Search Results - "Crabb, Beau"

Whole Exome Sequencing, Familial Genomic Triangulation, and Systems Biology Converge to Identify a Novel Nonsense Mutation in TAB2-encoded TGF-beta Activated Kinase 1 in a Child with Polyvalvular Syndrome by Ackerman, Jaeger P, Smestad, John A, Tester, David J, Qureshi, Muhammad Y, Crabb, Beau A, Mendelsohn, Nancy J, Ackerman, Michael J

“…To use whole exome sequencing (WES) of a family trio to identify a genetic cause for polyvalvular syndrome. A male child was born with mild pulmonary valve…”
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Impact of the third trophic level in an obligate mutualism: do yucca plants benefit from parasitoids of yucca moths? by Crabb, B.A, Pellmyr, O

“…In obligate pollination mutualism, selection should favor increased exploitation by either party at the expense of the other. One potential pathway to increase…”
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Preference and performance of a gall-inducing sawfly: plant vigor, sex, gall traits and phenology by Fritz, Robert S., Crabb, Beau A., Hochwender, Cris G.

“…We performed an experiment on preference and performance of the leaf galling sawfly, Phyllocolpa leavitti (Hymenoptera: Tenthredinidae), to test predictions of…”
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Defection by plants in the yucca-yucca moth association: a test of the cheater plant hypothesis for Yucca treculeana by Amadeus Crabb, Beau, Pellmyr, Olle

“…In mutualisms, an underlying conflict of interests may select for defection from providing benefits. In the obligate mutualism between yuccas and yucca moths,…”
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Preference and performance of a gall-inducing sawfly: a test of the plant vigor hypothesis [Phyllocolpa leavitii] by Fritz, Robert S., Crabb, Beau A., Hochwender, Cris G.

“…To test the Plant Vigor Hypothesis, we determined female oviposition preference of Phyllocolpa leavitii (Hymenoptera: Tenthredinidae) for shoot lengths on 20…”
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Chimerism for 20q11.2 microdeletion of GDF5 explains discordant phenotypes in monochorionic‐diamniotic twins by Meredith, Matthew M., Crabb, Beau, Vargas, Marcelo, Hirsch, Betsy A.

“…Microdeletions of 20q11.2 are rare but have been associated with characteristic clinical findings. A 1.6 Mb minimal critical region has been identified that…”
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The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants by Tatton-Brown, Katrina, Zachariou, Anna, Loveday, Chey, Renwick, Anthony, Mahamdallie, Shazia, Aksglaede, Lise, Baralle, Diana, Barge-Schaapveld, Daniela, Blyth, Moira, Bouma, Mieke, Breckpot, Jeroen, Crabb, Beau, Dabir, Tabib, Cormier-Daire, Valerie, Fauth, Christine, Fisher, Richard, Gener, Blanca, Goudie, David, Homfray, Tessa, Hunter, Matthew, Jorgensen, Agnete, Kant, Sarina G, Kirally-Borri, Cathy, Koolen, David, Kumar, Ajith, Labilloy, Anatalia, Lees, Melissa, Marcelis, Carlo, Mercer, Catherine, Mignot, Cyril, Miller, Kathryn, Neas, Katherine, Newbury-Ecob, Ruth, Pilz, Daniela T, Posmyk, Renata, Prada, Carlos, Ramsey, Keri, Randolph, Linda M, Selicorni, Angelo, Shears, Deborah, Suri, Mohnish, Temple, I Karen, Turnpenny, Peter, Val Maldergem, Lionel, Varghese, Vinod, Veenstra-Knol, Hermine E, Yachelevich, Naomi, Yates, Laura, Rahman, Nazneen

“…Tatton-Brown-Rahman syndrome (TBRS; OMIM 615879), also known as the DNMT3A-overgrowth syndrome, is an overgrowth intellectual disability syndrome first…”
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AT-16CASE REPORT OF METASTATIC ATYPICAL TERATOID RHABDOID TUMOR (ATRT) SECONDARY TO AN INHERITED GERMLINE MUTATION IN THE SMARCA4 GENE: LITERATURE REVIEW AND RECOMMENDATIONS FOR TUMOR SURVEILLANCE OF ASYMPTOMATIC CARRIERS by Bendel, Anne, Skrypek, Mary, Hansen, Melissa, Wein, Amy, Kebriaei, Meysam, Baldinger, Shari, Pacheco, M. Cristina, Helseth, Peter, Bhambhani, Vikas, Petronio, Joseph, Crabb, Beau

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