Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Te-Cheng Pan"'
Autor:
Dessislava Markova, Guiyun Zhang, Machiko Arita, Takako Sasaki, David E. Birk, Te-Cheng Pan, Mon-Li Chu, Rui-Zhu Zhang
Publikováno v:
Cell and Tissue Research. 364:637-646
Fibulin-4 is an extracellular matrix glycoprotein essential for elastic fiber formation. Mice deficient in fibulin-4 die perinatally due to severe pulmonary and vascular defects associated with lacking intact elastic fibers. Patients with fibulin-4 m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81a3f1c13c592b9b6cfaa19a7854e774
https://doi.org/10.1007/s00441-015-2346-x
https://doi.org/10.1007/s00441-015-2346-x
Autor:
Mon-Li Chu, David E. Birk, Tejvior S. Khurana, Te Cheng Pan, Raimund Wagener, Machiko Arita, Sheila M. Adams, Sasha Bogdanovich, Sudheer Kumar Gara, Rui Zhu Zhang
Publikováno v:
Journal of Biological Chemistry. 289:10293-10307
Dominant and recessive mutations in collagen VI genes, COL6A1, COL6A2, and COL6A3, cause a continuous spectrum of disorders characterized by muscle weakness and connective tissue abnormalities ranging from the severe Ullrich congenital muscular dystr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfba2e5232da5a7f272dc982960da276
https://doi.org/10.1074/jbc.m114.549311
https://doi.org/10.1074/jbc.m114.549311
Autor:
Suely Kazue Nagahashi Marie, Carsten G. Bönnemann, Ying Hu, Yaqun Zou, Mon-Li Chu, Stefano Squarzoni, Te Cheng Pan, Rui Zhu Zhang, Andrzej Fertala, Umbertina Conti Reed, Dessislava Markova
Publikováno v:
Journal of Biological Chemistry. 285:10005-10015
Ullrich congenital muscular dystrophy (UCMD) is a disabling and life-threatening disorder resulting from either recessive or dominant mutations in genes encoding collagen VI. Although the majority of the recessive UCMD cases have frameshift or nonsen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9a4ce7090d814a7c01d51f79ea40a2c
https://doi.org/10.1074/jbc.m109.093666
https://doi.org/10.1074/jbc.m109.093666
Autor:
Te-Cheng Pan1, Kluge, Matthias2, Rui-Zhu Zhang1, Mayer, Ulrike2, Timpl, Rupert2, Chu, Mon-Li1
Publikováno v:
European Journal of Biochemistry. 8/1/93, Vol. 215 Issue 3, p733-740. 8p.
Autor:
Te-Cheng Pan1, Qian-lin Hao1, Ting-Ting Yamin1, Pei-Hua Dai1, Bao-Sheng Chen1, Shiow-Ling Chen1, Kroon, Paulus A.1, Yu-Sheng Chao1
Publikováno v:
European Journal of Biochemistry. 12/30/87, Vol. 170 Issue 1/2, p99-104. 6p.
Autor:
Guglielmina Pepe, Betti Giusti, Laura Lucarini, Francesco Muntoni, Eugenio Mercuri, Cecilia Jimenez-Mallebrera, Mon-Li Chu, Rui-Zhu Zhang, Te-Cheng Pan
Publikováno v:
Human Genetics. 117:460-466
Ullrich congenital muscular dystrophy (UCMD) is a severe disorder caused, in most cases, by a deficiency in collagen VI microfibrils. Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have been identified in eight of the n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa79026ffd0d8be38911bad09a5eceda
https://doi.org/10.1007/s00439-005-1318-8
https://doi.org/10.1007/s00439-005-1318-8
Autor:
Mon-Li Chu, Carsten G. Bönnemann, Suely Kazue Nagahashi Marie, Dominick Sudano, Te-Cheng Pan, Rui-Zhu Zhang
Publikováno v:
The American Journal of Human Genetics. 73(2):355-369
Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3a63f54db76c4f0dc5ff5e110805e92
Publikováno v:
The Anatomical Record. :93-96
By mRNA differential display in mouse hearts, lysyl oxidase (Lox), a key enzyme catalyzing cross-links in elastin and collagens, was found to be up-regulated between embryonic days 11 (E11) and 13 (E13). This was confirmed by semiquantitative RT-PCR.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7301681053b5a5849bf6d55cbd8b5e27
https://doi.org/10.1002/ar.a.10002
https://doi.org/10.1002/ar.a.10002
Autor:
Enrico Bertini, Rui Zhu Zhang, Stefano Squarzoni, Te Cheng Pan, Mon-Li Chu, Guglielmina Pepe, Patrizia Sabatelli, Elisabetta Mattioli
Publikováno v:
Journal of Biological Chemistry. 277:43557-43564
We recently reported a severe deficiency in collagen type VI, resulting from recessive mutations of the COL6A2 gene, in patients with Ullrich congenital muscular dystrophy. Their parents, who are all carriers of one mutant allele, are unaffected, alt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f090a3554bd1a07787e458fd4c6114dc
https://doi.org/10.1074/jbc.m207696200
https://doi.org/10.1074/jbc.m207696200
Autor:
Rui-Zhu Zhang, Marie Dziadek, Mon-Li Chu, Jaqueline A. Hendrey, Te-Cheng Pan, Janette S. Kazenwadel
Publikováno v:
Matrix Biology. 21:227-241
Three distinct alpha chains form the collagen VI monomer, the alpha 3(VI) chain being much larger than the alpha 1(VI) and alpha 2(VI) chains. The alpha 3(VI) chain has 10 von Willebrand Factor type A domains of approximately 200 amino acids at the N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0a1bb5acfd5ef2ebfef3d7e0b6450e6
https://doi.org/10.1016/s0945-053x(02)00009-4
https://doi.org/10.1016/s0945-053x(02)00009-4