Early afferent signaling in the outer plexiform layer regulates development of horizontal cell morphology
Raven, Mary A., Orton, Noelle C., Nassar, Hadi, Williams, Gary A., Stell, William K., Jacobs, Gerald H., Bech-Hansen, N. Torben, Reese, Benjamin E.
Published in Journal of comparative neurology (1911) (10.02.2008)
Published in Journal of comparative neurology (1911) (10.02.2008)
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Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP)
Cummings, Kevin J, Klotz, Cherise, Liu, Wei-Qiao, Weese-Mayer, Debra E, Marazita, Mary L, Cooper, Margaret E, Berry-Kravis, Elizabeth M, Tobias, Rose, Goldie, Cameron, Bech-Hansen, N Torben, Wilson, Richard JA
Published in Acta Paediatrica (01.03.2009)
Published in Acta Paediatrica (01.03.2009)
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The CaV1.4 Calcium Channel Is a Critical Regulator of T Cell Receptor Signaling and Naive T Cell Homeostasis
Omilusik, Kyla, Priatel, John J., Chen, Xiaoxi, Wang, Yiwen Teresa, Xu, Hongjian, Choi, Kyung Bok, Gopaul, Rayshad, McIntyre-Smith, Adam, Teh, Hung-Sia, Tan, Rusung, Bech-Hansen, N. Torben, Waterfield, Douglas, Fedida, David, Hunt, Simon V., Jefferies, Wilfred A.
Published in Immunity (Cambridge, Mass.) (23.09.2011)
Published in Immunity (Cambridge, Mass.) (23.09.2011)
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ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison
Barclay, Sarah F, Rand, Casey M, Nguyen, Lisa, Wilson, Richard J A, Wevrick, Rachel, Gibson, William T, Bech-Hansen, N Torben, Weese-Mayer, Debra E
Published in Orphanet journal of rare diseases (20.07.2018)
Published in Orphanet journal of rare diseases (20.07.2018)
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Journal Article
Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina
Mansergh, Fiona, Orton, Noelle C., Vessey, John P., Lalonde, Melanie R., Stell, William K., Tremblay, Francois, Barnes, Steven, Rancourt, Derrick E., Bech-Hansen, N. Torben
Published in Human molecular genetics (15.10.2005)
Published in Human molecular genetics (15.10.2005)
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Amygdala responses to quetiapine XR and citalopram treatment in major depression: the role of 5-HTTLPR-S/Lg polymorphisms
Ramasubbu, Rajamannar, Burgess, Ashley, Gaxiola-Valdez, Ismael, Cortese, Filomeno, Clark, Darren, Kemp, Anne, Goodyear, Bradley, Macqueen, Glenda, Bech-Hansen, N. Torben, Foster, Jane, Diwadkar, Vaibhav A.
Published in Human psychopharmacology (01.03.2016)
Published in Human psychopharmacology (01.03.2016)
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Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness
BECH-HANSEN, N. T, NAYLOR, M. J, MAYBAUM, T. A, PEARCE, W. G, KOOP, B, FISHMAN, G. A, METS, M, MUSARELLA, M. A, BOYCOTT, K. M
Published in Nature genetics (01.07.1998)
Published in Nature genetics (01.07.1998)
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Journal Article
Analysis of PAC1 receptor gene variants in Caucasian and African American infants dying of sudden infant death syndrome
Barrett, Karlene T, Rodikova, Ekaterina, Weese-Mayer, Debra E, Rand, Casey M, Marazita, Mary L, Cooper, Margaret E, Berry-Kravis, Elizabeth M, Bech-Hansen, N Torben, Wilson, Richard JA
Published in Acta Paediatrica (01.12.2013)
Published in Acta Paediatrica (01.12.2013)
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Journal Article
Unique disease heritage of the Dutch-German Mennonite population
Orton, Noelle C., Innes, A. Micheil, Chudley, Albert E., Bech-Hansen, N. Torben
Published in American journal of medical genetics. Part A (15.04.2008)
Published in American journal of medical genetics. Part A (15.04.2008)
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Journal Article
The Ca(v)1.4 calcium channel is a critical regulator of T cell receptor signaling and naive T cell homeostasis
Omilusik, Kyla, Priatel, John J, Chen, Xiaoxi, Wang, Yiwen Teresa, Xu, Hongjian, Choi, Kyung Bok, Gopaul, Rayshad, McIntyre-Smith, Adam, Teh, Hung-Sia, Tan, Rusung, Bech-Hansen, N Torben, Waterfield, Douglas, Fedida, David, Hunt, Simon V, Jefferies, Wilfred A
Published in Immunity (Cambridge, Mass.) (23.09.2011)
Published in Immunity (Cambridge, Mass.) (23.09.2011)
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Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours
Barclay, Sarah F, Rand, Casey M, Borch, Lauren A, Nguyen, Lisa, Gray, Paul A, Gibson, William T, Wilson, Richard J A, Gordon, Paul M K, Aung, Zaw, Berry-Kravis, Elizabeth M, Ize-Ludlow, Diego, Weese-Mayer, Debra E, Bech-Hansen, N Torben
Published in Orphanet journal of rare diseases (25.08.2015)
Published in Orphanet journal of rare diseases (25.08.2015)
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Journal Article
Absence of mutations in HCRT , HCRTR1 and HCRTR2 in patients with ROHHAD
Barclay, Sarah F, Rand, Casey M, Gray, Paul A, Gibson, William T, Wilson, Richard J.A, Berry-Kravis, Elizabeth M, Ize-Ludlow, Diego, Bech-Hansen, N. Torben, Weese-Mayer, Debra E
Published in Respiratory physiology & neurobiology (15.01.2016)
Published in Respiratory physiology & neurobiology (15.01.2016)
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Journal Article
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism
Jacobson, Samuel G., Cideciyan, Artur V., Aleman, Tomas S., Sumaroka, Alexander, Roman, Alejandro J., Gardner, Leigh M., Prosser, Haydn M., Mishra, Monalisa, Bech-Hansen, N. Torben, Herrera, Waldo, Schwartz, Sharon B., Liu, Xue-Zhong, Kimberling, William J., Steel, Karen P., Williams, David S.
Published in Human molecular genetics (01.08.2008)
Published in Human molecular genetics (01.08.2008)
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Journal Article
A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD
Boycott, Kym M., Parslow, Malcolm I., Ross, Judith L., Miller, Ivan P., Bech‐Hansen, N. Torben, MacLeod, Patrick M.
Published in American journal of medical genetics. Part A (01.10.2003)
Published in American journal of medical genetics. Part A (01.10.2003)
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