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1p36
A chromosome band present on 1p
National Institutes of Health
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Related topics
Related topics
15 relations
CD52 wt Allele
CDK11B wt Allele
CLCN6 wt Allele
Chromosome 1 Short Arm
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Obstetric Care in the U.S. Military: Comparison of Direct and Purchased Care System Within TRICARE [11R]
A. Ranjit
,
Wei Jiang
,
A. Haider
,
C. Witkop
,
S. Little
,
J. Robinson
2016
Corpus ID: 75335953
INTRODUCTION: Pregnant women with TRICARE (universal insurance coverage to members of US Armed Services and their dependents) can…
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2011
2011
Hemangioendothelioma Identification of a Disease-Defining Gene Fusion in Epithelioid
M. Tanas
,
A. Sboner
,
+21 authors
B. Rubin
2011
Corpus ID: 34260231
control. researchers about the biology and prognosis of this rare cancer and eventually help bring the bad behavior under…
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2008
2008
KIF 1 B Functions as a Haploinsufficient Tumor Suppressor Gene Mapped to Chromosome 1 p 36 . 2 by Inducing Apoptotic Cell Death *
A. K. Munirajan
,
Kiyohiro Ando
,
+7 authors
A. Nakagawara
2008
Corpus ID: 36545749
Arasambattu K. Munirajan, Kiyohiro Ando, Akira Mukai, Masato Takahashi, Yusuke Suenaga, Miki Ohira, Tadayuki Koda, Toru Hirota…
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Review
2008
Review
2008
Clinical Report Prenatal Diagnosis of Monosomy 1p36: A Focus on Brain Abnormalities and a Review of the Literature
Philippe M. Campeau
,
N. Mew
,
+4 authors
M. A. Thomas
2008
Corpus ID: 80248161
Monosomy1p36 is anincreasingly recognizedchromosomalanomaly. We describe two patients with monosomy 1p36who had brain…
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2004
2004
Redundant skin over the nape in a girl with monosomy 1p36 caused by a de-novo satellited derivative chromosome: a possible new feature?
B.-T. Wang
,
M. Chen
Clinical Dysmorphology
2004
Corpus ID: 22415982
We present a case of monosomy 1p36 who, in addition to delayed growth and development, and mild facial dysmorphism also had…
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Review
2002
Review
2002
The two faces of p73
Tobias J. Grob
,
Martin F. Fey
,
Andreas Tobler
Cell Death and Differentiation
2002
Corpus ID: 19505934
In the present issue of Cell Death and Differentiation, Casciano et al., report that in neuroblastoma patients expression of the…
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2002
2002
Hornhautdystrophien im Licht moderner molekulargenetischer Forschung
C. Auw-Hädrich
,
H. Witschel
Der Ophthalmologe
2002
Corpus ID: 28262938
ZusammenfassungDie Ergebnisse molekulargenetischer Forschung erlauben neue Einsichten in Ursache und Pathogenese der erblichen…
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1999
1999
Risk factors for the development of malignant melanoma
Itin Ph
1999
Corpus ID: 68082627
Risikofaktoren fur die Entwicklung maligner Melanome sind vielfaltig. Sie werden sowohl durch genetische Faktoren als auch durch…
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1998
1998
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
Jin-Ren Ping
,
Y. Nakatsu
,
A. Goldstein
,
M. Tucker
,
K. Kraemer
,
K. Tanaka
Melanoma research
1998
Corpus ID: 22956884
Although some cases of dysplastic naevi (DN) and familial melanoma have been linked to anonymous markers on chromosome 1p36, the…
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1977
1977
The relationship between sister chromatid exchanges and chromosome aberrations in Bloom's syndrome.
Y. Shiraishi
,
A. Sandberg
Cytogenetics and Cell Genetics
1977
Corpus ID: 3268200
The distribution of the break points of sister chromatid exchanges (SCE) was compared with that of chromosome aberrations in…
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