福澤龍二 (Ryuji Fukuzawa) - マイポータル

基本情報

学位: 博士（医学）甲種(2000年5月慶應義塾大学)

ORCID iD: https://orcid.org/0000-0002-3996-3117
J-GLOBAL ID: 202101020858122605
researchmap会員ID: R000029243

論文

Coproporphyrinogen Oxidase Deficiency Causes Primary Adrenal Insufficiency and 46,XY DSD

Misa Honda, Satoshi Narumi, Kosei Hasegawa, Yoshimitsu Goto, Yusuke Kawashima, Osamu Ohara, Ryuji Fukuzawa, Tomohiro Ishii, Tomonobu Hasegawa

The Journal of Clinical Endocrinology & Metabolism 2025年12月18日
Identification and validation of DNA methylation changes in pre-eclampsia.

Suzan N Almomani, Abdulmonem A Alsaleh, Robert J Weeks, Aniruddha Chatterjee, Robert C Day, Izumi Honda, Hidekazu Homma, Ryuji Fukuzawa, Tania L Slatter, Noelyn A Hung …

Placenta 110 16-23 2021年7月
Human Papillomavirus E6/E7 Expression in Preeclampsia-Affected Placentae.

Ashley L Reily-Bell, Amanda Fisher, Bryony Harrison, Sara Bowie, Sankalita Ray, Mary Hawkes, Lyn M Wise, Ryuji Fukuzawa, Erin C Macaulay, Celia J Devenish …

Pathogens (Basel, Switzerland) 9(3) 2020年3月23日
Laparoscopic subtotal colectomy for a patient with chronic idiopathic colonic pseudo-obstruction: Report of a case.

Tsuyoshi Ozawa, Soichiro Ishihara, Yuka Okada, Kohei Ohno, Takahiro Yagi, Yoshihisa Fukushima, Ryu Shimada, Tamuro Hayama, Takeshi Tsuchiya, Keijiro Nozawa …

Asian journal of endoscopic surgery 12(4) 469-472 2019年10月
Selective Ablation of Tumorigenic Cells Following Human Induced Pluripotent Stem Cell-Derived Neural Stem/Progenitor Cell Transplantation in Spinal Cord Injury.

Kota Kojima, Hiroyuki Miyoshi, Narihito Nagoshi, Jun Kohyama, Go Itakura, Soya Kawabata, Masahiro Ozaki, Tsuyoshi Iida, Keiko Sugai, Shuhei Ito …

Stem cells translational medicine 8(3) 260-270 2019年3月
Ewing's Sarcoma with Extension into Superior Vena Cava and Right Atrium.

Yukari Atsumi, Yuya Saito, Hiroshi Hataya, Ryuji Fukuzawa, Yuki Yuza

Indian journal of surgical oncology 10(1) 98-100 2019年3月
A novel truncating mutation in MYH3 causes spondylocarpotarsal synostosis syndrome with basilar invagination.

Masaki Takagi, Satoshi Shimomura, Ryuji Fukuzawa, Satoshi Narumi, Gen Nishimura, Tomonobu Hasegawa

Journal of human genetics 63(12) 1277-1281 2018年12月
A Novel Mutation in NKX2-1 Shows Dominant-Negative Effects Only in the Presence of PAX8.

Hiroyuki Shinohara, Masaki Takagi, Kimiko Ito, Eri Shimizu, Ryuji Fukuzawa, Tomonobu Hasegawa

Thyroid : official journal of the American Thyroid Association 28(8) 1071-1073 2018年8月
Germline mutations and somatic inactivation of TRIM28 in Wilms tumour.

Benjamin J Halliday, Ryuji Fukuzawa, David M Markie, Richard G Grundy, Jackie L Ludgate, Michael A Black, Jane E Skeen, Robert J Weeks, Daniel R Catchpoole, Aedan G K Roberts …

PLoS genetics 14(6) e1007399 2018年6月
The Mosaicism Ratio of 45,X May Explain the Phenotype in a Case of Mixed Gonadal Dysgenesis.

Megumi Hatano, Ryuji Fukuzawa, Yukihiro Hasegawa

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 12(4) 175-179 2018年
MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency.

Hirohito Shima, Mie Hayashi, Takashi Tachibana, Makoto Oshiro, Naoko Amano, Tomohiro Ishii, Hidenori Haruna, Maki Igarashi, Masafumi Kon, Ryuji Fukuzawa …

PloS one 13(11) e0206184 2018年
A Novel Case of Somatic KCNJ5 Mutation in Pediatric-Onset Aldosterone-Producing Adenoma.

Noboru Uchida, Naoko Amano, Yui Yamaoka, Ayumi Uematsu, Yuji Sekine, Makoto Suzuki, Jun Watanabe, Koshiro Nishimoto, Kuniaki Mukai, Ryuji Fukuzawa …

Journal of the Endocrine Society 1(8) 1056-1061 2017年8月1日
A novel de novo germline mutation Glu40Lys in AKT3 causes megalencephaly with growth hormone deficiency.

Masaki Takagi, Kazushige Dobashi, Keiko Nagahara, Mitsuhiro Kato, Gen Nishimura, Ryuji Fukuzawa, Satoshi Narumi, Tomonobu Hasegawa

American journal of medical genetics. Part A 173(4) 1071-1076 2017年4月
A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency.

Masaki Takagi, Hotaka Kamasaki, Hiroko Yagi, Ryuji Fukuzawa, Satoshi Narumi, Tomonobu Hasegawa

Endocrine journal 64(2) 229-234 2017年2月27日
Syndromic disorder of sex development due to a novel hemizygous mutation in the carboxyl-terminal domain of ATRX.

Masaki Takagi, Hiroko Yagi, Ryuji Fukuzawa, Satoshi Narumi, Tomonobu Hasegawa

Human genome variation 4 17012-17012 2017年
The developmental programme for genesis of the entire kidney is recapitulated in Wilms tumour.

Ryuji Fukuzawa, Matthew R Anaka, Ian M Morison, Anthony E Reeve

PloS one 12(10) e0186333 2017年
Radiological findings of perivascular epithelioid cell tumour (PEComa) of the falciform ligament.

Atsuhiko Handa, Kazutoshi Fujita, Tatsuo Kono, Koji Komori, Seiichi Hirobe, Ryuji Fukuzawa

Journal of medical imaging and radiation oncology 60(6) 741-743 2016年12月
A case of transient neonatal diabetes due to a novel mutation in ABCC8.

Masaki Takagi, Ryojun Takeda, Hiroko Yagi, Daisuke Ariyasu, Ryuji Fukuzawa, Tomonobu Hasegawa

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 25(4) 139-141 2016年10月
Pathological classification of human iPSC-derived neural stem/progenitor cells towards safety assessment of transplantation therapy for CNS diseases.

Keiko Sugai, Ryuji Fukuzawa, Tomoko Shofuda, Hayato Fukusumi, Soya Kawabata, Yuichiro Nishiyama, Yuichiro Higuchi, Kenji Kawai, Miho Isoda, Daisuke Kanematsu …

Molecular brain 9(1) 85-85 2016年9月19日
Gonadal macrophage infiltration in congenital lipoid adrenal hyperplasia.

Tomohiro Ishii, Ryuji Fukuzawa, Takeshi Sato, Koji Muroya, Masanori Adachi, Kenji Ihara, Junko Igaki, Yukihiro Hasegawa, Seiji Sato, Toshikatsu Mitsui …

European journal of endocrinology 175(2) 127-32 2016年8月

もっとみる

MISC

Ovarian Macrophage Infiltration in Adult Women with Congenital Lipoid Adrenal Hyperplasia

Tomohiro Ishii, Ryuji Fukuzawa, Takeshi Sato, Koji Muroya, Masanori Adachi, Kenji Ihara, Junko Igaki, Yukihiro Hasegawa, Seiji Sato, Toshikatsu Mitsui …

ENDOCRINE REVIEWS 35(3) 2014年6月
NEPHROTOXICITY IN CHILDREN WITH FREQUENTLY RELAPSING NEPHROTIC SYNDROME (FRNS) RECEIVING LONG-TERM ADMINISTRATION OF CYCLOSPORINE (CSA)

Fumiyo Komaki, Yuko Hamasaki, Kenji Ishikura, Riku Hamada, Tomoyuki Sakai, Hiroshi Hataya, Kentaro Ogata, Ryuji Fukuzawa, Takashi Ando, Masataka Honda

NEPHROLOGY DIALYSIS TRANSPLANTATION 28 294-294 2013年5月

共同研究・競争的資金等の研究課題

ハイリスク型ヒトパピローマウイルスの先天性感染:胎児と母体の病理臨床像の解明

日本学術振興会科学研究費助成事業基盤研究(C) 2016年4月 - 2020年3月

福澤龍二
性腺の分化・形成異常と悪性腫瘍の多段階的発症機構の分子病理学的解明

日本学術振興会科学研究費助成事業基盤研究(C) 2013年4月 - 2016年3月

福澤龍二, 仁科範子
WT1遺伝子異常の病態―腎障害・泌尿生殖器系奇形および腫瘍発生機構解明を目指して―

日本学術振興会科学研究費助成事業基盤研究(C) 2000年 - 2001年

菊池春人, 福澤龍二, 秦順一
小児腫瘍におけるimprinted gene(KIP2/H19/IGF2)の異常

日本学術振興会科学研究費助成事業奨励研究(A) 1999年 - 2000年

福澤龍二