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European Journal of Human Genetics : EJHG
|
January 1, 1994
A systematic search for uniparental disomy in carriers of chromosome translocations
R S James, I K Temple, C Patch, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
March 22, 2001
Inducible nitric oxide synthase neutralizes carbamoylating potential of 1,3-bis(2-chloroethyl)-1-nitrosourea in c6 glioma cells
J H Yin, D I Yang, H Chou, et al.
Transgenic Research
|
December 22, 1998
Prediction of transgene integration by noninvasive bioluminescent screening of microinjected bovine embryos
M Menck, Y Mercier, E Campion, et al.
Journal of Cell Science
|
July 27, 2000
Somatic linker histone H1 is present throughout mouse embryogenesis and is not replaced by variant H1 degrees
P G Adenot, E Campion, E Legouy, et al.
Australian and New Zealand Journal of Medicine
|
October 20, 1998
The causes of sporadic and 'senile' chorea
J D Warren, F Firgaira, E M Thompson, et al.
Reproductive Biomedicine Online
|
December 6, 2003
Effects of cryopreservation on testicular sperm nuclear DNA fragmentation and its relationship with assisted conception outcome following ICSI with testicular spermatozoa
M E M Thompson-Cree, Neil McClure, Eilish T Donnelly, et al.
Fertility and Sterility
|
June 13, 2003
Effects of 24-hour incubation after freeze-thawing on DNA fragmentation of testicular sperm from infertile and fertile men
Lauren H Dalzell, Margaret E M Thompson-Cree, Neil McClure, et al.
Langmuir : the ACS Journal of Surfaces and Colloids
|
January 1, 2013
Hot embossed microtopographic gradients reveal morphological cues that guide the settlement of zoospores
Linlin Xiao, Stephanie E M Thompson, Michael Röhrig, et al.
American Journal of Human Genetics
|
August 16, 2001
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation
F Zhao, C G Weismann, M Satoda, et al.
Human Genetics
|
September 1, 1990
The incidence of delta F508 CF mutation, and associated haplotypes, in a sample of English CF families
E K Watson, E S Mayall, L Simova, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 123) with videos related to
Sort By:
Page
of 13
European Journal of Human Genetics : EJHG
|
January 1, 1994
A systematic search for uniparental disomy in carriers of chromosome translocations
R S James, I K Temple, C Patch, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
March 22, 2001
Inducible nitric oxide synthase neutralizes carbamoylating potential of 1,3-bis(2-chloroethyl)-1-nitrosourea in c6 glioma cells
J H Yin, D I Yang, H Chou, et al.
Transgenic Research
|
December 22, 1998
Prediction of transgene integration by noninvasive bioluminescent screening of microinjected bovine embryos
M Menck, Y Mercier, E Campion, et al.
Journal of Cell Science
|
July 27, 2000
Somatic linker histone H1 is present throughout mouse embryogenesis and is not replaced by variant H1 degrees
P G Adenot, E Campion, E Legouy, et al.
Australian and New Zealand Journal of Medicine
|
October 20, 1998
The causes of sporadic and 'senile' chorea
J D Warren, F Firgaira, E M Thompson, et al.
Reproductive Biomedicine Online
|
December 6, 2003
Effects of cryopreservation on testicular sperm nuclear DNA fragmentation and its relationship with assisted conception outcome following ICSI with testicular spermatozoa
M E M Thompson-Cree, Neil McClure, Eilish T Donnelly, et al.
Fertility and Sterility
|
June 13, 2003
Effects of 24-hour incubation after freeze-thawing on DNA fragmentation of testicular sperm from infertile and fertile men
Lauren H Dalzell, Margaret E M Thompson-Cree, Neil McClure, et al.
Langmuir : the ACS Journal of Surfaces and Colloids
|
January 1, 2013
Hot embossed microtopographic gradients reveal morphological cues that guide the settlement of zoospores
Linlin Xiao, Stephanie E M Thompson, Michael Röhrig, et al.
American Journal of Human Genetics
|
August 16, 2001
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation
F Zhao, C G Weismann, M Satoda, et al.
Human Genetics
|
September 1, 1990
The incidence of delta F508 CF mutation, and associated haplotypes, in a sample of English CF families
E K Watson, E S Mayall, L Simova, et al.
Page
of 13