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Journal De Genetique Humaine
|
September 1, 1989
[Biochemical and ultrastructural study of two familial cases of Winchester syndrome]
J C Lambert, J Y Jaffray, J C Michalski, et al.
Archives of Dermatological Research
|
January 1, 1986
In vitro study of the cell populations in two cases of Kaposi's sarcoma
J Gioanni, F Ettore, C Mazeau, et al.
Neuroreport
|
April 20, 1999
A new GTP-cyclohydrolase I mutation in an unusual dopa-responsive dystonia, familial form
S Brique, A Destée, J C Lambert, et al.
Clinical Genetics
|
November 22, 2008
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease
L Michel-Calemard, F Dijoud, M Till, et al.
British Journal of Cancer
|
July 1, 1990
Establishment and characterisation of a new tumorigenic cell line with a normal karyotype derived from a human breast adenocarcinoma
J Gioanni, D Le François, E Zanghellini, et al.
Bulletin Du Cancer
|
November 1, 1991
[Characterization of a human cell line from an anaplastic carcinoma of the thyroid gland]
J Gioanni, E Zanghellini, C Mazeau, et al.
Prenatal Diagnosis
|
May 1, 1994
Prenatal diagnosis of severe fetal toxoplasmosis as a result of toxoplasmic reactivation in an HIV-1 seropositive woman
P Marty, A Bongain, A Rahal, et al.
Cancer Research
|
March 1, 1985
Establishment, characterization, chemosensitivity, and radiosensitivity of two different cell lines derived from a human breast cancer biopsy
J Gioanni, A Courdi, C M Lalanne, et al.
Neuroscience Letters
|
June 19, 2001
Are the estrogen receptors involved in Alzheimer's disease?
J C Lambert, J M Harris, D Mann, et al.
Lancet (London, England)
|
September 18, 2001
Effect of the APOE promoter polymorphisms on cerebral amyloid peptide deposition in Alzheimer's disease
J C Lambert, D Mann, L Goumidi, et al.
Page
of 12
Search research articles
Search
Showing results (51-60 of 112) with videos related to
Sort By:
Page
of 12
Journal De Genetique Humaine
|
September 1, 1989
[Biochemical and ultrastructural study of two familial cases of Winchester syndrome]
J C Lambert, J Y Jaffray, J C Michalski, et al.
Archives of Dermatological Research
|
January 1, 1986
In vitro study of the cell populations in two cases of Kaposi's sarcoma
J Gioanni, F Ettore, C Mazeau, et al.
Neuroreport
|
April 20, 1999
A new GTP-cyclohydrolase I mutation in an unusual dopa-responsive dystonia, familial form
S Brique, A Destée, J C Lambert, et al.
Clinical Genetics
|
November 22, 2008
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease
L Michel-Calemard, F Dijoud, M Till, et al.
British Journal of Cancer
|
July 1, 1990
Establishment and characterisation of a new tumorigenic cell line with a normal karyotype derived from a human breast adenocarcinoma
J Gioanni, D Le François, E Zanghellini, et al.
Bulletin Du Cancer
|
November 1, 1991
[Characterization of a human cell line from an anaplastic carcinoma of the thyroid gland]
J Gioanni, E Zanghellini, C Mazeau, et al.
Prenatal Diagnosis
|
May 1, 1994
Prenatal diagnosis of severe fetal toxoplasmosis as a result of toxoplasmic reactivation in an HIV-1 seropositive woman
P Marty, A Bongain, A Rahal, et al.
Cancer Research
|
March 1, 1985
Establishment, characterization, chemosensitivity, and radiosensitivity of two different cell lines derived from a human breast cancer biopsy
J Gioanni, A Courdi, C M Lalanne, et al.
Neuroscience Letters
|
June 19, 2001
Are the estrogen receptors involved in Alzheimer's disease?
J C Lambert, J M Harris, D Mann, et al.
Lancet (London, England)
|
September 18, 2001
Effect of the APOE promoter polymorphisms on cerebral amyloid peptide deposition in Alzheimer's disease
J C Lambert, D Mann, L Goumidi, et al.
Page
of 12