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A F Markham

Showing results (221-230 of 231) with videos related to

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Bone Marrow Transplantation|November 11, 2008
Haematopoietic repopulating activity in human cord blood CD133+ quiescent cellsS A Boxall, G P Cook, D Pearce, et al.
The Journal of Clinical Investigation|February 22, 2001
Rheumatoid arthritis synovial T cells regulate transcription of several genes associated with antigen-induced anergyM Ali, F Ponchel, K E Wilson, et al.
Nucleic Acids Symposium Series|January 1, 1980
Total synthesis of tRNAfMetE Ohtsuka, A F Markham, S Tanaka, et al.
British Journal of Anaesthesia|January 5, 2000
Segregation of malignant hyperthermia, central core disease and chromosome 19 markersJ L Curran, W J Hall, P J Halsall, et al.
American Journal of Human Genetics|July 31, 1998
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pterA P Jackson, D P McHale, D A Campbell, et al.
Journal of Medical Genetics|January 16, 1998
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22D A Campbell, D P McHale, K A Brown, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
Human Molecular Genetics|July 7, 2001
Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophyC Toomes, N J Marchbank, D A Mackey, et al.
Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.
Human Molecular Genetics|July 27, 2001
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)A B McKie, J C McHale, T J Keen, et al.
Pageof 24

Showing results (221-230 of 231) with videos related to

Sort By:
Pageof 24
Bone Marrow Transplantation|November 11, 2008
Haematopoietic repopulating activity in human cord blood CD133+ quiescent cellsS A Boxall, G P Cook, D Pearce, et al.
The Journal of Clinical Investigation|February 22, 2001
Rheumatoid arthritis synovial T cells regulate transcription of several genes associated with antigen-induced anergyM Ali, F Ponchel, K E Wilson, et al.
Nucleic Acids Symposium Series|January 1, 1980
Total synthesis of tRNAfMetE Ohtsuka, A F Markham, S Tanaka, et al.
British Journal of Anaesthesia|January 5, 2000
Segregation of malignant hyperthermia, central core disease and chromosome 19 markersJ L Curran, W J Hall, P J Halsall, et al.
American Journal of Human Genetics|July 31, 1998
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pterA P Jackson, D P McHale, D A Campbell, et al.
Journal of Medical Genetics|January 16, 1998
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22D A Campbell, D P McHale, K A Brown, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
Human Molecular Genetics|July 7, 2001
Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophyC Toomes, N J Marchbank, D A Mackey, et al.
Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.
Human Molecular Genetics|July 27, 2001
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)A B McKie, J C McHale, T J Keen, et al.
Pageof 24