno T, Sakamoto M, Okazaki Y, Hasegawa F, Ogata-Kawata H, Namura S, Kojima K, Kikuya M, Matsubara K, Taniguchi K, Okamura K. Aoto S, et al. Among authors: taniguchi k. Sci Rep. 2022 Mar 8;12(1):3730. doi: 10.1038/s41598-022-07560-2. Sci Rep. 2022. PMID: 35260616 Free PMC article.
Isolation and characterization of fetal nucleated red blood cells from maternal blood as a target for single cell sequencing-based non-invasive genetic testing.
Ito N, Tsukamoto K, Taniguchi K, Takahashi K, Okamoto A, Aoki H, Otera-Takahashi Y, Kitagawa M, Ogata-Kawata H, Morita H, Hata K, Nakabayashi K. Ito N, et al. Among authors: taniguchi k. Reprod Med Biol. 2021 Jun 14;20(3):352-360. doi: 10.1002/rmb2.12392. eCollection 2021 Jul. Reprod Med Biol. 2021. PMID: 34262404 Free PMC article.
Improved library preparation protocols for amplicon sequencing-based noninvasive fetal genotyping for RHD-positive D antigen-negative alleles.
Hori A, Ogata-Kawata H, Sasaki A, Takahashi K, Taniguchi K, Migita O, Kawashima A, Okamoto A, Sekizawa A, Sago H, Takada F, Nakabayashi K, Hata K. Hori A, et al. Among authors: taniguchi k. BMC Res Notes. 2021 Sep 26;14(1):380. doi: 10.1186/s13104-021-05793-4. BMC Res Notes. 2021. PMID: 34565457 Free PMC article.
A novel FLNA variant in a fetus with skeletal dysplasia.
Oshina K, Kamei Y, Hori A, Hasegawa F, Taniguchi K, Migita O, Itakura A, Hata K. Oshina K, et al. Among authors: taniguchi k. Hum Genome Var. 2022 Dec 13;9(1):45. doi: 10.1038/s41439-022-00224-7. Hum Genome Var. 2022. PMID: 36509760 Free PMC article.
Pregnancy Outcome and Postnatal Chromosome Analysis of the Cord Blood and Chorionic Villi in Two Cases after Intrauterine Transfer of Mosaic Aneuploid Blastocysts.
Ito Y, Kamide T, Taniguchi K, Sato T, Yamamura M, Konishi A, Takahashi K, Kishi H, Hata K, Samura O, Okamoto A. Ito Y, et al. Among authors: taniguchi k. Case Rep Obstet Gynecol. 2022 Jul 19;2022:1763948. doi: 10.1155/2022/1763948. eCollection 2022. Case Rep Obstet Gynecol. 2022. PMID: 35909982 Free PMC article.
Congenital anaemia associated with loss-of-function variants in DNA polymerase epsilon 1.
Takeuchi I, Tanase-Nakao K, Ogawa A, Sugawara T, Migita O, Kashima M, Yamazaki T, Iguchi A, Naiki Y, Uchiyama T, Tamaoki J, Maeda H, Shimizu H, Kawai T, Taniguchi K, Hirata H, Kobayashi M, Matsumoto K, Naruse K, Hata K, Akutsu H, Kato T, Narumi S, Arai K, Ishiguro A. Takeuchi I, et al. Among authors: taniguchi k. J Med Genet. 2024 Feb 21;61(3):239-243. doi: 10.1136/jmg-2023-109444. J Med Genet. 2024. PMID: 37833059 Free article.
2,672 results