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J E Hewitt

Showing results (21-30 of 64) with videos related to

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Nucleic Acids Research|April 25, 1993
Sensitivity of HincII to CpG methylationL N Bull, J E Hewitt, D R Cox, et al.
Nature Genetics|May 31, 2001
Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouseP K Grewal, P J Holzfeind, R E Bittner, et al.
Meat Science|June 24, 2025
The impact of stockperson training on time to loss of posture in a minimal-handling high-concentration carbon dioxide stunning systemRobert J E Hewitt, Kate J Plush, Alan J Tilbrook, et al.
Chromosoma|September 1, 1996
Analysis of the organisation and localisation of the FSHD-associated tandem array in primates: implications for the origin and evolution of the 3.3 kb repeat familyL N Clark, U Koehler, D C Ward, et al.
Biochemical Society Transactions|May 1, 1996
A search for genes in the facioscapulohumeral muscular dystrophy regionP K Grewal, J C Van Deutekom, R R Frants, et al.
The American Journal of Physiology|May 1, 1991
Glycosylation is not required for ligand or receptor binding by expressed rat intrinsic factorM M Gordon, C Hu, H Chokshi, et al.
Cytogenetics and Cell Genetics|January 21, 2000
The murine urea transporter genes Slc14a1 and Slc14a2 occur in tandem on chromosome 18R A Fenton, J E Hewitt, A Howorth, et al.
Genomics|June 1, 1991
Human gastric intrinsic factor: characterization of cDNA and genomic clones and localization to human chromosome 11J E Hewitt, M M Gordon, R T Taggart, et al.
Gene|February 5, 1999
Recent amplification of the human FRG1 gene during primate evolutionP K Grewal, M van Geel, R R Frants, et al.
Gene|August 26, 1998
FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebratesP K Grewal, L C Todd, S van der Maarel, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
Nucleic Acids Research|April 25, 1993
Sensitivity of HincII to CpG methylationL N Bull, J E Hewitt, D R Cox, et al.
Nature Genetics|May 31, 2001
Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouseP K Grewal, P J Holzfeind, R E Bittner, et al.
Meat Science|June 24, 2025
The impact of stockperson training on time to loss of posture in a minimal-handling high-concentration carbon dioxide stunning systemRobert J E Hewitt, Kate J Plush, Alan J Tilbrook, et al.
Chromosoma|September 1, 1996
Analysis of the organisation and localisation of the FSHD-associated tandem array in primates: implications for the origin and evolution of the 3.3 kb repeat familyL N Clark, U Koehler, D C Ward, et al.
Biochemical Society Transactions|May 1, 1996
A search for genes in the facioscapulohumeral muscular dystrophy regionP K Grewal, J C Van Deutekom, R R Frants, et al.
The American Journal of Physiology|May 1, 1991
Glycosylation is not required for ligand or receptor binding by expressed rat intrinsic factorM M Gordon, C Hu, H Chokshi, et al.
Cytogenetics and Cell Genetics|January 21, 2000
The murine urea transporter genes Slc14a1 and Slc14a2 occur in tandem on chromosome 18R A Fenton, J E Hewitt, A Howorth, et al.
Genomics|June 1, 1991
Human gastric intrinsic factor: characterization of cDNA and genomic clones and localization to human chromosome 11J E Hewitt, M M Gordon, R T Taggart, et al.
Gene|February 5, 1999
Recent amplification of the human FRG1 gene during primate evolutionP K Grewal, M van Geel, R R Frants, et al.
Gene|August 26, 1998
FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebratesP K Grewal, L C Todd, S van der Maarel, et al.
Pageof 7