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Research 991–1000 of 1000+
- The atypical ‘hippocampal’ glutamate receptor coupled to phospholipase D that controls stretch‐sensitivity in primary mechanosensory nerve endings is homomeric purely metabotropic GluK2
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- Polymorphism of Exon V of prolactin gene and its association with Cashmere traits in Changthangi Pashmina goats
- A syndromic extreme insulin resistance caused by biallelic POC1A mutations in exon 10
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Polymorphism in the A2M gene associated with high-quality milk in Murrah buffaloes (Bubalus bubalis)
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review