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Diabetic Medicine : a Journal of the British Diabetic Association
|
June 1, 1997
Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population
J E Newkirk, R W Taylor, N Howell, et al.
Neuropathology and Applied Neurobiology
|
July 27, 2006
Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement
J Betts, E Jaros, R H Perry, et al.
Neurology
|
April 13, 2005
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations
S Winterthun, G Ferrari, L He, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
February 1, 1996
Human insulin receptor substrate-1: variant sequences in familial non-insulin-dependent diabetes mellitus
M Armstrong, F Haldane, R W Taylor, et al.
Journal of Dental Research
|
January 10, 2022
Axin2+ PDL Cells Directly Contribute to New Alveolar Bone Formation in Response to Orthodontic Tension Force
K Wang, C Xu, X Xie, et al.
Neurology
|
March 25, 2009
Fatal congenital myopathy and gastrointestinal pseudo-obstruction due to POLG1 mutations
C Giordano, H Powell, M Leopizzi, et al.
Nucleic Acids Research
|
May 9, 2001
Targeting peptide nucleic acid (PNA) oligomers to mitochondria within cells by conjugation to lipophilic cations: implications for mitochondrial DNA replication, expression and disease
A Muratovska, R N Lightowlers, R W Taylor, et al.
Molecular Microbiology
|
November 9, 2000
The quarternary molecular architecture of TetA, a secondary tetracycline transporter from Escherichia coli
C C Yin, M L Aldema-Ramos, M I Borges-Walmsley, et al.
Neuropathology and Applied Neurobiology
|
February 4, 2009
Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions
J Betts-Henderson, E Jaros, K J Krishnan, et al.
Neurology
|
April 23, 2003
Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)
A Agostino, L Valletta, P F Chinnery, et al.
Page
of 26
Search research articles
Search
Showing results (211-220 of 254) with videos related to
Sort By:
Page
of 26
Diabetic Medicine : a Journal of the British Diabetic Association
|
June 1, 1997
Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population
J E Newkirk, R W Taylor, N Howell, et al.
Neuropathology and Applied Neurobiology
|
July 27, 2006
Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement
J Betts, E Jaros, R H Perry, et al.
Neurology
|
April 13, 2005
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations
S Winterthun, G Ferrari, L He, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
February 1, 1996
Human insulin receptor substrate-1: variant sequences in familial non-insulin-dependent diabetes mellitus
M Armstrong, F Haldane, R W Taylor, et al.
Journal of Dental Research
|
January 10, 2022
Axin2+ PDL Cells Directly Contribute to New Alveolar Bone Formation in Response to Orthodontic Tension Force
K Wang, C Xu, X Xie, et al.
Neurology
|
March 25, 2009
Fatal congenital myopathy and gastrointestinal pseudo-obstruction due to POLG1 mutations
C Giordano, H Powell, M Leopizzi, et al.
Nucleic Acids Research
|
May 9, 2001
Targeting peptide nucleic acid (PNA) oligomers to mitochondria within cells by conjugation to lipophilic cations: implications for mitochondrial DNA replication, expression and disease
A Muratovska, R N Lightowlers, R W Taylor, et al.
Molecular Microbiology
|
November 9, 2000
The quarternary molecular architecture of TetA, a secondary tetracycline transporter from Escherichia coli
C C Yin, M L Aldema-Ramos, M I Borges-Walmsley, et al.
Neuropathology and Applied Neurobiology
|
February 4, 2009
Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions
J Betts-Henderson, E Jaros, K J Krishnan, et al.
Neurology
|
April 23, 2003
Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)
A Agostino, L Valletta, P F Chinnery, et al.
Page
of 26