Genetics of Human Growth

le Ogata, Tsutomu
Foilsithe 2006

Molecular Mechanisms Leading to the Phenotypic Development in Paternal and Maternal Uniparental Disomy for Chromosome 14

le Ogata, Tsutomu, Kagami, Masayo
Foilsithe 2008

A Novel A461S Mutation of PTPN11 in a Female with LEOPARD Syndrome

le Yoshida, Rie, Ogata, Tsutomu
Foilsithe 2008

Kagami–Ogata syndrome: a clinically recognizable upd(14)pat and related disorder affecting the chromosome 14q32.2 imprinted region

le Ogata, Tsutomu, Kagami, Masayo
Foilsithe in J Hum Genet (2016)

Molecular Bases and Phenotypic Determinants of Aromatase Excess Syndrome

le Fukami, Maki, Shozu, Makio, Ogata, Tsutomu
Foilsithe 2012

Glucose-6-Phosphate Dehydrogenase Deficiency and Adrenal Hemorrhage in a Filipino Neonate with Hyperbilirubinemia

le Ohishi, Akira, Ueno, Daizo, Ogata, Tsutomu
Foilsithe 2012

Aromatase excess syndromeas a model for genomic disorder: identification of molecular bases and phenotypic determinants

le Ogata, Tsutomu, Shozu, Makio, Fukami, Maki
Foilsithe 2013

MAMLD1 (CXorf6) is a New Gene for Hypospadias

le Ogata, Tsutomu, Fukami, Maki, Wada, Yuka
Foilsithe 2008

Target Height and Target Range for Japanese Children: Revisited

le Ogata, Tsutomu, Tanaka, Toshiaki, Kagami, Masayo
Foilsithe 2007

KRAS Analysis in 34 Noonan Syndrome Patients without PTPN11 Mutation

le Yamamoto, Kaoru, Yoshida, Rie, Ogata, Tsutomu
Foilsithe 2007

Understanding the pathological manifestations of aromatase excess syndrome: lessons for clinical diagnosis

le Shozu, Makio, Fukami, Maki, Ogata, Tsutomu
Foilsithe 2014

SHOX Haploinsufficiency as a Cause of Syndromic and Nonsyndromic Short Stature

le Fukami, Maki, Seki, Atsuhito, Ogata, Tsutomu
Foilsithe in Mol Syndromol (2016)

A Track Record on SHOX: From Basic Research to Complex Models and Therapy

le Marchini, Antonio, Ogata, Tsutomu, Rappold, Gudrun A.
Foilsithe in Endocr Rev (2016)

Transactivation Function of an ∼800-bp Evolutionarily Conserved Sequence at the SHOX 3′ Region: Implication for the Downstream Enhancer

le Fukami, Maki, Kato, Fumiko, Tajima, Toshihiro, Yokoya, Susumu, Ogata, Tsutomu
Foilsithe 2006

Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST

le Kagami, Masayo, Nagai, Toshiro, Fukami, Maki, Yamazawa, Kazuki, Ogata, Tsutomu
Foilsithe 2007

Human Spermatogenesis Tolerates Massive Size Reduction of the Pseudoautosomal Region

le Fukami, Maki, Fujisawa, Yasuko, Ono, Hiroyuki, Jinno, Tomoko, Ogata, Tsutomu
Foilsithe in Genome Biol Evol (2020)

Mosaic upd(14)pat in a patient with mild features of Kagami–Ogata syndrome

le Haug, Marte G., Brendehaug, Atle, Houge, Gunnar, Kagami, Masayo, Ogata, Tsutomu
Foilsithe in Clin Case Rep (2017)

Female Patient Showing Hypohidrotic Ectodermal Dysplasia and Immunodeficiency (HED-ID)

le Kosaki, Kenjiro, Shimasaki, Noriko, Fukushima, Hiroyuki, Hara, Mitsuhiro, Ogata, Tsutomu, Matsuo, Nobutake
Foilsithe 2001

Genetic screening of Wnt signaling factors in advanced retinopathy of prematurity

le Hiraoka, Miki, Takahashi, Hiroshi, Orimo, Hideo, Hiraoka, Miina, Ogata, Tsutomu, Azuma, Noriyuki
Foilsithe 2010

Mamld1 Knockdown Reduces Testosterone Production and Cyp17a1 Expression in Mouse Leydig Tumor Cells

le Nakamura, Michiko, Fukami, Maki, Sugawa, Fumihiro, Miyado, Mami, Nonomura, Katsuya, Ogata, Tsutomu
Foilsithe 2011