A one-dimensional Burridge-Knopoff spring-block model with slip-dependent friction was studied to explore the possibility of a solitary wave solution existing for the problem of earthquake faulting....
A one-dimensional Burridge-Knopoff spring-block model with slip-dependent friction was studied to explore the possibility of a solitary wave solution existing for the problem of earthquake faulting....
McGee, D J, Langford, M L, Watson, E L, Carter, J E, Chen, Y T, Ottemann, K M
Helicobacter pylori causes disease in the human stomach and in mouse and gerbil stomach models. Previous results have shown that motility is critical for H. pylori to colonize mice, gerbils, and...
Nomenclature of the GLUT/SLC2A family of sugar/polyol transport facilitators (2002)
Joost, Hans-Georg, Bell, Graeme I., Best, James D., Birnbaum, Morris J., Charron, Maureen J., Chen, Y. T., ...
The recent identification of several additional members of the family of sugar transport facilitators (gene symbol SLC2A, protein symbol GLUT) has created a heterogeneous and, in part, confusing...
A Study of the Effects of MnS Particle Size on the Fracture Toughness of Low Alloy P/M Steel. (1998)
Round compact tension (RCT) specimens and transverse rupture bars, made of R3755 low alloy steel with MnS additions of varying particle sizes and content, were sintered in a nitrogen atmosphere; the...
A one-dimensional Burridge-Knopoff spring-block model with slip-dependent friction was studied to explore the possibility of a solitary wave solution existing for the problem of earthquake faulting....
The China Digital Seismograph Network (1994)
Chen, Y. T., Mu, Q. D., Zhou, G. W.
The China Digital Seismograph Network (CDSN) program was initiated in May 1983. On October 1, 1986, the CDSN began to distribute the network-day tapes to the research community. On October 22, 1987,...
The China Digital Seismograph Network (1994)
Chen, Y. T.; Institute Of Geophysics, State Seismological Bureau, Beijing, China, Mu, Q. D.; Institute Of Geophysics, State Seismological Bureau, Beijing, China, Zhou, G. W.; Institute Of Geophysics, State Seismological Bureau, Beijing, China
The China Digital Seismograph Network (CDSN) program was initiated in May 1983. On October 1, 1986, the CDSN began to distribute the network-day tapes to the research community. On October 22, 1987,...
ANALYSIS OF THE $3^{1} A'$ STATE OF HCP (1994)
Rajaram, B., Wang, J., Chen, Y. T., Coy, Stephen L., Field, R. W.
$^{1}$S. P. Kama, P. J. Bruna, and F. Grein, Canad. J. Phys. 68 499 (1990)
Sub-barrier fusion of the oxygen isotopes: A more complete picture (1986)
Thomas, J., Chen, Y. T., Hinds, S., Meredith, D., Olson, M.
We have measured the sub-barrier fusion cross sections for 16,17,18O on 16O and we present the data and the experimental method in detail. The data were analyzed with a one-dimensional potential...
Sub-barrier fusion of 16O with 16,18O (1985)
Thomas, J., Chen, Y. T., Hinds, S., Langanke, K., Meredith, D., Olson, M., ...
We have measured the sub-barrier fusion cross sections for the 16O+ 16O and 16O+ 18O systems from Elab=13.5–25 MeV. We find no significant enhancement of the 16O+ 18O cross section compared with...
SUB-DOPPLER SPECTROSCOPY USING A MULTIPLE REFLECTION MIRROR SYSTEM (1985)
Chen, Y. T., Frye, J. M., Oka, T.
Author Institution: Department of Chemistry and Department of Astronomy and Astrophysics, University of Chicago
Gravitational Experiments in the Laboratory
Contenido: Introducción; Oscilador lineal manejado por ruido de termoagitación y amortiguamiento eléctrico; Fuentes externas del ruido y diseño de experimentos; El principio débil (interacción...
Gravitational Experiments in the Laboratory
Contenido: Introducción; Oscilador lineal manejado por ruido de termoagitación y amortiguamiento eléctrico; Fuentes externas del ruido y diseño de experimentos; El principio débil (interacción...
Amalfitano, A., McVie-Wylie, A. J., Hu, H., Dawson, T. L., Raben, N., Plotz, P., ...
This report demonstrates that a single intravenous administration of a gene therapy vector can potentially result in the correction of all affected muscles in a mouse model of a human genetic muscle...
Chen, Y T, Stockert, E, Jungbluth, A, Tsang, S, Coplan, K A, Scanlan, M J, ...
Recent progress in the structural identification of human melanoma antigens recognized by autologous cytotoxic T cells has led to the recognition of a new melanocyte differentiation antigen,...
Van Hove, J L, Yang, H W, Wu, J Y, Brady, R O, Chen, Y T
Infantile Pompe disease is a fatal genetic muscle disorder caused by a deficiency of acid alpha-glucosidase, a glycogen-degrading lysosomal enzyme. We constructed a plasmid containing a 5'-shortened...
Immunophenotyping of melanomas for tyrosinase: implications for vaccine development.
Chen, Y T, Stockert, E, Tsang, S, Coplan, K A, Old, L J
Tyrosinase (EC 1.14.18.1), the key enzyme in melanin synthesis, has been shown to be one of the targets for cytotoxic T-cell recognition in melanoma patients. To develop serological reagents useful...
Influence of interleukin 12 on p53 peptide vaccination against established Meth A sarcoma.
Noguchi, Y, Richards, E C, Chen, Y T, Old, L J
BALB/c murine sarcoma Meth A is known to have three missense point mutations in p53. We previously reported that a nonamer peptide containing the codon 234 mutational product (designated 234CM)...
A mouse mutant p53 product recognized by CD4+ and CD8+ T cells.
Noguchi, Y, Chen, Y T, Old, L J
The T-cell response to mutated and normal p53 products of BALB/c-derived Meth A sarcoma was analyzed. Meth A p53 is known to have three missense point mutations in codons 132, 168, and 234, and 24...
Chen, Y T, Holcomb, C, Moore, H P
Small GTP-binding proteins of the YPT/SEC4/Rab family have been shown to play an essential role in intracellular membrane trafficking. In mammals, Rab8 and Rab10 are the two small GTP-binding...
Chen, Y T, Rettig, W J, Yenamandra, A K, Kozak, C A, Chaganti, R S, Posner, J B, ...
Cerebellar degeneration-related antigen (designated CDR34) was previously cloned by antibody screening of a cDNA library and was shown to be one of the target molecules recognized by autoantibodies...
Influence of 5' flanking sequences on TL and H-2 expression in transfected L cells.
Obata, Y, Stockert, E, Chen, Y T, Takahashi, T, Old, L J
TL (thymus leukemia) antigens are encoded by genes in the major histocompatibility complex (MHC) of the mouse. Although similar in overall structure to other class I MHC antigens (H-2, Qa), TL...
Furneaux, H M, Dropcho, E J, Barbut, D, Chen, Y T, Rosenblum, M K, Old, L J, ...
Paraneoplastic cerebellar degeneration is a neurological disorder of unknown cause occurring in patients with an identified or occult cancer. An autoimmune etiology is likely since autoantibodies...
Lei, K J, Shelly, L L, Lin, B, Sidbury, J B, Chen, Y T, Nordlie, R C, ...
Glycogen storage disease (GSD) type 1, which is caused by the deficiency of glucose-6-phosphatase (G6Pase), is an autosomal recessive disease with heterogenous symptoms. Two models of G6Pase...
5'-structural analysis of genes encoding polymorphic antigens of chemically induced tumors.
Srivastava, P K, Chen, Y T, Old, L J
We have proposed that the distinct tumor rejection antigens of chemically induced sarcomas in inbred mice belong to a family of Mr 96,000 glycoproteins (gp96). An identical 14-amino acid sequence was...
Dropcho, E J, Chen, Y T, Posner, J B, Old, L J
Autoantibodies directed against neuronal proteins have been identified in some patients with paraneoplastic cerebellar degeneration. To identify the molecular targets for these autoantibodies, we...
Structural analysis of TL genes of the mouse.
Obata, Y, Chen, Y T, Stockert, E, Old, L J
Three Tla region-specific probes have been generated from the BALB/c genomic cosmid clone C6.3. One probe, pTL1, corresponds to 3' sequences of a thymus leukemia (TL)-encoding gene, whereas pTL2 and...
Hypertension and Impaired Glycine Handling in Mice Lacking the Orphan Transporter XT2
Quan, Hui, Athirakul, Krairerk, Wetsel, William C., Torres, Gonzalo E., Stevens, Robert, Chen, Y. T., ...
A family of orphan transporters has been discovered that are structurally related to the Na+-Cl−-dependent neurotransmitter transporters, including the dopamine transporter. One member of this...
Bao, Y, Kishnani, P, Wu, J Y, Chen, Y T
Glycogen storage disease type IV (GSD-IV) is an autosomal recessive disease resulting from deficient glycogen-branching enzyme (GBE) activity. The classic and most common form is progressive liver...
Shen, J, Bao, Y, Liu, H M, Lee, P, Leonard, J V, Chen, Y T
Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity. Most GSD-III patients are GDE deficient in both liver...
Kikuchi, T, Yang, H W, Pennybacker, M, Ichihara, N, Mizutani, M, Van Hove, J L, ...
Pompe disease is a fatal genetic muscle disorder caused by a deficiency of acid alpha-glucosidase (GAA), a glycogen degrading lysosomal enzyme. GAA-deficient (AMD) Japanese quails exhibit progressive...
Identification of the MAGE-1 gene product by monoclonal and polyclonal antibodies.
Chen, Y T, Stockert, E, Chen, Y, Garin-Chesa, P, Rettig, W J, ...
The human MAGE-1 gene encodes a melanoma peptide antigen recognized by autologous cytotoxic T lymphocytes. To produce antibodies against the MAGE-1 gene product, several approaches were taken. Three...
Gerin, I, Chen, Y T, De Barsy, T, De Lonlay, P, Dionisi-Vici, C, ...
Glycogen-storage diseases type I (GSD type I) are due to a deficiency in glucose-6-phosphatase, an enzymatic system present in the endoplasmic reticulum that plays a crucial role in blood glucose...
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood.
Van Hove, J L, Zhang, W, Kahler, S G, Roe, C R, Chen, Y T, Terada, N, ...
Medium-chain acyl-coenzyme A dehydrogenase (MCAD) deficiency is a disorder of fatty acid catabolism, with autosomal recessive inheritance. The disease is characterized by episodic illness associated...
Identification of a new mutation in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.
Ding, J H, Yang, B Z, Bao, Y, Roe, C R, Chen, Y T
A mutation involving an A-to-G nucleotide replacement at position 985 of the medium-chain acyl-CoA dehydrogenase (MCAD) cDNA was found in homozygous form in 18 unrelated MCAD-deficient families and...
Definitive prenatal diagnosis for type III glycogen storage disease.
Yang, B Z, Ding, J H, Brown, B I, Chen, Y T
Prenatal diagnosis for type III glycogen storage disease was performed by using (1) immunoblot analysis with a polyclonal antibody prepared against purified porcine-muscle debranching enzyme and (2)...
Chen, Y T, He, J K, Ding, J H, Brown, B I
Type III glycogen storage disease is caused by a deficiency of glycogen debranching-enzyme activity. Many patients with this disease have both liver and muscle involvement, whereas others have only...
Amalfitano, A., McVie-Wylie, A. J., Hu, H., Dawson, T. L., Raben, N., Plotz, P., ...
This report demonstrates that a single intravenous administration of a gene therapy vector can potentially result in the correction of all affected muscles in a mouse model of a human genetic muscle...
Chen, Y T, Stockert, E, Jungbluth, A, Tsang, S, Coplan, K A, Scanlan, M J, ...
Recent progress in the structural identification of human melanoma antigens recognized by autologous cytotoxic T cells has led to the recognition of a new melanocyte differentiation antigen,...
Van Hove, J L, Yang, H W, Wu, J Y, Brady, R O, Chen, Y T
Infantile Pompe disease is a fatal genetic muscle disorder caused by a deficiency of acid alpha-glucosidase, a glycogen-degrading lysosomal enzyme. We constructed a plasmid containing a 5'-shortened...
Immunophenotyping of melanomas for tyrosinase: implications for vaccine development.
Chen, Y T, Stockert, E, Tsang, S, Coplan, K A, Old, L J
Tyrosinase (EC 1.14.18.1), the key enzyme in melanin synthesis, has been shown to be one of the targets for cytotoxic T-cell recognition in melanoma patients. To develop serological reagents useful...
Influence of interleukin 12 on p53 peptide vaccination against established Meth A sarcoma.
Noguchi, Y, Richards, E C, Chen, Y T, Old, L J
BALB/c murine sarcoma Meth A is known to have three missense point mutations in p53. We previously reported that a nonamer peptide containing the codon 234 mutational product (designated 234CM)...
A mouse mutant p53 product recognized by CD4+ and CD8+ T cells.
Noguchi, Y, Chen, Y T, Old, L J
The T-cell response to mutated and normal p53 products of BALB/c-derived Meth A sarcoma was analyzed. Meth A p53 is known to have three missense point mutations in codons 132, 168, and 234, and 24...
Chen, Y T, Holcomb, C, Moore, H P
Small GTP-binding proteins of the YPT/SEC4/Rab family have been shown to play an essential role in intracellular membrane trafficking. In mammals, Rab8 and Rab10 are the two small GTP-binding...
Chen, Y T, Rettig, W J, Yenamandra, A K, Kozak, C A, Chaganti, R S, Posner, J B, ...
Cerebellar degeneration-related antigen (designated CDR34) was previously cloned by antibody screening of a cDNA library and was shown to be one of the target molecules recognized by autoantibodies...
Influence of 5' flanking sequences on TL and H-2 expression in transfected L cells.
Obata, Y, Stockert, E, Chen, Y T, Takahashi, T, Old, L J
TL (thymus leukemia) antigens are encoded by genes in the major histocompatibility complex (MHC) of the mouse. Although similar in overall structure to other class I MHC antigens (H-2, Qa), TL...
Furneaux, H M, Dropcho, E J, Barbut, D, Chen, Y T, Rosenblum, M K, Old, L J, ...
Paraneoplastic cerebellar degeneration is a neurological disorder of unknown cause occurring in patients with an identified or occult cancer. An autoimmune etiology is likely since autoantibodies...
Lei, K J, Shelly, L L, Lin, B, Sidbury, J B, Chen, Y T, Nordlie, R C, ...
Glycogen storage disease (GSD) type 1, which is caused by the deficiency of glucose-6-phosphatase (G6Pase), is an autosomal recessive disease with heterogenous symptoms. Two models of G6Pase...
5'-structural analysis of genes encoding polymorphic antigens of chemically induced tumors.
Srivastava, P K, Chen, Y T, Old, L J
We have proposed that the distinct tumor rejection antigens of chemically induced sarcomas in inbred mice belong to a family of Mr 96,000 glycoproteins (gp96). An identical 14-amino acid sequence was...
Dropcho, E J, Chen, Y T, Posner, J B, Old, L J
Autoantibodies directed against neuronal proteins have been identified in some patients with paraneoplastic cerebellar degeneration. To identify the molecular targets for these autoantibodies, we...
Structural analysis of TL genes of the mouse.
Obata, Y, Chen, Y T, Stockert, E, Old, L J
Three Tla region-specific probes have been generated from the BALB/c genomic cosmid clone C6.3. One probe, pTL1, corresponds to 3' sequences of a thymus leukemia (TL)-encoding gene, whereas pTL2 and...
Hypertension and Impaired Glycine Handling in Mice Lacking the Orphan Transporter XT2
Quan, Hui, Athirakul, Krairerk, Wetsel, William C., Torres, Gonzalo E., Stevens, Robert, Chen, Y. T., ...
A family of orphan transporters has been discovered that are structurally related to the Na+-Cl−-dependent neurotransmitter transporters, including the dopamine transporter. One member of this...
Bao, Y, Kishnani, P, Wu, J Y, Chen, Y T
Glycogen storage disease type IV (GSD-IV) is an autosomal recessive disease resulting from deficient glycogen-branching enzyme (GBE) activity. The classic and most common form is progressive liver...
Shen, J, Bao, Y, Liu, H M, Lee, P, Leonard, J V, Chen, Y T
Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity. Most GSD-III patients are GDE deficient in both liver...
Kikuchi, T, Yang, H W, Pennybacker, M, Ichihara, N, Mizutani, M, Van Hove, J L, ...
Pompe disease is a fatal genetic muscle disorder caused by a deficiency of acid alpha-glucosidase (GAA), a glycogen degrading lysosomal enzyme. GAA-deficient (AMD) Japanese quails exhibit progressive...
Identification of the MAGE-1 gene product by monoclonal and polyclonal antibodies.
Chen, Y T, Stockert, E, Chen, Y, Garin-Chesa, P, Rettig, W J, ...
The human MAGE-1 gene encodes a melanoma peptide antigen recognized by autologous cytotoxic T lymphocytes. To produce antibodies against the MAGE-1 gene product, several approaches were taken. Three...
Gerin, I, Chen, Y T, De Barsy, T, De Lonlay, P, Dionisi-Vici, C, ...
Glycogen-storage diseases type I (GSD type I) are due to a deficiency in glucose-6-phosphatase, an enzymatic system present in the endoplasmic reticulum that plays a crucial role in blood glucose...
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood.
Van Hove, J L, Zhang, W, Kahler, S G, Roe, C R, Chen, Y T, Terada, N, ...
Medium-chain acyl-coenzyme A dehydrogenase (MCAD) deficiency is a disorder of fatty acid catabolism, with autosomal recessive inheritance. The disease is characterized by episodic illness associated...