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Nature Genetics
|
October 4, 2000
Human-mouse genome comparisons to locate regulatory sites
W W Wasserman, M Palumbo, W Thompson, et al.
Cancer Letters
|
February 17, 2001
Polymorphic electrophile response elements in the mouse glutathione S-transferase GSTa1 gene that confer increased induction
M Zhu, W G Chapman, M J Oberley, et al.
Gene
|
July 17, 1998
Organization of the ABCR gene: analysis of promoter and splice junction sequences
R Allikmets, W W Wasserman, A Hutchinson, et al.
Optics Express
|
October 15, 2022
Cryogenic and hermetically sealed packaging of photonic chips for optomechanics
W W Wasserman, R A Harrison, G I Harris, et al.
Gene
|
May 23, 2001
Initial isolation and analysis of the human Kv1.7 (KCNA7) gene, a member of the voltage-gated potassium channel gene family
V I Kashuba, S M Kvasha, A I Protopopov, et al.
Neurogenetics
|
June 25, 2014
AIMP1 deficiency presents as a cortical neurodegenerative disease with infantile onset
L Armstrong, R Biancheri, C Shyr, et al.
Molecular and Cellular Biology
|
February 1, 2012
Retina restored and brain abnormalities ameliorated by single-copy knock-in of human NR2E1 in null mice
J-F Schmouth, K G Banks, A Mathelier, et al.
Clinical Genetics
|
October 17, 2013
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype
I Filges, E Nosova, E Bruder, et al.
European Journal of Medical Genetics
|
August 6, 2017
A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder
A M Matthews, M Tarailo-Graovac, E M Price, et al.
Clinical Genetics
|
August 9, 2017
Bone health and SATB2-associated syndrome
Y A Zarate, M Steinraths, A Matthews, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Nature Genetics
|
October 4, 2000
Human-mouse genome comparisons to locate regulatory sites
W W Wasserman, M Palumbo, W Thompson, et al.
Cancer Letters
|
February 17, 2001
Polymorphic electrophile response elements in the mouse glutathione S-transferase GSTa1 gene that confer increased induction
M Zhu, W G Chapman, M J Oberley, et al.
Gene
|
July 17, 1998
Organization of the ABCR gene: analysis of promoter and splice junction sequences
R Allikmets, W W Wasserman, A Hutchinson, et al.
Optics Express
|
October 15, 2022
Cryogenic and hermetically sealed packaging of photonic chips for optomechanics
W W Wasserman, R A Harrison, G I Harris, et al.
Gene
|
May 23, 2001
Initial isolation and analysis of the human Kv1.7 (KCNA7) gene, a member of the voltage-gated potassium channel gene family
V I Kashuba, S M Kvasha, A I Protopopov, et al.
Neurogenetics
|
June 25, 2014
AIMP1 deficiency presents as a cortical neurodegenerative disease with infantile onset
L Armstrong, R Biancheri, C Shyr, et al.
Molecular and Cellular Biology
|
February 1, 2012
Retina restored and brain abnormalities ameliorated by single-copy knock-in of human NR2E1 in null mice
J-F Schmouth, K G Banks, A Mathelier, et al.
Clinical Genetics
|
October 17, 2013
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype
I Filges, E Nosova, E Bruder, et al.
European Journal of Medical Genetics
|
August 6, 2017
A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder
A M Matthews, M Tarailo-Graovac, E M Price, et al.
Clinical Genetics
|
August 9, 2017
Bone health and SATB2-associated syndrome
Y A Zarate, M Steinraths, A Matthews, et al.
Page
of 2