Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Eve L. Bingham"'
Publikováno v:
The Chinese journal of dental research : the official journal of the Scientific Section of the Chinese Stomatological Association (CSA). 21(1)
To develop a bioreactor for automated culture, maintenance, and collection of normal human keratinocytes using an enzyme-free propagation method.The culture of normal human epithelial keratinocytes was compared in two culture methods - a study team-d
Publikováno v:
Tissue Engineering Part C: Methods. 21:872-880
The soft tissue reconstruction of significant avulsed and/or surgically created tissue defects requires the ability to manufacture substantial soft tissue constructs for repair of the resulting wounds. In this study, we detail the issues that need to
Autor:
Stephen E. Feinberg, Jack D. Wang, Eve L. Bingham, Sasha Cai Lesher-Perez, Shuichi Takayama, Mohamed E. H. ElSayed, Hady T. Sarhan, John P. Frampton, Brendan M. Leung
Publikováno v:
Advanced Functional Materials. 25:1694-1699
An entirely new approach to tissue engineering is presented that uses the interfacial forces between aqueous solutions of phase-separating polymers to confine cells and promote their assembly into interconnected, macroscopic tissue constructs. This s
Autor:
Atsuko Miyazawa, Stephen E. Feinberg, Eve L. Bingham, Cynthia L. Marcelo, Shiuhyang Kuo, Zhifa Wang, Hyungjin Myra Kim
Publikováno v:
Journal of tissue engineering and regenerative medicine. 12(4)
Immunologically inert allogeneic acellular dermal scaffolds provide a matrix with molecular architecture close to native tissues, which synthetic scaffolds cannot. Not all nature-derived scaffolds possess the same biological and physical properties.
Autor:
Laura E. Kakuk, F. Yesim Demirci, Michael Boehnke, Jiafan Liu, Eve L. Bingham, Radha Ayyagari, Julia E. Richards, Paul A. Sieving, Heather M. Stringham, Michael B. Gorin
Publikováno v:
Genomics. 80:166-171
We mapped a new X-linked recessive atrophic macular degeneration locus to Xp21.1-p11.4 and show allelic involvement of the gene RPGR, which normally causes severe peripheral retinal degeneration leading to global blindness. Ten affected males whom we
Autor:
Yumiko Toda, Paul A. Sieving, Eve L. Bingham, Jennifer A. Kemp, Janet J. Szczesny, Laura E. Kakuk, Joost Felius, Radha Ayyagari
Publikováno v:
Human Genetics. 107:75-82
Blue cone monochromacy (BCM) is an X-linked ocular disease characterized by poor visual acuity, nystagmus, and photodysphoria in males with severely reduced color discrimination. Deletions, rearrangements and point mutations in the red and green pigm
Autor:
Paul A. Sieving, Kent W. Small, Beverly M. Yashar, Richard G. Weleber, Kelaginamane Hiriyanna, David V. Weinberg, Richard A. Lewis, Julia E. Richards, Eve L. Bingham, Sten Andréasson, Gerald A. Fishman, Radha Ayyagari
Publikováno v:
Human Mutation. 14:423-427
Juvenile retinoschisis is an X-linked recessive disease caused by mutations in the XLRS1 gene. We screened 31 new unrelated patients and families for XLRS1 mutations in addition to previously reported mutations for 60 of our families (Retinoschisis C
Publikováno v:
American Journal of Ophthalmology. 128:179-184
PURPOSE: To present an Arg213Trp missense mutation in the XLRS1 gene in a family with juvenile X-linked retinoschisis in which one affected male had a normal electroretinogram scotopic b-wave amplitude. METHODS: Two affected males and one unaffected
Autor:
Mordechai Aladjem, Sung Han Kim, Wolfram Henn, Cigdem Altay, Terence P. Speed, Steven M. Haffner, John Blangero, Eve L. Bingham, Chi-Bew Chart, Jerry Pelletier, Katarzyna Dziechciowska, Sung Soo Hong, Paul A. Sieving, Kelaginamane Hiriyanna, Jean W. MacCluer, A. Gürgey, D. Castro de Guerra, Majid Ghahremani, Meridee Segal, Cashell E. Jaquish, Julia E. Richards, Chung Choo Lee, H. Arvelo, Young Bae Park, Francisco M. Salzano, Hemant Pawar, A. Rodríguez Larralde, Jae Jin Chae, Tzvy Bistritzer, Shili Lin, Yong Namkoong, Martin Tieder, André Reis, Michał Witt, Wojciech Cichy, M. P. Stern
Publikováno v:
Human Heredity. 46:I-IV
Autor:
Hemant Pawar, Eve L. Bingham, Julia E. Richards, Paul A. Sieving, Kelaginamane Hiriyanna, Meridee Segal
Publikováno v:
Human Heredity. 46:329-335
We studied 17 pedigrees with 108 affected males with X-linked juvenile retinoschisis (RS; McKusick No. 31270) and have analyzed all of the known polymorphic markers in the RS region of Xp22.1-p22.2 between DXS987 and DXS41. By haplotype analyses we f