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Mark Patterson
Mark Patterson
University of Manchester, Oxford, Stanford, Cambridge
Verifisert e-postadresse på elifesciences.org
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Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis
S Kenwrick, M Patterson, A Speer, K Fischbeck, K Davies
Cell 48 (2), 351-357, 1987
1961987
Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome
JA Batch, DM Williams, HR Davies, BD Brown, BAJ Evans, IA Hughes, ...
Human molecular genetics 1 (7), 497-503, 1992
1751992
Disorder-induced coherent scattering in slow-light photonic crystal waveguides
M Patterson, S Hughes, S Combrié, NVQ Tran, A De Rossi, R Gabet, ...
Physical review letters 102 (25), 253903, 2009
1722009
Molecular Characterization of Cell Cycle Gene CDC7 from Saccharomyces cerevisiae
M Patterson, RA Sclafani, WL Fangman, J Rosamond
Molecular and cellular biology 6 (5), 1590-1598, 1986
1721986
Ultrahigh Purcell factors and Lamb shifts in slow-light metamaterial waveguides
P Yao, C Van Vlack, A Reza, M Patterson, MM Dignam, S Hughes
Physical Review B 80 (19), 195106, 2009
1342009
Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs …
JS Waye, SJ Durfy, D Pinkel, S Kenwrick, M Patterson, KE Davies, ...
Genomics 1 (1), 43-51, 1987
1181987
Differential regulation of the yeast CDC7 gene during mitosis and meiosis
RA Sclafani, M Patterson, J Rosamond, WL Fangman
Molecular and cellular biology, 1988
1101988
Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UK
RM Viner, Y Teoh, DM Williams, MN Patterson, IA Hughes
Archives of Disease in Childhood 77 (4), 305-309, 1997
1001997
Disorder-induced incoherent scattering losses in photonic crystal waveguides: Bloch mode reshaping, multiple scattering, and breakdown of the Beer-Lambert law
M Patterson, S Hughes, S Schulz, DM Beggs, TP White, L O’Faolain, ...
Physical review B 80 (19), 195305, 2009
902009
Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndrome
CL Bevan, BB Brown, HR Davies, BAJ Evans, IA Hughes, MN Patterson
Human Molecular Genetics 5 (2), 265-273, 1996
891996
Phenotypic diversity in siblings with partial androgen insensitivity syndrome
BAJ Evans, IA Hughes, CL Bevan, MN Patterson, JW Gregory
Archives of disease in childhood 76 (6), 529-531, 1997
771997
Evidence that xeroderma pigmentosum cells from complementation group E are deficient in a homolog of yeast photolyase
M Patterson, G Chu
Molecular and cellular biology, 1989
771989
MASA syndrome: further clinical delineation and chromosomal localisation
RM Winter, KE Davies, MV Bell, SM Huson, MN Patterson
Human genetics 82, 367-370, 1989
751989
8 Androgen insensitivity syndrome
MN Patterson, MJ McPhaul, IA Hughes
Baillière's clinical endocrinology and metabolism 8 (2), 379-404, 1994
701994
Physical mapping studies on the human X chromosome in the region Xq27-Xqter
M Patterson, C Schwartz, M Bell, S Sauer, M Hofker, B Trask, ...
Genomics 1 (4), 297-306, 1987
661987
Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities.
PA Clarkson, HR Davies, DM Williams, R Chaudhary, IA Hughes, ...
Journal of medical genetics 30 (9), 767-772, 1993
631993
Mapping of DNA markers close to the fraglle site on the human X chromosome at Xq25–3
M Patterson, S Kenwrick, S Thibodeau, K Faulk, MG Mattei, JF Mattei, ...
Nucleic acids research 15 (6), 2639-2651, 1987
591987
Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28.
MV Bell, J Bloomfield, M McKinley, MN Patterson, MG Darlison, ...
American journal of human genetics 45 (6), 883, 1989
511989
Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndrome.
JA Batch, HR Davies, BA Evans, IA Hughes, MN Patterson
Archives of disease in childhood 68 (4), 453-457, 1993
501993
Mutations of the androgen receptor gene identified in perineal hypospadias.
JA Batch, BA Evans, IA Hughes, MN Patterson
Journal of medical genetics 30 (3), 198-201, 1993
481993
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Artikler 1–20