Search Results - "VERP, M. S"

HLA-G1 protein expression is not essential for fetal survival by Ober, C., Aldrich, C., Rosinsky, B., Robertson, A., Walker, M.A., Willadsen, S., Verp, M.S., Geraghty, D.E., Hunt, J.S.

“…HLA-G is a nonclassical, class I HLA gene that is primarily expressed by fetal cells at the maternal-fetal interface and is thought to play a key role in the…”
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A null mutation in HLA-G is not associated with preeclampsia or intrauterine growth retardation by Aldrich, Carrie, Verp, Marion S, Walker, Mary Ann, Ober, Carole

“…Modulation of the expression of genes of the major histocompatibility complex (MHC) in tissues at the maternal–fetal interface almost certainly plays a role in…”
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Genetic counseling : Clinical and ethical challenges by MAHOWALD, M. B, VERP, M. S, ANDERSON, R. R

“…After explaining the origin, nature, and goals of genetic counseling, we consider the impact of the Human Genome Project on its practice. In light of the…”
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Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis by Kubota, T, Aradhya, S, Macha, M, Smith, A C, Surh, L C, Satish, J, Verp, M S, Nee, H L, Johnson, A, Christan, S L, Ledbetter, D H

“…Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are distinct developmental disorders caused by absence of paternal or maternal contributions of the…”
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Cellular response in rabbit eyes after human fetal RPE cell transplantation by GABRIELIAN, K, OGANESIAN, A, PATEL, S. C, VERP, M. S, ERNEST, J. T

“…This study was carried out to study inflammatory and proliferative cellular responses in the rabbit eye after subretinal transplantation of human fetal retinal…”
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Choroid plexus cysts: Infant and early childhood developmental outcome by Digiovanni, Laura M., Quinlan, Maura Parker, Verp, Marion S.

“…To determine the infant and early childhood developmental outcome associated with choroid plexus cysts diagnosed prenatally. Between January 1990 and August…”
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Chimerism as the etiology of a 46,XX/46,XY fertile true hermaphrodite by Verp, M S, Harrison, H H, Ober, C, Oliveri, D, Amarose, A P, Lindgren, V, Talerman, A

“…To determine the conceptional events resulting in a 46,XX/46,XY true hermaphrodite and to report the first pregnancy in a 46,XX/46,XY true hermaphrodite with…”
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Preferences of pregnant women for amniocentesis or chorionic villus sampling for prenatal testing: comparison of patients' choices and those of a decision-analytic model by Heckerling, P S, Verp, M S, Hadro, T A

“…Decision analytic models have suggested that the choice of amniocentesis or chorionic villus sampling for prenatal genetic testing is a utility-driven…”
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Developmental regulation of the catalytic subunit of the apolipoprotein B mRNA editing enzyme (APOBEC-1) in human small intestine by Giannoni, F, Chou, S C, Skarosi, S F, Verp, M S, Field, F J, Coleman, R A, Davidson, N O

“…Apolipoprotein (apo) B mRNA editing is a site-specific cytidine deamination reaction responsible for the production of apoB-48 in mammalian small intestine…”
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Amniocentesis or chorionic villus sampling for prenatal genetic testing: a decision analysis by Heckerling, P S, Verp, M S

“…We used decision analysis to examine the strategies of amniocentesis, chorionic villus sampling, and no prenatal testing for a pregnant woman who would be 35…”
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Growth of human fetal retinal pigment epithelium as microspheres by GABRIELIAN, K, OGANESIAN, A, FARROKH-SIAR, L, REZAI, K. A, VERP, M. S, PATEL, S. C, ERNEST, J. T

“…The aim was to develop a three-dimensional cell culture system for human fetal retinal pigment epithelial (HFRPE) cells for in vitro cellular studies and for…”
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Prenatal testing for limb reduction defects : How patients' views affect their choice of CVS by HECKERLING, P. S, VERP, M. S, ALBERT, N

“…To determine the effect of reports and media coverage on chorionic villus sampling (CVS) and limb reduction defects (LRD) on patients' utilization of CVS for…”
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Maternal-fetal histocompatibility in intrauterine growth retarded and normal weight babies by Verp, M S, Sibul, M, Billstrand, C, Bellen, G, Hsu, M, Ober, C

“…To determine whether risk for intrauterine growth retardation (IUGR) is increased in HLA-DQA1 compatible pregnancies. Paired maternal and cord blood samples…”
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Cook obstetrics and gynecology catheter multicenter chorionic villus sampling trial: comparison of birth defects with expected rates by Blakemore, K, Filkins, K, Luthy, D A, Platt, L D, Medearis, A L, Carlson, D, Priest, J, Korotkin, J, Verp, M S, Padilla, L M

“…The null hypothesis was that offspring of women undergoing first-trimester chorionic villus sampling do not experience a rate of birth defects exceeding…”
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Posterior urethral valves in successive generations by Hanlon-Lundberg, K M, Verp, M S, Loy, G

“…Posterior urethral valves (PUV) are a frequent cause of urinary tract obstruction in infant males and may be diagnosed by antenatal ultrasound. PUV have been…”
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Inflammatory bowel disease and X chromosome abnormalities. A case report by VERP, M. S, AMAROSE, A. P

“…An abnormal sex chromosome constitution (45,X/46,XX) was observed in a woman with Crohn's disease and multiple spontaneous abortions. Immunologic disorders,…”
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Genetic risk and early versus late prenatal testing by Heckerling, P S, Verp, M S

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Fetal urinary tract obstruction and Trisomy 18 mosaicism: a case report by VERP, M. S, ISMAIL, M. A, SHEIKH, Z

“…Routine ultrasound examination has led increasingly to antepartum detection of fetal anomalies. Management decisions remain difficult, however, because…”
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Mucopolysaccharidosis type VII as a cause of recurrent non-immune hydrops fetalis by Cheng, Yvonne, Verp, Marion S, Knutel, Terri, Hibbard, Judith U

“…Mucopolysaccharidosis type VII (MPS VII) is a rare lysosomal storage disease first described by Sly in 1973. There are fewer than thirty reported cases world…”
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PRENATAL DIAGNOSIS OF UNIPARENTAL DISOMY 15 FOLLOWING TRISOMY 15 MOSAICISM by CHRISTIAN, SUSAN L., SMITH, ANN C. M., MACHA, MICHELLE, BLACK, SUSAN H., ELDER, FREDERICK F. B., JOHNSON, JAMIE M.-P., RESTA, ROBERT G., SURTI, URVASHI, SUSLAK, LORRAINE, VERP, MARION S., LEDBETTER, DAVID H.

“…Maternal uniparental disomy 15 (UPD15), responsible for approximately 25 per cent of Prader–Willi syndrome cases, is usually caused by maternal meiosis I…”
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