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1
Nell-1-Induced Bone Regeneration in Calvarial Defects
Nell-1-Induced Bone Regeneration in Calvarial Defects
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Nell-1-Induced Bone Regeneration in Calvarial Defects

Aghaloo, Tara ; Cowan, Catherine M. ; Chou, Yu-Fen ; Zhang, Xinli ; Lee, Haofu ; Miao, Steve ; Hong, Nichole ; Kuroda, Shun'ichi ; Wu, Benjamin ; Ting, Kang ; Soo, Chia

The American journal of pathology, 2006-09, Vol.169 (3), p.903-915 [Revista revisada por pares]

Bethesda, MD: Elsevier Inc

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2
Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability : A murine model of Waardenburg syndrome variation
Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability : A murine model of Waardenburg syndrome variation
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Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability : A murine model of Waardenburg syndrome variation

ASHER, J. H ; HARRISON, R. W ; MORELL, R ; CAREY, M. L ; FRIEDMAN, T. B

Genomics (San Diego, Calif.), 1996-06, Vol.34 (3), p.285-298 [Revista revisada por pares]

San Diego, CA: Elsevier

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3
Discovery and characterization of an antibody directed against exosite I of thrombin
Discovery and characterization of an antibody directed against exosite I of thrombin
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Discovery and characterization of an antibody directed against exosite I of thrombin

Baglin, T. P. ; Langdown, J. ; Frasson, R. ; Huntington, J. A.

Journal of thrombosis and haemostasis, 2016-01, Vol.14 (1), p.137-142 [Revista revisada por pares]

England: Wiley Subscription Services, Inc

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4
Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice
Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice
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Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice

Balemans, Monique C.M. ; Ansar, Muhammad ; Oudakker, Astrid R. ; van Caam, Arjan P.M. ; Bakker, Brenda ; Vitters, Elly L. ; van der Kraan, Peter M. ; de Bruijn, Diederik R.H. ; Janssen, Sanne M. ; Kuipers, Arthur J. ; Huibers, Manon M.H. ; Maliepaard, Eliza M. ; Walboomers, X. Frank ; Benevento, Marco ; Nadif Kasri, Nael ; Kleefstra, Tjitske ; Zhou, Huiqing ; Van der Zee, Catharina E.E.M. ; van Bokhoven, Hans

Developmental biology, 2014-02, Vol.386 (2), p.395-407 [Revista revisada por pares]

United States: Elsevier Inc

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5
Craniofacial abnormalities induced by ectopic expression of the homeobox gene Hox-1.1 in transgenic mice
Craniofacial abnormalities induced by ectopic expression of the homeobox gene Hox-1.1 in transgenic mice
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Craniofacial abnormalities induced by ectopic expression of the homeobox gene Hox-1.1 in transgenic mice

Balling, Rudi ; Mutter, George ; Gruss, Peter ; Kessel, Michael

Cell, 1989-07, Vol.58 (2), p.337-347 [Revista revisada por pares]

Cambridge, MA: Elsevier Inc

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6
A Twist Code Determines the Onset of Osteoblast Differentiation
A Twist Code Determines the Onset of Osteoblast Differentiation
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A Twist Code Determines the Onset of Osteoblast Differentiation

Bialek, Peter ; Kern, Britt ; Yang, Xiangli ; Schrock, Marijke ; Sosic, Drazen ; Hong, Nancy ; Wu, Hua ; Yu, Kai ; Ornitz, David M ; Olson, Eric N ; Justice, Monica J ; Karsenty, Gerard

Developmental cell, 2004-03, Vol.6 (3), p.423-435 [Revista revisada por pares]

United States: Elsevier Inc

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7
A Silicon Requirement for Normal Skull Formation in Chicks
A Silicon Requirement for Normal Skull Formation in Chicks
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A Silicon Requirement for Normal Skull Formation in Chicks

Carlisle, Edith M.

The Journal of nutrition, 1980-02, Vol.110 (2), p.352-359 [Revista revisada por pares]

United States: Elsevier Inc

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8
Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II
Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II
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Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II

Chen, Chih-Ping ; Chang, Tung-Yao ; Lin, Ming-Huei ; Chern, Schu-Rern ; Su, Jun-Wei ; Wang, Wayseen

Taiwanese journal of obstetrics & gynecology, 2013-09, Vol.52 (3), p.420-425 [Revista revisada por pares]

Elsevier B.V

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9
Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 7p (7p15.3→pter) and Partial Monosomy 13q (13q33.3→qter) Associated With Dandy-Walker Malformation, Abnormal Skull Development and Microcephaly
Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 7p (7p15.3→pter) and Partial Monosomy 13q (13q33.3→qter) Associated With Dandy-Walker Malformation, Abnormal Skull Development and Microcephaly
Material Type:
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Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 7p (7p15.3→pter) and Partial Monosomy 13q (13q33.3→qter) Associated With Dandy-Walker Malformation, Abnormal Skull Development and Microcephaly

Chen, Chih-Ping ; Chen, Ming ; Su, Yi-Ning ; Tsai, Fuu-Jen ; Chern, Schu-Rern ; Hsu, Chin-Yuan ; Wu, Pei-Chen ; Town, Dai-Dyi ; Lee, Dong-Jay ; Ma, Gwo-Chin ; Wang, Wayseen

Taiwanese journal of obstetrics & gynecology, 2010-09, Vol.49 (3), p.320-326 [Revista revisada por pares]

Elsevier B.V

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10
Craniofacial fibrous dysplasia: A 10-case series
Craniofacial fibrous dysplasia: A 10-case series
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Craniofacial fibrous dysplasia: A 10-case series

Couturier, A ; Aumaître, O ; Gilain, L ; Jean, B ; Mom, T ; André, M

European annals of otorhinolaryngology, head and neck diseases, 2017-09, Vol.134 (4), p.229-235 [Revista revisada por pares]

France: Elsevier Masson SAS

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