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Human Molecular Genetics
|
August 25, 2000
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21
S Kohl, B Baumann, M Broghammer, et al.
Genomics
|
August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11
B Wissinger, H Jägle, S Kohl, et al.
Biorxiv : the Preprint Server for Biology
|
January 7, 2026
Comprehensive Mapping of the Virus and Host Factors that Guide the Paths of HIV-1 Escape from a Therapeutic
Aaron N Gillman, Cassian M Birler, Rohith Rao Vujjini, et al.
Cell Reports
|
June 20, 2026
Comprehensive mapping of the virus and host factors that guide the paths of HIV-1 escape from a therapeutic
Aaron N Gillman, Cassian M Birler, Rohith Rao Vujjini, et al.
American Journal of Human Genetics
|
September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disorders
B Wissinger, D Gamer, H Jägle, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Human Molecular Genetics
|
August 25, 2000
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21
S Kohl, B Baumann, M Broghammer, et al.
Genomics
|
August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11
B Wissinger, H Jägle, S Kohl, et al.
Biorxiv : the Preprint Server for Biology
|
January 7, 2026
Comprehensive Mapping of the Virus and Host Factors that Guide the Paths of HIV-1 Escape from a Therapeutic
Aaron N Gillman, Cassian M Birler, Rohith Rao Vujjini, et al.
Cell Reports
|
June 20, 2026
Comprehensive mapping of the virus and host factors that guide the paths of HIV-1 escape from a therapeutic
Aaron N Gillman, Cassian M Birler, Rohith Rao Vujjini, et al.
American Journal of Human Genetics
|
September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disorders
B Wissinger, D Gamer, H Jägle, et al.
Page
of 2