Search Results - "Jenkins, C E"

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  1. 1

    Autism severity is associated with child and maternal MAOA genotypes by Cohen, IL, Liu, X, Lewis, MES, Chudley, A, Forster-Gibson, C, Gonzalez, M, Jenkins, EC, Brown, WT, Holden, JJA

    Published in Clinical genetics (01-04-2011)
    “…Cohen IL, Liu X, Lewis MES, Chudley A, Forster‐Gibson C, Gonzalez M, Jenkins EC, Brown WT, Holden JJA. Autism severity is associated with child and maternal…”
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    Journal Article
  2. 2

    Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH by Zhang, Y-X, Zhang, Y-P, Gu, Y, Guan, F-J, Li, S-L, Xie, J-S, Shen, Y, Wu, B-L, Ju, W, Jenkins, EC, Brown, WT, Zhong, N

    Published in Clinical genetics (01-02-2009)
    “…Miscarriage is the spontaneous loss of an embryo or fetus before the 20th week of pregnancy. Most miscarriages occur before the end of the first trimester (<13…”
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  3. 3

    Association of autism severity with a monoamine oxidase A functional polymorphism by Cohen, IL, Liu, X, Schutz, C, White, BN, Jenkins, EC, Brown, WT, Holden, JJA

    Published in Clinical genetics (01-09-2003)
    “…A functional polymorphism (the upstream variable‐number tandem repeat region, or uVNTR) in the monoamine oxidase A (MAOA) promoter region has been reported to…”
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  4. 4

    Textured growth of diamond on silicon via in situ carburization and bias-enhanced nucleation by WOLTER, S. D, STONER, B. R, GLASS, J. T, ELLIS, P. J, BUHAENKO, D. S, JENKINS, C. E, SOUTHWORTH, P

    Published in Applied physics letters (15-03-1993)
    “…Ordered diamond films have been deposited on single-crystal silicon substrates via an in situ carburization followed by bias-enhanced nucleation. Textured…”
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  5. 5

    Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype by Velinov, M., Kupferman, J., Gu, H., Macera, M.J., Babu, A., Jenkins, E.C., Kupchik, G.

    “…A three year-old boy was evaluated because of growth and developmental delay, hypotonia and dysmorphic features. G-banding analysis revealed a small…”
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  6. 6

    An improved method for detecting telomere size differences in T-lymphocyte interphases from older people with Down syndrome with and without mild cognitive impairment by Jenkins, E. C., Ye, L., Marchi, E., Krinsky-McHale, S. J., Zigman, W. B., Schupf, N., Silverman, W. P.

    Published in Biology methods and protocols (01-01-2017)
    “…Abstract Telomere size (quantified by fluorescence intensity and physical lengths) in short-term T-lymphocyte cultures from adults with Down syndrome (DS) with…”
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  7. 7

    Adult fragile X syndrome: clinico-neuropathologic findings by RUDELLI, R. D, BROWN, W. T, WISNIEWSKI, K, JENKINS, E. C, LAURE-KAMIONOWSKA, M, CONNELL, F, WISNIEWSKI, H. M

    Published in Acta neuropathologica (01-01-1985)
    “…Fragile X syndrome [fra (X)] is currently accepted as the second most frequent chromosomal disorder associated with developmental disability. Although next to…”
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  8. 8

    Viral pharmacovigilance study of haemophiliacs receiving porcine factor VIII by Giangrande, P. L. F., Kessler, C. M., Jenkins, C. E., Weatherill, P. J., Webb, P. D.

    “…Porcine factor VIII (FVIII; Hyate:C; Speywood Biopharm Ltd, UK) has been used since 1980 for the treatment both of patients with acquired haemophilia and those…”
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  9. 9

    Why are autism and the fragile-X syndrome associated ? conceptual and methodological issues by COHEN, I. L, SUDHALTER, V, PFADT, A, JENKINS, E. C, BROWN, W. T, VIETZE, P. M

    Published in American journal of human genetics (01-02-1991)
    “…Investigations of the association between autism and the fragile-X syndrome have yielded conflicting results with some studies indicating a strong correlation…”
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  10. 10

    Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies by Hsu, L Y, Kaffe, S, Jenkins, E C, Alonso, L, Benn, P A, David, K, Hirschhorn, K, Lieber, E, Shanske, A, Shapiro, L R

    Published in Prenatal diagnosis (01-07-1992)
    “…Currently, accepted protocol which has been developed at the Prenatal Diagnosis Laboratory of New York City (PDL) requires that when a chromosome abnormality…”
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  11. 11

    An enzyme-linked immunosorbent assay for detection of porcine parvovirus in fetal tissues by Jenkins, C E

    Published in Journal of virological methods (01-09-1992)
    “…An enzyme-linked immunosorbent assay for porcine parvovirus was developed for laboratory detection of parvovirus antigen in fetal tissues and compared with the…”
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  12. 12

    Parent-child dyadic gaze patterns in fragile X males and in non-fragile X males with autistic disorder by Cohen, I L, Vietze, P M, Sudhalter, V, Jenkins, E C, Brown, W T

    Published in Journal of child psychology and psychiatry (01-11-1989)
    “…Parent-child dyadic gaze patterns were examined in fragile X [fra(X)] males and in non-fra(X) autistic males across three age groups--early childhood, middle…”
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  13. 13

    LiverClear: A versatile protocol for mouse liver tissue clearing by Molina, Laura M., Krutsenko, Yekaterina, Jenkins, Nathaniel E.C., Smith, Megan C., Tao, Junyan, Wheeler, Travis B., Watkins, Simon C., Watson, Alan M., Monga, Satdarshan P.

    Published in STAR protocols (18-03-2022)
    “…Although there are numerous tissue clearing protocols, most are inadequate for clearing liver tissue. Here we present a flexible protocol for mouse liver…”
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  14. 14

    Mitotic index and Alzheimerʼs disease by Jenkins, Edmund C, Ye, Lingling, Gu, Hong, Wisniewski, Henryk M

    Published in Neuroreport (01-12-1998)
    “…ALZHEIMERʼS disease (AD), a progressive neurodegenerative disorder, is diagnosed definitively by increased numbers of β-amyloid plaques and neurofibrillary…”
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  15. 15

    Substrate Reduction Therapy in Four Patients with Milder CLN1 Mutations and Juvenile-Onset Batten Disease Using Cysteamine Bitartrate by Gavin, M., Wen, G. Y., Messing, J., Adelman, S., Logush, A., Jenkins, E. C., Brown, W. T., Velinov, M.

    Published in JIMD Reports - Volume 11 (01-01-2013)
    “…Homozygous mutations in the gene CLN1 typically result in infantile-onset neuronal ceroid lipofuscinosis, a severe progressive neurological disorder with early…”
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    Book Chapter Journal Article
  16. 16

    Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test by Brown, W. Ted, Houck, George E, Jeziorowska, Anna, Levinson, Faye N, Ding, Xiaohua, Dobkin, Carl, Zhong, Nan, Henderson, Jeanine, Brooks, Susan Sklower, Jenkins, Edmund C

    “…Objective.—To develop a rapid, nonradioactive test using the polymerase chain reaction (PCR) capable of detecting full fragile X mutations, premutations, and…”
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  17. 17

    Gamow's Cyclist: A New Look at Relativistic Measurements for a Binocular Observer by Cryer-Jenkins, E. C, Stevenson, P. D

    Published 26-06-2019
    “…The visualisation of objects moving at relativistic speeds has been a popular topic of study since Special Relativity's inception. While the standard…”
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  18. 18

    Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation by Miezejeski, Charles M., Heaney, Glenn, Belser, Richard, Brown, W. Ted, Jenkins, Edmund C., Sersen, Eugene A.

    Published in American journal of medical genetics (18-04-1997)
    “…Brainstem auditory evoked response latencies were studied in 75 males (13 with fragile X syndrome, 18 with mental retardation due to other causes, and 44 with…”
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  19. 19

    Polymerase chain reaction analysis of fragile X mutations by ERSTER, S. H, TED BROWN, W, GOONEWARDENA, P, DOBKIN, C. S, JENKINS, E. C, PERGOLIZZI, R. G

    Published in Human genetics (01-09-1992)
    “…The mutation that underlies the fragile X syndrome is presumed to be a large expansion in the number of CGG repeats within the gene FMR-1. The unusually…”
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  20. 20

    Further evidence for genetic heterogeneity in the fragile X syndrome by BROWN, W. T, JENKINS, E. C, GROSS, A. C, CHAN, C. B, KRAWCZUN, M. S, DUNCAN, C. J, SKOWLER, S. L, FISCH, G. S

    Published in Human genetics (01-04-1987)
    “…The X-linked fragile X [fra(X)] syndrome, associated with a fragile site at Xq27.3, is the most common Mendelian inherited form of mental deficiency…”
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