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A C Reed

Showing results (21-30 of 39) with videos related to

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Journal of Molecular Biology|July 16, 2003
Effects of domain dissection on the folding and stability of the 43 kDa protein PGK probed by NMRMichelle A C Reed, Andrea M Hounslow, K H Sze, et al.
Journal of Molecular Biology|January 25, 2006
The denatured state under native conditions: a non-native-like collapsed state of N-PGKMichelle A C Reed, Clare Jelinska, Karl Syson, et al.
The Journal of Endocrinology|July 10, 2009
Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiersManuel C Lemos, Brian Harding, Anita A C Reed, et al.
Laboratory Animals|May 12, 2010
Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cagesMichael J Stechman, Bushra N Ahmad, Nellie Y Loh, et al.
Human Molecular Genetics|May 26, 2009
Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulumSiân E Williams, Anita A C Reed, Juris Galvanovskis, et al.
Nucleic Acids Research|May 21, 2026
Combinatorial histone modifications direct ATP-dependent chromatin remodeling by NURF to promoter-proximal nucleosomesSo Yeon Kwon, Boyun Jang, Valentina Grisan, et al.
Endocrine-Related Cancer|July 22, 2009
Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemiaBrian Harding, Manuel C Lemos, Anita A C Reed, et al.
Endocrine Connections|April 30, 2020
Genetic background influences tumour development in heterozygous Men1 knockout miceKate E Lines, Mahsa Javid, Anita A C Reed, et al.
Human Genetics|October 27, 2010
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21Sian E Piret, Patrick Danoy, Karin Dahan, et al.
Cancer Research|August 24, 2012
MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary adenomasGerard V Walls, Manuel C Lemos, Mahsa Javid, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Journal of Molecular Biology|July 16, 2003
Effects of domain dissection on the folding and stability of the 43 kDa protein PGK probed by NMRMichelle A C Reed, Andrea M Hounslow, K H Sze, et al.
Journal of Molecular Biology|January 25, 2006
The denatured state under native conditions: a non-native-like collapsed state of N-PGKMichelle A C Reed, Clare Jelinska, Karl Syson, et al.
The Journal of Endocrinology|July 10, 2009
Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiersManuel C Lemos, Brian Harding, Anita A C Reed, et al.
Laboratory Animals|May 12, 2010
Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cagesMichael J Stechman, Bushra N Ahmad, Nellie Y Loh, et al.
Human Molecular Genetics|May 26, 2009
Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulumSiân E Williams, Anita A C Reed, Juris Galvanovskis, et al.
Nucleic Acids Research|May 21, 2026
Combinatorial histone modifications direct ATP-dependent chromatin remodeling by NURF to promoter-proximal nucleosomesSo Yeon Kwon, Boyun Jang, Valentina Grisan, et al.
Endocrine-Related Cancer|July 22, 2009
Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemiaBrian Harding, Manuel C Lemos, Anita A C Reed, et al.
Endocrine Connections|April 30, 2020
Genetic background influences tumour development in heterozygous Men1 knockout miceKate E Lines, Mahsa Javid, Anita A C Reed, et al.
Human Genetics|October 27, 2010
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21Sian E Piret, Patrick Danoy, Karin Dahan, et al.
Cancer Research|August 24, 2012
MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary adenomasGerard V Walls, Manuel C Lemos, Mahsa Javid, et al.
Pageof 4