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M Macek

Showing results (191-200 of 217) with videos related to

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Nature Genetics|November 1, 1993
A mutation in CFTR produces different phenotypes depending on chromosomal backgroundS Kiesewetter, M Macek, C Davis, et al.
Human Genetics|May 8, 2000
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East EuropeT Dörk, M Macek, F Mekus, et al.
Casopis Lekaru Ceskych|March 20, 2002
[Medical genetics in reproductive medicine]M Macek, S Vilímová, P Potuzníková, et al.
American Journal of Human Genetics|May 1, 1997
Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75%M Macek, A Mackova, A Hamosh, et al.
Molecular and Cellular Endocrinology|July 8, 2017
The polymorphic insertion of the luteinizing hormone receptor "insLQ" show a negative association to LHR gene expression and to the follicular fluid hormonal profile in human small antral folliclesT Borgbo, J Chrudimska, M Macek, et al.
Casopis Lekaru Ceskych|April 25, 1975
[Pregnancy hyperphenylalanemia and its diagnostic importance (author's transl)]J Hyánek, V Trnka, J Homolka, et al.
Casopis Lekaru Ceskych|April 8, 1977
[Results and possibilities of clinical cytogenetics in the Czech Socialist Republic (author's transl)]M Vrba, R Adámek, P Balícek, et al.
Human Molecular Genetics|February 1, 1995
Missense mutation (G480C) in the CFTR gene associated with protein mislocalization but normal chloride channel activityL S Smit, T V Strong, D J Wilkinson, et al.
American Journal of Human Genetics|July 31, 1998
Evidence for a common ethnic origin of cystic fibrosis mutation 3120+1G-->A in diverse populationsT Dörk, E H El-Harith, M Stuhrmann, et al.
Science (New York, N.Y.)|December 15, 1989
First plasma wave observations at neptuneD A Gurnett, W S Kurth, R L Poynter, et al.
Pageof 22

Showing results (191-200 of 217) with videos related to

Sort By:
Pageof 22
Nature Genetics|November 1, 1993
A mutation in CFTR produces different phenotypes depending on chromosomal backgroundS Kiesewetter, M Macek, C Davis, et al.
Human Genetics|May 8, 2000
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East EuropeT Dörk, M Macek, F Mekus, et al.
Casopis Lekaru Ceskych|March 20, 2002
[Medical genetics in reproductive medicine]M Macek, S Vilímová, P Potuzníková, et al.
American Journal of Human Genetics|May 1, 1997
Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75%M Macek, A Mackova, A Hamosh, et al.
Molecular and Cellular Endocrinology|July 8, 2017
The polymorphic insertion of the luteinizing hormone receptor "insLQ" show a negative association to LHR gene expression and to the follicular fluid hormonal profile in human small antral folliclesT Borgbo, J Chrudimska, M Macek, et al.
Casopis Lekaru Ceskych|April 25, 1975
[Pregnancy hyperphenylalanemia and its diagnostic importance (author's transl)]J Hyánek, V Trnka, J Homolka, et al.
Casopis Lekaru Ceskych|April 8, 1977
[Results and possibilities of clinical cytogenetics in the Czech Socialist Republic (author's transl)]M Vrba, R Adámek, P Balícek, et al.
Human Molecular Genetics|February 1, 1995
Missense mutation (G480C) in the CFTR gene associated with protein mislocalization but normal chloride channel activityL S Smit, T V Strong, D J Wilkinson, et al.
American Journal of Human Genetics|July 31, 1998
Evidence for a common ethnic origin of cystic fibrosis mutation 3120+1G-->A in diverse populationsT Dörk, E H El-Harith, M Stuhrmann, et al.
Science (New York, N.Y.)|December 15, 1989
First plasma wave observations at neptuneD A Gurnett, W S Kurth, R L Poynter, et al.
Pageof 22