Papers associated with gjb2 (and Disease Ontology)

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referenced by:

	Functional assessment of the "two-hit" model for neurodevelopmental defects in Drosophila and X. laevis., Pizzo L, Lasser M, Yusuff T, Jensen M, Ingraham P, Huber E, Singh MD, Monahan C, Iyer J, Desai I, Karthikeyan S, Gould DJ, Yennawar S, Weiner AT, Pounraja VK, Krishnan A, Rolls MM, Lowery LA, Girirajan S., PLoS Genet. April 5, 2021; 17 (4): e1009112.
	S-nitrosylation of connexin43 hemichannels elicits cardiac stress-induced arrhythmias in Duchenne muscular dystrophy mice., Lillo MA, Himelman E, Shirokova N, Xie LH, Fraidenraich D, Contreras JE., JCI Insight. December 19, 2019; 4 (24):
	The connexin26 human mutation N14K disrupts cytosolic intersubunit interactions and promotes channel opening., Valdez Capuccino JM, Chatterjee P, García IE, Botello-Smith WM, Zhang H, Harris AL, Luo Y, Contreras JE., J Gen Physiol. March 4, 2019; 151 (3): 328-341.
	A novel autosomal recessive GJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma., Youssefian L, Vahidnezhad H, Saeidian AH, Mahmoudi H, Karamzadeh R, Kariminejad A, Huang J, Li L, Jannace TF, Fortina P, Zeinali S, White TW, Uitto J., Hum Mutat. February 1, 2019; 40 (2): 217-229.
	The syndromic deafness mutation G12R impairs fast and slow gating in Cx26 hemichannels., García IE, Villanelo F, Contreras GF, Pupo A, Pinto BI, Contreras JE, Pérez-Acle T, Alvarez O, Latorre R, Martínez AD, González C., J Gen Physiol. May 7, 2018; 150 (5): 697-711.
	RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance., Ramírez-Gordillo D, Powers TR, van Velkinburgh JC, Trujillo-Provencio C, Schilkey F, Serrano EE., BMC Res Notes. November 18, 2015; 8 691.
	Aberrant connexin26 hemichannels underlying keratitis-ichthyosis-deafness syndrome are potently inhibited by mefloquine., Levit NA, Sellitto C, Wang HZ, Li L, Srinivas M, Brink PR, White TW., J Invest Dermatol. April 1, 2015; 135 (4): 1033-1042.
	Long-range gap junctional signaling controls oncogene-mediated tumorigenesis in Xenopus laevis embryos., Chernet BT, Fields C, Levin M., Front Physiol. January 19, 2015; 5 519.
	Resting potential, oncogene-induced tumorigenesis, and metastasis: the bioelectric basis of cancer in vivo., Lobikin M, Chernet B, Lobo D, Levin M., Phys Biol. December 1, 2012; 9 (6): 065002.
	Connexins in epidermal homeostasis and skin disease., Scott CA, Tattersall D, O'Toole EA, Kelsell DP., Biochim Biophys Acta. August 1, 2012; 1818 (8): 1952-61.
	Mechanism of inhibition of connexin channels by the quinine derivative N-benzylquininium., Rubinos C, Sánchez HA, Verselis VK, Srinivas M., J Gen Physiol. January 1, 2012; 139 (1): 69-82.
	GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf., Tekin M, Xia XJ, Erdenetungalag R, Cengiz FB, White TW, Radnaabazar J, Dangaasuren B, Tastan H, Nance WE, Pandya A., Ann Hum Genet. March 1, 2010; 74 (2): 155-64.
	Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss., Meşe G, Londin E, Mui R, Brink PR, White TW., Hum Genet. August 1, 2004; 115 (3): 191-9.
	Aberrant gating, but a normal expression pattern, underlies the recessive phenotype of the deafness mutant Connexin26M34T., Skerrett IM, Di WL, Kasperek EM, Kelsell DP, Nicholson BJ., FASEB J. May 1, 2004; 18 (7): 860-2.

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