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Journal of Clinical Microbiology
|
March 7, 2001
Identification of canine coronavirus strains from feces by S gene nested PCR and molecular characterization of a new Australian isolate
M J Naylor, G A Harrison, R P Monckton, et al.
British Journal of Sports Medicine
|
December 21, 2010
BJSM reviews: A-Z of nutritional supplements: dietary supplements, sports nutrition foods and ergogenic aids for health and performance--Part 16
M Manore, R Meeusen, B Roelands, et al.
Nature Genetics
|
July 14, 1998
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness
N T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Genes & Development
|
July 11, 2001
SOCS1 deficiency results in accelerated mammary gland development and rescues lactation in prolactin receptor-deficient mice
G J Lindeman, S Wittlin, H Lada, et al.
Human Genetics
|
April 3, 2001
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
K M Boycott, T A Maybaum, M J Naylor, et al.
The Journal of Clinical Investigation
|
April 1, 1989
Primer-mediated enzymatic amplification of cytomegalovirus (CMV) DNA. Application to the early diagnosis of CMV infection in marrow transplant recipients
S A Cassol, M C Poon, R Pal, et al.
Molecular Endocrinology (Baltimore, Md.)
|
June 4, 2010
The antiproliferative effects of progestins in T47D breast cancer cells are tempered by progestin induction of the ETS transcription factor Elf5
H N Hilton, M Kalyuga, M J Cowley, et al.
Nature Genetics
|
November 4, 2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
N T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Oncogene
|
September 24, 2013
c-Myc and Her2 cooperate to drive a stem-like phenotype with poor prognosis in breast cancer
R Nair, D L Roden, W S Teo, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Journal of Clinical Microbiology
|
March 7, 2001
Identification of canine coronavirus strains from feces by S gene nested PCR and molecular characterization of a new Australian isolate
M J Naylor, G A Harrison, R P Monckton, et al.
British Journal of Sports Medicine
|
December 21, 2010
BJSM reviews: A-Z of nutritional supplements: dietary supplements, sports nutrition foods and ergogenic aids for health and performance--Part 16
M Manore, R Meeusen, B Roelands, et al.
Nature Genetics
|
July 14, 1998
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness
N T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Genes & Development
|
July 11, 2001
SOCS1 deficiency results in accelerated mammary gland development and rescues lactation in prolactin receptor-deficient mice
G J Lindeman, S Wittlin, H Lada, et al.
Human Genetics
|
April 3, 2001
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
K M Boycott, T A Maybaum, M J Naylor, et al.
The Journal of Clinical Investigation
|
April 1, 1989
Primer-mediated enzymatic amplification of cytomegalovirus (CMV) DNA. Application to the early diagnosis of CMV infection in marrow transplant recipients
S A Cassol, M C Poon, R Pal, et al.
Molecular Endocrinology (Baltimore, Md.)
|
June 4, 2010
The antiproliferative effects of progestins in T47D breast cancer cells are tempered by progestin induction of the ETS transcription factor Elf5
H N Hilton, M Kalyuga, M J Cowley, et al.
Nature Genetics
|
November 4, 2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
N T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Oncogene
|
September 24, 2013
c-Myc and Her2 cooperate to drive a stem-like phenotype with poor prognosis in breast cancer
R Nair, D L Roden, W S Teo, et al.
Page
of 2