論文・総説 - 森　崇寧

41. Fujimaru T, Kawanishi K, Mori T, Mishima E, Sekine A, Chiga M, Mizui M, Sato N, Yanagita M, Ooki Y, Nagahama K, Ohnuki Y, Hamano N, Watanabe S, Mochizuki T, Nagatsuji K, Tanaka K, Tsukamoto T, Tsushima H, Shimamoto M, Tsuji T, Kuyama T, Kawamoto S, Maki K, Katsuma A, Oishi M, Yamamoto K, Mandai S, Kikuchi H, Ando F, Mori Y, Susa K, Iimori S, Naito S, Rai T, Hoshino J, Ubara Y, Miyazaki M, Nagata M, Uchida S, Sohara E. Genetic Background and Clinicopathologic Features of Adult-onset Nephronophthisis. Kidney international reports. 2021.05; 6 (5): 1346-1354. ( PubMed, DOI )

42. Oe Y, Mishima E, Mori T, Okamoto K, Honkura Y, Nagasawa T, Yoshida M, Sato H, Suzuki J, Ikeda R, Sohara E, Uchida S, Katori Y, Miyazaki M. A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype. Internal medicine (Tokyo, Japan). 2021.04; 60 (18): 2991-2996. ( PubMed, DOI )

43. Mori Takehiko, Saburi Masuho, Hagihara Maki, Mori Masaaki, Yamazaki Rie, Kato Jun. Long-term remission of cryopyrin-associated periodic syndrome after allogeneic haematopoietic stem cell transplantation ANNALS OF THE RHEUMATIC DISEASES. 2021.04; 80 (4): 542-+. ( DOI )

44. Ota Yoshihide, Noguchi Tadahide, Ariji Eiichiro, Fushimi Chihiro, Fuwa Nobukazu, Harada Hiroyuki, Hayashi Takafumi, Hayashi Ryuichi, Honma Yoshitaka, Miura Masahiko, Mori Taisuke, Nagatsuka Hitoshi, Okura Masaya, Ueda Michihiro, Uzawa Narikazu, Yagihara Kazuhiro, Yagishita Hisao, Yamashiro Masashi, Yanamoto Souichi, Kirita Tadaaki. General rules for clinical and pathological studies on oral cancer (2nd edition): a synopsis INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY. 2021.04; 26 (4): 623-635. ( DOI )

45. Tao K, Awazu M, Honda M, Shibata H, Mori T, Uchida S, Hasegawa T, Ishii T. An infant with congenital nephrogenic diabetes insipidus presenting with hypercalcemia and hyperphosphatemia. Endocrinology, diabetes & metabolism case reports. 2021.04; 2021 ( PubMed, DOI )

46. Onoe Tamehito, Hara Satoshi, Yamada Kazunori, Zoshima Takeshi, Mizushima Ichiro, Ito Kiyoaki, Mori Takayasu, Daimon Shoichiro, Muramoto Hiroaki, Shimizu Maki, Iguchi Akira, Kuma Akihiro, Ubara Yoshifumi, Mitobe Michihiro, Tsuruta Hiroaki, Kishimoto Nao, Imura Junko, Konoshita Tadashi, Kawano Mitsuhiro. Significance of kidney biopsy in autosomal dominant tubulointerstitial kidney disease-UMOD: is kidney biopsy truly nonspecific? BMC NEPHROLOGY. 2021.01; 22 (1): 1. ( PubMed, DOI )

47. Yohei Arai, Kenichi Asano, Shintaro Mandai, Fumiaki Ando, Koichiro Susa, Takayasu Mori, Naohiro Nomura, Tatemitsu Rai, Masato Tanaka, Shinichi Uchida, Eisei Sohara. WNK1-TAK1 signaling suppresses lipopolysaccharide-induced cytokine production and classical activation in macrophages. Biochem Biophys Res Commun. 2020.12; 533 (4): 1290-1297. ( PubMed, DOI )

48. Takayasu Mori, Motoko Chiga, Takuya Fujimaru, Ryosuke Kawamoto, Shintaro Mandai, Azuma Nanamatsu, Naohiro Nomura, Fumiaki Ando, Koichiro Susa, Eisei Sohara, Tatemitsu Rai, Shinichi Uchida. Phenotypic differences of mutation-negative cases in Gitelman syndrome clinically diagnosed in adulthood. Hum Mutat. 2020.12; ( PubMed, DOI )

49. Fukano Reiji, Mori Tetsuya, Sekimizu Masahiro, Choi Ilseung, Kada Akiko, Saito Akiko Moriya, Asada Ryuta, Takeuchi Kengo, Terauchi Takashi, Tateishi Ukihide, Horibe Keizo, Nagai Hirokazu. Alectinib for relapsed or refractory anaplastic lymphoma kinase-positive anaplastic large cell lymphoma: An open-label phase II trial CANCER SCIENCE. 2020.12; 111 (12): 4540-4547. ( DOI )

50. Shirai Ryota, Osumi Tomoo, Mori Takeshi, Kohri Mika, Ishihara Takashi, Yasue Shiho, Imamura Toshihiko, Endo Mikiya, Takagi Masatoshi, Kato Motohiro. Genomic Analysis of B-Lymphoblastic Lymphoma with TCF3-PBX1 PEDIATRIC BLOOD & CANCER. 2020.12; 67

51. Takashi Iijima, Takayasu Mori, Eisei Sohara, Tatsuya Suwabe, Junichi Hoshino, Yoshifumi Ubara. A patient with congenital nephrogenic diabetes insipidus due to AVPR2 mutation complicated by persisting polydipsia under hemodialysis treatment. CEN Case Rep. 2020.10; ( PubMed, DOI )

52. Fujii Shinya, Kikuchi Eriko, Watanabe Yuko, Suzuyama Honoka, Ishigami-Yuasa Mari, Mori Takayasu, Isobe Kiyoshi, Uchida Shinichi, Kagechika Hiroyuki. Structural development of N-(4-phenoxyphenyl)benzamide derivatives as novel SPAK inhibitors blocking WNK kinase signaling BIOORGANIC & MEDICINAL CHEMISTRY LETTERS. 2020.09; 30 (17): 127408. ( PubMed, DOI )

53. Nakano Kiyoshi, Kubota Yasuo, Mori Takayuki, Chiga Motoko, Mori Takayasu, Sonoda Shyunya, Ueda Daisuke, Asakura Isao, Ikegaya Takeshi, Kagawa Jiro, Uchida Shinichi, Kubota Akira. Familial cases of pseudohypoaldosteronism typeIIharboring a novel mutation in theCullin 3gene NEPHROLOGY. 2020.08; 25 (11): e13752-821. ( PubMed, DOI )

54. Mishima E, Mori T, Nakajima Y, Toyohara T, Kikuchi K, Oikawa Y, Matsuhashi T, Maeda Y, Suzuki T, Kudo M, Ito S, Sohara E, Uchida S, Abe T. HPRT-related hyperuricemia with a novel p.V35M mutation in HPRT1 presenting familial juvenile gout. CEN case reports. 2020.08; 9 (3): 210-214. ( PubMed, DOI )

55. Sekine A, Hoshino J, Fujimaru T, Suwabe T, Mizuno H, Kawada M, Hiramatsu R, Hasegawa E, Yamanouchi M, Hayami N, Mandai S, Chiga M, Kikuchi H, Ando F, Mori T, Sohara E, Uchida S, Sawa N, Takaichi K, Ubara Y. Genetics May Predict Effectiveness of Tolvaptan in Autosomal Dominant Polycystic Kidney Disease. American journal of nephrology. 2020.08; 51 (9): 1-7. ( PubMed, DOI )

56. Murata Yoichi, Uchida Soshi, Utsunomiya Hajime, Hatakeyama Akihisa, Nakashima Hirotaka, Mori Toshiharu, Yamanaka Yoshiaki, Tsukamoto Manabu, Sekiya Ichiro, Huard Johnny, Philippon Marc J., Sakai Akinori. Differentiation Potential of Synovial Mesenchymal Stem Cells Isolated From Hip Joints Affected by Femoroacetabular Impingement Syndrome Versus Osteoarthritis ARTHROSCOPY-THE JOURNAL OF ARTHROSCOPIC AND RELATED SURGERY. 2020.08; 36 (8): 2122-2133. ( DOI )

57. Tsuji Kiyokazu, Kitamura Mineaki, Muta Kumiko, Mochizuki Yasushi, Mori Takayasu, Sohara Eisei, Uchida Shinichi, Sakai Hideki, Mukae Hiroshi, Nishino Tomoya. Transplantation of a kidney with a heterozygous mutation in the SLC22A12 (URAT1) gene causing renal hypouricemia: a case report BMC NEPHROLOGY. 2020.07; 21 (1): 282. ( PubMed, DOI )

58. Moena Ishikawa, Yumi Tada, Hiromu Tanaka, Wataru Morii, Masako Inaba, Hidetoshi Takada, Takayasu Mori, Emiko Noguchi. A Family with Gitelman Syndrome with Asymptomatic Phenotypes while Carrying Reported SLC12A3 Mutations. Case Rep Nephrol Dial. 2020.07; 10 (2): 71-78. ( PubMed, DOI )

59. Shigemizu Daichi, Mori Taiki, Akiyama Shintaro, Higaki Sayuri, Watanabe Hiroshi, Sakurai Takashi, Niida Shumpei, Ozaki Kouichi. Identification of potential blood biomarkers for early diagnosis of Alzheimer's disease through RNA sequencing analysis ALZHEIMERS RESEARCH & THERAPY. 2020.07; 12 (1): ( DOI )

60. Shoda Wakana, Nomura Naohiro, Ando Fumiaki, Tagashira Hideaki, Iwamoto Takahiro, Ohta Akihito, Isobe Kiyoshi, Mori Takayasu, Susa Koichiro, Sohara Eisei, Rai Tatemitsu, Uchida Shinichi. Sodium-calcium exchanger 1 is the key molecule for urinary potassium excretion against acute hyperkalemia PLOS ONE. 2020.06; 15 (6): e0235360. ( PubMed, DOI )