Irvine, California
United States
28
2026-06-18
The entities that hold a legal rights for patent applications filed by inventor Sun Weimin:
Weimin Sun from Irvine, US has applied for patents for these inventions. The list has both pending applications and granted patents:
METHODS FOR DETECTING HEREDITARY CANCERS
#2 | 2023-08-24METHOD TO DETECT REPEAT SEQUENCE MOTIFS IN NUCLEIC ACID
#3 | 2022-09-01METHODS FOR DETECTING HEREDITARY CANCERS
#4 | 2021-05-06METHOD FOR DETECTING CYSTIC FIBROSIS
#5 | 2021-04-01CYSTIC FIBROSIS GENE MUTATIONS
#6 | 2020-08-27Cystic fibrosis transmembrane conductance regulator gene mutations
#7 | 2019-12-12Method to detect repeat sequence motifs in nucleic acid
#8 | 2019-06-13METHOD FOR DETECTING CYSTIC FIBROSIS
#9 | 2018-07-12Cystic fibrosis transmembrane conductance regulator gene mutations
#10 | 2018-04-05Cystic fibrosis gene mutations
#11 | 2017-11-16Aptamers and diagnostic methods for detecting the EGF receptor
#12 | 2017-01-05Cystic fibrosis transmembrane conductance regulator gene mutations
#13 | 2017-01-05Method to detect repeat sequence motifs in nucleic acid
#14 | 2016-06-09Cystic fibrosis gene mutations
#15 | 2015-03-26Aptamers and diagnostic methods for detecting the EGF receptor
#16 | 2015-01-08Cystic fibrosis transmembrane conductance regulator gene mutations
#17 | 2014-06-26Cystic fibrosis gene mutations
#18 | 2013-05-09Method to detect repeat sequence motifs in nucleic acid
#19 | 2012-12-25Cystic fibrosis gene mutations
#20 | 2012-06-07Cystic fibrosis transmembrane conductance regulator gene mutations
#21 | 2012-04-05Cystic fibrosis gene mutations
#22 | 2011-01-13Cystic fibrosis transmembrane conductance regulator gene mutations
#23 | 2010-12-16Cystic fibrosis gene mutations
#24 | 2010-09-28Methods for diagnosing cystic fibrosis
#25 | 2009-12-10METHOD OF DETECTING CYP2A6 GENE VARIANTS
#26 | 2008-07-17Cystic fibrosis transmembrane conductance regulator gene mutations
#27 | 2008-05-29Alpha globin gene dosage assay
#28 | 2005-07-14Methods and compositions for the detection of mucolipidosis IV mutations
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