Search Results - "Menold, Marisa M."

novel role for Lsc/p115 RhoGEF and LARG in regulating RhoA activity downstream of adhesion to fibronectin by Dubash, Adi D, Wennerberg, Krister, García-Mata, Rafael, Menold, Marisa M, Arthur, William T, Burridge, Keith

“…Adhesion of cells to extracellular matrix proteins such as fibronectin initiates signaling cascades that affect cell morphology, migration and survival. Some…”
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Genomic screen and follow-up analysis for autistic disorder by Shao, Yujun, Wolpert, Chantelle M., Raiford, Kimberly L., Menold, Marisa M., Donnelly, Shannon L., Ravan, Sarah A., Bass, Meredyth P., McClain, Cate, von Wendt, Lennart, Vance, Jeffery M., Abramson, Ruth H., Wright, Harry H., Ashley-Koch, Allison, Gilbert, John R., DeLong, Robert G., Cuccaro, Michael L., Pericak-Vance, Margaret A.

“…Autistic disorder (AutD) is a neurodevelopmental disorder characterized by significant impairment in social, communicative, and behavioral functioning. A…”
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Chapter 1 Focal Adhesions: New Angles on an Old Structure by Dubash, Adi D., Menold, Marisa M., Samson, Thomas, Boulter, Etienne, García-Mata, Rafael, Doughman, Renee, Burridge, Keith

“…Focal adhesions have been intensely studied ever since their discovery in 1971. The last three decades have seen major advances in understanding the structure…”
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Autistic Disorder and Chromosome 15q11–q13: Construction and Analysis of a BAC/PAC Contig by Maddox, Lewis O., Menold, Marisa M., Bass, Meredyth P., Rogala, Allison R., Pericak-Vance, Margaret A., Vance, Jeffery M., Gilbert, John R.

“…Autistic disorder (AD) is a neurodevelopmental disorder that affects approximately 2–10/10,000 individuals. Chromosome 15q11–q13 has been implicated in the…”
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Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromes by Menold, M M, Sadeh, M, Lennon, F, Blatt, I, Goldhammer, Y, Yamaoka, L H, Vance, J M, Pericak-Vance, M A

“…Congenital myasthenic syndromes (CMS) define a diverse group of disorders, all of which compromise neuromuscular transmission. Symptoms can be present at birth…”
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Association Analysis of Chromosome 15 GABAA Receptor Subunit Genes in Autistic Disorder by Menold, Marisa M., Shao, Yujun, Wolpert, Chantelle M., Donnelly, Shannon L., Raiford, Kimberly L., Martin, Eden R., Ravan, Sarah A., Abramson, Ruth K., Wright, Harry H., Delong, G. Robert, Cuccaro, Michael L., Pericak-Vance, Margaret A., Gilbert, John R.

“…Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the brain, acting via the GABAA receptors. The GABAA receptors are comprised of…”
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Three probands with autistic disorder and isodicentric chromosome 15 by Wolpert, Chantelle M., Menold, Marisa M., Bass, Meredyth P., Qumsiyeh, Mazin B., Donnelly, Shannon L., Ravan, Sarah A., Vance, Jeffery M., Gilbert, John R., Abramson, Ruth K., Wright, Harry H., Cuccaro, Michael L., Pericak-Vance, Margaret A.

“…We have identified three unrelated probands with autistic disorder (AD) and isodicentric chromosomes that encompass the proximal region of 15q11.2. All three…”
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Association Analysis of Chromosome 15 GABA A Receptor Subunit Genes in Autistic Disorder by Menold, Marisa M., Shao, Yujun, Wolpert, Chantelle M., Donnelly, Shannon L., Raiford, Kimberly L., Martin, Eden R., Ravan, Sarah A., Abramson, Ruth K., Wright, Harry H., Delong, G. Robert, Cuccaro, Michael L., Pericak-Vance, Margaret A., Gilbert, John R.

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Female with autistic disorder and monosomy X (Turner syndrome): Parent-of-origin effect of the X chromosome by Donnelly, Shannon L., Wolpert, Chantelle M., Menold, Marisa M., Bass, Meredyth P., Gilbert, John R., Cuccaro, Michael L., Delong, G. Robert, Pericak-Vance, Margaret A.

“…We have ascertained and examined a patient with autistic disorder (AD) and monosomy X (Turner syndrome). The patient met Diagnostic and Statistical Manual of…”
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Genetic studies in autistic disorder and chromosome 15 by BASS, M. P, MENOLD, M. M, GILBERT, J. R, CUCCARO, M. L, DELONG, G. R, PERICAK-VANCE, M. A, WOLPERT, C. M, DONNELLY, S. L, RAVAN, S. A, HAUSER, E. R, MADDOX, L. O, VANCE, J. M, ABRAMSON, R. K, WRIGHT, H. H

“…Autistic disorder (AD) is a developmental disorder affecting social interactions, communication, and behavior. AD is a disease of complex genetic architecture…”
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Casein kinase I-like protein kinases encoded by YCK1 and YCK2 are required for yeast morphogenesis by ROBINSON, L. C, MENOLD, M. M, GARRETT, S, CULBERTSON, M. R

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SMS1, a high-copy suppressor of the yeast mas6 mutant, encodes an essential inner membrane protein required for mitochondrial protein import by Ryan, K R, Menold, M M, Garrett, S, Jensen, R E

“…MAS6 encodes an essential inner membrane protein required for mitochondrial protein import in the yeast Saccharomyces cerevisiae (Emtage and Jensen, 1993). To…”
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The Saccharomyces cerevisiae YAK1 gene encodes a protein kinase that is induced by arrest early in the cell cycle by GARRETT, S, MENOLD, M. M, BROACH, J. R

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Focal Adhesions: New Angles on an Old Structure

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Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity by Pericak-Vance, M A, Speer, M C, Lennon, F, West, S G, Menold, M M, Stajich, J M, Wolpert, C M, Slotterbeck, B D, Saito, M, Tim, R W, Rozear, M P, Middleton, L T, Tsuji, S, Vance, J M

“…The Charcot-Marie-Tooth (CMT) neuropathies are a group of disorders exhibiting neurophysical, pathological and genetic heterogeneity. CMT2 is a diagnostic…”
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Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia by Scott, W K, Gaskell, P C, Lennon, F, Wolpert, C M, Menold, M M, Aylsworth, A S, Warner, C, Farrell, C D, Boustany, R M, Albright, S G, Boyd, E, Kingston, H M, Cumming, W J, Vance, J M, Pericak-Vance, M A

“…We examined 11 Caucasian pedigrees with autosomal dominant 'uncomplicated' familial spastic paraplegia (SPG) for linkage to the previously identified loci on…”
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The Saccharomyces cerevisiae YAK1 Gene Encodes a Protein Kinase That Is Induced by Arrest Early in the Cell Cycle by Garrett, Stephen, Menold, Marisa M., Broach, James R.

“…Null mutations in the gene YAK1, which encodes a protein with sequence homology to known protein kinases, suppress the cell cycle arrest phenotype of mutants…”
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Casein Kinase I-Like Protein Kinases Encoded by YCK1 and YCK2 are Required for Yeast Morphogenesis by Robinson, Lucy C., Menold, Marisa M., Garrett, Stephen, Culbertson, Michael R.

“…Casein kinase I is an acidotropic protein kinase class that is widely distributed among eukaryotic cell types. In the yeast Saccharomyces cerevisiae, the…”
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Heterogeneity of spectrin distribution among avian muscle fiber types by Menold, M M, Repasky, E A

“…Muscle spectrin has been examined in avian fast, slow, and mixed muscles using the techniques of immunofluorescence microscopy and immunoautoradiography. By…”
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Increased concentration of spectrin is observed in avian dystrophic muscle by Repasky, E.A, Pollina, C.M, Menold, M.M, Hudecki, M.S

“…A significant increase in the concentration of spectrin has been observed in dystrophic chicken pectoralis major muscle when compared to normal fast-twitch…”
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