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1.
Long-Read DNA Sequencing: Recent Advances and Remaining Challenges.
Annu Rev Genomics Hum Genet
; 24: 109-132, 2023 08 25.
Article
in English
| MEDLINE | ID: mdl-37075062
2.
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Nat Genet
; 55(7): 1149-1163, 2023 07.
Article
in English
| MEDLINE | ID: mdl-37386251
3.
Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeres.
Chromosoma
; 120(6): 621-32, 2011 Dec.
Article
in English
| MEDLINE | ID: mdl-21826412
4.
Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.
Hum Mol Genet
; 19(17): 3383-93, 2010 Sep 01.
Article
in English
| MEDLINE | ID: mdl-20570968
5.
Duplication of the ZIC2 gene is not associated with holoprosencephaly.
Am J Med Genet A
; 158A(1): 103-8, 2012 Jan.
Article
in English
| MEDLINE | ID: mdl-22105922
6.
Analysis of transposon interruptions suggests selection for L1 elements on the X chromosome.
PLoS Genet
; 4(8): e1000172, 2008 Aug 29.
Article
in English
| MEDLINE | ID: mdl-18769724
7.
Biased distributions and decay of long interspersed nuclear elements in the chicken genome.
Genetics
; 178(1): 573-81, 2008 Jan.
Article
in English
| MEDLINE | ID: mdl-17947446
8.
Analysis of the largest tandemly repeated DNA families in the human genome.
BMC Genomics
; 9: 533, 2008 Nov 07.
Article
in English
| MEDLINE | ID: mdl-18992157
9.
Evolutionary history of mammalian transposons determined by genome-wide defragmentation.
PLoS Comput Biol
; 3(7): e137, 2007 Jul.
Article
in English
| MEDLINE | ID: mdl-17630829
10.
DNA modification and functional delivery into human cells using Escherichia coli DH10B.
Nucleic Acids Res
; 31(9): e51, 2003 May 01.
Article
in English
| MEDLINE | ID: mdl-12711696
11.
CP248, a derivative of exisulind, causes growth inhibition, mitotic arrest, and abnormalities in microtubule polymerization in glioma cells.
Mol Cancer Ther
; 1(6): 393-404, 2002 Apr.
Article
in English
| MEDLINE | ID: mdl-12477052
12.
Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay.
Am J Med Genet
; 108(3): 198-204, 2002 Mar 15.
Article
in English
| MEDLINE | ID: mdl-11891685
13.
Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence.
Am J Med Genet
; 113(3): 263-7, 2002 Dec 01.
Article
in English
| MEDLINE | ID: mdl-12439894
14.
Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.
Am J Med Genet
; 110(3): 258-67, 2002 Jul 01.
Article
in English
| MEDLINE | ID: mdl-12116235
15.
The octamer is the major form of CENP-A nucleosomes at human centromeres.
Nat Struct Mol Biol
; 20(6): 687-95, 2013 Jun.
Article
in English
| MEDLINE | ID: mdl-23644596
16.
Neocentric X-chromosome in a girl with Turner-like syndrome.
Mol Cytogenet
; 5(1): 29, 2012 Jun 09.
Article
in English
| MEDLINE | ID: mdl-22682421
17.
A paucity of heterochromatin at functional human neocentromeres.
Epigenetics Chromatin
; 3(1): 6, 2010 Mar 08.
Article
in English
| MEDLINE | ID: mdl-20210998
18.
Recombineering linear DNA that replicate stably in E. coli.
Plasmid
; 59(1): 63-71, 2008 Jan.
Article
in English
| MEDLINE | ID: mdl-17988739
19.
The mouse X chromosome is enriched for multicopy testis genes showing postmeiotic expression.
Nat Genet
; 40(6): 794-9, 2008 Jun.
Article
in English
| MEDLINE | ID: mdl-18454149
20.
Co-localization of CENP-C and CENP-H to discontinuous domains of CENP-A chromatin at human neocentromeres.
Genome Biol
; 8(7): R148, 2007.
Article
in English
| MEDLINE | ID: mdl-17651496