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The specific expression during male germ cell development and its characteristic localization suggest that it may play an important role in male meiosis.. De plus, nous expédions et beaucoup plus de produits pour cette protéine.
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RSPH1 mutations in primary ciliary dyskinesia cause structural defects in the cilia.
Milder disease in patients with biallelic mutations in RSPH1 provides evidence of a unique genotype-phenotype relationship in primary ciliary dyskinesia, suggesting that mutations in RSPH1 may be associated with residual ciliary function.
RSPH1 mutations thus appear as a major etiology for primary ciliary dyskinesia phenotype.
Tsga2 fulfills many of the prerequisites required to make it a strong candidate for Ccub1, an element of Cucb positioned within a genomic interval spanning approximately 0.6 Mb immediately distal to Dnahc8.
Tsga2 is most abundantly expressed in tissues rich in highly ciliated cells, such as olfactory sensory neurons, and is predicted to be important to cilia.
The specific expression during male germ cell development and its characteristic localization suggest that it may play an important role in male meiosis.
radial spoke head 1 homolog (Chlamydomonas)
, testes specific A2 homolog
, testis specific A2 homolog
, cancer/testis antigen 79
, male meiotic metaphase chromosome-associated acidic protein
, radial spoke head 1 homolog
, testes specific gene A2 homolog
, testis-specific gene A2 protein
, testis-specific gene A2
, TSGA2 epididymal isoform
, testis specific gene A2