المؤلفون: Kim, H.W., Cho, T.J., Kim, S.A., Rhee, M.S.

المصدر: Journal of Food Protection ; volume 85, issue 12, page 1883-1889 ; ISSN 0362-028X

الاتاحة: http://dx.doi.org/10.4315/jfp-22-022
https://api.elsevier.com/content/article/PII:S0362028X2211080X?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0362028X2211080X?httpAccept=text/plain
https://meridian.allenpress.com/jfp/article-pdf/85/12/1883/3151650/i1944-9097-85-12-1883.pdf

المؤلفون: Kim, H.W., Kim, N.H., Cho, T.J., Park, S.M., Kim, S.H., Rhee, M.S.

المصدر: Journal of Food Protection ; volume 81, issue 11, page 1838-1843 ; ISSN 0362-028X

الاتاحة: http://dx.doi.org/10.4315/0362-028x.jfp-18-219
https://api.elsevier.com/content/article/PII:S0362028X22088202?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0362028X22088202?httpAccept=text/plain
http://meridian.allenpress.com/jfp/article-pdf/81/11/1838/1996252/0362-028x_jfp-18-219.pdf

المؤلفون: Choi, J.H., Choe, Y.J., Hong, K.B., Lee, J., Yoo, W.J., Kim, H.S., Park, M.S., Cho, T.J., Chung, C.Y., Lee, H.J., Choi, I.H., Choi, E.H.

المساهمون: Yoo, W.J., Park, M.S., Choi, E.H.

مصطلحات موضوعية: Arthritis, Children, Osteomyelitis, Pyogenic osteoarthritis, Staphylococcus aureus

Relation: Pediatric Infection and Vaccine, Vol.18 No.1, pp.31-39; https://hdl.handle.net/10371/192114; 2-s2.0-84869117517; 182132; ART001559386

الاتاحة: https://hdl.handle.net/10371/192114

المؤلفون: Park, S.W., Cho, T.J., Rhee, M.S.

المساهمون: Ministry of Science and ICT, South Korea, National Research Foundation of Korea

المصدر: Food Research International ; volume 156, page 111332 ; ISSN 0963-9969

الاتاحة: http://dx.doi.org/10.1016/j.foodres.2022.111332
https://api.elsevier.com/content/article/PII:S0963996922003891?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0963996922003891?httpAccept=text/plain

المؤلفون: Wade, E.M., Daniel, P.B., Jenkins, Z.A., McInerney-Leo, A., Leo, P., Morgan, T., Addor, M.C., Adès, L.C., Bertola, D., Bohring, A., Carter, E., Cho, T.J., Duba, H.C., Fletcher, E., Kim, C.A., Krakow, D., Morava, E., Neuhann, T., Superti-Furga, A., Veenstra-Knol, I., Wieczorek, D., Wilson, L.C., Hennekam, R.C., Sutherland-Smith, A.J., Strom, T.M., Wilkie, A.O., Brown, M.A., Duncan, E.L., Markie, D.M., Robertson, S.P.

المصدر: American journal of human genetics, vol. 99, no. 2, pp. 392-406

مصطلحات موضوعية: Adaptor Proteins, Signal Transducing/genetics, Signal Transducing/metabolism, Female, Filamins/genetics, Forehead/abnormalities, Humans, MAP Kinase Kinase Kinases/genetics, MAP Kinase Kinase Kinases/metabolism, MAP Kinase Signaling System/genetics, Male, Mutation/genetics, NF-kappa B/metabolism, Osteochondrodysplasias/genetics, Osteochondrodysplasias/metabolism, Phosphorylation, Protein Binding, Protein Multimerization, Signal Transduction/genetics

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/27426733; info:eu-repo/semantics/altIdentifier/eissn/1537-6605; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_CD2DAF16D0862; https://serval.unil.ch/notice/serval:BIB_CD2DAF16D086; https://serval.unil.ch/resource/serval:BIB_CD2DAF16D086.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_CD2DAF16D086
https://doi.org/10.1016/j.ajhg.2016.05.024
https://serval.unil.ch/resource/serval:BIB_CD2DAF16D086.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_CD2DAF16D0862

المؤلفون: Royer-Bertrand, B., Castillo-Taucher, S., Moreno-Salinas, R., Cho, T.J., Chae, J.H., Choi, M., Kim, O.H., Dikoglu, E., Campos-Xavier, B., Girardi, E., Superti-Furga, G., Bonafé, L., Rivolta, C., Unger, S., Superti-Furga, A.

المصدر: Scientific Reports, vol. 5, pp. 17154

مصطلحات موضوعية: Abnormalities, Multiple/genetics, Multiple/radiography, Bone Diseases, Developmental/genetics, Developmental/radiography, Child, Preschool, DNA Mutational Analysis, Female, Genetic Association Studies, HSP70 Heat-Shock Proteins/genetics, Humans, Mitochondrial Proteins/genetics, Musculoskeletal Abnormalities/genetics, Musculoskeletal Abnormalities/radiography, Mutation, Missense, Syndrome

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/26598328; info:eu-repo/semantics/altIdentifier/eissn/2045-2322; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_825739ACCA7E9; https://serval.unil.ch/notice/serval:BIB_825739ACCA7E; https://serval.unil.ch/resource/serval:BIB_825739ACCA7E.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_825739ACCA7E
https://doi.org/10.1038/srep17154
https://serval.unil.ch/resource/serval:BIB_825739ACCA7E.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_825739ACCA7E9

المؤلفون: Kim, S.A., Jeon, S.H., Kim, N.H., Kim, H.W., Lee, N.Y., Cho, T.J., Jung, Y.M., Lee, S.H., Hwang, I.G., Rhee, M.S.

المصدر: Journal of Food Protection ; volume 78, issue 12, page 2233-2239 ; ISSN 0362-028X

الاتاحة: http://dx.doi.org/10.4315/0362-028x.jfp-15-261
https://api.elsevier.com/content/article/PII:S0362028X23059604?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0362028X23059604?httpAccept=text/plain
http://meridian.allenpress.com/jfp/article-pdf/78/12/2233/1688162/0362-028x_jfp-15-261.pdf

المؤلفون: Dai, J., Kim, O.H., Cho, T.J., Schmidt-Rimpler, M., Tonoki, H., Takikawa, K., Haga, N., Miyoshi, K., Kitoh, H., Yoo, W.J., Choi, I.H., Song, H.R., Jin, D.K., Kim, H.T., Kamasaki, H., Bianchi, P., Grigelioniene, G., Nampoothiri, S., Minagawa, M., Miyagawa, S.I., Fukao, T., Marcelis, C., Jansweijer, M.C.E., Hennekam, R.C.M., Bedeschi, F., Mustonen, A., Jiang, Q., Ohashi, H., Furuichi, T., Unger, S., Zabel, B., Lausch, E., Superti-Furga, A., Nishimura, G., Ikegawa, S.

المصدر: Dai , J , Kim , O H , Cho , T J , Schmidt-Rimpler , M , Tonoki , H , Takikawa , K , Haga , N , Miyoshi , K , Kitoh , H , Yoo , W J , Choi , I H , Song , H R , Jin , D K , Kim , H T , Kamasaki , H , Bianchi , P , Grigelioniene , G , Nampoothiri , S , Minagawa , M , Miyagawa , S I , Fukao , T , Marcelis , C , Jansweijer , M ....

وصف الملف: application/pdf

Relation: https://dare.uva.nl/personal/pure/en/publications/novel-and-recurrent-trpv4-mutations-and-their-association-with-distinct-phenotypes-within-the-trpv4-dysplasia-family(db57a3e6-c982-4f3e-bd68-4c2617662e1a).html

الاتاحة: https://dare.uva.nl/personal/pure/en/publications/novel-and-recurrent-trpv4-mutations-and-their-association-with-distinct-phenotypes-within-the-trpv4-dysplasia-family(db57a3e6-c982-4f3e-bd68-4c2617662e1a).html
https://doi.org/10.1136/jmg.2009.075358
https://pure.uva.nl/ws/files/1257940/93555_339667.pdf

المؤلفون: Kim, H.W., Jang, J.J., Kim, N.H., Lee, N.Y., Cho, T.J., Kim, S.H., Rhee, M.S.

المساهمون: Korea Ministry of Food and Drug Safety

المصدر: Food Control ; volume 87, page 1-8 ; ISSN 0956-7135

الاتاحة: http://dx.doi.org/10.1016/j.foodcont.2017.12.009
https://api.elsevier.com/content/article/PII:S0956713517305881?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0956713517305881?httpAccept=text/plain

المؤلفون: Wade, E.M., Jenkins, Z.A., Daniel, P.B., Morgan, T., Addor, M.C., Adés, L.C., Bertola, D., Bohring, A., Carter, E., Cho, T.J., de Geus, C.M., Duba, H.C., Fletcher, E., Hadzsiev, K., Hennekam, RCM, Kim, C.A., Krakow, D., Morava, E., Neuhann, T., Sillence, D., Superti-Furga, A., Veenstra-Knol, H.E., Wieczorek, D., Wilson, L.C., Markie, D.M., Robertson, S.P.

المصدر: American journal of medical genetics. Part A, vol. 173, no. 7, pp. 1730-1746

مصطلحات موضوعية: Frontometaphyseal dysplasia, TAB2, TAK1, keloid, locus heterogeneity, scoliosis

Relation: info:eu-repo/semantics/altIdentifier/pmid/28498505; info:eu-repo/semantics/altIdentifier/eissn/1552-4833; https://serval.unil.ch/notice/serval:BIB_1A54928B107C

الاتاحة: https://serval.unil.ch/notice/serval:BIB_1A54928B107C
https://doi.org/10.1002/ajmg.a.38267

المؤلفون: Moosa, S., Haagerup, A., Gregersen, P.A., Petersen, K.K., Altmüller, J., Thiele, H., Nürnberg, P., Cho, T.J., Kim, O.H., Nishimura, G., Wollnik, B., Vogel, I.

مصطلحات موضوعية: Technology Platforms

Relation: Confirmation of CAGSSS syndrome as a distinct entity in a Danish patient with a novel homozygous mutation in IARS2. Moosa, S. and Haagerup, A. and Gregersen, P.A. and Petersen, K.K. and Altmüller, J. and Thiele, H. and Nürnberg, P. and Cho, T.J. and Kim, O.H. and Nishimura, G. and Wollnik, B. and Vogel, I. American Journal of Medical Genetics Part A 173 (4): 1102-1108. April 2017

الاتاحة: http://edoc.mdc-berlin.de/20642/
https://edoc.mdc-berlin.de/20642/
https://doi.org/10.1002/ajmg.a.38116

المؤلفون: Cho, S.Y., Bae, J.S., Kim, N.K., Forzano, F., Girisha, K.M., Baldo, C., Faravelli, F., Cho, T.J., Kim, D., Lee, K.Y., Ikegawa, S., Shim, J.S., Ko, A.R., Miyake, N., Nishimura, G., Superti-Furga, A., Spranger, J., Kim, O.H., Park, W.Y., Jin, D.K.

المصدر: American journal of human genetics, vol. 98, no. 6, pp. 1243-1248

مصطلحات موضوعية: Adult, Aged, Amino Acid Sequence, Biglycan/chemistry, Biglycan/genetics, Biglycan/metabolism, Child, Preschool, Female, Genetic Diseases, X-Linked/genetics, Humans, Infant, Newborn, Male, Middle Aged, Mutation/genetics, Osteochondrodysplasias/genetics, Pedigree, Protein Binding, Protein Conformation, Sequence Homology, Amino Acid, Transforming Growth Factor beta/chemistry, Transforming Growth Factor beta/genetics, Transforming Growth Factor beta/metabolism

Relation: info:eu-repo/semantics/altIdentifier/pmid/27236923; info:eu-repo/semantics/altIdentifier/eissn/1537-6605; https://serval.unil.ch/notice/serval:BIB_D3A1222A286B

الاتاحة: https://serval.unil.ch/notice/serval:BIB_D3A1222A286B
https://doi.org/10.1016/j.ajhg.2016.04.004

المؤلفون: Cho, T.J., Kim, N.H., Kim, S.A., Song, J.H., Rhee, M.S.

المساهمون: Korea University

المصدر: International Journal of Food Microbiology ; volume 238, page 50-55 ; ISSN 0168-1605

الاتاحة: http://dx.doi.org/10.1016/j.ijfoodmicro.2016.08.041
https://api.elsevier.com/content/article/PII:S0168160516304536?httpAccept=text/plain
https://api.elsevier.com/content/article/PII:S0168160516304536?httpAccept=text/xml

المؤلفون: Dikoglu, E., Alfaiz, A., Gorna, M., Bertola, D., Chae, J.H., Cho, T.J., Derbent, M., Alanay, Y., Guran, T., Kim, O.H., Llerenar, J.C., Yamamoto, G., Superti-Furga, G., Reymond, A., Xenarios, I., Stevenson, B., Campos-Xavier, B., Bonafé, L., Superti-Furga, A., Unger, S.

المصدر: American Journal of Medical Genetics. Part A, vol. 167, no. 7, pp. 1501-1509

مصطلحات موضوعية: ATP-Dependent Proteases/genetics, Base Sequence, Craniofacial Abnormalities/genetics, Exome/genetics, Eye Abnormalities/genetics, Genes, Recessive/genetics, Growth Disorders/genetics, Hip Dislocation, Congenital/genetics, Humans, Mitochondrial Proteins/genetics, Models, Genetic, Molecular Sequence Data, Mutation/genetics, Osteochondrodysplasias/genetics, Sequence Analysis, DNA, Switzerland, Tooth Abnormalities/genetics

Relation: info:eu-repo/semantics/altIdentifier/pmid/25808063; info:eu-repo/semantics/altIdentifier/eissn/1552-4833; https://serval.unil.ch/notice/serval:BIB_5FC5887518A1

الاتاحة: https://serval.unil.ch/notice/serval:BIB_5FC5887518A1
https://doi.org/10.1002/ajmg.a.37029

المؤلفون: Kim, S.A., Yun, S.J., Jeon, S.H., Kim, N.H., Kim, H.W., Cho, T.J., Lee, S.H., Hwang, I.G., Rhee, M.S.

المساهمون: Ministry of Food and Drug Safety

المصدر: Food Control ; volume 53, page 1-8 ; ISSN 0956-7135

الاتاحة: http://dx.doi.org/10.1016/j.foodcont.2015.01.002
https://api.elsevier.com/content/article/PII:S0956713515000043?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0956713515000043?httpAccept=text/plain

المؤلفون: Cho, T.J., Ahn, E.C., Lyu, J.H., Chung, M.G., Oh, S.Y.

المصدر: Twenty Fourth IEEE/CPMT International Electronics Manufacturing Technology Symposium (Cat. No.99CH36330) ; page 230-233

الاتاحة: http://dx.doi.org/10.1109/iemt.1999.804825
http://xplorestaging.ieee.org/ielx5/6537/17443/00804825.pdf?arnumber=804825

المؤلفون: Moon, H.J., Chung, T.G., Lee, H., Ahn, E.C., Cho, T.J., Oh, S.Y.

المصدر: ICVC '99. 6th International Conference on VLSI and CAD (Cat. No.99EX361) ; page 510-513

الاتاحة: http://dx.doi.org/10.1109/icvc.1999.820988
http://xplorestaging.ieee.org/ielx5/6645/17744/00820988.pdf?arnumber=820988

المؤلفون: Daniel, P.B., Morgan, T., Alanay, Y., Bijlsma, E., Cho, T.J., Cole, T., Collins, F., David, A., Devriendt, K., Faivre, L., Ikegawa, S., Jacguemont, S., Jesic, M., Krakow, D., Liebrecht, D., Maitz, S., Marlin, S., Morin, G., Nishikubo, T., Nishimura, G., Prescott, T., Scarano, G., Shafeghati, Y., Skovby, F., Tsutsumi, S., Whiteford, M., Zenker, M., Robertson, S.P.

المصدر: Human Mutation

مصطلحات موضوعية: FLNB, FLNA, atelosteogenesis, boomerang dysplasia, Larsen syndrome

Relation: lumc-id: 3739711; https://hdl.handle.net/1887/102695

الاتاحة: https://hdl.handle.net/1887/102695
https://doi.org/10.1002/humu.22012

المؤلفون: Choo, H.J., Cho, T.J., Song, J., Tiller, G.E., Lee, S.H., Park, G., Lee, I.S., Lachman, R., Superti-Furga, A., Kim, O.H.

المصدر: Skeletal Radiology, vol. 41, no. 11, pp. 1479-1487

Relation: info:eu-repo/semantics/altIdentifier/pmid/22639207; info:eu-repo/semantics/altIdentifier/eissn/1432-2161; https://serval.unil.ch/notice/serval:BIB_63CE7E74D072

الاتاحة: https://serval.unil.ch/notice/serval:BIB_63CE7E74D072
https://doi.org/10.1007/s00256-012-1442-1

المؤلفون: Vissers, L.E.L.M., Fano, V., Martinelli, D., Campos-Xavier, B., Barbuti, D., Cho, T.J., Dursun, A., Kim, O.H., Lee, S., Timpani, G., Nishimura, G., Unger, S., Sass, J.O., Veltman, J.A., Brunner, H.G., Bonafe, L., Dionisi-Vici, C., Superti-Furga, A.

المصدر: American Journal of Medical Genetics. Part A, 155A, 11, pp. 2609-16

مصطلحات موضوعية: NCMLS 6: Genetics and epigenetic pathways of disease IGMD 3: Genomic disorders and inherited multi-system disorders

Relation: http://hdl.handle.net/2066/97516; https://doi.org/10.1002/ajmg.a.34325

الاتاحة: http://hdl.handle.net/2066/97516
https://doi.org/10.1002/ajmg.a.34325