Peter Rogan
Zitiert von
Zitiert von
Hepatic CYP2B6 expression: gender and ethnic differences and relationship to CYP2B6 genotype and CAR (constitutive androstane receptor) expression
V Lamba, J Lamba, K Yasuda, S Strom, J Davila, ML Hancock, ...
Journal of Pharmacology and Experimental Therapeutics 307 (3), 906-922, 2003
Imprinting-mutation mechanisms in Prader-Willi syndrome
T Ohta, TA Gray, PK Rogan, K Buiting, JM Gabriel, S Saitoh, B Muralidhar, ...
The American Journal of Human Genetics 64 (2), 397-413, 1999
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints
JM Amos-Landgraf, Y Ji, W Gottlieb, T Depinet, AE Wandstrat, SB Cassidy, ...
The American Journal of Human Genetics 65 (2), 370-386, 1999
The frequency of uniparental disomy in Prader-Willi syndrome: implications for molecular diagnosis
MJ Mascari, W Gottlieb, PK Rogan, MG Butler, DA Waller, JAL Armour, ...
New England Journal of Medicine 326 (24), 1599-1607, 1992
Ancient DNA: recovery and analysis of genetic material from paleontological, archaeological, museum, medical, and forensic specimens
B Herrmann, S Hummel
Springer Science & Business Media, 1994
Information analysis of human splice site mutations
PK Rogan, BM Faux, TD Schneider
Human mutation 12 (3), 153-171, 1998
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
S Saitoh, K Buiting, PK Rogan, JL Buxton, DJ Driscoll, J Arnemann, ...
Proceedings of the National Academy of Sciences 93 (15), 7811-7815, 1996
Automated splicing mutation analysis by information theory
VK Nalla, PK Rogan
Human mutation 25 (4), 334-342, 2005
Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the bA3/A1-crystallin gene
C Kannabiran, PK Rogan, L Olmos, S Basti, GN Rao, M Kaiser-Kupfer, ...
Mol Vis 4, 21, 1998
AB initio generation of single copy genomic probes
PK Rogan
US Patent 8,407,013, 2013
Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns
Z Michael, R Jacobs, Patricia, James, P Rogan, S Sherman, T Hassold
Human Genetics 94, 411-417, 1994
Mutations that alter RNA splicing of the human HPRT gene: a review of the spectrum
JP O'Neill, PK Rogan, N Cariello, JA Nicklas
Mutation Research/Reviews in Mutation Research 411 (3), 179-214, 1998
Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis
N Caminsky, EJ Mucaki, PK Rogan
F1000Research 3, 2014
Clinical spectrum and molecular diagnosis of Angelman and Prader‐Willi syndrome patients with an imprinting mutation
S Saitoh, K Buiting, SB Cassidy, JM Conroy, DJ Driscoll, JM Gabriel, ...
American journal of medical genetics 68 (2), 195-206, 1997
Genomic signatures for paclitaxel and gemcitabine resistance in breast cancer derived by machine learning
SN Dorman, K Baranova, JHM Knoll, BL Urquhart, G Mariani, ...
Molecular oncology 10, 85-100, 2015
Method for rapid identification of prokaryotic and eukaryotic organisms
PK Rogan
US Patent 5,849,492, 1998
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor
P Peterlongo, I Catucci, M Colombo, L Caleca, E Mucaki, M Bogliolo, ...
Human molecular genetics 24 (18), 5345-5355, 2015
Organization of the ABCR gene: analysis of promoter and splice junction sequences.
R Allikmets, WW Wasserman, A Hutchinson, P Smallwood, J Nathans, ...
Gene 215 (1), 111-122, 1998
Human SP-A locus: allele frequencies and linkage disequilibrium between the two surfactant protein A genes.
J Floros, S DiAngelo, M Koptides, AM Karinch, PK Rogan, H Nielsen, ...
American journal of respiratory cell and molecular biology 15 (4), 489-498, 1996
Study of nucleic acids isolated from ancient remains
PK Rogan, JJ Salvo
American Journal of Physical Anthropology 33 (S11), 195-214, 1990
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