Search Results - "Kapfhamer, D."

Protein Phosphatase 2a and glycogen synthase kinase 3 signaling modulate prepulse inhibition of the acoustic startle response by altering cortical M-Type potassium channel activity by Kapfhamer, David, Berger, Karen H, Hopf, F Woodward, Seif, Taban, Kharazia, Viktor, Bonci, Antonello, Heberlein, Ulrike

“…There is considerable interest in the regulation of sensorimotor gating, since deficits in this process could play a critical role in the symptoms of…”
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Taok2 controls behavioral response to ethanol in mice by Kapfhamer, D., Taylor, S., Zou, M. E., Lim, J. P., Kharazia, V., Heberlein, U.

“…Nervous system‐specific loss of Taok2 in mice alters ethanol‐induced sedation and consumption. Despite recent advances in the understanding of ethanol's…”
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Loss of RAB‐3/A in Caenorhabditis elegans and the mouse affects behavioral response to ethanol by Kapfhamer, D., Bettinger, J. C., Davies, A. G., Eastman, C. L., Smail, E. A., Heberlein, U., McIntire, S. L.

“…The mechanisms by which ethanol induces changes in behavior are not well understood. Here, we show that Caenorhabditis elegans loss‐of‐function mutations in…”
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Lmo4 in the nucleus accumbens regulates cocaine sensitivity by Lasek, A. W., Kapfhamer, D., Kharazia, V., Gesch, J., Giorgetti, F., Heberlein, U.

“…An estimated 2 million Americans use cocaine, resulting in large personal and societal costs. Discovery of the genetic factors that contribute to cocaine abuse…”
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Abnormal behavior in mice mutant for the Disc1 binding partner, Dixdc1 by Kivimäe, S, Martin, P-M, Kapfhamer, D, Ruan, Y, Heberlein, U, Rubenstein, J L R, Cheyette, B N R

“…Disrupted-in-Schizophrenia-1 ( DISC1 ) is a genetic susceptibility locus for major mental illness, including schizophrenia and depression. The Disc1 protein…”
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An automated system for recording and analysis of sleep in mice by VEASEY, Sigrid C, VALLADARES, Otto, FENIK, Polina, KAPFHAMER, David, SANFORD, Larry, BENINGTON, Joel, BUCAN, Maja

“…Significant differences in many aspects of sleep/wake activity among inbred strains of mice suggest genetic influences on the control of sleep. A number of…”
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Biochemical, molecular and behavioral phenotypes of Rab3A mutations in the mouse by Yang, S., Farias, M., Kapfhamer, D., Tobias, J., Grant, G., Abel, T., Bućan, M.

“…Ras‐associated binding (Rab) protein 3A is a neuronal guanosine triphosphate (GTP)‐binding protein that binds synaptic vesicles and regulates synaptic…”
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Difference between mean gestational sac diameter and crown-rump length as a marker of first-trimester pregnancy loss after in vitro fertilization by Kapfhamer, Joshua D., Palaniappan, Sruthi, Summers, Karen, Kassel, Kristen, Mancuso, Abigail C., Ryan, Ginny L., Shah, Divya K.

“…To investigate whether the difference between mean gestational sac diameter and crown-rump length (mGSD − CRL) is associated with first-trimester pregnancy…”
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Random Mutagenesis Screen for Dominant Behavioral Mutations in Mice by Nolan, P.M., Kapfhamer, D., Bućan, M.

“…Large-scale mutagenesis and screening for altered phenotypes have been used effectively in many (lower) model organisms to identify mutations in genes that…”
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The Importance of Risk Tolerance in Maternal Autonomy by Kapfhamer, Joshua D., Menon, Seema, Spellecy, Ryan

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Genetic map of the region around grizzled (gr) and mocha (mh) on mouse chromosome 10, homologous to human 19p13.3 by Kapfhamer, D, Burmeister, M

“…Grizzled (gr) is a recessive mouse mutation resulting in a gray coat color and reduced perinatal viability. Mocha (mh) is one of several recessive mouse…”
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The Neurological Mouse Mutations Jittery and Hesitant Are Allelic and Map to the Region of Mouse Chromosome 10 Homologous to 19p13.3 by Kapfhamer, David, Sweet, Hope O., Sufalko, Damaris, Warren, Sarah, Johnson, Ken R., Burmeister, M.

“…Jittery (ji) is a recessive mouse mutation on Chromosome 10 characterized by progressive ataxic gait, dystonic movements, spontaneus seizures, and death by…”
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Mutation in AP-3 δ in the mocha Mouse Links Endosomal Transport to Storage Deficiency in Platelets, Melanosomes, and Synaptic Vesicles by Kantheti, Prameela, Qiao, Xiaoxi, Diaz, Maria E, Peden, Andrew A, Meyer, Gary E, Carskadon, Shannon L, Kapfhamer, David, Sufalko, Damaris, Robinson, Margaret S, Noebels, Jeffrey L, Burmeister, Margit

“…The mouse mutant mocha, a model for the Hermansky-Pudlak storage pool deficiency syndrome, is characterized by defective platelets, coat and eye color…”
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Mutations in Rab3a alter circadian period and homeostatic response to sleep loss in the mouse by Bu an, Maja, Kapfhamer, David, Valladares, Otto, Sun, Yi, Nolan, Patrick M, Rux, John J, Arnold, Steven E, Veasey, Sigrid C

“…Rab3a is the most abundant Rab (ras-associated binding) protein in the brain and has a regulatory role in synaptic vesicle trafficking. Mice with a targeted…”
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A Sperm-Associated WD Repeat Protein Orthologous to Chlamydomonas PF20 Associates with Spag6, the Mammalian Orthologue of Chlamydomonas PF16 by Zhang, Zhibing, Sapiro, Rossana, Kapfhamer, David, Bucan, Maja, Bray, Jeff, Chennathukuzhi, Vargheese, McNamara, Peter, Curtis, Anne, Zhang, Mei, Blanchette-Mackie, E. Joan, Strauss, Jerome F.

“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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DIFFERENCE BETWEEN MEAN GESTATIONAL SAC AND CROWN-RUMP LENGTH AS A MARKER OF FIRST TRIMESTER PREGNANCY LOSS AFTER IN VITRO FERTILIZATION by Kapfhamer, Joshua D, Palaniappan, Sruthi, Summers, Karen, Kassel, Kristen, Mancuso, Abigail C, Ryan, Ginny L, Shah, Divya K

“…A small mean gestational sac diameter to crown rump length difference is associated with a significantly increased risk of first trimester pregnancy loss in…”
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Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints by Puttagunta, R, Gordon, L A, Meyer, G E, Kapfhamer, D, Lamerdin, J E, Kantheti, P, Portman, K M, Chung, W K, Jenne, D E, Olsen, A S, Burmeister, M

“…A cosmid/bacterial artificial chromosome (BAC) contiguous (contig) map of human chromosome (HSA) 19p13.3 has been constructed, and over 50 genes have been…”
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Chromosomal localization of the ankyrinG gene (ANK3/Ank3) to human 10q21 and mouse 10 by KAPFHAMER, D, MILLER, D. E, LAMBERT, S, BENNETT, V, GLOVER, T. W, BURMEISTER, M

“…The ankyrin3 gene encodes a novel form of ankyrin, AnkyrinG, expressed in multiple tissues but characteristically present at the axonal initial segment and…”
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