LIFTON; Richard P.

Patent Applications and Registrations

Patent applications and USPTO patent grants for LIFTON; Richard P..The latest application filed is for "loss of function mutations in kcnj10 cause sesame, a human syndrome with sensory, neurological, and renal deficits".

Company Profile

1.8.7

LIFTON; Richard P. - North Haven CT
Lifton, Richard P. - Guilford CT
Lifton; Richard P. - Salt Lake City UT

*profile and listings may contain filings by different individuals or companies with the same name. Review application materials to confirm ownership/assignment.

Patent Activity

Patent	Date
Loss of Function mutations in KCNJ10 cause SeSAME, a human syndrome with sensory, neurological, and renal deficits App 20200362008 - LIFTON; Richard P. ; et al.	2020-11-19
Loss of function mutations in KCNJ10 cause SeSAME, a human syndrome with sensory, neurological, and renal deficits Grant 10,696,729 - Lifton , et al. June 30, 2	2020-06-30
Compositions and methods for assessing and treating adrenal diseases and disorders Grant 9,982,026 - Lifton , et al. May 29, 2	2018-05-29
Loss of Function mutations in KCNJ10 cause SeSAME, a human syndrome with sensory, neurological, and renal deficits App 20170298114 - LIFTON; Richard P. ; et al.	2017-10-19
Loss of function mutations in KCNJ10 cause SeSAME, a human syndrome with sensory, neurological, and renal deficits Grant 9,732,138 - Lifton , et al. August 15, 2	2017-08-15
Compositions and Methods for Assessing and Treating Adrenal Diseases and Disorders App 20140127126 - Lifton; Richard P. ; et al.	2014-05-08
Loss of Function mutations in KCNJ10 cause SeSAME, a human syndrome with sensory, neurological, and renal deficits App 20110195863 - Lifton; Richard P. ; et al.	2011-08-11
Mutations in Contaction Associated Protein 2 (CNTNAP2) are Associated with Increased Risk for Ideopathic Autism App 20110118135 - State; Matthew W. ; et al.	2011-05-19
Compositions methods and kits relating to treating and diagnosing hypertension App 20030082720 - Lifton, Richard P. ; et al.	2003-05-01
Method to diagnose and treat pathological conditions resulting from deficient ion transport such as pseudohypoaldosteronism type-1 Grant 6,551,775 - Lifton , et al. April 22, 2	2003-04-22
Method to determine predisposition to hypertension Grant 6,165,727 - Lalouel , et al. December 26, 2	2000-12-26
Methods to determine predisposition to hypertension and association of variant angiotensinogen gene and hypertension Grant 5,374,525 - Lalouel , et al. December 20, 1	1994-12-20

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