CHD7 promotes neural progenitor differentiation in embryonic stem cells via altered chromatin accessibility and nascent gene expression von Yao, Hui, Hannum, Douglas F., Zhai, Yiwen, Hill, Sophie F., Albanus, Ricardo D.’Oliveira, Lou, Wenjia, Skidmore, Jennifer M., Sanchez, Gilson, Saiakhova, Alina, Bielas, Stephanie L., Scacheri, Peter, Ljungman, Mats, Parker, Stephen C. J., Martin, Donna M.

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CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome von Micucci, Joseph A, Layman, Wanda S, Hurd, Elizabeth A, Sperry, Ethan D, Frank, Sophia F, Durham, Mark A, Swiderski, Donald L, Skidmore, Jennifer M, Scacheri, Peter C, Raphael, Yehoash, Martin, Donna M

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GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function von Guo, Jingying, Ma, Xiaobo, Skidmore, Jennifer M., Cimerman, Jelka, Prieskorn, Diane M., Beyer, Lisa A., Swiderski, Donald L., Dolan, David F., Martin, Donna M., Raphael, Yehoash

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Characterization of progenitor domains in the developing mouse thalamus von Vue, Tou Yia, Aaker, Joshua, Taniguchi, Aya, Kazemzadeh, Christina, Skidmore, Jennifer M., Martin, Donna M., Martin, James F., Treier, Mathias, Nakagawa, Yasushi

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CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development von Yao, Hui, Hill, Sophie F, Skidmore, Jennifer M, Sperry, Ethan D, Swiderski, Donald L, Sanchez, Gilson J, Bartels, Cynthia F, Raphael, Yehoash, Scacheri, Peter C, Iwase, Shigeki, Martin, Donna M

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Nestin-Lineage Cells Contribute to the Microvasculature but Not Endocrine Cells of the Islet von TRENTELAAR, Mary Kay, SKIDMORE, Jennifer M, DIAS-LEME, Claudia L, HARA, Manami, LIZHI ZHANG, SIMEONE, Diane, MARTIN, Donna M, BURANT, Charles F

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Genetic specification of left-right asymmetry in the diaphragm muscles and their motor innervation von Charoy, Camille, Dinvaut, Sarah, Chaix, Yohan, Morlé, Laurette, Sanyas, Isabelle, Bozon, Muriel, Kindbeiter, Karine, Durand, Bénédicte, Skidmore, Jennifer M, De Groef, Lies, Seki, Motoaki, Moons, Lieve, Ruhrberg, Christiana, Martin, James F, Martin, Donna M, Falk, Julien, Castellani, Valerie

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A novel TaulacZ allele reveals a requirement for Pitx2 in formation of the mammillothalamic tract von Skidmore, Jennifer M., Waite, Mindy R., Alvarez-Bolado, Gonzalo, Puelles, Luis, Martin, Donna M.

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Chromatin remodeler CHD7 is critical for cochlear morphogenesis and neurosensory patterning von Balendran, Vinodh, Skidmore, Jennifer M., Ritter, K. Elaine, Gao, Jingxia, Cimerman, Jelka, Beyer, Lisa A., Hurd, Elizabeth A., Raphael, Yehoash, Martin, Donna M.

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Pleiotropic and isoform-specific functions for Pitx2 in superior colliculus and hypothalamic neuronal development von Waite, Mindy R., Skidmore, Jennifer M., Micucci, Joseph A., Shiratori, Hidetaka, Hamada, Hiroshi, Martin, James F., Martin, Donna M.

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CHD7 and SOX2 act in a common gene regulatory network during mammalian semicircular canal and cochlear development von Gao, Jingxia, Skidmore, Jennifer M, Cimerman, Jelka, Ritter, K Elaine, Qiu, Jingyun, Wilson, Lindsey M Q, Raphael, Yehoash, Kwan, Kelvin Y, Martin, Donna M

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The Caulobacter crescentus GTPase CgtAC is required for progression through the cell cycle and for maintaining 50S ribosomal subunit levels von Datta, Kaustuv, Skidmore, Jennifer M., Pu, Kun, Maddock, Janine R.

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Chromatin remodeler Chd7 regulates photoreceptor development and outer segment length von Krueger, Laura A., Bills, Jessica D., Lim, Zun Yi, Skidmore, Jennifer M., Martin, Donna M., Morris, Ann C.

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Genetic analysis of CHARGE syndrome identifies overlapping molecular biology von Moccia, Amanda, Srivastava, Anshika, Skidmore, Jennifer M, Bernat, John A, Wheeler, Marsha, Chong, Jessica X, Nickerson, Deborah, Bamshad, Michael, Hefner, Margaret A, Martin, Donna M, Bielas, Stephanie L

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Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder von Bedoyan, Jirair Krikor, Schaibley, Valerie M, Peng, Weiping, Bai, Yongsheng, Mondal, Kajari, Shetty, Amol C, Durham, Mark, Micucci, Joseph A, Dhiraaj, Arti, Skidmore, Jennifer M, Kaplan, Julie B, Skinner, Cindy, Schwartz, Charles E, Antonellis, Anthony, Zwick, Michael E, Cavalcoli, James D, Li, Jun Z, Martin, Donna M

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Cre fate mapping reveals lineage specific defects in neuronal migration with loss of Pitx2 function in the developing mouse hypothalamus and subthalamic nucleus von Skidmore, Jennifer M., Cramer, John D., Martin, James F., Martin, Donna M.

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Distinct populations of GABAergic neurons in mouse rhombomere 1 express but do not require the homeodomain transcription factor PITX2 von Waite, Mindy R., Skaggs, Kaia, Kaviany, Parisa, Skidmore, Jennifer M., Causeret, Frédéric, Martin, James F., Martin, Donna M.

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PITX2 is required for normal development of neurons in the mouse subthalamic nucleus and midbrain von Martin, Donna M, Skidmore, Jennifer M, Philips, Steven T, Vieira, Claudia, Gage, Philip J, Condie, Brian G, Raphael, Yehoash, Martinez, Salvador, Camper, Sally A

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Nestin-Cre mediated deletion of Pitx2 in the mouse von Sclafani, Anthony M., Skidmore, Jennifer M., Ramaprakash, Hemanth, Trumpp, Andreas, Gage, Philip J., Martin, Donna M.

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Pitx2 Distinguishes Subtypes of Terminally Differentiated Neurons in the Developing Mouse Neuroepithelium von Martin, Donna M., Skidmore, Jennifer M., Fox, Sharon E., Gage, Philip J., Camper, Sally A.

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