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S Hart

Showing results (481-490 of 590) with videos related to

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Gastroenterology|September 13, 2000
SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitisR H Pfützer, M M Barmada, A P Brunskill, et al.
Journal of Medical Genetics|December 14, 1999
Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndromeT C Hart, P S Hart, D W Bowden, et al.
Biomedicines|December 23, 2022
A Subset Screen of the Compounds Australia Scaffold Library Identifies 7-Acylaminodibenzoxazepinones as Potent and Selective Hits for Anti-<i>Giardia</i> Drug DiscoveryChristopher J S Hart, Andrew G Riches, Snigdha Tiash, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|September 26, 2025
Practice patterns of Canadian neurosurgeons in laparoscopic-assisted placement of ventriculoperitoneal shuntsJ M Heppner, B Ajlan, S Hart, et al.
Eneuro|March 2, 2019
The Role of the Voltage-Gated Potassium Channel Proteins Kv8.2 and Kv2.1 in Vision and Retinal Disease: Insights from the Study of Mouse Gene Knock-Out MutationsNathan S Hart, Jessica K Mountford, Valentina Voigt, et al.
Journal of Medical Genetics|March 4, 2005
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfectaJ-W Kim, J P Simmer, T C Hart, et al.
Clinical Genetics|February 18, 2009
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfectaP S Hart, S Becerik, D Cogulu, et al.
Journal of Medical Genetics|February 9, 2000
Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutationT C Hart, P S Hart, M D Michalec, et al.
Cell Cycle (Georgetown, Tex.)|January 8, 2010
The p53 target Plk2 interacts with TSC proteins impacting mTOR signaling, tumor growth and chemosensitivity under hypoxic conditionsElizabeth M Matthew, Lori S Hart, Aristotelis Astrinidis, et al.
Cancer Research|June 11, 1998
Ataxia-telangiectasia and T-cell leukemias: no evidence for somatic ATM mutation in sporadic T-ALL or for hypermethylation of the ATM-NPAT/E14 bidirectional promoter in T-PLLL Luo, F M Lu, S Hart, et al.
Pageof 59

Showing results (481-490 of 590) with videos related to

Sort By:
Pageof 59
Gastroenterology|September 13, 2000
SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitisR H Pfützer, M M Barmada, A P Brunskill, et al.
Journal of Medical Genetics|December 14, 1999
Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndromeT C Hart, P S Hart, D W Bowden, et al.
Biomedicines|December 23, 2022
A Subset Screen of the Compounds Australia Scaffold Library Identifies 7-Acylaminodibenzoxazepinones as Potent and Selective Hits for Anti-<i>Giardia</i> Drug DiscoveryChristopher J S Hart, Andrew G Riches, Snigdha Tiash, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|September 26, 2025
Practice patterns of Canadian neurosurgeons in laparoscopic-assisted placement of ventriculoperitoneal shuntsJ M Heppner, B Ajlan, S Hart, et al.
Eneuro|March 2, 2019
The Role of the Voltage-Gated Potassium Channel Proteins Kv8.2 and Kv2.1 in Vision and Retinal Disease: Insights from the Study of Mouse Gene Knock-Out MutationsNathan S Hart, Jessica K Mountford, Valentina Voigt, et al.
Journal of Medical Genetics|March 4, 2005
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfectaJ-W Kim, J P Simmer, T C Hart, et al.
Clinical Genetics|February 18, 2009
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfectaP S Hart, S Becerik, D Cogulu, et al.
Journal of Medical Genetics|February 9, 2000
Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutationT C Hart, P S Hart, M D Michalec, et al.
Cell Cycle (Georgetown, Tex.)|January 8, 2010
The p53 target Plk2 interacts with TSC proteins impacting mTOR signaling, tumor growth and chemosensitivity under hypoxic conditionsElizabeth M Matthew, Lori S Hart, Aristotelis Astrinidis, et al.
Cancer Research|June 11, 1998
Ataxia-telangiectasia and T-cell leukemias: no evidence for somatic ATM mutation in sporadic T-ALL or for hypermethylation of the ATM-NPAT/E14 bidirectional promoter in T-PLLL Luo, F M Lu, S Hart, et al.
Pageof 59