| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Highly Efficient Escherichia coli-Based Chromosome Engineering System Adapted for Recombinogenic Targeting and Subcloning of BAC DNA
|
Lee, E-Chiang
|
|
2001
|
73 |
1 |
p. 56-65
10 p.
|
artikel
|
| 2 |
Characterization of the Human NDRG Gene Family: A Newly Identified Member, NDRG4, Is Specifically Expressed in Brain and Heart
|
Zhou, Rui-Hai
|
|
2001
|
73 |
1 |
p. 86-97
12 p.
|
artikel
|
| 3 |
Characterization of the Human Xq21.3/Yp11 Homology Block and Conservation of Organization in Primates
|
Sargent, Carole A.
|
|
2001
|
73 |
1 |
p. 77-85
9 p.
|
artikel
|
| 4 |
Complex Arrangement of Genes within a 220-kb Region of Double-Duplicated DNA on Human 2q37.1
|
Rump, Andreas
|
|
2001
|
73 |
1 |
p. 50-55
6 p.
|
artikel
|
| 5 |
Elucidation of the Minimal Sequence Required to Imprint H19 Transgenes
|
Cranston, Melanie J.
|
|
2001
|
73 |
1 |
p. 98-107
10 p.
|
artikel
|
| 6 |
Genomic Organization of the CC Chemokine MIP-3α/CCL20/LARC/EXODUS/SCYA20, Showing Gene Structure, Splice Variants, and Chromosome Localization
|
Nelson, Robin T.
|
|
2001
|
73 |
1 |
p. 28-37
10 p.
|
artikel
|
| 7 |
Human and Mouse ABCA1 Comparative Sequencing and Transgenesis Studies Revealing Novel Regulatory Sequences
|
Qiu, Yang
|
|
2001
|
73 |
1 |
p. 66-76
11 p.
|
artikel
|
| 8 |
Identification and Characterization of KLK14, a Novel Kallikrein Serine Protease Gene Located on Human Chromosome 19q13.4 and Expressed in Prostate and Skeletal Muscle
|
Hooper, John D.
|
|
2001
|
73 |
1 |
p. 117-122
6 p.
|
artikel
|
| 9 |
Identification of Genes from a Schizophrenia-Linked Translocation Breakpoint Region
|
Semple, C.A.M.
|
|
2001
|
73 |
1 |
p. 123-126
4 p.
|
artikel
|
| 10 |
Identification of Serhl, a New Member of the Serine Hydrolase Family Induced by Passive Stretch of Skeletal Muscle in Vivo
|
Sadusky, T.J.
|
|
2001
|
73 |
1 |
p. 38-49
12 p.
|
artikel
|
| 11 |
Integration of a c-myc Transgene Results in Disruption of the Mouse Gtf2ird1 Gene, the Homologue of the Human GTF2IRD1 Gene Hemizygously Deleted in Williams–Beuren Syndrome
|
Durkin, Marian E.
|
|
2001
|
73 |
1 |
p. 20-27
8 p.
|
artikel
|
| 12 |
Low Mutational Burden of Individual Acquired Mitochondrial DNA Mutations in Brain
|
Simon, D.K.
|
|
2001
|
73 |
1 |
p. 113-116
4 p.
|
artikel
|
| 13 |
Maternal and Paternal Chromosomes 7 Show Differential Methylation of Many Genes in Lymphoblast DNA
|
Hannula, Katariina
|
|
2001
|
73 |
1 |
p. 1-9
9 p.
|
artikel
|
| 14 |
The Human Contactin-Associated Protein-like 2 Gene (CNTNAP2) Spans over 2 Mb of DNA at Chromosome 7q35
|
Nakabayashi, Kazuhiko
|
|
2001
|
73 |
1 |
p. 108-112
5 p.
|
artikel
|
| 15 |
The LZTFL1 Gene Is a Part of a Transcriptional Map Covering 250 kb within the Common Eliminated Region 1 (C3CER1) in 3p21.3
|
Kiss, Hajnalka
|
|
2001
|
73 |
1 |
p. 10-19
10 p.
|
artikel
|
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