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Genome-Wide Methylation Study Identifies an IL-13-induced Epigenetic Signature in Asthmatic Airways 全基因组甲基化研究确定哮喘气道中的IL-13-induced表观遗传特征 Nicodemus-Johnson, Jessie; Naughton, Katherine A.; Sudi, Jyotsna; Hogarth, Kyle; Naurekas, Edward T.; Nicolae, Dan L.; Sperling, Anne I.; Solway, Julian; White, Steven R.; Ober, Carole 分享 收藏
Maternal asthma and microRNA regulation of soluble HLA-G in the airway Nicodemus-Johnson, Jessie; Laxman, Bharathi; Stern, Randi K.; Sudi, Jyotsna; Tierney, Courtney N.; Norwick, Lourdes; Hogarth, Douglas K.; McConville, John F.; Naureckas, Edward T.; Sperling, Anne I.; Solway, Julian; Krishnan, Jerry A.; Nicolae, Dan L.; White, Steven R.; Ober, Carole 分享 收藏
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Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7q Pavone, Piero; Ruggieri, Martino; Lombardo, Ilaria; Sudi, Jyotsna; Biancheri, Roberta; Castellano-Chiodo, Danilo; Rossi, Andrea; Incorpora, Gemma; Nowak, Norma J.; Christian, Susan L.; Pavone, Lorenzo; Dobyns, William B. 分享 收藏
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism Kumar, Ravinesh A.; Sudi, Jyotsna; Babatz, Timothy D.; Brune, Camille W.; Oswald, Donald; Yen, Mayon; Nowak, Norma J.; Cook, Edwin H.; Christian, Susan L.; Dobyns, William B. 分享 收藏
Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females Marsh, Eric; Fulp, Carl; Gomez, Ernest; Nasrallah, Ilya; Minarcik, Jeremy; Sudi, Jyotsna; Christian, Susan L.; Mancini, Grazia; Labosky, Patricia; Dobyns, William; Brooks-Kayal, Amy; Golden, Jeffrey A. 分享 收藏
Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum (vol 40, pg 1065, 2008) Najm, Juliane; Horn, Denise; Wimplinger, Isabella; Golden, Jeffrey A.; Chizhikov, Victor V.; Sudi, Jyotsna; Christian, Susan L.; Ullmann, Reinhard; Kuechler, Alma; Haas, Carola A.; Flubacher, Armin; Charnas, Lawrence R.; Uyanik, Goekhan; Frank, Ulrich; Klopocki, Eva; Dobyns, William B.; Kutsche, Kerstin 分享 收藏
Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum Najm, Juliane; Horn, Denise; Wimplinger, Isabella; Golden, Jeffrey A.; Chizhikov, Victor V.; Sudi, Jyotsna; Christian, Susan L.; Ullmann, Reinhard; Kuechler, Alma; Haas, Carola A.; Flubacher, Armin; Charnas, Lawrence R.; Uyanik, Goekhan; Frank, Ulrich; Klopocki, Eva; Dobyns, William B.; Kutsche, Kerstin 分享 收藏
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder Christian, Susan L.; Brune, Camille W.; Sudi, Jyotsna; Kumar, Ravinesh A.; Liu, Shaung; Karamohamed, Samer; Badner, Judith A.; Matsui, Seiichi; Conroy, Jeffrey; McQuaid, Devin; Gergel, James; Hatchwell, Eli; Gilliam, T. Conrad; Gershon, Elliot S.; Nowak, Norma J.; Dobyns, William B.; Cook, Edwin H., Jr. 分享 收藏
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Recurrent 16p11.2 microdeletions in autism Kumar, Ravinesh A.; KaraMohamed, Samer; Sudi, Jyotsna; Conrad, Donald F.; Brune, Camille; Badner, Judith A.; Gilliam, T. Conrad; Nowak, Norma J.; Cook, Edwin H., Jr.; Dobyns, William B.; Christian, Susan L. 分享 收藏