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Phenotypic and molecular analyses of A/WySn mice

The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association

Aug 28, 2001

S G Gong

Abstract

Since its first description, the A strain of mice have been utilized extensively as models to study the processes involved in clefting of the midfacial region. Of the A substrains, the A/WySn has a spontaneous rate of clefting of the lip of about 20% to 30%. The A/WySn mouse model was u...read more

Mentioned in this Paper

Embryo
Biochemical Pathway
Structure of Papilla Incisiva of Mouth
MSX1
Bone Structure of Face
Maxilla
Retinoic acid receptor alpha
Candidate Disease Gene
MSX1 wt Allele
Skeletal System
Paper Details
References
  • References24
  • Citations13
123
  • References24
  • Citations13
12

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Phenotypic and molecular analyses of A/WySn mice

The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association

Aug 28, 2001

S G Gong

PMID: 11522170

DOI: 10.1597/1545-1569(2001)038<0486:pamaoa>2.0.co;2

Abstract

Since its first description, the A strain of mice have been utilized extensively as models to study the processes involved in clefting of the midfacial region. Of the A substrains, the A/WySn has a spontaneous rate of clefting of the lip of about 20% to 30%. The A/WySn mouse model was u...read more

Mentioned in this Paper

Embryo
Biochemical Pathway
Structure of Papilla Incisiva of Mouth
MSX1
Bone Structure of Face
Maxilla
Retinoic acid receptor alpha
Candidate Disease Gene
MSX1 wt Allele
Skeletal System

Similar Papers Found In These Feeds

Hox Gene Family

The homeobox genes (Hox gene family) encode for homeodomain-containing transcription factors, which are important in the regulation of embryonic development and cell differentiation. They have a conserved DNA binding domain that are found in the family of hox genes. Discover the latest research on hox gene family here.

Birth Defects

Birth defects encompass structural and functional alterations that occur during embryonic or fetal development and are present since birth. The cause may be genetic, environmental or unknown and can result in physical and/or mental impairment. Here is the latest research on birth defects.

Related Papers

Differentiation; Research in Biological Diversity

Bmp4 gene is expressed at the putative site of fusion in the midfacial region

Differentiation; Research in Biological DiversityApril 16, 2003
Siew-Gong Gong, Chiao Guo
Developmental Biology

Shh and Fgf8 act synergistically to drive cartilage outgrowth during cranial development

Developmental BiologyAugust 11, 2004
Arhat Abzhanov, Clifford J Tabin
Paper Details
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  • References24
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123
  • References24
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12
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