N. Bech-Hansen

发表

Construction of a 1.5-Mb bacterial artificial chromosome contig in Xp11.23, a region of high gene content.

K. Boycott, C. G. Russell, R. Zahorchak, 1998, Genomics.

Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

Kym M. Boycott, G. Fishman, B. Koop, 1998, Nature Genetics.

Congenital stationary night blindness: mutation update and clinical variability.

C. Beaulieu, J. Parboosingh, N. Bech-Hansen, 2012, Advances in experimental medicine and biology.

Saccharomyces cerevisiae petite mitochondrial DNA of suppressive and neutral haploids and of [rho-] diploids obtained from crossing [rho+] to a neutral petite.

G. H. Rank, A. Robertson, N. Bech-Hansen, 1975, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

A 2-megabase physical contig incorporating 43 DNA markers on the human X chromosome at p11.23-p11.22 from ZNF21 to DXS255.

D. Schlessinger, K. Boycott, N. Bech-Hansen, 1996, Genomics.

TRANSMISSION OF IN-VITRO RADIORESISTANCE IN A CANCER-PRONE FAMILY

J. Fraumeni, B. Lampkin, N. Bech-Hansen, 1981, The Lancet.

Clustered organization of Krüppel zinc-finger genes at Xp11.23, flanking a translocation breakpoint at OATL1: a physical map with locus assignments for ZNF21, ZNF41, ZNF81, and ELK1.

C. Fletcher, G. Grimaldi, H. Thiesen, 1994, Genomics.

Selective messenger RNA reduction in Alzheimer's disease.

C. Bergeron, W. Lukiw, D. McLachlan, 1988, Brain research.

Development of a 1.4-Mb BAC/PAC contig and physical map within the critical region for complete X-linked congenital stationary night blindness in Xp11.4.

K. Boycott, R. Sparkes, R. Zahorchak, 2000, Genomics.

A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD

K. Boycott, J. Ross, N. Bech-Hansen, 2003, American journal of medical genetics. Part A.

Amygdala responses to quetiapine XR and citalopram treatment in major depression: the role of 5‐HTTLPR‐S/Lg polymorphisms

R. Ramasubbu, G. MacQueen, V. Diwadkar, 2016, Human psychopharmacology.

Pleiotropic phenotype of colchicine‐resistant CHO cells: Cross‐resistance and collateral sensitivity

J. Till, V. Ling, N. Bech-Hansen, 1976, Journal of cellular physiology.

Restriction fragment length polymorphisms associated with immunoglobulin C gamma genes reveal linkage disequilibrium and genomic organization.

P. Linsley, D. Cox, N. Bech-Hansen, 1983, Proceedings of the National Academy of Sciences of the United States of America.

TaqI RFLP in human adenylate kinase-1 (AK1) gene region on chromosome 9.

N. Bech-Hansen, K. J. Marshall, S. Kraus, 1989, Nucleic acids research.

Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locus.

P. Linsley, L. Siminovitch, D. Cox, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.

W. Stell, S. Bonfield, Y. Sauve, 2010, Advances in experimental medicine and biology.

Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase‐activating polypeptide (PACAP)

M. Marazita, R. Tobias, E. Berry-Kravis, 2009, Acta paediatrica.

Avian Adeno-Associated Viral Transduction of the Postembryonic Chicken Retina

W. Stell, N. Bech-Hansen, A. Fischer, 2019, Translational vision science & technology.

Single nuclear gene inherited cross resistance and collateral sensitivity to 17 inhibitors of mitochondrial function in S. cerevisiae

G. H. Rank, N. Bech-Hansen, N. Bech‐Hansen, 1973, Molecular and General Genetics MGG.

Mutation of the Calcium Channel Gene Cacna1f Disrupts Calcium Signaling and Synaptic Transmission in Mouse Retina

W. Stell, F. Tremblay, D. Rancourt, 2004 .