Vitamin B(12) Metabolism during Pregnancy and in Embryonic Mouse Models

por Moreno-Garcia, Maira A., Rosenblatt, David S., Jerome-Majewska, Loydie A.
Publicado 2013

Transmembrane emp24 domain proteins in development and disease.

por Aber, Rachel, Chan, Wesley, Mugisha, Sevane, Jerome-Majewska, Loydie A.
Publicado 2019

Alternative splicing is frequent during early embryonic development in mouse

por Revil, Timothée, Gaffney, Daniel, Dias, Christel, Majewski, Jacek, Jerome-Majewska, Loydie A
Publicado 2010

Non-alcoholic fatty liver disease in mice with heterozygous mutation in TMED2

por Hou, Wenyang, Gupta, Swati, Beauchamp, Marie-Claude, Yuan, Libin, Jerome-Majewska, Loydie A.
Publicado 2017

Craniofacial Defects in Embryos with Homozygous Deletion of Eftud2 in Their Neural Crest Cells Are Not Rescued by Trp53 Deletion

por Beauchamp, Marie-Claude, Boucher, Alexia, Dong, Yanchen, Aber, Rachel, Jerome-Majewska, Loydie A.
Publicado 2022

TMED2 binding restricts SMO to the ER and Golgi compartments

por Di Minin, Giulio, Holzner, Markus, Grison, Alice, Dumeau, Charles E., Chan, Wesley, Monfort, Asun, Jerome-Majewska, Loydie A., Roelink, Henk, Wutz, Anton
Publicado 2022

Somatic overgrowth associated with homozygous mutations in both MAN1B1 and SEC23A

por Gupta, Swati, Fahiminiya, Somayyeh, Wang, Tracy, Dempsey Nunez, Laura, Rosenblatt, David S., Gibson, William T., Gilfix, Brian, Bergeron, John J. M., Jerome-Majewska, Loydie A.
Publicado 2016

Snrpb is required in murine neural crest cells for proper splicing and craniofacial morphogenesis

por Alam, Sabrina Shameen, Kumar, Shruti, Beauchamp, Marie-Claude, Bareke, Eric, Boucher, Alexia, Nzirorera, Nadine, Dong, Yanchen, Padilla, Reinnier, Zhang, Si Jing, Majewski, Jacek, Jerome-Majewska, Loydie A.
Publicado 2022

Snap29 mutant mice recapitulate neurological and ophthalmological abnormalities associated with 22q11 and CEDNIK syndrome

por Keser, Vafa, Lachance, Jean-François Boisclair, Alam, Sabrina Shameen, Lim, Youngshin, Scarlata, Eleonora, Kaur, Apinder, Zhang, Tian Fang, Lv, Shasha, Lachapelle, Pierre, O’Flaherty, Cristian, Golden, Jeffrey A., Jerome-Majewska, Loydie A.
Publicado 2019

Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS

por McDonald-McGinn, Donna M, Fahiminiya, Somayyeh, Revil, Timothée, Nowakowska, Beata A, Suhl, Joshua, Bailey, Alice, Mlynarski, Elisabeth, Lynch, David R, Yan, Albert C, Bilaniuk, Larissa T, Sullivan, Kathleen E, Warren, Stephen T, Emanuel, Beverly S, Vermeesch, Joris R, Zackai, Elaine H, Jerome-Majewska, Loydie A
Publicado 2013

Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro–costo–mandibular syndrome

por Lynch, Danielle C., Revil, Timothée, Schwartzentruber, Jeremy, Bhoj, Elizabeth J., Innes, A. Micheil, Lamont, Ryan E., Lemire, Edmond G., Chodirker, Bernard N., Taylor, Juliet P., Zackai, Elaine H., McLeod, D. Ross, Kirk, Edwin P., Hoover-Fong, Julie, Fleming, Leah, Savarirayan, Ravi, Majewski, Jacek, Jerome-Majewska, Loydie A., Parboosingh, Jillian S., Bernier, Francois P.
Publicado 2014

Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation

por Gurumurthy, Channabasavaiah B., O’Brien, Aidan R., Quadros, Rolen M., Adams, John, Alcaide, Pilar, Ayabe, Shinya, Ballard, Johnathan, Batra, Surinder K., Beauchamp, Marie-Claude, Becker, Kathleen A., Bernas, Guillaume, Brough, David, Carrillo-Salinas, Francisco, Chan, Wesley, Chen, Hanying, Dawson, Ruby, DeMambro, Victoria, D’Hont, Jinke, Dibb, Katharine M., Eudy, James D., Gan, Lin, Gao, Jing, Gonzales, Amy, Guntur, Anyonya R., Guo, Huiping, Harms, Donald W., Harrington, Anne, Hentges, Kathryn E., Humphreys, Neil, Imai, Shiho, Ishii, Hideshi, Iwama, Mizuho, Jonasch, Eric, Karolak, Michelle, Keavney, Bernard, Khin, Nay-Chi, Konno, Masamitsu, Kotani, Yuko, Kunihiro, Yayoi, Lakshmanan, Imayavaramban, Larochelle, Catherine, Lawrence, Catherine B., Li, Lin, Lindner, Volkhard, Liu, Xian-De, Lopez-Castejon, Gloria, Loudon, Andrew, Lowe, Jenna, Jerome-Majewska, Loydie A., Matsusaka, Taiji, Miura, Hiromi, Miyasaka, Yoshiki, Morpurgo, Benjamin, Motyl, Katherine, Nabeshima, Yo-ichi, Nakade, Koji, Nakashiba, Toshiaki, Nakashima, Kenichi, Obata, Yuichi, Ogiwara, Sanae, Ouellet, Mariette, Oxburgh, Leif, Piltz, Sandra, Pinz, Ilka, Ponnusamy, Moorthy P., Ray, David, Redder, Ronald J., Rosen, Clifford J., Ross, Nikki, Ruhe, Mark T., Ryzhova, Larisa, Salvador, Ane M., Alam, Sabrina Shameen, Sedlacek, Radislav, Sharma, Karan, Smith, Chad, Staes, Katrien, Starrs, Lora, Sugiyama, Fumihiro, Takahashi, Satoru, Tanaka, Tomohiro, Trafford, Andrew W., Uno, Yoshihiro, Vanhoutte, Leen, Vanrockeghem, Frederique, Willis, Brandon J., Wright, Christian S., Yamauchi, Yuko, Yi, Xin, Yoshimi, Kazuto, Zhang, Xuesong, Zhang, Yu, Ohtsuka, Masato, Das, Satyabrata, Garry, Daniel J., Hochepied, Tino, Thomas, Paul, Parker-Thornburg, Jan, Adamson, Antony D., Yoshiki, Atsushi, Schmouth, Jean-Francois, Golovko, Andrei, Thompson, William R., Lloyd, K. C. Kent, Wood, Joshua A., Cowan, Mitra, Mashimo, Tomoji, Mizuno, Seiya, Zhu, Hao, Kasparek, Petr, Liaw, Lucy, Miano, Joseph M., Burgio, Gaetan
Publicado 2019