Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Teresa L. Yang-Feng"'
Autor:
Lisa H. Plumley, Denise Yan, Teresa L. Yang-Feng, Yukun Yuan, Bret A. Hughes, Anuradha Swaminathan, A. K. Sharma, Gyanendra Kumar, Anand Swaroop
Publikováno v:
Scopus-Elsevier
To identify novel potassium channel genes expressed in the retina, we screened a human retina cDNA library with an EST sequence showing partial homology to inwardly rectifying potassium (Kir) channel genes. The isolated cDNA yielded a 2,961-base pair
Autor:
Frederick H. Leibach, Haiping Wang, Teresa L. Yang-Feng, Vadivel Ganapathy, You Jun Fei, Ramesh Kekuda, Puttur D. Prasad, Lawrence D. Devoe
Publikováno v:
American Journal of Physiology-Cell Physiology. 278:C1019-C1030
We have cloned and functionally characterized the human Na+-dependent high-affinity dicarboxylate transporter (hNaDC3) from placenta. The hNaDC3 cDNA codes for a protein of 602 amino acids with 12 transmembrane domains. When expressed in mammalian ce
Autor:
Vadivel Ganapathy, Frederick H. Leibach, Puttur D Prasad, Wei Huang, Haiping Wang, You Jun Fei, Lawrence D. Devoe, Hong Xia, Teresa L. Yang-Feng
Publikováno v:
Journal of Biological Chemistry. 274:14875-14883
We have cloned the human Na+-dependent multivitamin transporter (SMVT), which transports the water-soluble vitamins pantothenate, biotin, and lipoate, from a placental choriocarcinoma cell line (JAR). The cDNA codes for a protein of 635 amino acids w
Publikováno v:
Prenatal Diagnosis. 18:384-389
Trisomy 22 mosaicism diagnosed at 20 weeks' gestation by amniocentesis in a 35-year-old woman was not confirmed by fetal blood sampling. Subsequent fetal skin biopsy revealed trisomy 22 in 7 of the 15 fibroblasts analysed. We conclude that, depending
Autor:
Teresa L. Yang-Feng, Kathy Scott, Cathleen M. Lutz, Srish Sinha, Julia E. Richards, Wayne N. Frankel, Debra A. Thompson
Publikováno v:
Genomics. 46:287-290
Ppyr1, Npy5r,andNpy6r,the genes encoding mouse type 4, type 5, and type 6 members of the neuropeptide Y receptor family, have been mapped by interspecific backcross analysis to conserved linkage groups on mouse Chr 14, Chr 8, and Chr 18, respectively
Autor:
Yen-Ying Ma, Wen-Hwa Lee, Wen-Hai Chou, Yumay Chen, Kai-Hsuan Chang, Teresa L. Yang-Feng, Ming-Jer Tsai, Xiaohua Leng, Tung-Ti Chen, Bert W. O'Malley, Phang Lang Chen
Publikováno v:
Proceedings of the National Academy of Sciences. 94:9040-9045
The retinoblastoma protein (Rb) plays a critical role in cell proliferation, differentiation, and development. To decipher the mechanism of Rb function at the molecular level, we have systematically characterized a number of Rb-interacting proteins,
Autor:
Lisa H. Gibson, Jui-Der Liou, Hua Su, Yen-Ying Ma, Teresa L. Yang-Feng, Yun-Fai Chris Lau, Nancy J. Charest
Publikováno v:
American Journal of Medical Genetics. 70:134-137
Here we describe the first reported case of a patient with a familial paracentric inversion in the long arm of the Y chromosome and ambiguous genitalia. FISH analyses with Y chromosome YACs demonstrated that the inversion breakpoints of the patients
Publikováno v:
American Journal of Medical Genetics. 68:417-420
A newborn infant with multiple congenital anomalies was diagnosed with an unbalanced translocation of chromosomes 1 and 5. Studies of parental chromosomes revealed a complex rearrangement in the patient's mother involving the exchange of terminal lon
Autor:
Viviana Torres-Zamorano, Vadivel Ganapathy, Teresa L. Yang-Feng, Frederick H. Leibach, Srish Sinha, You Jun Fei, Puttur D. Prasad, Ramesh Kekuda
Publikováno v:
Journal of Biological Chemistry. 271:18657-18661
We have isolated a cDNA from a human placental choriocarcinoma cell cDNA library which, when expressed in HeLa cells, induces a Na+-dependent amino acid transport system with preference for zwitterionic amino acids. Anionic amino acids, cationic amin
Autor:
W. Roy Breg, Te-Yao Hsu, Teresa L. Yang-Feng, Jui-Der Liou, Joshua A. Copel, Maurice J. Mahoney
Publikováno v:
Prenatal Diagnosis. 16:169-172
We present a prenatal case of mosaicism with at least two monosomy cell lines : one with monosomy 21 (45,XY, - 21) and one missing the Y (45,X) and a possible third 46,XY in chorionic villus cell culture. Cytogenetic studies were initiated following