Chloroplast DNA sequence utility for the lowest phylogenetic and phylogeographic inferences in angiosperms: The tortoise and the hare IV von Shaw, Joey, Shafer, Hayden L, Leonard, O. Rayne, Kovach, Margaret J, Schorr, Mark, Morris, Ashley B

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Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein von Kimonis, Virginia E, Watts, Giles D J, Wymer, Jill, Kovach, Margaret J, Mehta, Sarju G, Mumm, Steven, Darvish, Daniel, Pestronk, Alan, Whyte, Michael P

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Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Fronto... von Kovach, Margaret J., Waggoner, Brook, Leal, Suzanne M., Gelber, David, Khardori, Romesh, Levenstien, Mark A., Shanks, Christy A., Gregg, Gregory, Al-Lozi, Muhammad T., Miller, Timothy, Rakowicz, Wojtek, Lopate, Glenn, Florence, Juliane, Glosser, Guila, Simmons, Zachary, Morris, John C., Whyte, Michael P., Pestronk, Alan, Kimonis, Virginia E.

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Genetic heterogeneity in autosomal dominant essential tremor von Kovach, Margaret J, Ruiz, Jimmy, Kimonis, Katerina, Mueed, Sajjad, Sinha, Shobhit, Higgins, Connie, Elble, Suzanne, Elble, Rodger, Kimonis, Virginia E

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Site-specific Photo-cross-linking between λ Integrase and Its DNA Recombination Target von Kovach, Margaret J., Tirumalai, Radhakrishna, Landy, Arthur

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Stable transformation of a mosquito cell line results in extraordinarily high copy numbers of the plasmid von Monroe, T.J. (Colorado State University, Fort Collins, CO), Muhlmann-Diaz, M.C, Kovach, M.J, Carlson, J.O, Bedford, J.S, Beaty, B.J

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Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone von Kimonis, V E, Kovach, M J, Waggoner, B, Leal, S, Salam, A, Rimer, L, Davis, K, Khardori, R, Gelber, D

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A Unique Point Mutation in the PMP22 Gene Is Associated with Charcot-Marie-Tooth Disease and Deafness von Kovach, Margaret J., Lin, Jing-Ping, Boyadjiev, Simeon, Campbell, Kathleen, Mazzeo, Larry, Herman, Kristin, Rimer, Lisa A., Frank, William, Llewellyn, Barbara, Wang Jabs, Ethylin, Gelber, David, Kimonis, Virginia E.

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Site-specific Photo-cross-linking between λ Integrase and Its DNA Recombination Target von Margaret J. Kovach, Radhakrishna Tirumalai, Arthur Landy

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Heterogeneity in familial dominant Paget disease of bone and muscular dystrophy von Waggoner, Brook, Kovach, Margaret J., Winkelman, Marc, Cai, Dan, Khardori, Romesh, Gelber, David, Kimonis, Virginia E.

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Kousseff syndrome caused by deletion of chromosome 22q11‐13 von Forrester, Shawnia, Kovach, Margaret J., Smith, Randell E., Rimer, Lisa, Wesson, Melissa, Kimonis, Virginia E.

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Clinical heterogeneity in autosomal dominant optic atrophy in two 3q28-qter linked central Illinois families von Chen, A S, Kovach, M J, Herman, K, Avakian, A, Frank, W, Forrester, S, Lin, J P, Kimonis, V

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Kousseff syndrome caused by deletion of chromosome 22q11-13 von Forrester, Shawnia, Kovach, Margaret J., Smith, Randell E., Rimer, Lisa, Wesson, Melissa, Kimonis, Virginia E.

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Expression of oncogenic HRAS in human Rh28 and RMS-YM rhabdomyosarcoma cells leads to oncogene-induced senescence von Li, Jenny J., Kovach, Alexander R., DeMonia, Margaret, Slemmons, Katherine K., Oristian, Kristianne M., Chen, Candy, Linardic, Corinne M.

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A Consensus Approach for Targeted Muscle Reinnervation in Amputees von Eberlin, Kyle R., Brown, David A., Gaston, R. Glenn, Kleiber, Grant M., Ko, Jason H., Kovach, Stephen J., Loeffler, Bryan J., MacKay, Brendan J., Potter, Benjamin K., Roubaud, Margaret S., Souza, Jason M., Valerio, Ian L., Dumanian, Gregory A.

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Progression Rate From Intermediate to Advanced Age-Related Macular Degeneration Is Correlated With the Number of Risk Alleles at the CFH Locus von Sardell, Rebecca J, Persad, Patrice J, Pan, Samuel S, Whitehead, Patrice, Adams, Larry D, Laux, Reneé A, Fortun, Jorge A, Brantley, Jr, Milam A, Kovach, Jaclyn L, Schwartz, Stephen G, Agarwal, Anita, Haines, Jonathan L, Scott, William K, Pericak-Vance, Margaret A

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Vision Loss Reduction with Avacincaptad Pegol for Geographic Atrophy: A 12-Month Post Hoc Analysis of the GATHER1 and GATHER2 Trials von Danzig, Carl J, Khanani, Arshad M, Kaiser, Peter K, Chang, Margaret A, Kovach, Jaclyn L, Lally, David R, Rachitskaya, Aleksandra, Sheth, Veeral S, Vajzovic, Lejla, Clark, Julie, Tang, Justin, Zhu, Liansheng, Desai, Dhaval, Chakravarthy, Usha

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Molecular Classification of MYC-Driven B-Cell Lymphomas by Targeted Gene Expression Profiling of Fixed Biopsy Specimens von Carey, Christopher D, Gusenleitner, Daniel, Chapuy, Bjoern, Kovach, Alexandra E, Kluk, Michael J, Sun, Heather H, Crossland, Rachel E, Bacon, Chris M, Rand, Vikki, Cin, Paola Dal, Le, Long P, Neuberg, Donna, Sohani, Aliyah R, Shipp, Margaret A, Monti, Stefano, Rodig, Scott J

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Whole exome sequencing of extreme age-related macular degeneration phenotypes von Sardell, Rebecca J, Bailey, Jessica N Cooke, Courtenay, Monique D, Whitehead, Patrice, Laux, Reneé A, Adams, Larry D, Fortun, Jorge A, Brantley, Jr, Milam A, Kovach, Jaclyn L, Schwartz, Stephen G, Agarwal, Anita, Scott, William K, Haines, Jonathan L, Pericak-Vance, Margaret A

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Vision Loss Reduction with Avacincaptad Pegol for Geographic Atrophy von Danzig, Carl J., Khanani, Arshad M., Kaiser, Peter K., Chang, Margaret A., Kovach, Jaclyn L., Lally, David R., Rachitskaya, Aleksandra, Sheth, Veeral S., Vajzovic, Lejla, Clark, Julie, Tang, Justin, Zhu, Liansheng, Desai, Dhaval, Chakravarthy, Usha

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