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                             44 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A high-resolution map of the chromosomal region surrounding the nude gene Blackburn, C.C.
1995
26 2 p. 308-317
10 p.
artikel
2 Analysis of randomly amplified flow-sorted chromosomes using the polymerase chain reaction Hui, Stephanie M.
1995
26 2 p. 364-371
8 p.
artikel
3 Analysis of the structural integrity of YACs comprising human immunoglobulin genes in yeast and in embryonic stem cells Mendez, Michael J.
1995
26 2 p. 294-307
14 p.
artikel
4 A set of inter-Alu PCR markers for chromosome 21 generated from pulsed-field gel-fractionated NotI restriction fragments Wang, Denan
1995
26 2 p. 318-326
9 p.
artikel
5 Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with tourette syndrome Gelernter, Joel
1995
26 2 p. 207-209
3 p.
artikel
6 A widely distributed putative mammalian transcriptional regulator containing multiple paired amphipathic helices, with similarity to yeast SIN3 Halleck, Margaret S.
1995
26 2 p. 403-406
4 p.
artikel
7 A YAC contig map of Plasmodium falciparum chromosome 4: characterization of a DNA amplification between two recently separated isolates Rubio, Justin P.
1995
26 2 p. 192-198
7 p.
artikel
8 Chromosomal mapping of the human proteinase inhibitor 6 (PI6) gene to 6p25 by fluorescence in situ hybridization Coughlin, Paul
1995
26 2 p. 431-433
3 p.
artikel
9 Cloning and characterization of the human invasion suppressor gene E-cadherin (CDH1) Berx, Geert
1995
26 2 p. 281-289
9 p.
artikel
10 Cloning and mapping of the mouse α7-neuronal nicotinic acetylcholine receptor Orr-Urtreger, Avi
1995
26 2 p. 399-402
4 p.
artikel
11 Cloning of the human heparan sulfate-N-deacetylase/N-sulfotransferase gene from the treacher Collins syndrome candidate region at 5q32–q33.1 Dixon, Jill
1995
26 2 p. 239-244
6 p.
artikel
12 Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis Tahvanainen, Esa
1995
26 2 p. 290-293
4 p.
artikel
13 EMR1, an unusual member in the family of hormone receptors with seven transmembrane segments Baud, Véronique
1995
26 2 p. 334-344
11 p.
artikel
14 Exon organization of the mouse entactin gene corresponds to the structural domains of the polypeptide and has regional homology to the low-density lipoprotein receptor gene Durkin, Marian E.
1995
26 2 p. 219-228
10 p.
artikel
15 High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1) Wang, Irène
1995
26 2 p. 229-238
10 p.
artikel
16 Human protein synthesis initiation factor eIF-4γ is encoded by a single gene (EIF4G) that maps to chromosome 3q27—qter Yan, Riqiang
1995
26 2 p. 394-398
5 p.
artikel
17 Identification of a YAC spanning the translocation breakpoints in uterine leiomyomata, pulmonary chondroid hamartoma, and lipoma: physical mapping of the 12q14–q15 breakpoint region in uterine leiomyomata Fejzo, Marlena Schoenberg
1995
26 2 p. 265-271
7 p.
artikel
18 Identification of the human ERK gene as a putative receptor tyrosine kinase and its chromosomal localization to 1p36.1: a comparative mapping of human, mouse, and rat chromosomes Saito, Toshiyuki
1995
26 2 p. 382-384
3 p.
artikel
19 Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15 Kohrman, David C.
1995
26 2 p. 171-177
7 p.
artikel
20 Isolation and characterization of a human pseudogene (CTNNAP1) for αE-catenin (CTNNA1): assignment of the pseudogene to 5q22 and the αE-catenin gene to 5q31 Nollet, Friedel
1995
26 2 p. 410-413
4 p.
artikel
21 Isolation of 115 human chromosome 8-specific expressed-sequence tags by Exon amplification Koyama, Kumiko
1995
26 2 p. 245-253
9 p.
artikel
22 Isolation of the human genomic brain-2/N-Oct 3 gene (POUF3) and assignment to chromosome 6q16 Atanasoski, S.
1995
26 2 p. 272-280
9 p.
artikel
23 Large-scale cloning of human chromosome 2-specific yeast artificial chromosomes (YACs) using an interspersed repetitive sequences (IRS)-PCR approach Liu, Jing
1995
26 2 p. 178-191
14 p.
artikel
24 Localization of the adenosine A1 receptor subtype gene (ADORA1) to chromosome 1q32.1 Townsend-Nicholson, Andrea
1995
26 2 p. 423-425
3 p.
artikel
25 Localization of the human B-type natriuretic peptide precursor (NPPB) gene to chromosome 1p36 Arden, Karen C.
1995
26 2 p. 385-389
5 p.
artikel
26 Mapping of guanylin to murine chromosome 4 and human chromosome 1p34–p35 Sciaky, Daniela
1995
26 2 p. 427-429
3 p.
artikel
27 Mapping of the human gene for a melanocyte protein Pmel 17 (D12S53E) to chromosome 12q13–q14 Kubota, Ryo
1995
26 2 p. 430-431
2 p.
artikel
28 Mouse Elk oncogene maps to chromosome X and a novel Elk oncogene (Elk3) maps to chromosome 10 Tamai, Yoshitaka
1995
26 2 p. 414-416
3 p.
artikel
29 Multiplex genotype determination at a DNA sequence polymorphism cluster in the human immunoglobulin heavy-chain region Li, Honghua
1995
26 2 p. 199-206
8 p.
artikel
30 Organization and sequence of the human P gene and identification of a new family of transport proteins Lee, Seung-Taek
1995
26 2 p. 354-363
10 p.
artikel
31 Pairwise end sequencing: a unified approach to genomic mapping and sequencing Roach, Jared C.
1995
26 2 p. 345-353
9 p.
artikel
32 Physical mapping of the human glutamine:fructose-6-phosphate amidotransferase gene (GFPT) to chromosome 2p13 Whitmore, T.E.
1995
26 2 p. 422-423
2 p.
artikel
33 Rapid physical mapping of the human trk protooncogene (NTRK1) to human chromosome 1q21–q22 by P1 clone selection, fluorescence in situ hybridization (FISH), and computer-assisted microscopy Weier, Heinz-Ulrich G.
1995
26 2 p. 390-393
4 p.
artikel
34 Rat phenol-preferring sulfotransferase genes (Stp and stp2): localization to mouse chromosomes 7 and 17 Khan, Akbar S.
1995
26 2 p. 417-419
3 p.
artikel
35 Structure and organization of the human galactocerebrosidase (GALC) gene Luzi, Paola
1995
26 2 p. 407-409
3 p.
artikel
36 The γ-aminobutyric acid receptor γ3 subunit gene (GABRG3) is tightly linked to the α5 subunit gene (GABRA5) on human chromosome 15q11–q13 and is transcribed in the same orientation Greger, V.
1995
26 2 p. 258-264
7 p.
artikel
37 The BAT1 gene in the MHC encodes an evolutionarily conserved putative nuclear RNA helicase of the DEAD family Peelman, Luc J.
1995
26 2 p. 210-218
9 p.
artikel
38 The DAD1 protein, whose defect causes apoptotic cell death, maps to human chromosome 14 Ylug, Isik G.
1995
26 2 p. 433-435
3 p.
artikel
39 The human NACP/α-synuclein gene: chromosome assignment to 4q21.3–q22 and TaqI RFLP analysis Chen, Xiaohua
1995
26 2 p. 425-427
3 p.
artikel
40 The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the tw18 or tth20 deletions Pilz, Alison
1995
26 2 p. 420-421
2 p.
artikel
41 The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease Campion, Dominique
1995
26 2 p. 254-257
4 p.
artikel
42 The PML gene is linked to a megabase-scale insertion/deletion restriction fragment length polymorphism Goy, André
1995
26 2 p. 327-333
7 p.
artikel
43 Thioredoxin, a mediator of growth inhibition, maps to 9q31 Heppell-Parton, Amanda
1995
26 2 p. 379-381
3 p.
artikel
44 Visualization of the conservation of synteny between humans and pigs by heterologous chromosomal painting Rettenberger, G.
1995
26 2 p. 372-378
7 p.
artikel
                             44 gevonden resultaten
 
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