Papillary Thyroid Carcinoma Associated with Familial Adenomatous Polyposis: Molecular Analysis of Pathogenesis in a Family and Review of the Literature
LEE, Sihoon, HONG, Soon Won, SHIN, Sung Jae, KIM, Yoo Mee, RHEE, Yumie, JEON, Bu Il, MOON, Woo Chul, OH, Myung Ryurl, LIM, Sung-Kil
Published in Endocrine Journal (01.06.2004)
Published in Endocrine Journal (01.06.2004)
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Journal Article
High prevalence of c-RET expression in papillary thyroid carcinomas from the Korean population
Lee, Sihoon, Hong, Soon Won, Moon, Woo Chul, Oh, Myung Ryurl, Lee, Jin Kyung, Ahn, Chul Woo, Cha, Bong Soo, Kim, Kyung Rae, Lee, Hyun Chul, Lim, Sung-Kil
Published in Thyroid (New York, N.Y.) (01.03.2005)
Published in Thyroid (New York, N.Y.) (01.03.2005)
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Frequency of spinocerebellar ataxia types 1, 2, 3, 6, 7 and dentatorubral pallidoluysian atrophy mutations in Korean patients with spinocerebellar ataxia
DONG KYU JIN, MYUNG RYURL OH, MYUNG JONG LEE, JAE WOO KIM, MYUNG SIK LEE, SENG MI SONG, SI WHAN KOH, LEE, M, GYEONG MOON KIM, LEE, W.-Y, CHUNG, C.-S, KWANG HO LEE, JOO HYUK IM
Published in Journal of neurology (01.03.1999)
Published in Journal of neurology (01.03.1999)
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Journal Article
DNA testing for fragile X syndrome in school for severely emotionally handicapped children in Korea
Hong, Sung-Do David, Lee, So-Young, Oh, Myung-Ryurl, Jin, Dong-Kyu
Published in Journal of genetic medicine (30.12.1998)
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Published in Journal of genetic medicine (30.12.1998)
Journal Article
CAG repeats of CTG18.1 and KCNN3 in Korean patients with bipolar affective disorder
Jin, Dong Kyu, Hwang, Hye Zin, Oh, Myung Ryurl, Kim, Jung Shim, Lee, Munhyang, Kim, Seonwoo, Lim, Shinn-Won, Seo, Min Young, Kim, Ji-Hae, Kim, Doh Kwan
Published in Journal of affective disorders (01.09.2001)
Published in Journal of affective disorders (01.09.2001)
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Frequency Analysis and Clinical Characterization of Spinocerebellar Ataxia Types 1, 2, 3, 6, and 7 in Korean Patients
Lee, Won Yong, Jin, Dong Kyu, Oh, Myung Ryurl, Lee, Ji Eun, Song, Seng Mi, Lee, Eun Ah, Kim, Gyeong-moon, Chung, Jin Sang, Lee, Kwang Ho
Published in Archives of neurology (Chicago) (01.06.2003)
Published in Archives of neurology (Chicago) (01.06.2003)
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Duplication and deletion of 21 hydroxylase gene among the normal Korean subjects and in adrenogenital syndrome patients
Jin, Dong-Kyu, Beck, Nam-Seon, Oh, Phil-Soo, Whang, Hye-Zin, Koh, Si-Whan, Kim, Jung-Sim, Oh, Myung-Ryurl
Published in Journal of genetic medicine (1997)
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Published in Journal of genetic medicine (1997)
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Droplet digital PCR-based EGFR mutation detection with an internal quality control index to determine the quality of DNA
Kim, Sung-Su, Choi, Hyun-Jeung, Kim, Jin Ju, Kim, M. Sun, Lee, In-Seon, Byun, Bohyun, Jia, Lina, Oh, Myung Ryurl, Moon, Youngho, Park, Sarah, Choi, Joon-Seok, Chae, Seoung Wan, Nam, Byung-Ho, Kim, Jin-Soo, Kim, Jihun, Min, Byung Soh, Lee, Jae Seok, Won, Jae-Kyung, Cho, Soo Youn, Choi, Yoon-La, Shin, Young Kee
Published in Scientific reports (11.01.2018)
Published in Scientific reports (11.01.2018)
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Employing Digital Droplet PCR to Detect BRAF V600E Mutations in Formalin-fixed Paraffin-embedded Reference Standard Cell Lines
Rajasekaran, Nirmal, Oh, Myung Ryurl, Kim, Sung-Su, Kim, Si Eun, Kim, Young Deug, Choi, Hyun-Jeung, Byun, Bohyun, Shin, Young Kee
Published in Journal of visualized experiments (08.10.2015)
Published in Journal of visualized experiments (08.10.2015)
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Journal Article
Employing Digital Droplet PCR to Detect BRAF V600E Mutations in Formalin-fixed Paraffin-embedded Reference Standard Cell Lines
Rajasekaran, Nirmal, Oh, Myung Ryurl, Kim, Sung-Su, Kim, Si Eun, Kim, Young Deug, Choi, Hyun-Jeung, Byun, Bohyun, Shin, Young Kee
Published in Journal of visualized experiments (08.10.2015)
Published in Journal of visualized experiments (08.10.2015)
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Journal Article
Six novel mutations of the fibrillin-1 gene in Korean patients with Marfan syndrome
Oh, Myung Ryurl, Kim, Jung Sim, Beck, Nam Seon, Yoo, Han Wook, Lee, Heung Jae, Kohsaka, Takao, Jin, Dong Kyu
Published in Pediatrics international (01.10.2000)
Published in Pediatrics international (01.10.2000)
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Activating Mutation of GSα in McCune-Albright Syndrome Causes Skin Pigmentation by Tyrosinase Gene Activation on Affected Melanocytes
Kim, Il-Soo, Kim, Eun Ryoung, Nam, Hye Jung, Chin, Mi Ok, Moon, Young Ho, Oh, Myung Ryurl, Yeo, Un Cheol, Song, Seng Mi, Kim, Jung Sim, Uhm, Mee Ryung, Beck, Nam Seon, Jin, Dong Kyu
Published in Hormone research (1999)
Published in Hormone research (1999)
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Journal Article
Activating Mutation of GS[alpha] in McCune-Albright Syndrome Causes Skin Pigmentation by Tyrosinase Gene Activation on Affected Melanocytes
Kim, Il-soo, Kim, Eun Ryoung, Nam, Hye Jung, Chin, Mi Ok, Moon, Young Ho, Oh, Myung Ryurl, Yeo, Un Cheol, Song, Seng Mi, Kim, Jung Sim, Uhm, Mee Ryung, Beck, Nam Seon, Jin, Dong Kyu
Published in Hormone research in paediatrics (01.11.1999)
Published in Hormone research in paediatrics (01.11.1999)
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Probe of human papillomavirus and DNA chip comprising the same
Moon, Woo-Chul, Oh, Myung-Ryurl, Yim, Su-Bin, Eum, Tae-Han, Jung, Eun-Hae, Ko, Jung-Eun, Bae, Jae-Han
Year of Publication 02.03.2010
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Year of Publication 02.03.2010
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