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Volumn 169, Issue 2, 2001, Pages
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The Booroola (FecB) phenotype is associated with a mutation in the bone morphogenetic receptor type 1 B (BMPR1B) gene
a
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINO ACID;
ARGININE;
BONE MORPHOGENETIC PROTEIN RECEPTOR;
BONE MORPHOGENETIC PROTEIN RECEPTOR TYPE 1B;
BOOROOLA PROTEIN;
COMPLEMENTARY DNA;
CYTOSINE;
DNA;
GENE PRODUCT;
GLUTAMINE;
PROTEIN KINASE;
UNCLASSIFIED DRUG;
AMINO ACID SEQUENCE;
ANIMAL CELL;
ARTICLE;
AUTOSOME;
BRAZIL;
BREEDING;
CHROMOSOMAL LOCALIZATION;
CHROMOSOME 6;
CONTROLLED STUDY;
FEMALE;
GENE MAPPING;
GENE MUTATION;
GENETIC ASSOCIATION;
GENETIC CODE;
GENETIC LINKAGE;
GENETIC SCREENING;
GENETIC VARIABILITY;
GENOTYPE;
HETEROZYGOTE;
HOMOZYGOTE;
MOLECULAR CLONING;
NONHUMAN;
NUCLEOTIDE SEQUENCE;
OVARY;
OVARY FOLLICLE;
OVULATION;
PHENOTYPE;
POINT MUTATION;
PRECOCIOUS PUBERTY;
PRIORITY JOURNAL;
PROTEIN DOMAIN;
PROTEIN PHOSPHORYLATION;
SHEEP;
SYNTENY;
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EID: 0035024936
PISSN: 00220795
EISSN: None
Source Type: Journal
DOI: 10.1677/joe.0.169R001 Document Type: Article |
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Times cited : (362)
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References (32)
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