| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromes.
|
Science
|
1992
|
2.23
|
|
2
|
High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A gene.
|
Nature
|
1995
|
1.91
|
|
3
|
Molecular cloning of an activated human oncogene, homologous to v-raf, from primary stomach cancer.
|
Proc Natl Acad Sci U S A
|
1985
|
1.83
|
|
4
|
DNA repair protein XPA binds replication protein A (RPA).
|
J Biol Chem
|
1995
|
1.63
|
|
5
|
High-frequency genetic reversion mediated by a DNA duplication: the mouse pink-eyed unstable mutation.
|
Proc Natl Acad Sci U S A
|
1993
|
1.61
|
|
6
|
African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism.
|
Nat Genet
|
1994
|
1.50
|
|
7
|
A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice.
|
Proc Natl Acad Sci U S A
|
1998
|
1.46
|
|
8
|
Identification of a melanosomal membrane protein encoded by the pink-eyed dilution (type II oculocutaneous albinism) gene.
|
Proc Natl Acad Sci U S A
|
1994
|
1.35
|
|
9
|
Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse.
|
Proc Natl Acad Sci U S A
|
1992
|
1.30
|
|
10
|
A novel cytoplasmic GTPase XAB1 interacts with DNA repair protein XPA.
|
Nucleic Acids Res
|
2000
|
1.23
|
|
11
|
Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes.
|
Proc Natl Acad Sci U S A
|
2001
|
1.15
|
|
12
|
Enhancement of damage-specific DNA binding of XPA by interaction with the ERCC1 DNA repair protein.
|
Biochem Biophys Res Commun
|
1995
|
1.04
|
|
13
|
Mutations in the XPD gene leading to xeroderma pigmentosum symptoms.
|
Hum Mutat
|
1997
|
0.98
|
|
14
|
The original pink-eyed dilution mutation (p) arose in Asiatic mice: implications for the H4 minor histocompatibility antigen, Myod1 regulation and the origin of inbred strains.
|
Genetics
|
1994
|
0.93
|
|
15
|
The gamma-aminobutyric acid receptor gamma 3 subunit gene (GABRG3) is tightly linked to the alpha 5 subunit gene (GABRA5) on human chromosome 15q11-q13 and is transcribed in the same orientation.
|
Genomics
|
1995
|
0.93
|
|
16
|
Isolation and characterization of cDNA and genomic sequences for mouse O6-methylguanine-DNA methyltransferase.
|
Carcinogenesis
|
1992
|
0.88
|
|
17
|
Mutational analysis of a function of xeroderma pigmentosum group A (XPA) protein in strand-specific DNA repair.
|
Nucleic Acids Res
|
1998
|
0.88
|
|
18
|
The mouse pink-eyed dilution gene: association with hypopigmentation in Prader-Willi and Angelman syndromes and with human OCA2.
|
Pigment Cell Res
|
1994
|
0.87
|
|
19
|
Specific amino acid sequences required for O6-methylguanine-DNA methyltransferase activity: analyses of three residues at or near the methyl acceptor site.
|
Carcinogenesis
|
1992
|
0.87
|
|
20
|
UV-induced skin carcinogenesis in xeroderma pigmentosum group A (XPA) gene-knockout mice with nucleotide excision repair-deficiency.
|
Mutat Res
|
2001
|
0.86
|
|
21
|
Structure of the activated c-raf-1 gene from human stomach cancer.
|
Cold Spring Harb Symp Quant Biol
|
1986
|
0.85
|
|
22
|
Structure of the activated c-raf-1 gene from human stomach cancer.
|
Princess Takamatsu Symp
|
1986
|
0.83
|
|
23
|
Strand specificity and absence of hot spots for p53 mutations in ultraviolet B-induced skin tumors of XPA-deficient mice.
|
Cancer Res
|
1998
|
0.82
|
|
24
|
A novel protein, MAPO1, that functions in apoptosis triggered by O6-methylguanine mispair in DNA.
|
Oncogene
|
2009
|
0.82
|
|
25
|
Action of T4 endonuclease V on polydeoxyribonucleotides with apyrimidinic or apurinic sites.
|
J Biochem
|
1982
|
0.82
|
|
26
|
Assay of repair enzyme activity by reactivation of ultraviolet-irradiated infective viral DNA.
|
J Biochem
|
1980
|
0.81
|
|
27
|
[Activated c-raf-1 gene from human stomach cancer].
|
Gan To Kagaku Ryoho
|
1987
|
0.80
|
|
28
|
Decreased UV sensitivity, mismatch repair activity and abnormal cell cycle checkpoints in skin cancer cell lines derived from UVB-irradiated XPA-deficient mice.
|
Mutat Res
|
2000
|
0.80
|
|
29
|
Long-term forskolin stimulation induces AMPK activation and thereby enhances tight junction formation in human placental trophoblast BeWo cells.
|
Placenta
|
2008
|
0.80
|
|
30
|
Studies of in vivo mutations in rpsL transgene in UVB-irradiated epidermis of XPA-deficient mice.
|
Mutat Res
|
2000
|
0.79
|
|
31
|
Bovine and water buffalo Mx2 genes: polymorphism and antiviral activity.
|
Immunogenetics
|
2006
|
0.78
|
|
32
|
Loss of the xeroderma pigmentosum group A gene (XPA) enhances apoptosis of cultured cerebellar neurons induced by UV but not by low-K+ medium.
|
J Neurochem
|
1997
|
0.78
|
|
33
|
[Diagnostic methods of ectopic pregnancy, information for practioners].
|
Sanfujinka No Jissai
|
1969
|
0.75
|
|
34
|
[Shock due to hemorrhage of the internal female genitalia].
|
Sanfujinka No Jissai
|
1967
|
0.75
|
|
35
|
RPA2, a gene for the 32 kDa subunit of replication protein A on chromosome 1p35-36, is not mutated in patients with familial melanoma linked to chromosome 1p36.
|
Melanoma Res
|
1998
|
0.75
|
|
36
|
[Statistical observations and countermeasures in uterine rupture in legal abortion].
|
Sanfujinka No Jissai
|
1967
|
0.75
|