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Leukemia
|
January 20, 2009
Molecular recognition of acute myeloid leukemia using aptamers
K Sefah, Z W Tang, D H Shangguan, et al.
Human Genetics
|
January 27, 2000
Germline origins in the human F9 gene: frequent G:C-->A:T mosaicism and increased mutations with advanced maternal age
R P Ketterling, E Vielhaber, X Li, et al.
Human Biology
|
August 1, 1997
Cystic fibrosis in the Brazilian population: DF508 mutation and KM-19/XV-2C haplotype distribution
S Raskin, J A Phillips, M R Krishnamani, et al.
Nature Genetics
|
February 14, 1998
Mutations in PROP1 cause familial combined pituitary hormone deficiency
W Wu, J D Cogan, R W Pfäffle, et al.
Molecular Cell
|
February 20, 1999
Role of the angiotensin type 2 receptor gene in congenital anomalies of the kidney and urinary tract, CAKUT, of mice and men
H Nishimura, E Yerkes, K Hohenfellner, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 20, 1999
Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene
R Salvatori, C Y Hayashida, M H Aguiar-Oliveira, et al.
Nature Genetics
|
March 1, 1997
Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32
W C Nichols, D L Koller, B Slovis, et al.
Journal of Bacteriology
|
March 6, 2024
HtrA, fatty acids, and membrane protein interplay in <i>Chlamydia trachomatis</i> to impact stress response and trigger early cellular exit
Natalie Strange, Laurence Luu, Vanissa Ong, et al.
Genetica
|
February 5, 2017
Cystic fibrosis in Afro-Brazilians: XK haplotypes analysis supports the European origin of p.F508del mutation
D A S de Souza, F R Faucz, R B de Alexandre, et al.
Hypertension (Dallas, Tex. : 1979)
|
July 25, 2000
Combinations of variations in multiple genes are associated with hypertension
S M Williams, J H Addy, J A Phillips, et al.
Page
of 20
Search research articles
Search
Showing results (181-190 of 197) with videos related to
Sort By:
Page
of 20
Leukemia
|
January 20, 2009
Molecular recognition of acute myeloid leukemia using aptamers
K Sefah, Z W Tang, D H Shangguan, et al.
Human Genetics
|
January 27, 2000
Germline origins in the human F9 gene: frequent G:C-->A:T mosaicism and increased mutations with advanced maternal age
R P Ketterling, E Vielhaber, X Li, et al.
Human Biology
|
August 1, 1997
Cystic fibrosis in the Brazilian population: DF508 mutation and KM-19/XV-2C haplotype distribution
S Raskin, J A Phillips, M R Krishnamani, et al.
Nature Genetics
|
February 14, 1998
Mutations in PROP1 cause familial combined pituitary hormone deficiency
W Wu, J D Cogan, R W Pfäffle, et al.
Molecular Cell
|
February 20, 1999
Role of the angiotensin type 2 receptor gene in congenital anomalies of the kidney and urinary tract, CAKUT, of mice and men
H Nishimura, E Yerkes, K Hohenfellner, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 20, 1999
Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene
R Salvatori, C Y Hayashida, M H Aguiar-Oliveira, et al.
Nature Genetics
|
March 1, 1997
Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32
W C Nichols, D L Koller, B Slovis, et al.
Journal of Bacteriology
|
March 6, 2024
HtrA, fatty acids, and membrane protein interplay in <i>Chlamydia trachomatis</i> to impact stress response and trigger early cellular exit
Natalie Strange, Laurence Luu, Vanissa Ong, et al.
Genetica
|
February 5, 2017
Cystic fibrosis in Afro-Brazilians: XK haplotypes analysis supports the European origin of p.F508del mutation
D A S de Souza, F R Faucz, R B de Alexandre, et al.
Hypertension (Dallas, Tex. : 1979)
|
July 25, 2000
Combinations of variations in multiple genes are associated with hypertension
S M Williams, J H Addy, J A Phillips, et al.
Page
of 20