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Showing results (1301-1310 of 1,876) with videos related to
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Oncogene
|
November 11, 1999
Stable overexpression of MEN1 suppresses tumorigenicity of RAS
Y S Kim, A L Burns, P K Goldsmith, et al.
Cell
|
November 15, 1996
Failure of embryonic hematopoiesis and lethal hemorrhages in mouse embryos heterozygous for a knocked-in leukemia gene CBFB-MYH11
L H Castilla, C Wijmenga, Q Wang, et al.
The Laryngoscope
|
January 1, 1994
Surgical variables affecting postoperative swallowing efficiency in oral cancer patients: a pilot study
F M McConnel, J A Logemann, A W Rademaker, et al.
Cancer Research
|
October 7, 2004
Pancreatic insulinomas in multiple endocrine neoplasia, type I knockout mice can develop in the absence of chromosome instability or microsatellite instability
Peter C Scacheri, Alyssa L Kennedy, Koei Chin, et al.
American Journal of Human Genetics
|
October 1, 1989
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21
D E Merry, J G Lesko, D M Sosnoski, et al.
Nature Communications
|
September 20, 2025
Multiple lines of evidence for a hypervelocity impact origin for the Silverpit Crater
Uisdean Nicholson, Iain de Jonge-Anderson, Alex Gillespie, et al.
BMJ (Clinical Research Ed.)
|
March 28, 2020
Artificial intelligence versus clinicians: systematic review of design, reporting standards, and claims of deep learning studies
Myura Nagendran, Yang Chen, Christopher A Lovejoy, et al.
Military Medicine
|
August 25, 2010
Substantiation of spouse and child maltreatment reports as a function of referral source and maltreatment type
Rachel E Foster, Fred P Stone, David J Linkh, et al.
American Journal of Human Genetics
|
February 1, 1991
Two frameshift mutations in the cystic fibrosis gene
M C Iannuzzi, R C Stern, F S Collins, et al.
Human Heredity
|
June 12, 1999
Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus. Finland-United States Investigation of NIDDM Genetics (FUSION) Study investigators
R M Watanabe, T Valle, E R Hauser, et al.
Page
of 188
Search research articles
Search
Showing results (1301-1310 of 1,876) with videos related to
Sort By:
Page
of 188
Oncogene
|
November 11, 1999
Stable overexpression of MEN1 suppresses tumorigenicity of RAS
Y S Kim, A L Burns, P K Goldsmith, et al.
Cell
|
November 15, 1996
Failure of embryonic hematopoiesis and lethal hemorrhages in mouse embryos heterozygous for a knocked-in leukemia gene CBFB-MYH11
L H Castilla, C Wijmenga, Q Wang, et al.
The Laryngoscope
|
January 1, 1994
Surgical variables affecting postoperative swallowing efficiency in oral cancer patients: a pilot study
F M McConnel, J A Logemann, A W Rademaker, et al.
Cancer Research
|
October 7, 2004
Pancreatic insulinomas in multiple endocrine neoplasia, type I knockout mice can develop in the absence of chromosome instability or microsatellite instability
Peter C Scacheri, Alyssa L Kennedy, Koei Chin, et al.
American Journal of Human Genetics
|
October 1, 1989
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21
D E Merry, J G Lesko, D M Sosnoski, et al.
Nature Communications
|
September 20, 2025
Multiple lines of evidence for a hypervelocity impact origin for the Silverpit Crater
Uisdean Nicholson, Iain de Jonge-Anderson, Alex Gillespie, et al.
BMJ (Clinical Research Ed.)
|
March 28, 2020
Artificial intelligence versus clinicians: systematic review of design, reporting standards, and claims of deep learning studies
Myura Nagendran, Yang Chen, Christopher A Lovejoy, et al.
Military Medicine
|
August 25, 2010
Substantiation of spouse and child maltreatment reports as a function of referral source and maltreatment type
Rachel E Foster, Fred P Stone, David J Linkh, et al.
American Journal of Human Genetics
|
February 1, 1991
Two frameshift mutations in the cystic fibrosis gene
M C Iannuzzi, R C Stern, F S Collins, et al.
Human Heredity
|
June 12, 1999
Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus. Finland-United States Investigation of NIDDM Genetics (FUSION) Study investigators
R M Watanabe, T Valle, E R Hauser, et al.
Page
of 188