Jinno T - Search Results

1

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: jinno t. Sci Rep. 2022 Mar 8;12(1):3730. doi: 10.1038/s41598-022-07560-2. Sci Rep. 2022. PMID: 35260616 Free PMC article.

2

SHOX far-downstream copy-number variations involving cis-regulatory nucleotide variants in two sisters with Leri-Weill dyschondrosteosis.

Ogushi K, Muroya K, Shima H, Jinno T, Miyado M, Fukami M. Ogushi K, et al. Among authors: jinno t. Am J Med Genet A. 2019 Sep;179(9):1778-1782. doi: 10.1002/ajmg.a.61275. Epub 2019 Jun 22. Am J Med Genet A. 2019. PMID: 31228230

3

Skeletal Deformity Associated with SHOX Deficiency.

Seki A, Jinno T, Suzuki E, Takayama S, Ogata T, Fukami M. Seki A, et al. Among authors: jinno t. Clin Pediatr Endocrinol. 2014 Jul;23(3):65-72. doi: 10.1297/cpe.23.65. Epub 2014 Aug 6. Clin Pediatr Endocrinol. 2014. PMID: 25110390 Free PMC article. Review.

4

Human Spermatogenesis Tolerates Massive Size Reduction of the Pseudoautosomal Region.

Fukami M, Fujisawa Y, Ono H, Jinno T, Ogata T. Fukami M, et al. Among authors: jinno t. Genome Biol Evol. 2020 Nov 3;12(11):1961-1964. doi: 10.1093/gbe/evaa168. Genome Biol Evol. 2020. PMID: 32785664 Free PMC article.

5

Hypogonadotropic hypogonadism in a female patient previously diagnosed as having waardenburg syndrome due to a sox10 mutation.

Izumi Y, Musha I, Suzuki E, Iso M, Jinno T, Horikawa R, Amemiya S, Ogata T, Fukami M, Ohtake A. Izumi Y, et al. Among authors: jinno t. Endocrine. 2015 Jun;49(2):553-6. doi: 10.1007/s12020-014-0434-4. Epub 2014 Oct 2. Endocrine. 2015. PMID: 25273316 No abstract available.

6

Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short stature.

Fukami M, Naiki Y, Muroya K, Hamajima T, Soneda S, Horikawa R, Jinno T, Katsumi M, Nakamura A, Asakura Y, Adachi M, Ogata T, Kanzaki S; Japanese SHOX study group. Fukami M, et al. Among authors: jinno t. J Hum Genet. 2015 Sep;60(9):553-6. doi: 10.1038/jhg.2015.53. Epub 2015 Jun 4. J Hum Genet. 2015. PMID: 26040210

7

Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosis.

Shima H, Tanaka T, Kamimaki T, Dateki S, Muroya K, Horikawa R, Kanno J, Adachi M, Naiki Y, Tanaka H, Mabe H, Yagasaki H, Kure S, Matsubara Y, Tajima T, Kashimada K, Ishii T, Asakura Y, Fujiwara I, Soneda S, Nagasaki K, Hamajima T, Kanzaki S, Jinno T, Ogata T, Fukami M; Japanese SHOX study group. Shima H, et al. Among authors: jinno t. J Hum Genet. 2016 Jul;61(7):585-91. doi: 10.1038/jhg.2016.18. Epub 2016 Mar 17. J Hum Genet. 2016. PMID: 26984564

8

Compound heterozygous deletions in pseudoautosomal region 1 in an infant with mild manifestations of langer mesomelic dysplasia.

Tsuchiya T, Shibata M, Numabe H, Jinno T, Nakabayashi K, Nishimura G, Nagai T, Ogata T, Fukami M. Tsuchiya T, et al. Among authors: jinno t. Am J Med Genet A. 2014 Feb;164A(2):505-10. doi: 10.1002/ajmg.a.36284. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311385

9

SOX10 Mutation Screening for 117 Patients with Kallmann Syndrome.

Shima H, Tokuhiro E, Okamoto S, Nagamori M, Ogata T, Narumi S, Nakamura A, Izumi Y, Jinno T, Suzuki E, Fukami M. Shima H, et al. Among authors: jinno t. J Endocr Soc. 2021 Mar 30;5(7):bvab056. doi: 10.1210/jendso/bvab056. eCollection 2021 Jul 1. J Endocr Soc. 2021. PMID: 34095692 Free PMC article.

10

Analysis of survivorship following periacetabular osteotomy for hip dysplasia based on three-dimensional acetabular coverage.

Tachibana T, Koga H, Katagiri H, Ogawa T, Takada R, Miyatake K, Jinno T. Tachibana T, et al. Among authors: jinno t. J Hip Preserv Surg. 2023 Nov 11;11(1):30-37. doi: 10.1093/jhps/hnad044. eCollection 2024 Jan. J Hip Preserv Surg. 2023. PMID: 38606334 Free PMC article.

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