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Oncogene
|
February 3, 2000
UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients
M D'Errico, A Calcagnile, F Canzona, et al.
Lancet (London, England)
|
August 28, 1993
Absence of xid mutation in X-linked agammaglobulinaemia
I Vorechovsky, J N Zhou, L Hammarström, et al.
Human Molecular Genetics
|
April 1, 1995
Identification of Btk mutations in 20 unrelated patients with X-linked agammaglobulinaemia (XLA)
H Jin, A D Webster, M Vihinen, et al.
Leukemia
|
January 30, 2004
Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia
M D Tischkowitz, N V Morgan, D Grimwade, et al.
The Journal of Biological Chemistry
|
May 24, 1996
A mammalian patched homolog is expressed in target tissues of sonic hedgehog and maps to a region associated with developmental abnormalities
H Hahn, J Christiansen, C Wicking, et al.
Human Genetics
|
July 1, 1994
Identification of deletions in the btk gene allows unambiguous assessment of carrier status in families with X-linked agammaglobulinaemia
R C Lovering, A Sweatman, S A Genet, et al.
Breast Cancer Research : BCR
|
April 18, 2001
Low frequency of E-cadherin alterations in familial breast cancer
S Salahshor, L Haixin, H Huo, et al.
Oncogene
|
March 14, 2000
Low frequency of alterations of the alpha (PPP2R1A) and beta (PPP2R1B) isoforms of the subunit A of the serine-threonine phosphatase 2A in human neoplasms
G A Calin, M G di Iasio, E Caprini, et al.
Nature Genetics
|
September 11, 2001
Does 77C-->G in PTPRC modify autoimmune disorders linked to the major histocompatibility locus?
I Vorechovsky, J Kralovicova, E Tchilian, et al.
Nucleic Acids Research
|
January 1, 1997
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
M Vihinen, B H Belohradsky, R N Haire, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Oncogene
|
February 3, 2000
UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients
M D'Errico, A Calcagnile, F Canzona, et al.
Lancet (London, England)
|
August 28, 1993
Absence of xid mutation in X-linked agammaglobulinaemia
I Vorechovsky, J N Zhou, L Hammarström, et al.
Human Molecular Genetics
|
April 1, 1995
Identification of Btk mutations in 20 unrelated patients with X-linked agammaglobulinaemia (XLA)
H Jin, A D Webster, M Vihinen, et al.
Leukemia
|
January 30, 2004
Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia
M D Tischkowitz, N V Morgan, D Grimwade, et al.
The Journal of Biological Chemistry
|
May 24, 1996
A mammalian patched homolog is expressed in target tissues of sonic hedgehog and maps to a region associated with developmental abnormalities
H Hahn, J Christiansen, C Wicking, et al.
Human Genetics
|
July 1, 1994
Identification of deletions in the btk gene allows unambiguous assessment of carrier status in families with X-linked agammaglobulinaemia
R C Lovering, A Sweatman, S A Genet, et al.
Breast Cancer Research : BCR
|
April 18, 2001
Low frequency of E-cadherin alterations in familial breast cancer
S Salahshor, L Haixin, H Huo, et al.
Oncogene
|
March 14, 2000
Low frequency of alterations of the alpha (PPP2R1A) and beta (PPP2R1B) isoforms of the subunit A of the serine-threonine phosphatase 2A in human neoplasms
G A Calin, M G di Iasio, E Caprini, et al.
Nature Genetics
|
September 11, 2001
Does 77C-->G in PTPRC modify autoimmune disorders linked to the major histocompatibility locus?
I Vorechovsky, J Kralovicova, E Tchilian, et al.
Nucleic Acids Research
|
January 1, 1997
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
M Vihinen, B H Belohradsky, R N Haire, et al.
Page
of 4