Search Results - "SCHULZ, T. C"

Latent profiles of impulsivity facets and associations with drinking behaviors by Stamates, A.L., Schulz, C.T., Ehlke, S.J., Thompson, L., Lau-Barraco, C., Kelley, M.L.

“…•Latent profile analysis examined typologies across UPPS-P facets.•A 3-profile solution was found with Low, Moderate, and Highest levels of UPPS-P…”
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Transient pluripotent cell populations during primitive ectoderm formation: correlation of in vivo and in vitro pluripotent cell development by Pelton, T A, Sharma, S, Schulz, T C, Rathjen, J, Rathjen, P D

“…Formation and differentiation of a pluripotent cell population is central to mammalian development, and the isolation, identification and manipulation of human…”
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Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome by HORIKE, S.-I, MITSUYA, K, MEGURO, M, KOTOBUKI, N, KASHIWAGI, A, NOTSU, T, SCHULZ, T. C, SHIRAYOSHI, Y, OSHIMURA, M

“…Human chromosome 11p15.5 harbors an intriguing imprinted gene cluster of 1 Mb. This imprinted domain is implicated in a wide variety of malignancies and…”
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Subtypes of Alcohol Expectancies Are Differentially Associated With Alcohol Use for Bisexual and Heterosexual Women by Stamates, A L, Schulz, C T, Rothstein, M C, Todaro, S M, Ehlke, S J, Kelley, M L

“…: Bisexual women, compared to heterosexual women, report greater amounts of alcohol use and heavy drinking. Alcohol expectancies (i.e., beliefs about alcohol…”
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LIT1, an Imprinted Antisense RNA in the Human KvLQT1 Locus Identified by Screening for Differentially Expressed Transcripts Using Monochromosomal Hybrids by Mitsuya, Kohzoh, Meguro, Makiko, Lee, Maxwell P., Katoh, Motonobu, Schulz, Thomas C., Kugoh, Hiroyuki, Yoshida, Mitsuaki A., Niikawa, Norio, Feinberg, Andrew P., Oshimura, Mitsuo

“…Mammalian imprinted genes are frequently arranged in clusters on particular chromosomes. The imprinting cluster on human chromosome 11p15 is associated with…”
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Multipoint imprinting analysis in sporadic colorectal cancers with and without microsatellite instability by Nishihara, S, Hayashida, T, Mitsuya, K, Schulz, T C, Ikeguchi, M, Kaibara, N, Oshimura, M

“…Disrupted imprinting is implicated in certain tumorigenesis. Since aberrant methylation has been described for a majority of microsatellite instability…”
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Construction of 700 human/mouse A9 monochromosomal hybrids and analysis of imprinted genes on human chromosome 6 by Inoue, J, Mitsuya, K, Maegawa, S, Kugoh, H, Kadota, M, Okamura, D, Shinohara, T, Nishihara, S, Takehara, S, Yamauchi, K, Schulz, T C, Oshimura, M

“…As an in vitro assay system for the identification of human imprinted genes, a library of human/mouse A9 monochromosomal hybrids containing a single, intact…”
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The mouse homeobox gene, Gbx2 : Genomic organization and expression in pluripotent cells in vitro and in vivo by CHAPMAN, G, REMISZEWSKI, J. L, WEBB, G. C, SCHULZ, T. C, BOTTEMA, C. D. K, RATHJEN, P. D

“…The Gbx2 homeodomain is widely conserved in metazoans. We investigated the mouse Gbx2 locus by isolation and characterization of genomic clones and by physical…”
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Histone variant H2A.Z is required for early mammalian development by Faast, Renate, Thonglairoam, Varaporn, Schulz, Thomas C, Beall, Jacquie, Wells, Julian R.E, Taylor, Helen, Matthaei, Klaus, Rathjen, Peter D, Tremethick, David J, Lyons, Ian

“…Fundamental to the process of mammalian development is the timed and coordinated regulation of gene expression. This requires transcription of a precise subset…”
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An unusual arrangement of 13 zinc fingers in the vertebrate gene Z13 by Schulz, T C, Hopwood, B, Rathjen, P D, Wells, J R

“…The zinc finger is a protein domain that imparts specific nucleic acid-binding activity on a wide range of functionally important proteins. In this paper we…”
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A new mouse model for Down syndrome by Kazuki, Y, Schulz, T C, Shinohara, T, Kadota, M, Nishigaki, R, Inoue, T, Kimura, M, Kai, Y, Abe, S, Shirayoshi, Y, Oshimura, M

“…Trisomy 21 (Ts21) is the most common live-born human aneuploidy and results in a constellation of features known as Down syndrome (DS). Ts21 is a frequent…”
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Human chromosome 21q22.2-qter carries a gene(s) responsible for downregulation of mlc2a and PEBP in Down syndrome model mice by Kazuki, Yasuhiro, Kimura, Motoshi, Nishigaki, Ryuichi, Kai, Yoshiteru, Abe, Satoshi, Okita, Chiga, Shirayoshi, Yasuaki, Schulz, Thomas C, Tomizuka, Kazuma, Hanaoka, Kazunori, Inoue, Toshiaki, Oshimura, Mitsuo

“…Congenital heart disease (CHD) is a major clinical manifestation of Down syndrome (DS). We recently showed that chimeric mice containing a human chromosome 21…”
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A family of RS domain proteins with novel subcellular localization and trafficking by Kavanagh, Steven J., Schulz, Thomas C., Davey, Philippa, Claudianos, Charles, Russell, Carrie, Rathjen, Peter D.

“…We report the sequence, conservation and cell biology of a novel protein, Psc1, which is expressed and regulated within the embryonic pluripotent cell…”
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Epigenetic reprogramming of the human H19 gene in mouse embryonic cells does not erase the primary parental imprint by Mitsuya, Kohzoh, Meguro, Makiko, Sui, Hajime, Schulz, Thomas C., Kugoh, Hiroyuki, Hamada, Hiroshi, Oshimura, Mitsuo

“…Background Genomic imprinting in mammals is thought to result from epigenetic modifications to chromosomes during gametogenesis, which leads to differential…”
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Cellular Senescence of a Human Bladder Carcinoma Cell Line (JTC-32) Induced by a Normal Chromosome 11 by Kugoh, Hiroyuki, Fujiwara, Mutsunori, Kihara, Kazunori, Fukui, Iwao, Horikawa, Izumi, Schulz, Thomas C, Oshimura, Mitsuo

“…Human chromosome 11 is expected to carry tumor suppressor genes for a variety of human cancers, including bladder carcinoma. To examine the functional role of…”
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Briareolate esters from the gorgonian Briareum asbestinum by Meginley, Rian J, Gupta, Prasoon, Schulz, Thomas C, McLean, Amanda B, Robins, Allan J, West, Lyndon M

“…Two new briarane diterpenoids briareolate esters J (1) and K (2) were isolated from the methanolic extract of the octocoral Briareum asbestinum collected off…”
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Genomic alterations in cultured human embryonic stem cells by Rao, Mahendra, Chakravarti, Aravinda, Maitra, Anirban, Arking, Dan E, Shivapurkar, Narayan, Ikeda, Morna, Stastny, Victor, Kassauei, Keyaunoosh, Sui, Guoping, Cutler, David J, Liu, Ying, Brimble, Sandii N, Noaksson, Karin, Hyllner, Johan, Schulz, Thomas C, Zeng, Xianmin, Freed, William J, Crook, Jeremy, Abraham, Suman, Colman, Alan, Sartipy, Peter, Matsui, Sei-Ichi, Carpenter, Melissa, Gazdar, Adi F

“…Cultured human embryonic stem cell (hESC) lines are an invaluable resource because they provide a uniform and stable genetic system for functional analyses and…”
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Differentiation of Human Embryonic Stem Cells to Dopaminergic Neurons in Serum‐Free Suspension Culture by Schulz, Thomas C., Noggle, Scott A., Palmarini, Gail M., Weiler, Deb A., Lyons, Ian G., Pensa, Kate A., Meedeniya, Adrian C.B., Davidson, Bruce P., Lambert, Nevin A., Condie, Brian G.

“…The use of human embryonic stem cells (hESCs) as a source of dopaminergic neurons for Parkinson's disease cell therapy will require the development of simple…”
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Karyotypic stability, genotyping, differentiation, feeder-free maintenance, and gene expression sampling in three human embryonic stem cell lines derived prior to August 9, 2001 by Brimble, Sandii N, Zeng, Xianmin, Weiler, Deborah A, Luo, Yongquan, Liu, Ying, Lyons, Ian G, Freed, William J, Robins, Allan J, Rao, Mahendra S, Schulz, Thomas C

“…The number of human embryonic stem cell (hESC) lines available to federally funded U.S. researchers is currently limited. Thus, determining their basic…”
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Mouse A9 cells containing single human chromosomes for analysis of genomic imprinting by Kugoh, H, Mitsuya, K, Meguro, M, Shigenami, K, Schulz, T C, Oshimura, M

“…To develop an systematic in vitro approach for the study of genomic imprinting, we generated a new library of human/mouse A9 monochromosomal hybrids. We used…”
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