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Genomics
|
April 15, 1996
The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3
M D Lalioti, A Gos, M R Green, et al.
Genomics
|
April 18, 1998
Identification and characterization of two putative human arginine methyltransferases (HRMT1L1 and HRMT1L2)
H S Scott, S E Antonarakis, M D Lalioti, et al.
Nature
|
April 24, 1997
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy
M D Lalioti, H S Scott, C Buresi, et al.
American Journal of Human Genetics
|
February 1, 1997
Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1)
M D Lalioti, M Mirotsou, C Buresi, et al.
Genomics
|
February 18, 1998
Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis
H S Scott, D S Kyriakou, P Peterson, et al.
Human Genetics
|
December 18, 1998
Identification and characterization of a novel cyclic nucleotide phosphodiesterase gene (PDE9A) that maps to 21q22.3: alternative splicing of mRNA transcripts, genomic structure and sequence
M Guipponi, H S Scott, J Kudoh, et al.
Genomics
|
August 22, 2000
Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat protein
J Michaud, J Kudoh, A Berry, et al.
American Journal of Human Genetics
|
June 13, 1998
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset
M D Lalioti, H S Scott, P Genton, et al.
Nature Genetics
|
December 17, 1997
Positional cloning of the APECED gene
K Nagamine, P Peterson, H S Scott, et al.
Molecular Endocrinology (Baltimore, Md.)
|
August 26, 1998
Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins
H S Scott, M Heino, P Peterson, et al.
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 20 results.
Genomics
|
April 15, 1996
The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3
M D Lalioti, A Gos, M R Green, et al.
Genomics
|
April 18, 1998
Identification and characterization of two putative human arginine methyltransferases (HRMT1L1 and HRMT1L2)
H S Scott, S E Antonarakis, M D Lalioti, et al.
Nature
|
April 24, 1997
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy
M D Lalioti, H S Scott, C Buresi, et al.
American Journal of Human Genetics
|
February 1, 1997
Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1)
M D Lalioti, M Mirotsou, C Buresi, et al.
Genomics
|
February 18, 1998
Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis
H S Scott, D S Kyriakou, P Peterson, et al.
Human Genetics
|
December 18, 1998
Identification and characterization of a novel cyclic nucleotide phosphodiesterase gene (PDE9A) that maps to 21q22.3: alternative splicing of mRNA transcripts, genomic structure and sequence
M Guipponi, H S Scott, J Kudoh, et al.
Genomics
|
August 22, 2000
Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat protein
J Michaud, J Kudoh, A Berry, et al.
American Journal of Human Genetics
|
June 13, 1998
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset
M D Lalioti, H S Scott, P Genton, et al.
Nature Genetics
|
December 17, 1997
Positional cloning of the APECED gene
K Nagamine, P Peterson, H S Scott, et al.
Molecular Endocrinology (Baltimore, Md.)
|
August 26, 1998
Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins
H S Scott, M Heino, P Peterson, et al.
Page
of 2