Peter Pearson
Peter Pearson
Visiting Professor Human Genetics, Dept Genetics and Evolutionary Biology, University of Sao Paulo
Preverjeni e-poštni naslov na ib.usp.br
The variability of female reproductive ageing
ER Te Velde, PL Pearson
Human reproduction update 8 (2), 141-154, 2002
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16
ST Reeders, MH Breuning, KE Davies, RD Nicholls, AP Jarman, ...
Nature 317 (6037), 542-544, 1985
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.
JT Den Dunnen, PM Grootscholten, E Bakker, LA Blonden, HB Ginjaar, ...
American journal of human genetics 45 (6), 835, 1989
Technique for Identifying Y Chromosomes in Human Interphase Nuclei
PL Pearson, M Bobrow, CG Vosa
Nature 226 (5240), 78-80, 1970
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome
U Francke, HD Ochs, B de Martinville, J Giacalone, V Lindgren, ...
American journal of human genetics 37 (2), 250, 1985
Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization …
T Cremer, J Landegent, A Brückner, HP Scholl, M Schardin, HD Hager, ...
Human genetics 74, 346-352, 1986
Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome
KE Davies, PL Pearson, PS Harper, JM Murray, T O'Brien, M Sarfarazi, ...
Nucleic Acids Research 11 (8), 2303-2312, 1983
Identification of a new copper metabolism gene by positional cloning in a purebred dog population
B van De Sluis, J Rothuizen, PL Pearson, BA van Oost, C Wijmenga
Human molecular genetics 11 (2), 165-173, 2002
Introduction and expression of the 400 kilobase precursor amyloid protein gene in transgenic mice
BT Lamb, SS Sisodia, AM Lawler, HH Slunt, CA Kitt, WG Kearns, ...
Nature genetics 5 (1), 22-30, 1993
The role of genetic factors in age at natural menopause
JP De Bruin, H Bovenhuis, PAH Van Noord, PL Pearson, ...
Human reproduction 16 (9), 2014-2018, 2001
A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q
SC Bakker, EM Van der Meulen, JK Buitelaar, LA Sandkuijl, DL Pauls, ...
The American Journal of Human Genetics 72 (5), 1251-1260, 2003
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1. 28
SS Bhattacharya, AF Wright, JF Clayton, WH Price, CI Phillips, ...
Nature 309 (5965), 253-255, 1984
Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9
M Bobrow, K Madan, PL Pearson
Nature New Biology 238 (82), 122-124, 1972
Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes
P Devilee, RF Thierry, T Kievits, R Kolluri, AHN Hopman, HF Willard, ...
Cancer Research 48 (20), 5825-5830, 1988
Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q.
P Devilee, M Van Vliet, P Van Sloun, J Hermans, PL Pearson, ...
Oncogene 6 (9), 1705-1711, 1991
At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma
P Devilee, M van den Broek, N Kuipers-Dukshoorn, R Kolluri, PM Khan, ...
Genomics 5 (3), 554-560, 1989
Heart disease risk determines menopausal age rather than the reverse
HS Kok, KM van Asselt, YT van der Schouw, I van der Tweel, ...
Journal of the American College of Cardiology 47 (10), 1976-1983, 2006
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs
E Bakker, N Goor, K Wrogemann, LM Kunkel, WA Fenton, ...
The Lancet 325 (8430), 655-658, 1985
Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy
MH Hofker, MC Wapenaar, N Goor, E Bakker, GJB van Ommen, ...
Human genetics 70, 148-156, 1985
Germinal mosaicism increases the recurrence risk for'new'Duchenne muscular dystrophy mutations.
E Bakker, H Veenema, JT Den Dunnen, C Van Broeckhoven, ...
Journal of medical genetics 26 (9), 553-559, 1989
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