Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Human homolog of patched, a candidate gene for the basal cell nevus syndrome.
|
Science
|
1996
|
8.06
|
2
|
Activating Smoothened mutations in sporadic basal-cell carcinoma.
|
Nature
|
1998
|
7.43
|
3
|
Epidermolysis bullosa simplex: evidence in two families for keratin gene abnormalities.
|
Science
|
1991
|
3.93
|
4
|
Basal cell carcinomas in mice overexpressing sonic hedgehog.
|
Science
|
1997
|
3.84
|
5
|
(Alpha1(3))3 human skin collagen. Release by pepsin digestion and preponderance in fetal life.
|
J Biol Chem
|
1974
|
3.83
|
6
|
Identification of three genetically distinct collagens by cyanogen bromide cleavage of insoluble human skin and cartilage collagen.
|
Biochem Biophys Res Commun
|
1971
|
2.63
|
7
|
Ultraviolet and ionizing radiation enhance the growth of BCCs and trichoblastomas in patched heterozygous knockout mice.
|
Nat Med
|
1999
|
2.39
|
8
|
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease.
|
Nat Genet
|
2000
|
2.09
|
9
|
Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome.
|
J Invest Dermatol
|
1998
|
2.00
|
10
|
Isolation and characterization of CNBr peptides of human (alpha 1 (III) )3 collagen and tissue distribution of (alpha 1 (I) )2 alpha 2 and (alpha 1 (III) )3 collagens.
|
J Biol Chem
|
1975
|
1.92
|
11
|
Mycosis fungoides. Survival, prognostic features, response to therapy, and autopsy findings.
|
Medicine (Baltimore)
|
1972
|
1.91
|
12
|
Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors.
|
Cancer Res
|
1997
|
1.83
|
13
|
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis.
|
Nat Genet
|
1998
|
1.82
|
14
|
Activation of expression of hedgehog target genes in basal cell carcinomas.
|
J Invest Dermatol
|
2001
|
1.77
|
15
|
Precursors of collagen secreted by cultured human fibroblasts.
|
Proc Natl Acad Sci U S A
|
1972
|
1.73
|
16
|
Isolation and characterization of the peptides derived from soluble human and baboon skin collagen after cyanogen bromide cleavage.
|
J Biol Chem
|
1971
|
1.72
|
17
|
Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5).
|
Nat Genet
|
1994
|
1.63
|
18
|
Keratin 14 gene mutations in patients with epidermolysis bullosa simplex.
|
J Invest Dermatol
|
1995
|
1.57
|
19
|
Hailey-Hailey disease is not allelic to Darier's disease.
|
J Invest Dermatol
|
1994
|
1.40
|
20
|
Stratum corneum lipids in disorders of cornification. Steroid sulfatase and cholesterol sulfate in normal desquamation and the pathogenesis of recessive X-linked ichthyosis.
|
J Clin Invest
|
1984
|
1.38
|
21
|
Staphylococcal scalded skin syndrome. Clinical features, pathogenesis, and recent microbiological and biochemical developments.
|
Arch Dermatol
|
1977
|
1.37
|
22
|
X-linked ichthyosis: increased blood cholesterol sulfate and electrophoretic mobility of low-density lipoprotein.
|
Science
|
1981
|
1.26
|
23
|
Lamellar body-enriched fractions from neonatal mice: preparative techniques and partial characterization.
|
J Invest Dermatol
|
1985
|
1.19
|
24
|
Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis.
|
Proc Natl Acad Sci U S A
|
1987
|
1.18
|
25
|
Steroid sulfatase of human leukocytes and epidermis and the diagnosis of recessive X-linked ichthyosis.
|
J Clin Invest
|
1981
|
1.16
|
26
|
Biosynthesis of type I and III collagens by cultured smooth muscle cells from human aorta.
|
Proc Natl Acad Sci U S A
|
1977
|
1.14
|
27
|
Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients.
|
Hum Mol Genet
|
1994
|
1.12
|
28
|
Ultraviolet B(UVB)-induced cox-2 expression in murine skin: an immunohistochemical study.
|
Biochem Biophys Res Commun
|
2001
|
1.11
|
29
|
Bart's syndrome. Ultrastructure and genetic linkage.
|
Arch Dermatol
|
1995
|
1.02
|
30
|
Popsicle panniculitis.
|
N Engl J Med
|
1970
|
1.02
|
31
|
Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma.
|
Exp Dermatol
|
2000
|
0.98
|
32
|
The epidermal cholesterol sulfate cycle.
|
J Am Acad Dermatol
|
1984
|
0.95
|
33
|
Clinical staging for cutaneous T-cell lymphoma.
|
Ann Intern Med
|
1984
|
0.95
|
34
|
Evidence against keratin gene mutations in a family with ichthyosis hystrix Curth-Macklin.
|
J Invest Dermatol
|
1993
|
0.93
|
35
|
Steroid sulfatase, X-linked ichthyosis, and stratum corneum cell cohesion.
|
Arch Dermatol
|
1981
|
0.93
|
36
|
Cirrhosis following methotrexate administration for psoriasis.
|
Arch Dermatol
|
1969
|
0.92
|
37
|
Topical carmustine (BCNU) for cutaneous T cell lymphoma: a 15-year experience in 143 patients.
|
J Am Acad Dermatol
|
1990
|
0.92
|
38
|
Adult toxic epidermal necrolysis with fatal staphylococcal septicemia.
|
JAMA
|
1974
|
0.91
|
39
|
Human skin collagen. Presence of type I and type III at all levels of the dermis.
|
J Biol Chem
|
1978
|
0.91
|
40
|
A novel three-nucleotide deletion in the helix 2B region of keratin 14 in epidermolysis bullosa simplex: delta E375.
|
Hum Mol Genet
|
1993
|
0.89
|
41
|
Genetic basis of Bart's syndrome: a glycine substitution mutation in type VII collagen gene.
|
J Invest Dermatol
|
1996
|
0.88
|
42
|
Status report of 376 mycosis fungoides patients at 4 years: Mycosis Fungoides Cooperative Group.
|
Cancer Treat Rep
|
1979
|
0.88
|
43
|
Isolation and identification of the antigenic determinants of human collagen.
|
Isr J Med Sci
|
1971
|
0.87
|
44
|
Recessive X-linked ichthyosis: lack of immunologically detectable steroid sulfatase enzyme protein.
|
Hum Genet
|
1985
|
0.86
|
45
|
Genetic basis of Bart's syndrome: a glycine substitution mutation in the type VII collagen gene.
|
J Invest Dermatol
|
1996
|
0.86
|
46
|
Ultraviolet radiation mutagenesis of hedgehog pathway genes in basal cell carcinomas.
|
J Investig Dermatol Symp Proc
|
1999
|
0.86
|
47
|
Localization of the gene whose mutations underlie Hailey-Hailey disease to chromosome 3q.
|
Hum Mol Genet
|
1994
|
0.84
|
48
|
Glucocorticoid receptors of normal human epidermis.
|
J Invest Dermatol
|
1982
|
0.84
|
49
|
Severe vasculitis during isotretinoin therapy.
|
Arch Dermatol
|
1987
|
0.83
|
50
|
Mutations of keratin 9 in two families with palmoplantar epidermolytic hyperkeratosis.
|
J Invest Dermatol
|
1994
|
0.83
|
51
|
Urinary excretion of 3',5'-AMP in syndromes considered refractory to parathyroid hormone.
|
Metabolism
|
1970
|
0.83
|
52
|
Topical carmustine (BCNU) for mycosis fungoides and related disorders: a 10-year experience.
|
J Am Acad Dermatol
|
1983
|
0.82
|
53
|
Regional assignment of the human keratin 5 (KRT5) gene to chromosome 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridization.
|
Genomics
|
1992
|
0.82
|
54
|
Linkage of the epidermolytic hyperkeratosis phenotype and the region of the type II keratin gene cluster on chromosome 12.
|
J Invest Dermatol
|
1992
|
0.82
|
55
|
Lipids in the pathogenesis of ichthyosis: topical cholesterol sulfate-induced scaling in hairless mice.
|
J Invest Dermatol
|
1984
|
0.82
|
56
|
Low-dose methotrexate for the Sézary syndrome.
|
J Am Acad Dermatol
|
1989
|
0.81
|
57
|
Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site.
|
Cancer Res
|
1992
|
0.81
|
58
|
Dithiothreitol separation of newborn rodent dermis and epidermis.
|
J Invest Dermatol
|
1979
|
0.81
|
59
|
Cholesterol sulfotransferase of newborn mouse epidermis.
|
J Invest Dermatol
|
1984
|
0.80
|
60
|
Chemoprevention of basal cell carcinomas in the ptc1+/- mouse--green and black tea.
|
Skin Pharmacol Appl Skin Physiol
|
2001
|
0.80
|
61
|
Combined total body X-ray irradiation and total skin electron beam radiotherapy with an improved technique for mycosis fungoides.
|
Int J Radiat Oncol Biol Phys
|
1989
|
0.79
|
62
|
Localization of the Darier disease gene to a 2-cM portion of 12q23-24.1.
|
J Invest Dermatol
|
1996
|
0.78
|
63
|
Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis.
|
Exp Dermatol
|
2000
|
0.78
|
64
|
Glucocorticoid receptors of mouse epidermis and dermis.
|
Endocrinology
|
1981
|
0.78
|
65
|
Treatment of mycosis fungoides with topical BCNU.
|
Cancer Treat Rep
|
1979
|
0.77
|
66
|
Biochemical abnormalities in the ichthyoses.
|
Curr Probl Dermatol
|
1987
|
0.76
|
67
|
Biochemical identification of alpha-fodrin and protein 4.1 in human keratinocytes.
|
J Invest Dermatol
|
1991
|
0.76
|
68
|
Topical carmustine therapy for lymphomatoid papulosis.
|
Arch Dermatol
|
1985
|
0.76
|
69
|
Topical chemotherapy of mycosis fungoides.
|
Cutis
|
1979
|
0.75
|
70
|
Keratoacanthoma recurrent after surgical excision.
|
J Dermatol Surg Oncol
|
1978
|
0.75
|
71
|
Failure of steroid sulfatase to desulfate vitamin D3 sulfate.
|
J Invest Dermatol
|
1983
|
0.75
|
72
|
Mycosis fungoides presenting as areas of hypopigmentation: a report of three cases.
|
J Am Acad Dermatol
|
1982
|
0.75
|
73
|
Dermatome shaving in the treatment of xeroderma pigmentosum.
|
Arch Dermatol
|
1972
|
0.75
|
74
|
Partial dominance of a keratin 14 mutation in epidermolysis bullosa simplex--increased severity of disease in a homozygote.
|
J Invest Dermatol
|
1997
|
0.75
|
75
|
Mycosis fungoides: clinical course and cellular abnormalities.
|
J Invest Dermatol
|
1980
|
0.75
|
76
|
Treatment of mycosis fungoides with topical nitrosourea compounds: Further studies.
|
Arch Dermatol
|
1975
|
0.75
|
77
|
A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of Siemens.
|
J Invest Dermatol
|
1999
|
0.75
|
78
|
Mycosis fungoides of the mastoid, middle ear, and CNS. Literature review of mycosis fungoides of the CNS.
|
Arch Dermatol
|
1983
|
0.75
|
79
|
Folliculitis induced by actinomycin D.
|
N Engl J Med
|
1969
|
0.75
|
80
|
Detection of carriers for X-linked ichthyosis by Southern blot analysis and identification of one family with a de novo mutation.
|
J Invest Dermatol
|
1990
|
0.75
|