关注
Tomonobu Hasegawa
Tomonobu Hasegawa
未知所在单位机构
在 keio.jp 的电子邮件经过验证
标题
引用次数
引用次数
年份
Field test of quantum key distribution in the Tokyo QKD Network
M Sasaki, M Fujiwara, H Ishizuka, W Klaus, K Wakui, M Takeoka, S Miki, ...
Optics express 19 (11), 10387-10409, 2011
12432011
Mullerian inhibiting substance in humans: normal levels from infancy to adulthood
MM Lee, PK Donahoe, T Hasegawa, B Silverman, GB Crist, S Best, ...
The Journal of Clinical Endocrinology & Metabolism 81 (2), 571-576, 1996
5811996
Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome
Y Aoki, T Niihori, T Banjo, N Okamoto, S Mizuno, K Kurosawa, T Ogata, ...
The American Journal of Human Genetics 93 (1), 173-180, 2013
3552013
SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7
S Narumi, N Amano, T Ishii, N Katsumata, K Muroya, M Adachi, ...
Nature genetics 48 (7), 792-797, 2016
3342016
Developmental roles of the steroidogenic acute regulatory protein (StAR) as revealed by StAR knockout mice
T Hasegawa, L Zhao, KM Caron, G Majdic, T Suzuki, S Shizawa, ...
Molecular Endocrinology 14 (9), 1462-1471, 2000
2982000
Clinical Assessment and Mutation Analysis of Kallmann Syndrome 1 (KAL1) and Fibroblast Growth Factor Receptor 1 (FGFR1, or KAL2) in Five Families and 18 …
N Sato, N Katsumata, M Kagami, T Hasegawa, N Hori, S Kawakita, ...
The Journal of Clinical Endocrinology & Metabolism 89 (3), 1079-1088, 2004
2772004
Measurements of serum Müllerian inhibiting substance in the evaluation of children with nonpalpable gonads
MM Lee, PK Donahoe, BL Silverman, T Hasegawa, Y Hasegawa, ...
New England Journal of Medicine 336 (21), 1480-1486, 1997
2581997
Reduced phototoxicity of a fluoroquinolone antibacterial agent with a methoxy group at the 8 position in mice irradiated with long-wavelength UV light
K Marutani, M Matsumoto, Y Otabe, M Nagamuta, K Tanaka, A Miyoshi, ...
Antimicrobial agents and chemotherapy 37 (10), 2217-2223, 1993
2111993
Phenotypic spectrum of CHARGE syndrome with CHD7 mutations
M Aramaki, T Udaka, R Kosaki, Y Makita, N Okamoto, H Yoshihashi, H Oki, ...
The Journal of pediatrics 148 (3), 410-414, 2006
1962006
GATA3 abnormalities and the phenotypic spectrum of HDR syndrome
K Muroya, T Hasegawa, Y Ito, T Nagai, H Isotani, Y Iwata, K Yamamoto, ...
Journal of medical genetics 38 (6), 374-380, 2001
1782001
Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients
M Fukami, R Horikawa, T Nagai, T Tanaka, Y Naiki, N Sato, T Okuyama, ...
The Journal of Clinical Endocrinology & Metabolism 90 (1), 414-426, 2005
1692005
Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosterone
K Homma, T Hasegawa, T Nagai, M Adachi, R Horikawa, I Fujiwara, ...
The Journal of Clinical Endocrinology & Metabolism 91 (7), 2643-2649, 2006
1662006
CXorf6 is a causative gene for hypospadias
M Fukami, Y Wada, K Miyabayashi, I Nishino, T Hasegawa, ...
Nature genetics 38 (12), 1369-1371, 2006
1632006
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly
S W. Scherer, P Poorka], H Massa, S Soder, T Allen, M Nunes, D Geshurl, ...
Human molecular genetics 3 (8), 1345-1354, 1994
1411994
PTPN11 (Protein-Tyrosine Phosphatase, Nonreceptor-Type 11) Mutations in Seven Japanese Patients with Noonan Syndrome
K Kosaki, T Suzuki, K Muroya, T Hasegawa, S Sato, N Matsuo, R Kosaki, ...
The Journal of Clinical Endocrinology & Metabolism 87 (8), 3529-3533, 2002
1372002
Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature
GA Vasques, N Amano, AJ Docko, MFA Funari, EPS Quedas, MY Nishi, ...
The Journal of Clinical Endocrinology & Metabolism 98 (10), E1636-E1644, 2013
1352013
Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients
M Fukami, G Nishimura, K Homma, T Nagai, K Hanaki, A Uematsu, T Ishii, ...
The Journal of Clinical Endocrinology & Metabolism 94 (5), 1723-1731, 2009
1332009
Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome
R Yoshida, T Hasegawa, Y Hasegawa, T Nagai, E Kinoshita, Y Tanaka, ...
The Journal of Clinical Endocrinology & Metabolism 89 (7), 3359-3364, 2004
1302004
An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14
P Lichtner, R König, T Hasegawa, H Van Esch, T Meitinger, ...
Journal of medical genetics 37 (1), 33-37, 2000
1292000
Transcription factor mutations and congenital hypothyroidism: systematic genetic screening of a population-based cohort of Japanese patients
S Narumi, K Muroya, Y Asakura, M Adachi, T Hasegawa
The Journal of Clinical Endocrinology & Metabolism 95 (4), 1981-1985, 2010
1272010
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