CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome
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
Published in Human molecular genetics (15.01.2014)
Published in Human molecular genetics (15.01.2014)
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The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development
Sperry, Ethan D., Hurd, Elizabeth A., Durham, Mark A., Reamer, Elyse N., Stein, Adam B., Martin, Donna M.
Published in Developmental dynamics (01.09.2014)
Published in Developmental dynamics (01.09.2014)
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CHD7 functions in the nucleolus as a positive regulator of ribosomal RNA biogenesis
Zentner, Gabriel E., Hurd, Elizabeth A., Schnetz, Michael P., Handoko, Lusy, Wang, Chuanping, Wang, Zhenghe, Wei, Chialin, Tesar, Paul J., Hatzoglou, Maria, Martin, Donna M., Scacheri, Peter C.
Published in Human molecular genetics (15.09.2010)
Published in Human molecular genetics (15.09.2010)
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Polarity Proteins Control Ciliogenesis via Kinesin Motor Interactions
Fan, Shuling, Hurd, Toby W., Liu, Chia-Jen, Straight, Samuel W., Weimbs, Thomas, Hurd, Elizabeth A., Domino, Steven E., Margolis, Ben
Published in Current biology (24.08.2004)
Published in Current biology (24.08.2004)
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Chromatin remodeler CHD7 is critical for cochlear morphogenesis and neurosensory patterning
Balendran, Vinodh, Skidmore, Jennifer M., Ritter, K. Elaine, Gao, Jingxia, Cimerman, Jelka, Beyer, Lisa A., Hurd, Elizabeth A., Raphael, Yehoash, Martin, Donna M.
Published in Developmental biology (01.09.2021)
Published in Developmental biology (01.09.2021)
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Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndrome
Layman, Wanda S., Hurd, Elizabeth A., Martin, Donna M.
Published in Human molecular genetics (15.08.2011)
Published in Human molecular genetics (15.08.2011)
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Corrigendum to “Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient mice” [Mech. Dev. 129 (9–12) (2012) 308–23 (PMID 22705977)]
Hurd, Elizabeth A., Micucci, Joseph A., Reamer, Elyse N., Martin, Donna M.
Published in Cells & development (01.06.2022)
Published in Cells & development (01.06.2022)
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Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues
Hurd, Elizabeth A, Capers, Patrice L, Blauwkamp, Marsha N, Adams, Meredith E, Raphael, Yehoash, Poucher, Heather K, Martin, Donna M
Published in Mammalian genome (01.02.2007)
Published in Mammalian genome (01.02.2007)
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Defects in vestibular sensory epithelia and innervation in mice with loss of Chd7 function: Implications for human CHARGE syndrome
Adams, Meredith E., Hurd, Elizabeth A., Beyer, Lisa A., Swiderski, Donald L., Raphael, Yehoash, Martin, Donna M.
Published in Journal of comparative neurology (1911) (10.10.2007)
Published in Journal of comparative neurology (1911) (10.10.2007)
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Mature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome
Hurd, Elizabeth A., Adams, Meredith E., Layman, Wanda S., Swiderski, Donald L., Beyer, Lisa A., Halsey, Karin E., Benson, Jennifer M., Gong, Tzy-Wen, Dolan, David F., Raphael, Yehoash, Martin, Donna M.
Published in Hearing research (01.12.2011)
Published in Hearing research (01.12.2011)
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Cervical mucins carry α(1,2)fucosylated glycans that partly protect from experimental vaginal candidiasis
Domino, Steven E, Hurd, Elizabeth A, Thomsson, Kristina A, Karnak, David M, Holmén Larsson, Jessica M, Thomsson, Elisabeth, Bäckström, Malin, Hansson, Gunnar C
Published in Glycoconjugate journal (01.12.2009)
Published in Glycoconjugate journal (01.12.2009)
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